Fermentative production of self-toxic fungal secondary metabolites
Fungi are well known for their vast diversity of secondary metabolites that include many life-saving drugs and highly toxic mycotoxins. In general, fungal cultures producing such metabolites are immune to their toxic effects. However, some are known to produce self-toxic compounds that can pose prod...
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description | Fungi are well known for their vast diversity of secondary metabolites that include many life-saving drugs and highly toxic mycotoxins. In general, fungal cultures producing such metabolites are immune to their toxic effects. However, some are known to produce self-toxic compounds that can pose production optimization challenges if the metabolites are needed in large amounts for chemical modification. One such culture, LV-2841, was identified as the lead for one of our exploratory projects. This culture was found to be a slow grower that produced trace amounts of a known metabolite, cercosporamide, under the standard flask fermentation conditions, and extensive medium optimization studies failed to yield higher titers. Poor growth of the culture in liquid media was attributed to the self-toxicity of cercosporamide to the producing organism, and the minimum inhibitory concentration (MIC) of cercosporamide was estimated to be in the range of 8-16 μg/ml. Fermentations carried out in media containing Diaion® HP20 resin afforded significantly higher titers of the desired compound. While several examples of resin-based fermentations of soil streptomyces have been published, this approach has rarely been used for fungal fermentations. Over a 100-fold increase in the production titer of cercosporamide, a self-toxic secondary metabolite, was achieved by supplementing the production medium with a commercially available neutral adsorbent resin. |
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In general, fungal cultures producing such metabolites are immune to their toxic effects. However, some are known to produce self-toxic compounds that can pose production optimization challenges if the metabolites are needed in large amounts for chemical modification. One such culture, LV-2841, was identified as the lead for one of our exploratory projects. This culture was found to be a slow grower that produced trace amounts of a known metabolite, cercosporamide, under the standard flask fermentation conditions, and extensive medium optimization studies failed to yield higher titers. Poor growth of the culture in liquid media was attributed to the self-toxicity of cercosporamide to the producing organism, and the minimum inhibitory concentration (MIC) of cercosporamide was estimated to be in the range of 8-16 μg/ml. Fermentations carried out in media containing Diaion® HP20 resin afforded significantly higher titers of the desired compound. While several examples of resin-based fermentations of soil streptomyces have been published, this approach has rarely been used for fungal fermentations. Over a 100-fold increase in the production titer of cercosporamide, a self-toxic secondary metabolite, was achieved by supplementing the production medium with a commercially available neutral adsorbent resin.</description><identifier>ISSN: 1367-5435</identifier><identifier>EISSN: 1476-5535</identifier><identifier>DOI: 10.1007/s10295-009-0678-9</identifier><identifier>PMID: 20033470</identifier><language>eng</language><publisher>Berlin/Heidelberg: Berlin/Heidelberg : Springer-Verlag</publisher><subject>Antifungal Agents - metabolism ; Antifungal Agents - toxicity ; Benzofurans - metabolism ; Benzofurans - toxicity ; Biochemistry ; Bioinformatics ; Biological and medical sciences ; Biomedical and Life Sciences ; Biotechnology ; Culture Media - chemistry ; Fermentation ; Fundamental and applied biological sciences. Psychology ; Fungi ; Fungi - drug effects ; Fungi - metabolism ; Genetic Engineering ; Inorganic Chemistry ; Ion Exchange Resins - metabolism ; Life Sciences ; Metabolites ; Methods. Procedures. Technologies ; Microbial engineering. Fermentation and microbial culture technology ; Microbial Sensitivity Tests ; Microbiology ; Mycotoxins ; Natural products ; Optimization ; Original Paper ; Polystyrenes - metabolism ; Resins ; Secondary metabolites ; Studies ; Toxicity ; Yeast</subject><ispartof>Journal of industrial microbiology & biotechnology, 2010-04, Vol.37 (4), p.335-340</ispartof><rights>Society for Industrial Microbiology 2009</rights><rights>2015 INIST-CNRS</rights><rights>Society for Industrial Microbiology 2010</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c533t-8377fff51011689d6661afc9183d92782c42c193b16c6644573f584f01f5d66c3</citedby><cites>FETCH-LOGICAL-c533t-8377fff51011689d6661afc9183d92782c42c193b16c6644573f584f01f5d66c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s10295-009-0678-9$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10295-009-0678-9$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27903,27904,41467,42536,51297</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=22592902$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20033470$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Singh, Maya P</creatorcontrib><creatorcontrib>Leighton, Margaret M</creatorcontrib><creatorcontrib>Barbieri, Laurel R</creatorcontrib><creatorcontrib>Roll, Deborah M</creatorcontrib><creatorcontrib>Urbance, Susan E</creatorcontrib><creatorcontrib>Hoshan, Linda</creatorcontrib><creatorcontrib>McDonald, Leonard A</creatorcontrib><title>Fermentative production of self-toxic fungal secondary metabolites</title><title>Journal of industrial microbiology & biotechnology</title><addtitle>J Ind Microbiol Biotechnol</addtitle><addtitle>J Ind Microbiol Biotechnol</addtitle><description>Fungi are well known for their vast diversity of secondary metabolites that include many life-saving drugs and highly toxic mycotoxins. In general, fungal cultures producing such metabolites are immune to their toxic effects. However, some are known to produce self-toxic compounds that can pose production optimization challenges if the metabolites are needed in large amounts for chemical modification. One such culture, LV-2841, was identified as the lead for one of our exploratory projects. This culture was found to be a slow grower that produced trace amounts of a known metabolite, cercosporamide, under the standard flask fermentation conditions, and extensive medium optimization studies failed to yield higher titers. Poor growth of the culture in liquid media was attributed to the self-toxicity of cercosporamide to the producing organism, and the minimum inhibitory concentration (MIC) of cercosporamide was estimated to be in the range of 8-16 μg/ml. Fermentations carried out in media containing Diaion® HP20 resin afforded significantly higher titers of the desired compound. While several examples of resin-based fermentations of soil streptomyces have been published, this approach has rarely been used for fungal fermentations. Over a 100-fold increase in the production titer of cercosporamide, a self-toxic secondary metabolite, was achieved by supplementing the production medium with a commercially available neutral adsorbent resin.</description><subject>Antifungal Agents - metabolism</subject><subject>Antifungal Agents - toxicity</subject><subject>Benzofurans - metabolism</subject><subject>Benzofurans - toxicity</subject><subject>Biochemistry</subject><subject>Bioinformatics</subject><subject>Biological and medical sciences</subject><subject>Biomedical and Life Sciences</subject><subject>Biotechnology</subject><subject>Culture Media - chemistry</subject><subject>Fermentation</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Fungi</subject><subject>Fungi - drug effects</subject><subject>Fungi - metabolism</subject><subject>Genetic Engineering</subject><subject>Inorganic Chemistry</subject><subject>Ion Exchange Resins - metabolism</subject><subject>Life Sciences</subject><subject>Metabolites</subject><subject>Methods. Procedures. Technologies</subject><subject>Microbial engineering. 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A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Fermentative production of self-toxic fungal secondary metabolites</atitle><jtitle>Journal of industrial microbiology & biotechnology</jtitle><stitle>J Ind Microbiol Biotechnol</stitle><addtitle>J Ind Microbiol Biotechnol</addtitle><date>2010-04-01</date><risdate>2010</risdate><volume>37</volume><issue>4</issue><spage>335</spage><epage>340</epage><pages>335-340</pages><issn>1367-5435</issn><eissn>1476-5535</eissn><abstract>Fungi are well known for their vast diversity of secondary metabolites that include many life-saving drugs and highly toxic mycotoxins. In general, fungal cultures producing such metabolites are immune to their toxic effects. However, some are known to produce self-toxic compounds that can pose production optimization challenges if the metabolites are needed in large amounts for chemical modification. One such culture, LV-2841, was identified as the lead for one of our exploratory projects. This culture was found to be a slow grower that produced trace amounts of a known metabolite, cercosporamide, under the standard flask fermentation conditions, and extensive medium optimization studies failed to yield higher titers. Poor growth of the culture in liquid media was attributed to the self-toxicity of cercosporamide to the producing organism, and the minimum inhibitory concentration (MIC) of cercosporamide was estimated to be in the range of 8-16 μg/ml. Fermentations carried out in media containing Diaion® HP20 resin afforded significantly higher titers of the desired compound. While several examples of resin-based fermentations of soil streptomyces have been published, this approach has rarely been used for fungal fermentations. Over a 100-fold increase in the production titer of cercosporamide, a self-toxic secondary metabolite, was achieved by supplementing the production medium with a commercially available neutral adsorbent resin.</abstract><cop>Berlin/Heidelberg</cop><pub>Berlin/Heidelberg : Springer-Verlag</pub><pmid>20033470</pmid><doi>10.1007/s10295-009-0678-9</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Antifungal Agents - metabolism Antifungal Agents - toxicity Benzofurans - metabolism Benzofurans - toxicity Biochemistry Bioinformatics Biological and medical sciences Biomedical and Life Sciences Biotechnology Culture Media - chemistry Fermentation Fundamental and applied biological sciences. Psychology Fungi Fungi - drug effects Fungi - metabolism Genetic Engineering Inorganic Chemistry Ion Exchange Resins - metabolism Life Sciences Metabolites Methods. Procedures. Technologies Microbial engineering. Fermentation and microbial culture technology Microbial Sensitivity Tests Microbiology Mycotoxins Natural products Optimization Original Paper Polystyrenes - metabolism Resins Secondary metabolites Studies Toxicity Yeast |
title | Fermentative production of self-toxic fungal secondary metabolites |
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