<?xml version="1.0" encoding="UTF-8" ?>

    <journal>
    <language>en</language>
    <journal_id_issn>2008-2835</journal_id_issn>
    <journal_id_issn_online>2008-4625</journal_id_issn_online>
    <journal_id_pii></journal_id_pii>
    <journal_id_doi></journal_id_doi>
    <journal_id_isnet></journal_id_isnet>
    <journal_id_iranmedex>276</journal_id_iranmedex>
    <journal_id_magiran>5669</journal_id_magiran>
    <journal_id_sid>11181</journal_id_sid>
    <pubdate>
	    <type>gregorian</type>
	    <year>>2016</year>
	    <month>>October-December</month>
	    <day></day>
    </pubdate>
    <volume>8</volume>
    <number>4</number>
    <publish_type>online</publish_type>
    <publish_edition>1</publish_edition>
    <article_type>fulltext</article_type>
    <articleset>

<article>
	<language>en</language>
	<article_id_issn></article_id_issn>
	<article_id_issn_online></article_id_issn_online>
	<article_id_pubmed>27920887</article_id_pubmed>
	<article_id_pii></article_id_pii>
	<article_id_doi></article_id_doi>
	<article_id_iranmedex></article_id_iranmedex>
	<article_id_magiran></article_id_magiran>
	<article_id_sid></article_id_sid>
	<title_fa></title_fa>
	<title>Preliminary Study on Cost-effective L-Tryptophan Production from Indole and L-Serine by E. coli Cells</title>
	<subject_fa></subject_fa>
	<subject></subject>
	<content_type_fa></content_type_fa>
	<content_type></content_type>
	<abstract_fa></abstract_fa>
	<abstract>&lt;p&gt;Background: L-tryptophan is used widespread in the pharmaceutical industry. The majority of L-Trp production depends on microbial processes that produce L-tryptophan from indole and L-serine. These processes are very costly due to the costs of precursors, especially L-serine. Use of inexpensive substitutions as the L-serine source of L-tryptophan production enables us to reach a cost-effective process. In this paper, effect of Triton X-100 on L-Trp production and the ability to use Iranian cane molasses as inexpensive L-serine source was investigated.&lt;br /&gt;
Methods: &lt;em&gt;Escherichia coli (E. coli)&lt;/em&gt; &lt;em&gt;ATCC 11303&lt;/em&gt; cells were grown in 10-L fermenter containing minimal medium supplemented with beet molasses as an inexpensive carbon source and indole as tryptophan synthase inducer. Whole cells of stationary phase were used as biocatalyst for L-Trp production. Triton X-100 addition to the production medium as indole reservoir was investigated. Then, cane molasses was used as L-Ser source in L-Trp production medium. Amount of L-Tryptophan and theoretical yield of L-Trp production was determined by HPLC and by a colorimetrically method on the basis of remaining indole assay, respectively.&lt;br /&gt;
Results: As a result, triton X-100 increased L-Trp production three times.&amp;nbsp; Also, the result showed that 0.68 &lt;em&gt;mM&lt;/em&gt; L-Tryptophan was produced in the presence of cane molasses at 37&lt;sup&gt;o&lt;/sup&gt;&lt;em&gt;C&lt;/em&gt; for 8 &lt;em&gt;hr&lt;/em&gt;.&lt;br /&gt;
Conclusion: This result showed that cane molasses of Qazvin sugar factory includes significant amounts of L-Ser that makes it a suitable substitution for L-Ser in L-Trp production. Therefore, it has the potential to be used for cost-effective L-Trp production in industrial scale.&lt;/p&gt;
</abstract>
	<keyword_fa></keyword_fa>
	<keyword>Molasses, PLP, Tryptophan synthase, Tryptophanase</keyword>
	<start_page>188</start_page>
	<end_page>192</end_page>
	<web_url>https://www.ajmb.org/En/Article.aspx?id=256</web_url>
    <pdf_url>https://www.ajmb.org/PDF/En/FullText/256.pdf</pdf_url>
	<author_list><author><first_name>Tahereh</first_name><middle_name></middle_name><last_name>Sadeghiyan-Rizi</last_name><suffix></suffix><affiliation>Department of Pharmaceutical Biotechnology, Faculty of Pharmacy, Isfahan University of Medical Sciences, Isfahan, Iran</affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>1043</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Jamshid</first_name><middle_name></middle_name><last_name>Fooladi</last_name><suffix></suffix><affiliation>National Laboratory of Industrial Microbiology, Department of Biology, Faculty of Science, Alzahra University, Tehran, Iran</affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>1044</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Sima</first_name><middle_name></middle_name><last_name>Sadrai</last_name><suffix></suffix><affiliation>Department of Pharmaceutics, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran</affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>1045</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author></author_list>
</article>

</articleset>
</journal>

