<?xml version="1.0" encoding="utf-8"?>
<journal>
<title>Journal of Medicinal Plants</title>
<title_fa>فصلنامه گياهان دارویی</title_fa>
<short_title>J. Med. Plants</short_title>
<subject>Medical Sciences</subject>
<web_url>http://jmp.ir</web_url>
<journal_hbi_system_id>1</journal_hbi_system_id>
<journal_hbi_system_user>admin</journal_hbi_system_user>
<journal_id_issn>2717-204X</journal_id_issn>
<journal_id_issn_online>2717-2058</journal_id_issn_online>
<journal_id_pii></journal_id_pii>
<journal_id_doi>10.61882/jmp</journal_id_doi>
<journal_id_iranmedex></journal_id_iranmedex>
<journal_id_magiran></journal_id_magiran>
<journal_id_sid>14</journal_id_sid>
<journal_id_nlai>8888</journal_id_nlai>
<journal_id_science>13</journal_id_science>
<language>en</language>
<pubdate>
	<type>jalali</type>
	<year>1392</year>
	<month>12</month>
	<day>1</day>
</pubdate>
<pubdate>
	<type>gregorian</type>
	<year>2014</year>
	<month>3</month>
	<day>1</day>
</pubdate>
<volume>13</volume>
<number>49</number>
<publish_type>online</publish_type>
<publish_edition>1</publish_edition>
<article_type>fulltext</article_type>
<articleset>
	<article>


	<language>en</language>
	<article_id_doi></article_id_doi>
	<title_fa>The Effect of Chitosan and Chitin Oligomers on Gene Expression and Lignans Production in &lt;i&gt;Linum album&lt;/i&gt; Cell Cultures</title_fa>
	<title>The Effect of Chitosan and Chitin Oligomers on Gene Expression and Lignans Production in &lt;i&gt;Linum album&lt;/i&gt; Cell Cultures</title>
	<subject_fa>بيوتكنولوژی</subject_fa>
	<subject>Biotechnology</subject>
	<content_type_fa>پژوهشی</content_type_fa>
	<content_type>Research</content_type>
	<abstract_fa>&lt;div dir=&quot;ltr&quot; style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; &lt;em&gt;Linum album&lt;/em&gt;, a herbaceous and medicinal plant, has been shown to accumulate anti-tumor podophyllotoxin (PTOX) and related lignans. &lt;strong&gt;Objective:&lt;/strong&gt; In this study, we have verified the time-course of cell growth, lignan production in cells treated with chitosan and chitin oligomers. To study mechanism of chitosan and chitin oligomers action, expression of phenylalanine ammonio-lyase (PAL), cinnamoyl-CoA reductase (CCR), cinnamyl alcohol dehydrogenase (CAD) and pinoresinol lariciresinol reductase (PLR) genes were investigated. &lt;strong&gt;Methods:&lt;/strong&gt; The cells were treated with 100 mg l-1 chitin and chitosan oligomers. Cells were harvested for 5 days after elicitation. lignans quantified by reverse-phase high-performance liquid chromatography (HPLC). Cell samples frozen with liquid N2 were used to elucidate the expression level of genes by quantitative PCR (qPCR). &lt;strong&gt;Results:&lt;/strong&gt; Cells elicited with chitosan hexamer for 5 days yielded the highest amount of PTOX (73.5 &amp;micro;g/g dry weight) and lariciresinol (96 &amp;micro;g/g DW) which were about 3-fold and 2-fold higher than control, respectively. The expression of genes by oligomers was increased, reaching a peak at 3 day after treatment. &lt;strong&gt;Conclusion:&lt;/strong&gt; Chitosan and chitin oligomers up-regulate the production of PTOX, by effecting on gene expression of PTOX biosynthesis pathway.&lt;/div&gt;</abstract_fa>
	<abstract>&lt;div dir=&quot;ltr&quot; style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; &lt;em&gt;Linum album&lt;/em&gt;, a herbaceous and medicinal plant, has been shown to accumulate anti-tumor podophyllotoxin (PTOX) and related lignans. &lt;strong&gt;Objective:&lt;/strong&gt; In this study, we have verified the time-course of cell growth, lignan production in cells treated with chitosan and chitin oligomers. To study mechanism of chitosan and chitin oligomers action, expression of phenylalanine ammonio-lyase (PAL), cinnamoyl-CoA reductase (CCR), cinnamyl alcohol dehydrogenase (CAD) and pinoresinol lariciresinol reductase (PLR) genes were investigated. &lt;strong&gt;Methods:&lt;/strong&gt; The cells were treated with 100 mg l-1 chitin and chitosan oligomers. Cells were harvested for 5 days after elicitation. lignans quantified by reverse-phase high-performance liquid chromatography (HPLC). Cell samples frozen with liquid N2 were used to elucidate the expression level of genes by quantitative PCR (qPCR). &lt;strong&gt;Results:&lt;/strong&gt; Cells elicited with chitosan hexamer for 5 days yielded the highest amount of PTOX (73.5 &amp;micro;g/g dry weight) and lariciresinol (96 &amp;micro;g/g DW) which were about 3-fold and 2-fold higher than control, respectively. The expression of genes by oligomers was increased, reaching a peak at 3 day after treatment. &lt;strong&gt;Conclusion:&lt;/strong&gt; Chitosan and chitin oligomers up-regulate the production of PTOX, by effecting on gene expression of PTOX biosynthesis pathway.&lt;/div&gt;</abstract>
	<keyword_fa>,Linum album, Chitosan oligomers, Gene expression, Podophyllotoxin</keyword_fa>
	<keyword>Linum album, Chitosan oligomers, Gene expression, Podophyllotoxin</keyword>
	<start_page>46</start_page>
	<end_page>53</end_page>
	<web_url>http://jmp.ir/browse.php?a_code=A-10-68-1&amp;slc_lang=en&amp;sid=1</web_url>


<author_list>
	<author>
	<first_name>S </first_name>
	<middle_name></middle_name>
	<last_name>Esmaeilzadeh Bahabadi </last_name>
	<suffix></suffix>
	<first_name_fa>S</first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa>Esmaeilzadeh Bahabadi</last_name_fa>
	<suffix_fa></suffix_fa>
	<email>shirin_esm@yahoo.com</email>
	<code>100319475328460041937</code>
	<orcid>100319475328460041937</orcid>
	<coreauthor>Yes
</coreauthor>
	<affiliation>Department of Biology, Faculty of Basic Sciences, University of Zabol, Zabol, Iran</affiliation>
	<affiliation_fa>Department of Biology, Faculty of Basic Sciences, University of Zabol, Zabol, Iran</affiliation_fa>
	 </author>


	<author>
	<first_name>M</first_name>
	<middle_name></middle_name>
	<last_name>Sharifi  </last_name>
	<suffix></suffix>
	<first_name_fa>M</first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa>Sharifi</last_name_fa>
	<suffix_fa></suffix_fa>
	<email></email>
	<code>100319475328460041938</code>
	<orcid>100319475328460041938</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Department of Plant Biology, Faculty of Biological Sciences, Tarbiat Modares University, Tehran, Iran</affiliation>
	<affiliation_fa>Department of Plant Biology, Faculty of Biological Sciences, Tarbiat Modares University, Tehran, Iran</affiliation_fa>
	 </author>


	<author>
	<first_name>J</first_name>
	<middle_name></middle_name>
	<last_name>Murata </last_name>
	<suffix></suffix>
	<first_name_fa>J</first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa>Murata</last_name_fa>
	<suffix_fa></suffix_fa>
	<email></email>
	<code>100319475328460041939</code>
	<orcid>100319475328460041939</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Suntory Foundation for Life Sciences, Bioorganic Research Institute, Osaka, Japan</affiliation>
	<affiliation_fa>Suntory Foundation for Life Sciences, Bioorganic Research Institute, Osaka, Japan</affiliation_fa>
	 </author>


	<author>
	<first_name>H</first_name>
	<middle_name></middle_name>
	<last_name>Satake  </last_name>
	<suffix></suffix>
	<first_name_fa>H</first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa>Satake</last_name_fa>
	<suffix_fa></suffix_fa>
	<email></email>
	<code>100319475328460041940</code>
	<orcid>100319475328460041940</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Suntory Foundation for Life Sciences, Bioorganic Research Institute, Osaka, Japan</affiliation>
	<affiliation_fa>Suntory Foundation for Life Sciences, Bioorganic Research Institute, Osaka, Japan</affiliation_fa>
	 </author>


</author_list>


	</article>
</articleset>
</journal>
