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<!DOCTYPE ArticleSet PUBLIC "-//NLM//DTD PubMed 2.7//EN" "https://dtd.nlm.nih.gov/ncbi/pubmed/in/PubMed.dtd">
<ArticleSet>
<Article>
<Journal>
				<PublisherName>University of Tehran Press</PublisherName>
				<JournalTitle>Progress in Biological Sciences</JournalTitle>
				<Issn>1016-1058</Issn>
				<Volume>3</Volume>
				<Issue>1</Issue>
				<PubDate PubStatus="epublish">
					<Year>2013</Year>
					<Month>03</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Perspectives in taxonomy and phylogeny of the genus Astragalus
(Fabaceae): a review</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>1</FirstPage>
			<LastPage>6</LastPage>
			<ELocationID EIdType="pii">32086</ELocationID>
			
<ELocationID EIdType="doi">10.22059/pbs.2013.32086</ELocationID>
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Shahin</FirstName>
					<LastName>Zarre</LastName>
<Affiliation>Center of Excellence in Phylogeny of Living Organisms and Department of Plant Science, School of Biology, College of
Science, University of Tehran, Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Nasim</FirstName>
					<LastName>Azani</LastName>
<Affiliation>Center of Excellence in Phylogeny of Living Organisms and Department of Plant Science, School of Biology, College of
Science, University of Tehran, Tehran, Iran</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2012</Year>
					<Month>11</Month>
					<Day>10</Day>
				</PubDate>
			</History>
		<Abstract>The genus &lt;em&gt;&lt;span style=&quot;font-family: Times New Roman; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: Times New Roman; font-size: small;&quot;&gt;Astragalus &lt;/span&gt;&lt;/span&gt;&lt;/em&gt;&lt;span style=&quot;font-family: Times New Roman; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: Times New Roman; font-size: small;&quot;&gt;L. (Fabaceae) is reviewed from both phyloenetic and taxonomic&lt;/span&gt;&lt;/span&gt;
points of view. As the largest genus of flowering plants it has attracted many researchers,
but much work remains to be done. A short taxonomic history with special focus on
infrageneric classification of the genus, a list of phylogenetic studies including the applied
markers and sampling strategies as well as a short discussion on evolution of
morphological characters are presented.</Abstract>
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			<Param Name="value">Astragalus</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Fabaceae</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Taxonomy</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">phylogeny</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://pbiosci.ut.ac.ir/article_32086_ae39c323e05d6bbc7f22523a550e5374.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>University of Tehran Press</PublisherName>
				<JournalTitle>Progress in Biological Sciences</JournalTitle>
				<Issn>1016-1058</Issn>
				<Volume>3</Volume>
				<Issue>1</Issue>
				<PubDate PubStatus="epublish">
					<Year>2013</Year>
					<Month>03</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>New data on spider fauna from Golestan province, Iran (Arachnida, Araneae)</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>7</FirstPage>
			<LastPage>22</LastPage>
			<ELocationID EIdType="pii">32087</ELocationID>
			
<ELocationID EIdType="doi">10.22059/pbs.2013.32087</ELocationID>
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Roya</FirstName>
					<LastName>Kashefi</LastName>
<Affiliation>Department of Biology, Faculty of Sciences, Ferdowsi University of Mashhad, Mashhad, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Fereshteh</FirstName>
					<LastName>Ghassemzadeh</LastName>
<Affiliation>Department of Biology, Faculty of Sciences, Ferdowsi University of Mashhad, Mashhad, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Haji Gholi</FirstName>
					<LastName>Kami</LastName>
<Affiliation>Department of Biology, Faculty of Sciences, Golestan University, Gorgan, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Omid</FirstName>
					<LastName>Mirshamsi</LastName>
<Affiliation>Department of Biology, Faculty of Sciences, Ferdowsi University of Mashhad, Mashhad, Iran</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2012</Year>
					<Month>10</Month>
					<Day>08</Day>
				</PubDate>
			</History>
		<Abstract>Spiders are poorly studied in Iran, based on the latest studies the spider fauna of Iran includes 394 species in 126 genera belonging to 36 families. Considering the climatic and geographical variation of Iran, it can be assumed that Iran has a rich spider fauna compared to the adjacent countries. The present study seeks to take a new step in the ongoing active research of Iranian spider fauna. Therefore, the spider fauna of Golestan Province were studied here. The main purpose of this study is to present new data on twenty-five new faunistic records for Golestan Province. According to previous studies 90 spider species were known in Golestan. This study was conducted during a period of two years. Samplings were performed using hand collecting and pitfall traps. As a result, twenty five species were identified as new records for Golestan Province, ten of which are new records for Iran including &lt;em&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;Araneus marmoreus &lt;/span&gt;&lt;/span&gt;&lt;/em&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;Clerck, 1757, &lt;/span&gt;&lt;/span&gt;&lt;em&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;Cyclosa sierra &lt;/span&gt;&lt;/span&gt;&lt;/em&gt;Simon, 1870, &lt;em&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;Gibbaranea &lt;/span&gt;&lt;/span&gt;&lt;/em&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;sp., &lt;/span&gt;&lt;/span&gt;&lt;em&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;Singa semiatra &lt;/span&gt;&lt;/span&gt;&lt;/em&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;L. Koch, 1867, &lt;/span&gt;&lt;/span&gt;&lt;em&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;Castianeira arnoldii &lt;/span&gt;&lt;/span&gt;&lt;/em&gt;Charitonov, 1946, &lt;em&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;Drassyllus praeficus &lt;/span&gt;&lt;/span&gt;&lt;/em&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;(L. Koch, 1866), &lt;/span&gt;&lt;/span&gt;&lt;em&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;Drassodex &lt;/span&gt;&lt;/span&gt;&lt;/em&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;sp., &lt;/span&gt;&lt;/span&gt;&lt;em&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;Alopecosa &lt;/span&gt;&lt;/span&gt;&lt;/em&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;cf. &lt;/span&gt;&lt;/span&gt;albofasciata &lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;(Brullé, 1832), &lt;/span&gt;&lt;/span&gt;&lt;em&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;Metellina &lt;/span&gt;&lt;/span&gt;&lt;/em&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;cf. &lt;/span&gt;&lt;/span&gt;&lt;em&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;mengei &lt;/span&gt;&lt;/span&gt;&lt;/em&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;(Blackwall, 1870), and &lt;/span&gt;&lt;/span&gt;&lt;em&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;Parasteatoda &lt;/span&gt;&lt;/span&gt;&lt;/em&gt;lunata &lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;(Clerck, 1757). Furthermore, the family Corinnidae and the genus &lt;/span&gt;&lt;/span&gt;&lt;em&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;Castianeira, &lt;/span&gt;&lt;/span&gt;&lt;/em&gt;were recorded for the first time from Iran.</Abstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">Araneae</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Spider</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">New record</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Fauna</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Iran</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">golestan</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://pbiosci.ut.ac.ir/article_32087_ce14a21841578c3da84c006eefc895f3.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>University of Tehran Press</PublisherName>
				<JournalTitle>Progress in Biological Sciences</JournalTitle>
				<Issn>1016-1058</Issn>
				<Volume>3</Volume>
				<Issue>1</Issue>
				<PubDate PubStatus="epublish">
					<Year>2013</Year>
					<Month>03</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Effect of single additive bivalent metal ions on the growth of
Streptomyces clavuligerus and clavulanic acid production</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>23</FirstPage>
			<LastPage>30</LastPage>
			<ELocationID EIdType="pii">32088</ELocationID>
			
<ELocationID EIdType="doi">10.22059/pbs.2013.32088</ELocationID>
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Javad</FirstName>
					<LastName>Hamedi</LastName>
<Affiliation>Microbial Biotechnology Lab., Dept. of Microbiology, School of Biology, College of Science</Affiliation>

</Author>
<Author>
					<FirstName>Sara</FirstName>
					<LastName>Goomeshi Nobary</LastName>
<Affiliation>University of Tehran Microorganisms Collection (UTMC), Microbial Technology and Product Research Center
University of Tehran, Tehran, Iran</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2012</Year>
					<Month>10</Month>
					<Day>14</Day>
				</PubDate>
			</History>
		<Abstract>Metal ions are the main impurities of water and media ingredients used in fermentation processes. In this research, the effect of Ca&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: xx-small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: xx-small;&quot;&gt;+2&lt;/span&gt;&lt;/span&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;, Co&lt;/span&gt;&lt;/span&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: xx-small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: xx-small;&quot;&gt;+2&lt;/span&gt;&lt;/span&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;, Cu&lt;/span&gt;&lt;/span&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: xx-small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: xx-small;&quot;&gt;+2&lt;/span&gt;&lt;/span&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;, Fe&lt;/span&gt;&lt;/span&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: xx-small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: xx-small;&quot;&gt;+2&lt;/span&gt;&lt;/span&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;, Mg&lt;/span&gt;&lt;/span&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: xx-small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: xx-small;&quot;&gt;+2&lt;/span&gt;&lt;/span&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;, Mn&lt;/span&gt;&lt;/span&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: xx-small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: xx-small;&quot;&gt;+2 &lt;/span&gt;&lt;/span&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;and Zn&lt;/span&gt;&lt;/span&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: xx-small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: xx-small;&quot;&gt;+2 &lt;/span&gt;&lt;/span&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;as &lt;/span&gt;&lt;/span&gt;chloride and sulfate salts was studied on the clavulanic acid production and &lt;em&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;Streptomyces &lt;/span&gt;&lt;/span&gt;&lt;/em&gt;clavuligerus &lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;growth. All chloride salts had negative effect on clavulanic acid production &lt;/span&gt;&lt;/span&gt;and no clavulanic acid was produced in the media containing more than 1.5 mM ZnCl&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: xx-small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: xx-small;&quot;&gt;2 &lt;/span&gt;&lt;/span&gt;and 18 mM FeCl&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: xx-small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: xx-small;&quot;&gt;2&lt;/span&gt;&lt;/span&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;. CuCl&lt;/span&gt;&lt;/span&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: xx-small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: xx-small;&quot;&gt;2 &lt;/span&gt;&lt;/span&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;and CaCl&lt;/span&gt;&lt;/span&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: xx-small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: xx-small;&quot;&gt;2 &lt;/span&gt;&lt;/span&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;increased biomass production, while the other &lt;/span&gt;&lt;/span&gt;chloride salts decreased it. Concentration of clavulanic acid in the 0.2 mM MnSO&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: xx-small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: xx-small;&quot;&gt;4 &lt;/span&gt;&lt;/span&gt;containing medium was 1.21 times more than that of control. There was no significant difference in antibiotic concentration in the medium containing 0.41 mM MgSO&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: xx-small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: xx-small;&quot;&gt;4 &lt;/span&gt;&lt;/span&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;and &lt;/span&gt;&lt;/span&gt;control. Other sulfate salts decreased antibiotic production. MgSO&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: xx-small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: xx-small;&quot;&gt;4&lt;/span&gt;&lt;/span&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;, CuSO&lt;/span&gt;&lt;/span&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: xx-small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: xx-small;&quot;&gt;4 &lt;/span&gt;&lt;/span&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;and FeSO&lt;/span&gt;&lt;/span&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: xx-small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: xx-small;&quot;&gt;4 &lt;/span&gt;&lt;/span&gt;increased the biomass, while other sulfate salts decreased it. Minimum and maximum specific consumption rate of glycerol were seen in the medium containing CuSO&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: xx-small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: xx-small;&quot;&gt;4&lt;/span&gt;&lt;/span&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;, and &lt;/span&gt;&lt;/span&gt;MnSO&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: xx-small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: xx-small;&quot;&gt;4&lt;/span&gt;&lt;/span&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;, respectively.&lt;/span&gt;&lt;/span&gt;</Abstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">β-lactamase inhibitor</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Clavulanic acid</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Metal ions</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Streptomyces
clavuligerus</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Fermentation water quality</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://pbiosci.ut.ac.ir/article_32088_40a709da2815a8345a94a4c2bc512c9b.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>University of Tehran Press</PublisherName>
				<JournalTitle>Progress in Biological Sciences</JournalTitle>
				<Issn>1016-1058</Issn>
				<Volume>3</Volume>
				<Issue>1</Issue>
				<PubDate PubStatus="epublish">
					<Year>2013</Year>
					<Month>03</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Improvement of some physiological responses of alfalfa
(Medicago sativa L.) under in vitro salt stress using Triadimefon</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>31</FirstPage>
			<LastPage>40</LastPage>
			<ELocationID EIdType="pii">32089</ELocationID>
			
<ELocationID EIdType="doi">10.22059/pbs.2013.32089</ELocationID>
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Leila</FirstName>
					<LastName>Arab</LastName>
<Affiliation>Department of Biology, Faculty of Science, University of Isfahan, Isfahan, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Ali Akbar</FirstName>
					<LastName>Ehsanpour</LastName>
<Affiliation>Department of Biology, Faculty of Science, University of Isfahan, Isfahan, Iran</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2012</Year>
					<Month>10</Month>
					<Day>20</Day>
				</PubDate>
			</History>
		<Abstract>This study was carried out to investigation the possibility of using Triadimefon (TRD) in order to decrease the adverse effects of salt stress on &lt;em&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;Medicago &lt;/span&gt;&lt;/span&gt;&lt;/em&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;plant. Triadimefon is a &lt;/span&gt;&lt;/span&gt;member of Triazol compounds which enhances stress tolerance through physiological processes. Two cultivars of &lt;em&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;Medicago sitiva &lt;/span&gt;&lt;/span&gt;&lt;/em&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;including Hamedani and Yazdi were used in &lt;/span&gt;&lt;/span&gt;this study. Plants were treated with 1, 2 and 4 mg/l TRD and 0, 100 and 140 mM NaCl. Salinity reduced fresh and dry weight of plants in both cultivars with the result of higher reduction in cv. Hamedani significantly. Salt stress also increased proline, MDA and H&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: xx-small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: xx-small;&quot;&gt;2&lt;/span&gt;&lt;/span&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;O&lt;/span&gt;&lt;/span&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: xx-small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: xx-small;&quot;&gt;2 &lt;/span&gt;&lt;/span&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;contents and also the activity of SOD and P5CS, and the level of P5CS ranscripts, &lt;/span&gt;&lt;/span&gt;while decreased the activity of CAT and POX in both cultivars. When plants were treated with TRD and NaCl, less proline, MDA and H&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: xx-small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: xx-small;&quot;&gt;2&lt;/span&gt;&lt;/span&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;O&lt;/span&gt;&lt;/span&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: xx-small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: xx-small;&quot;&gt;2 &lt;/span&gt;&lt;/span&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;accumulation occurred. Interaction of &lt;/span&gt;&lt;/span&gt;NaCl and TRD increased SOD but reduced P5CS and CAT activity. Both NaCl and TRD treatments increased P5CS transcription in cultivar Yazdi while showed less effect in Hamadani cultivar. Interaction of TRD and NaCl alleviated the negative effects of salt stress on plant growth, especially at 2 mg/l TRD. The results of the present study showed that 2 mg/l TRD was the most effective level to alleviate the negative effects of NaCl treatment on &lt;em&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;Medicago sativa &lt;/span&gt;&lt;/span&gt;&lt;/em&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;plants.&lt;/span&gt;&lt;/span&gt;</Abstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">antioxidant enzyme</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Medicago</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">salt stress</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Triadimefon</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://pbiosci.ut.ac.ir/article_32089_7514ff61e68925663b9ab8e3700126ec.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>University of Tehran Press</PublisherName>
				<JournalTitle>Progress in Biological Sciences</JournalTitle>
				<Issn>1016-1058</Issn>
				<Volume>3</Volume>
				<Issue>1</Issue>
				<PubDate PubStatus="epublish">
					<Year>2013</Year>
					<Month>03</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Normalization of qPCR array data: a novel method based on procrustes superimposition</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>41</FirstPage>
			<LastPage>46</LastPage>
			<ELocationID EIdType="pii">32090</ELocationID>
			
<ELocationID EIdType="doi">10.22059/pbs.2013.32090</ELocationID>
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Ali</FirstName>
					<LastName>Mohammadian</LastName>
<Affiliation>Department of Biotechnology, College of Science, University of Tehran, Tehran, Iran.</Affiliation>

</Author>
<Author>
					<FirstName>Mohammad Reza</FirstName>
					<LastName>Nourani</LastName>
<Affiliation>Chemical Injury Research Center, Baqiatallah Medical Sciences University, Tehran, Iran.</Affiliation>

</Author>
<Author>
					<FirstName>Seyed Javad</FirstName>
					<LastName>Mowla</LastName>
<Affiliation>Molecular Genetics Department, Faculty of Biological Sciences, Tarbiat Modares University, Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Mahmood</FirstName>
					<LastName>Tavallaei</LastName>
<Affiliation>Human Genetic Research Center, Baqiatallah Medical Sciences University, Tehran, Iran.</Affiliation>

</Author>
<Author>
					<FirstName>Yu</FirstName>
					<LastName>Liang</LastName>
<Affiliation>Division of Molecular Medicine, Life Technologies, Foster City, CA 94404, USA.</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2012</Year>
					<Month>10</Month>
					<Day>30</Day>
				</PubDate>
			</History>
		<Abstract>MicroRNAs (miRNAs) are short, endogenous non-coding RNAs that function as guide molecules to regulate transcription of their target messenger RNAs. Several methods including low-density qPCR arrays are being increasingly used to profile the expression of these molecules in a variety of different biological conditions. Reliable analysis of expression profiles demands removal of technical variations in data, which is achieved via applying normalization techniques. Most normalization techniques have been developed for mRNA microarrays and new and modified methods should be used or miRNA studies in general and RT-qPCR miRNA arrays in particular, because of low number of miRNAs. Here, we introduce a new method based on Procrustes superimposition of arrays to be normalized on a reference array. To assess the performance of our normalization method, we compared this method to the common miRNA normalization methods. Removal of technical variation was assessed by robust modeling of mean square error (MSE) in different subsets of real miRNA datasets before and after applying normalization. We show that our method outperforms the other normalization methods in concurrent reduction of technical variation and retention of biological variability.</Abstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">miRNA</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Low-density qPCR array</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Normalization</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Procrustes superimposition</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://pbiosci.ut.ac.ir/article_32090_7709c257be05f7218bdb9319c0031b2e.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>University of Tehran Press</PublisherName>
				<JournalTitle>Progress in Biological Sciences</JournalTitle>
				<Issn>1016-1058</Issn>
				<Volume>3</Volume>
				<Issue>1</Issue>
				<PubDate PubStatus="epublish">
					<Year>2013</Year>
					<Month>03</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Study of promoter CpG island hypermethylation of cyclindependent
kinase inhibitor gene p21waf1/cip1 on some breast
carcinoma cell lines</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>47</FirstPage>
			<LastPage>52</LastPage>
			<ELocationID EIdType="pii">32091</ELocationID>
			
<ELocationID EIdType="doi">10.22059/pbs.2013.32091</ELocationID>
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Mohsen</FirstName>
					<LastName>Alipour</LastName>
<Affiliation>Department of Cell &amp; Molecular Biology, School of Biology, College of Science, University of Tehran, Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Seyed Jalal</FirstName>
					<LastName>Zargar</LastName>
<Affiliation>Department of Cell &amp; Molecular Biology, School of Biology, College of Science, University of Tehran, Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Shahrokh</FirstName>
					<LastName>Safarian</LastName>
<Affiliation>Department of Cell &amp; Molecular Biology, School of Biology, College of Science, University of Tehran, Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Shamileh</FirstName>
					<LastName>Fouladdel</LastName>
<Affiliation>Department of Pharmacology and Toxicology, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Ebrahim</FirstName>
					<LastName>Azizi</LastName>
<Affiliation>Department of Pharmacology and Toxicology, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran.
Biotechnology Research Center, Tehran University of Medical Sciences, Tehran, Iran.</Affiliation>

</Author>
<Author>
					<FirstName>Naser</FirstName>
					<LastName>Jafargholizadeh</LastName>
<Affiliation>Department of Cell &amp; Molecular Biology, School of Biology, College of Science, University of Tehran, Tehran, Iran</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2012</Year>
					<Month>11</Month>
					<Day>05</Day>
				</PubDate>
			</History>
		<Abstract>The &lt;em&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;p21 &lt;/span&gt;&lt;/span&gt;&lt;/em&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;belongs to the CIP/KIP family of CDK inhibitors involved in cell cycle arrest at &lt;/span&gt;&lt;/span&gt;specific stages of the cell cycle progression. DNA methylation is the best studied epigenetic mark that have been evidently associated to chromatin condensation, and repression of gene transcription. The CpG island hypermethylation in promoter region of certain genes occurs in cancer cells and affects tumorigenesis. The aim of the current study was to assess DNA methylation pattern of &lt;em&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;p21 &lt;/span&gt;&lt;/span&gt;&lt;/em&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;gene promoter region in the MCF7, T47D, &lt;/span&gt;&lt;/span&gt;MDA-MB-231 and MDA-MB-468 human breast carcinoma cell lines. The methylation status of cancer associated gene, &lt;em&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;p21&lt;/span&gt;&lt;/span&gt;&lt;/em&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: xx-small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: xx-small;&quot;&gt;waf1/cip1 &lt;/span&gt;&lt;/span&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;was analyzed at CpG sites in the promoter &lt;/span&gt;&lt;/span&gt;region using a sensitive methylation-specific PCR (MSP) technique. The total genomic DNA from each cell line was isolated and subjected to the sodium bisulfite treatment to differentiate between methylated and unmethylated CpG islands. Then MSP was performed using designed primers for methylated (M-MSP) and unmethylated (U-MSP) forms of CpG islands in the promoter region of &lt;em&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;p21 &lt;/span&gt;&lt;/span&gt;&lt;/em&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;gene. The results of the MSP indicated &lt;/span&gt;&lt;/span&gt;that promoter of &lt;em&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;p21 &lt;/span&gt;&lt;/span&gt;&lt;/em&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;gene was consistently unmethylated in tested human breast cancer &lt;/span&gt;&lt;/span&gt;cell lines. Therefore, methylation inactivation of the &lt;em&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;p21&lt;/span&gt;&lt;/span&gt;&lt;/em&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: xx-small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: xx-small;&quot;&gt;waf1/cip1 &lt;/span&gt;&lt;/span&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;does not commonly &lt;/span&gt;&lt;/span&gt;happen in all cancer cell lines.</Abstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">p21waf1/cip1</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Tumor suppressor gene</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">DNA methylation</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">MSP</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Breast Cancer</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://pbiosci.ut.ac.ir/article_32091_d009755fd137e64a069b35d88002b00c.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>University of Tehran Press</PublisherName>
				<JournalTitle>Progress in Biological Sciences</JournalTitle>
				<Issn>1016-1058</Issn>
				<Volume>3</Volume>
				<Issue>1</Issue>
				<PubDate PubStatus="epublish">
					<Year>2013</Year>
					<Month>03</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Enzymatic detoxification of Don in transgenic plants via expression
of Fusarium graminearum Tri101 gene</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>53</FirstPage>
			<LastPage>59</LastPage>
			<ELocationID EIdType="pii">32092</ELocationID>
			
<ELocationID EIdType="doi">10.22059/pbs.2013.32092</ELocationID>
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Akram</FirstName>
					<LastName>Ahmadizadeh</LastName>
<Affiliation>National Institute of Genetic Engineering and Biotechnology</Affiliation>

</Author>
<Author>
					<FirstName>Forough</FirstName>
					<LastName>Sanjarian</LastName>
<Affiliation>National Institute of Genetic Engineering and Biotechnology</Affiliation>

</Author>
<Author>
					<FirstName>Kamahldin</FirstName>
					<LastName>Haghbeen</LastName>
<Affiliation>National Institute of Genetic Engineering and Biotechnology</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2012</Year>
					<Month>11</Month>
					<Day>10</Day>
				</PubDate>
			</History>
		<Abstract>Fusarium graminearum &lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;is causal agent of economically catastrophic disease of cereal &lt;/span&gt;&lt;/span&gt;Fusarium Head Blight (FHB) around the world. In addition to causing a loss of yield, this fungus causes serious threats to humans and animals due to the contamination of grain with the trichothecene mycotoxin. &lt;em&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;TRI101 &lt;/span&gt;&lt;/span&gt;&lt;/em&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;gene, a &lt;/span&gt;&lt;/span&gt;&lt;em&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;Fusarium &lt;/span&gt;&lt;/span&gt;&lt;/em&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;spp. gene, encodes an &lt;/span&gt;&lt;/span&gt;enzyme that transfers an acetyl group to the C3 hydroxyl of trichothecenes. We introduced TRI101 &lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;gene from &lt;/span&gt;&lt;/span&gt;&lt;em&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;F. graminearum &lt;/span&gt;&lt;/span&gt;&lt;/em&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;to tobacco to test its usefulness for decontamination &lt;/span&gt;&lt;/span&gt;of mycotoxins. The acetyltransferase activity of this gene was detected in transgenic plants. The growth pattern of T1 seedling was examined at present of deoxynivalenol (DON) and crude extract of mycotoxin. A significant difference in growth rate was seen in plants expressing TRI101 as compared to wild type in DON assay. There was no significant difference in growth rate of the wild type and transgenic plants in presence of a mixture of mycotoxins. According to the results, it seems although FgTRI101 enzyme is suitable for detoxification of DON, more studies are required to evaluate its performance in detoxification of mixture of Fusarium toxins.</Abstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">detoxification</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">DON</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">fusarium head blight</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">F.gTRI101</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Mycotoxin</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://pbiosci.ut.ac.ir/article_32092_426e4cd9650410f1b0b387bf1c84186c.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>University of Tehran Press</PublisherName>
				<JournalTitle>Progress in Biological Sciences</JournalTitle>
				<Issn>1016-1058</Issn>
				<Volume>3</Volume>
				<Issue>1</Issue>
				<PubDate PubStatus="epublish">
					<Year>2013</Year>
					<Month>03</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Regeneration and Agrobacterium-mediated transformation of three
economically important strawberry cultivars Kurdistan, Camarosa and Paros</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>60</FirstPage>
			<LastPage>66</LastPage>
			<ELocationID EIdType="pii">32093</ELocationID>
			
<ELocationID EIdType="doi">10.22059/pbs.2013.32093</ELocationID>
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Sirwan</FirstName>
					<LastName>Nasri</LastName>
<Affiliation>Department of Agricultural Biotechnology, Faculty of Agriculture, University of Kurdistan, Sanandaj, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Bahman</FirstName>
					<LastName>Bahramnejad</LastName>
<Affiliation>Department of Agricultural Biotechnology, Faculty of Agriculture, University of Kurdistan, Sanandaj, Iran</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2012</Year>
					<Month>11</Month>
					<Day>15</Day>
				</PubDate>
			</History>
		<Abstract>Genetic transformation studies were carried out to standardize a protocol for Agrobacterium &lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;-mediated genetic transformation of three economically important &lt;/span&gt;&lt;/span&gt;strawberry (&lt;em&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;Fragaria &lt;/span&gt;&lt;/span&gt;&lt;/em&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;x &lt;/span&gt;&lt;/span&gt;&lt;em&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;ananassa &lt;/span&gt;&lt;/span&gt;&lt;/em&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;Duch) cultivars Kurdistan’, Camarosa’, and ‘Paros’. &lt;/span&gt;&lt;/span&gt;Shoot regeneration frequency 72, 65 and 30% was obtained on MS (1) basal medium supplemented with 2% glucose and 4 mg/l TDZ for Camarosa, Kurdistan and Paros, respectively. To optimize the concentration of kanamycin for these cultivars, we observed the responses of leaf explants to different concentration of kanamycin (0-100 mg/l) in the media. Our results showed that 75 mg/l was an effective concentration of kanamycin. For genetic transformation, &lt;em&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;Agrobacterium tumefaciens &lt;/span&gt;&lt;/span&gt;&lt;/em&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;strain C58C1RifR (pGV2260) &lt;/span&gt;&lt;/span&gt;harbouring the binary vector pTJK136 containing &lt;em&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;uidA &lt;/span&gt;&lt;/span&gt;&lt;/em&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;gene with intron along with &lt;/span&gt;&lt;/span&gt;kanamycin resistance gene (&lt;em&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;npt-II&lt;/span&gt;&lt;/span&gt;&lt;/em&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;) was used. After five days pre-incubation and 72 h &lt;/span&gt;&lt;/span&gt;co-cultivation, transformed cells (explants) were able to grow on the selective regeneration medium containing 75 mg/l kanamycin and 500 mg/l cefotaxime, while, control explants failed to grow. The regenerated putative transgenic shoots were analyzed by histochemical GUS assay and PCR analysis. Transformation efficiency based on inoculated explants number was 2, 1 and 3% for ‘, Camarosa’, ‘Paros ’, and ‘Kurdistan’, respectively. The standardized protocol would be useful for &lt;em&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;Agrobacterium&lt;/span&gt;&lt;/span&gt;&lt;/em&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;-mediated &lt;/span&gt;&lt;/span&gt;genetic transformation of these cultivars with important agronomic genes.</Abstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">Agrobacterium tumifaciens</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">genetic transformation</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">gus</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">strawberry</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://pbiosci.ut.ac.ir/article_32093_4e3642799be890c0604d6b92e11ad4af.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>University of Tehran Press</PublisherName>
				<JournalTitle>Progress in Biological Sciences</JournalTitle>
				<Issn>1016-1058</Issn>
				<Volume>3</Volume>
				<Issue>1</Issue>
				<PubDate PubStatus="epublish">
					<Year>2013</Year>
					<Month>03</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>iProsite: an improved prosite database achieved by replacing
ambiguous positions with more informative representations</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>67</FirstPage>
			<LastPage>71</LastPage>
			<ELocationID EIdType="pii">32094</ELocationID>
			
<ELocationID EIdType="doi">10.22059/pbs.2013.32094</ELocationID>
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Mohammad-Hadi</FirstName>
					<LastName>Foroughmand-Araabi</LastName>
<Affiliation>Institute of Biochemistry and Biophysics, University of Tehran, Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Bahram</FirstName>
					<LastName>Goliaei</LastName>
<Affiliation>Institute of Biochemistry and Biophysics, University of Tehran, Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Mehdi</FirstName>
					<LastName>Sadeghi</LastName>
<Affiliation>National Institute of Genetic Engineering and Biotechnology (NIGEB), Tehran 14155-6346, Iran</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2012</Year>
					<Month>12</Month>
					<Day>15</Day>
				</PubDate>
			</History>
		<Abstract>PROSITE database contains a set of entries corresponding to protein families, which are used to identify the family of a protein from its sequence. Although patterns and profiles are developed to be very selective, each may have false positive or negative hits. Considering false positives as items that reduce the selectiveness of a pattern, then, the more selective pattern we have, a more accuracy in protein family detection we will get. In this paper, we have provided a method for improving the PROSITE patterns by reconstructing them in a manner that they not only still match to true positive hits, but also match to less false positive hits. From 973 PROSITE patterns, 283 have been improved by our method. We have applied the provided method on the PROSITE database and the improved resulting database is available at http://cbp.ut.ac.ir/iPROSITE.</Abstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">Protein sequence pattern</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Protein database</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Protein family</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">PROSITE</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://pbiosci.ut.ac.ir/article_32094_74709f41295c390d6235e625df0a4935.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>University of Tehran Press</PublisherName>
				<JournalTitle>Progress in Biological Sciences</JournalTitle>
				<Issn>1016-1058</Issn>
				<Volume>3</Volume>
				<Issue>1</Issue>
				<PubDate PubStatus="epublish">
					<Year>2013</Year>
					<Month>03</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Quantitative expression analysis of candidate genes for Septoria
tritici blotch resistance in wheat (Triticum aestivum L.)</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>72</FirstPage>
			<LastPage>78</LastPage>
			<ELocationID EIdType="pii">32095</ELocationID>
			
<ELocationID EIdType="doi">10.22059/pbs.2013.32095</ELocationID>
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Laleh</FirstName>
					<LastName>Karimi Farsad</LastName>
<Affiliation>Genomics Department, Agricultural Biotechnology Research Institute of Iran (ABRII), Karaj, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Mohsen</FirstName>
					<LastName>Mardi</LastName>
<Affiliation>Genomics Department, Agricultural Biotechnology Research Institute of Iran (ABRII), Karaj, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Mohammad Ali</FirstName>
					<LastName>Ebrahimi</LastName>
<Affiliation>Department of Biotechnology, Payame Noor University, Tehran, Iran.</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2012</Year>
					<Month>12</Month>
					<Day>30</Day>
				</PubDate>
			</History>
		<Abstract>Septoria tritici blotch (STB), caused by the ascomycete fungus &lt;em&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;Mycosphaerella &lt;/span&gt;&lt;/span&gt;&lt;/em&gt;graminicola &lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;(asexual stage: &lt;/span&gt;&lt;/span&gt;&lt;em&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;Septoria tritici&lt;/span&gt;&lt;/span&gt;&lt;/em&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;), is one of the most important foliar diseases &lt;/span&gt;&lt;/span&gt;of wheat. In this research, quantitative expression analysis of five candidate genes for the induction of resistance to STB (&lt;em&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;PR-1&lt;/span&gt;&lt;/span&gt;&lt;/em&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;, &lt;/span&gt;&lt;/span&gt;&lt;em&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;Bsi&lt;/span&gt;&lt;/span&gt;&lt;/em&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;, &lt;/span&gt;&lt;/span&gt;&lt;em&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;Msr, Per&lt;/span&gt;&lt;/span&gt;&lt;/em&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;, and &lt;/span&gt;&lt;/span&gt;&lt;em&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;Ppi&lt;/span&gt;&lt;/span&gt;&lt;/em&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;) was conducted in the wheat &lt;/span&gt;&lt;/span&gt;cultivars ‘Seri 82’ (susceptible) and ‘Frontana’ (resistant). The study used a randomized complete block design with three replications and five time-points (0, 3, 6, 12, and 24hours after inoculation). Evaluation of the expression of five candidate genes by real-time PCR showed that expression of &lt;em&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;Per, pr-1, Bsi, Msr &lt;/span&gt;&lt;/span&gt;&lt;/em&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;genes was higher than 5, 3, 3 and 2 &lt;/span&gt;&lt;/span&gt;fold in treatment &lt;em&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;vs. &lt;/span&gt;&lt;/span&gt;&lt;/em&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;control samples in ‘Frontana’ at 12 hours after inoculation &lt;/span&gt;&lt;/span&gt;respectively. The results indicated the effectiveness of these genes in the conferral of resistance to STB in wheat.</Abstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">Septoria tritici</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Wheat</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Real-time PCR analysis</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Resistance gene</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://pbiosci.ut.ac.ir/article_32095_af8b1963a0d79c27a674900c3b547415.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>University of Tehran Press</PublisherName>
				<JournalTitle>Progress in Biological Sciences</JournalTitle>
				<Issn>1016-1058</Issn>
				<Volume>3</Volume>
				<Issue>1</Issue>
				<PubDate PubStatus="epublish">
					<Year>2013</Year>
					<Month>03</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Identification and toxigenic potential of a cyanobacterial strain
(Stigomena sp.)</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>79</FirstPage>
			<LastPage>85</LastPage>
			<ELocationID EIdType="pii">32096</ELocationID>
			
<ELocationID EIdType="doi">10.22059/pbs.2013.32096</ELocationID>
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Bahareh</FirstName>
					<LastName>Nowruzi</LastName>
<Affiliation>Faculty of Biological Sciences, Kharazmi University, Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Ramazan Ali</FirstName>
					<LastName>Khavari-Nejad</LastName>
<Affiliation>1Faculty of Biological Sciences, Kharazmi University, Tehran, Iran. Department of Biology, Science and Research Branch, Islamic Azad University, Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Karina</FirstName>
					<LastName>Sivonen</LastName>
<Affiliation>Department of Applied Chemistry and Microbiology, University of Helsinki, Helsinki, Finland</Affiliation>

</Author>
<Author>
					<FirstName>Bahram</FirstName>
					<LastName>Kazemi</LastName>
<Affiliation>Department of Biotechnology, Shahid Beheshti University of Medical Sciences, Tehran, Iran. 5Cellular and Molecular Biology Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Farzaneh</FirstName>
					<LastName>Najafi</LastName>
<Affiliation>Faculty of Biological Sciences, Kharazmi University, Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Taher</FirstName>
					<LastName>Nejadsattari</LastName>
<Affiliation>Department of Biology, Science and Research Branch, Islamic Azad University, Tehran, Iran</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2013</Year>
					<Month>01</Month>
					<Day>15</Day>
				</PubDate>
			</History>
		<Abstract>Cyanobacteria are well known for their production of a multitude of highly toxic substances &lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;. The genus &lt;/span&gt;&lt;/span&gt;&lt;em&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;Stigomena &lt;/span&gt;&lt;/span&gt;&lt;/em&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;is regarded as good candidates for producing &lt;/span&gt;&lt;/span&gt;biologically active secondary metabolites, which are highly toxic to humans and other animals. The carcass of a dog was found at the shore of Lake Ali-Abad, Iran. Biomass from the discovery site appeared to be of cyanobacterial nature. We identified the strain as freshwater bloom-forming representative of the &lt;em&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;Stigomena &lt;/span&gt;&lt;/span&gt;&lt;/em&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;genus on the basis of its &lt;/span&gt;&lt;/span&gt;16S rRNA sequence. It carried the &lt;em&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;mcyE &lt;/span&gt;&lt;/span&gt;&lt;/em&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;gene, as well as a potential cryptic &lt;/span&gt;&lt;/span&gt;&lt;em&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;hassallidin &lt;/span&gt;&lt;/span&gt;&lt;/em&gt;gene cluster. These results suggest that microcystin-induced liver damage may have significantly ontributed to the death of the dog. This case is thus the first reported incident of potential microcystin intoxication in a dog in Iran.</Abstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">Cyanobacteria</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Stigomena sp</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Natural bioactive compound</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Toxicity</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://pbiosci.ut.ac.ir/article_32096_9b43cc4961df536be57860d6d78319ab.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>University of Tehran Press</PublisherName>
				<JournalTitle>Progress in Biological Sciences</JournalTitle>
				<Issn>1016-1058</Issn>
				<Volume>3</Volume>
				<Issue>1</Issue>
				<PubDate PubStatus="epublish">
					<Year>2013</Year>
					<Month>03</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Preliminary study of rodents’ fauna (mammalia; rodentia) of Khaf
township, southeast of Khorasan Razavi province, Iran, using pellets
of birds of prey</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>86</FirstPage>
			<LastPage>89</LastPage>
			<ELocationID EIdType="pii">32097</ELocationID>
			
<ELocationID EIdType="doi">10.22059/pbs.2013.32097</ELocationID>
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Kordiyeh</FirstName>
					<LastName>Hamidi</LastName>
<Affiliation>Department of Biology, Faculty of Sciences, Ferdowsi University of Mashhad, Mashhad, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Hamidreza</FirstName>
					<LastName>Mehraban</LastName>
<Affiliation>Department of Biology, Faculty of Sciences, Ferdowsi University of Mashhad, Mashhad, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Jamshid</FirstName>
					<LastName>Darvish</LastName>
<Affiliation>Department of Biology, Faculty of Sciences, Ferdowsi University of Mashhad, Mashhad, Iran. 
Rodentology Research Department, Ferdowsi University of Mashhad, Mashhad, Iran</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2013</Year>
					<Month>02</Month>
					<Day>10</Day>
				</PubDate>
			</History>
		<Abstract>The rodents’ fauna of boundary zones of Iran are still poorly known. In this research rodents fauna of Khaf township in northeast of Iran have been reported mainly based on pellets of birds of prey. Alive samples and also rodent’s remains from pellet materials of birds of prey in the present study was collected from 46 localities in Khaf, northeast of KhorasanRazavi province and different specimens were collected during the period of April, 2011 until September, 2012. A total of 718 prey bird pellet material and six complete (living) samples were identified based on morphological methods on external anatomy (in complete samples), teeth, cranial and dentary bones (in pellets) and as a result of the study, the rodents fauna of Khaf consists of twelve species belonging to nine genera and three families including; 1) dae (&lt;em&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;Allactaga elater&lt;/span&gt;&lt;/span&gt;&lt;/em&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;), 2) Cricetidae (&lt;/span&gt;&lt;/span&gt;&lt;em&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;Cricetulus &lt;/span&gt;&lt;/span&gt;&lt;/em&gt;migratorius&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;), 3) Muridae (&lt;/span&gt;&lt;/span&gt;&lt;em&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;Tatera indica, Gerbillus nanus, Meriones persicus, Meriones &lt;/span&gt;&lt;/span&gt;&lt;/em&gt;libycus, Meriones crassus, Meriones meridianus, Rhombomys opimus, Mus musculus, Nesokia indica &lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;), and also one species of Lagomorpha (Ochotonidae: &lt;/span&gt;&lt;/span&gt;&lt;em&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;Ochotona &lt;/span&gt;&lt;/span&gt;&lt;/em&gt;rufescense &lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;) and Soricomorpha (Soricidae: &lt;/span&gt;&lt;/span&gt;&lt;em&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;Crocidura gmelini&lt;/span&gt;&lt;/span&gt;&lt;/em&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;).&lt;/span&gt;&lt;/span&gt;</Abstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">Rodent’s Fauna</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Pellets</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Khaf</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Iran</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://pbiosci.ut.ac.ir/article_32097_69b5fe6e3858350cf28478bc64434e52.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>University of Tehran Press</PublisherName>
				<JournalTitle>Progress in Biological Sciences</JournalTitle>
				<Issn>1016-1058</Issn>
				<Volume>3</Volume>
				<Issue>1</Issue>
				<PubDate PubStatus="epublish">
					<Year>2013</Year>
					<Month>03</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Relationship among AFLP, RAPD marker diversity and
Agromorphological traits in safflower (Carthamus tinctorius L.)</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>90</FirstPage>
			<LastPage>99</LastPage>
			<ELocationID EIdType="pii">32098</ELocationID>
			
<ELocationID EIdType="doi">10.22059/pbs.2013.32098</ELocationID>
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Bahman</FirstName>
					<LastName>Panahi</LastName>
<Affiliation>Department of Biotechnology and Plant Breeding, University of Tabriz, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Rahim</FirstName>
					<LastName>Afzal</LastName>
<Affiliation>Department of Biotechnology and Plant Breeding, Ferdowsi University of mashhad, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Mahmoud</FirstName>
					<LastName>Ghorbanzadeh Neghab</LastName>
<Affiliation>Department of Biotechnology and Plant Breeding, Ferdowsi University of mashhad, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Mohsen</FirstName>
					<LastName>Mahmoodnia</LastName>
<Affiliation>Department of Agronomy and Plant Breeding, Valieasr University of Rafsanjan, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Behzad</FirstName>
					<LastName>Paymard</LastName>
<Affiliation>Department of Biotechnology and Plant Breeding, University of Tabriz, Iran</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2013</Year>
					<Month>02</Month>
					<Day>10</Day>
				</PubDate>
			</History>
		<Abstract>of high-quality vegetable and industrial oil. 9 RAPD primers, 6 AFLP primer combinations and 12 agro-morphological traits were used to assess the genetic diversity of 20 accessions of saf &lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;fl&lt;/span&gt;&lt;/span&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;ower representing global germplasm variability. Jacquards’ &lt;/span&gt;&lt;/span&gt;similarity coef &lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;fi&lt;/span&gt;&lt;/span&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;cient were used to understanding the genetic relationships among &lt;/span&gt;&lt;/span&gt;ccessions, for AFLP and RAPD markers and Euclidian similarity coefficient for agromorphological markers. UPGMA clustering algorithm was used for all markers. RAPD and AFLP markers grouped accessions into two main clusters whereas dendrogram of morphology data delineated the accessions into three clusters. Correlation coef &lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;fi&lt;/span&gt;&lt;/span&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;cient &lt;/span&gt;&lt;/span&gt;comparisons between similarity matrices and co-phenetic matrices obtained with the three markers revealed that AFLP displayed no congruence vis-a-vis RAPD and agromorphological data.</Abstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">AFLP</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Carthamus tinctorius L</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Genetic diversity</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">RAPD</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">marker</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://pbiosci.ut.ac.ir/article_32098_0b9b014b1dc1b19dfa9240fd7f57b19b.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>University of Tehran Press</PublisherName>
				<JournalTitle>Progress in Biological Sciences</JournalTitle>
				<Issn>1016-1058</Issn>
				<Volume>3</Volume>
				<Issue>1</Issue>
				<PubDate PubStatus="epublish">
					<Year>2013</Year>
					<Month>03</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Effects of exogenous ornithine enantiomers on tobacco cells under
salinity conditions</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>100</FirstPage>
			<LastPage>107</LastPage>
			<ELocationID EIdType="pii">32099</ELocationID>
			
<ELocationID EIdType="doi">10.22059/pbs.2013.32099</ELocationID>
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Mina</FirstName>
					<LastName>Ghahremani</LastName>
<Affiliation>Department of Plant Biology, Faculty of Biological Science, Tarbiat Modares University, Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Faezeh</FirstName>
					<LastName>Ghanati</LastName>
<Affiliation>Department of Plant Biology, Faculty of Biological Science, Tarbiat Modares University, Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Francoise</FirstName>
					<LastName>Bernard</LastName>
<Affiliation>Department of Plant Biology, Faculty of Biological Science, Shahid Beheshti University, Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Morteza</FirstName>
					<LastName>Gholami</LastName>
<Affiliation>Medicinal Plants and Drugs Research Institute (MPDRI), Shahid Beheshti University, G.C., Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Taha</FirstName>
					<LastName>Azad</LastName>
<Affiliation>Department of Biochemistry, Faculty of Biological Science, Tarbiat Modares University, Tehran, Iran</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2013</Year>
					<Month>02</Month>
					<Day>16</Day>
				</PubDate>
			</History>
		<Abstract>Ornithine is a non-proteinogenic amino acid, which plays an essential role in the metabolism of plants. Regard to the chirality of the molecule, physiological response of the plant cells to its two enantiomers have not been widely investigated yet. In the present study, suspension-cultured tobacco cells were treated with 1 mM of D- and Lenantiomers of ornithine in normal conditions as well as under stress of 50 mM NaCl. Differential effects of L- and D-enanthiomers were observed either in normal or under salinity stress conditions. L-ornithin adversely affected the growth of tobacco cells in normal conditions and its detrimental effect was intensified by salinity. Treatment with D-ornithine however, not only did not change the growth but also alleviated it under salt stress. Physiological response of tobacco cells to D-ornithine in normal conditions was accompanied by increasing of polyamines. Under salinity stress however, D-ornithine treatment increased the activity of major antioxidant enzymes i.e., superoxide dismutase, catalase, and peroxidase and also increased proline content of the cells, all together resulted in lowering H&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: xx-small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: xx-small;&quot;&gt;2&lt;/span&gt;&lt;/span&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;O&lt;/span&gt;&lt;/span&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: xx-small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: xx-small;&quot;&gt;2 &lt;/span&gt;&lt;/span&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;and maintenance of cells membrane integrity. The results &lt;/span&gt;&lt;/span&gt;suggested that D-ornithine is a potent compound for activation of anti-oxidant system of plant cells and alleviation of stress condition.</Abstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">Antioxidant Enzymes</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">(D/L)-ornithine</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">polyamines</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">proline</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">salt stress</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://pbiosci.ut.ac.ir/article_32099_c3e26c5d5fbcd8338230b4e6e4682c9d.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>University of Tehran Press</PublisherName>
				<JournalTitle>Progress in Biological Sciences</JournalTitle>
				<Issn>1016-1058</Issn>
				<Volume>3</Volume>
				<Issue>1</Issue>
				<PubDate PubStatus="epublish">
					<Year>2013</Year>
					<Month>03</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Comparison of biochemical properties of recombinant
endoglucanase II of Trichoderma reesei in methylotrophic yeasts,
Pichia pastoris and Hansenula polymorpha</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>108</FirstPage>
			<LastPage>117</LastPage>
			<ELocationID EIdType="pii">32100</ELocationID>
			
<ELocationID EIdType="doi">10.22059/pbs.2013.32100</ELocationID>
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Ali</FirstName>
					<LastName>Akbarzadeh</LastName>
<Affiliation>Department of Plant Biotechnology, National Institute of Genetic Engineering and Biotechnology (NIGEB); 
Nanobiotechnology Engineering Laboratory, Faculty of Energy Engineering and New Technologies, Shahid Beheshti
University, GC,</Affiliation>

</Author>
<Author>
					<FirstName>Seyed Omid</FirstName>
					<LastName>Ranaei Siadat</LastName>
<Affiliation>Nanobiotechnology Engineering Laboratory, Faculty of Energy Engineering and New Technologies, Shahid Beheshti
University, GC, Tehran, Islamic Republic of Iran</Affiliation>

</Author>
<Author>
					<FirstName>Mohammad Reza</FirstName>
					<LastName>Zamani</LastName>
<Affiliation>Department of Plant Biotechnology, National Institute of Genetic Engineering and Biotechnology (NIGEB), Tehran, Islamic
Republic of Iran</Affiliation>

</Author>
<Author>
					<FirstName>Mostafa</FirstName>
					<LastName>Motallebi</LastName>
<Affiliation>Department of Plant Biotechnology, National Institute of Genetic Engineering and Biotechnology (NIGEB), Tehran, Islamic
Republic of Iran</Affiliation>

</Author>
<Author>
					<FirstName>Mohammad</FirstName>
					<LastName>Barshan Tashnizi</LastName>
<Affiliation>Department of Life Science Engineering, Faculty of New Science and Technologies, University of Tehran, Tehran, Islamic
Republic of Iran</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2013</Year>
					<Month>02</Month>
					<Day>22</Day>
				</PubDate>
			</History>
		<Abstract>Bioconversion of cellulosic material into bioethanol needs cellulase complex enzymesthat contain endoglucanase, exoglucanase and beta glucosidase. One of the most important organisms that produce cellulases is the filamentous fungi, &lt;em&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;Trichoderma reesei &lt;/span&gt;&lt;/span&gt;&lt;/em&gt;which able to secrete large amounts of different cellulases. These enzymes are probably the most widely used cellulases industrially, however, the cellulases excreted from fungi are not stable at high pH or high temperatures. In this study methylotrophic yeasts, &lt;em&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;Pichia &lt;/span&gt;&lt;/span&gt;&lt;/em&gt;pastoris &lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;and &lt;/span&gt;&lt;/span&gt;&lt;em&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;Hansenula polymorpha &lt;/span&gt;&lt;/span&gt;&lt;/em&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;were used for the comparative heterologous &lt;/span&gt;&lt;/span&gt;production of endoglucanase II. Two synthetic &lt;em&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;egII &lt;/span&gt;&lt;/span&gt;&lt;/em&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;genes with &lt;/span&gt;&lt;/span&gt;&lt;em&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;P. pastoris &lt;/span&gt;&lt;/span&gt;&lt;/em&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;and &lt;/span&gt;&lt;/span&gt;H. polymorpha &lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;codon preferences were transferred into the yeasts. In addition, both &lt;/span&gt;&lt;/span&gt;expression vectors contained the pre-pro-sequence of &lt;em&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;Saccharomyces cerevisiae &lt;/span&gt;&lt;/span&gt;&lt;/em&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;mating &lt;/span&gt;&lt;/span&gt;factor alpha to allow secretion of protein. Enzymes characterization demonstrated increasing thermal stability in both recombinants EGII compare with native enzyme from T. reesei &lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;and the &lt;/span&gt;&lt;/span&gt;&lt;em&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;Hansenula &lt;/span&gt;&lt;/span&gt;&lt;/em&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;enzyme was more stable than &lt;/span&gt;&lt;/span&gt;&lt;em&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;Pichia &lt;/span&gt;&lt;/span&gt;&lt;/em&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;in higher temperature. &lt;/span&gt;&lt;/span&gt;Biochemical properties determination on different substrates showed higher binding site affinity in &lt;em&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;Pichia &lt;/span&gt;&lt;/span&gt;&lt;/em&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;than &lt;/span&gt;&lt;/span&gt;&lt;em&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;Hansenula &lt;/span&gt;&lt;/span&gt;&lt;/em&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;and native one. We can conclude that &lt;/span&gt;&lt;/span&gt;&lt;em&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPS-ItalicMT; font-size: small;&quot;&gt;P. pastoris &lt;/span&gt;&lt;/span&gt;&lt;/em&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;and &lt;/span&gt;&lt;/span&gt;H. polymorpha &lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;&lt;span style=&quot;font-family: TimesNewRomanPSMT; font-size: small;&quot;&gt;are appropriate hosts for expression and production of endoglucanase with &lt;/span&gt;&lt;/span&gt;improved thermal stability.</Abstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">Hansenula polymorpha</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Pichia pastoris</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Recombinant protein</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">endoglucanase</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://pbiosci.ut.ac.ir/article_32100_cd518e484dd59ed45e64b03005f46bc6.pdf</ArchiveCopySource>
</Article>
</ArticleSet>
