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Biosynthesis of the Halogenated Mycotoxin Aspirochlorine in Koji Mold Involves a Cryptic Amino Acid Conversion
Aspirochlorine (1) is an epidithiodiketopiperazine (ETP) toxin produced from koji mold (Aspergillus oryzae), which has been used in the oriental cuisine for over two millennia. Considering its potential risk for food safety, we have elucidated the molecular basis of aspirochlorine biosynthesis. By a...
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Published in: | Angewandte Chemie International Edition 2014-12, Vol.53 (49), p.13409-13413 |
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creator | Chankhamjon, Pranatchareeya Boettger-Schmidt, Daniela Scherlach, Kirstin Urbansky, Barbara Lackner, Gerald Kalb, Daniel Dahse, Hans-Martin Hoffmeister, Dirk Hertweck, Christian |
description | Aspirochlorine (1) is an epidithiodiketopiperazine (ETP) toxin produced from koji mold (Aspergillus oryzae), which has been used in the oriental cuisine for over two millennia. Considering its potential risk for food safety, we have elucidated the molecular basis of aspirochlorine biosynthesis. By a combination of genetic and chemical analyses we found the acl gene locus and identified the key role of AclH as a chlorinase. Stable isotope labeling, biotransformation, and mutational experiments, analysis of intermediates and an in vitro adenylation domain assay gave totally unexpected insights into the acl pathway: Instead of one Phe and one Gly, two Phe units are assembled by an iterative non‐ribosomal peptide synthetase (NRPS, AclP), followed by halogenation and an unprecedented Phe to Gly amino acid conversion. Biological assays showed that both amino acid transformations are required to confer cytotoxicity and antifungal activity to the mycotoxin.
A delicious riddle: The koji mold Aspergillus oryzae is used for the production of Asian delicacies like soy sauce and sake. The biosynthesis of the toxin aspirochlorine (1) in A. oryzae was elucidated by mutagenesis, in vitro adenylation, and isotope labeling. It was found that its peptide core is not assembled from Phe and Gly, but from two Phe units: one Phe undergoes chlorination and oxygenation whereas the other one is transformed into Gly. |
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A delicious riddle: The koji mold Aspergillus oryzae is used for the production of Asian delicacies like soy sauce and sake. The biosynthesis of the toxin aspirochlorine (1) in A. oryzae was elucidated by mutagenesis, in vitro adenylation, and isotope labeling. It was found that its peptide core is not assembled from Phe and Gly, but from two Phe units: one Phe undergoes chlorination and oxygenation whereas the other one is transformed into Gly.</description><edition>International ed. in English</edition><identifier>ISSN: 1433-7851</identifier><identifier>EISSN: 1521-3773</identifier><identifier>DOI: 10.1002/anie.201407624</identifier><identifier>PMID: 25302411</identifier><identifier>CODEN: ACIEAY</identifier><language>eng</language><publisher>Weinheim: WILEY-VCH Verlag</publisher><subject>Amino acids ; Aspergillus oryzae ; Aspergillus oryzae - chemistry ; Aspergillus oryzae - enzymology ; Aspergillus oryzae - genetics ; Aspergillus oryzae - metabolism ; Biosynthesis ; Biosynthetic Pathways ; CC cleavage ; epidithiodiketopiperazine ; Food Microbiology ; Genetic Loci ; halogenases ; Halogenation ; Koji ; Marking ; Molds ; Mycotoxins ; Mycotoxins - chemistry ; Mycotoxins - genetics ; Mycotoxins - metabolism ; Peptide Synthases - chemistry ; Peptide Synthases - genetics ; Peptide Synthases - metabolism ; Peptides ; Spiro Compounds - chemistry ; Spiro Compounds - metabolism ; Toxins</subject><ispartof>Angewandte Chemie International Edition, 2014-12, Vol.53 (49), p.13409-13413</ispartof><rights>2014 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim</rights><rights>2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.</rights><rights>2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5474-54898455845ecefc6c858fa2a389d619cd020a25069ee85177bcef308b7a0dad3</citedby><cites>FETCH-LOGICAL-c5474-54898455845ecefc6c858fa2a389d619cd020a25069ee85177bcef308b7a0dad3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25302411$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chankhamjon, Pranatchareeya</creatorcontrib><creatorcontrib>Boettger-Schmidt, Daniela</creatorcontrib><creatorcontrib>Scherlach, Kirstin</creatorcontrib><creatorcontrib>Urbansky, Barbara</creatorcontrib><creatorcontrib>Lackner, Gerald</creatorcontrib><creatorcontrib>Kalb, Daniel</creatorcontrib><creatorcontrib>Dahse, Hans-Martin</creatorcontrib><creatorcontrib>Hoffmeister, Dirk</creatorcontrib><creatorcontrib>Hertweck, Christian</creatorcontrib><title>Biosynthesis of the Halogenated Mycotoxin Aspirochlorine in Koji Mold Involves a Cryptic Amino Acid Conversion</title><title>Angewandte Chemie International Edition</title><addtitle>Angew. Chem. Int. Ed</addtitle><description>Aspirochlorine (1) is an epidithiodiketopiperazine (ETP) toxin produced from koji mold (Aspergillus oryzae), which has been used in the oriental cuisine for over two millennia. Considering its potential risk for food safety, we have elucidated the molecular basis of aspirochlorine biosynthesis. By a combination of genetic and chemical analyses we found the acl gene locus and identified the key role of AclH as a chlorinase. Stable isotope labeling, biotransformation, and mutational experiments, analysis of intermediates and an in vitro adenylation domain assay gave totally unexpected insights into the acl pathway: Instead of one Phe and one Gly, two Phe units are assembled by an iterative non‐ribosomal peptide synthetase (NRPS, AclP), followed by halogenation and an unprecedented Phe to Gly amino acid conversion. Biological assays showed that both amino acid transformations are required to confer cytotoxicity and antifungal activity to the mycotoxin.
A delicious riddle: The koji mold Aspergillus oryzae is used for the production of Asian delicacies like soy sauce and sake. The biosynthesis of the toxin aspirochlorine (1) in A. oryzae was elucidated by mutagenesis, in vitro adenylation, and isotope labeling. It was found that its peptide core is not assembled from Phe and Gly, but from two Phe units: one Phe undergoes chlorination and oxygenation whereas the other one is transformed into Gly.</description><subject>Amino acids</subject><subject>Aspergillus oryzae</subject><subject>Aspergillus oryzae - chemistry</subject><subject>Aspergillus oryzae - enzymology</subject><subject>Aspergillus oryzae - genetics</subject><subject>Aspergillus oryzae - metabolism</subject><subject>Biosynthesis</subject><subject>Biosynthetic Pathways</subject><subject>CC cleavage</subject><subject>epidithiodiketopiperazine</subject><subject>Food Microbiology</subject><subject>Genetic Loci</subject><subject>halogenases</subject><subject>Halogenation</subject><subject>Koji</subject><subject>Marking</subject><subject>Molds</subject><subject>Mycotoxins</subject><subject>Mycotoxins - chemistry</subject><subject>Mycotoxins - genetics</subject><subject>Mycotoxins - metabolism</subject><subject>Peptide Synthases - chemistry</subject><subject>Peptide Synthases - genetics</subject><subject>Peptide Synthases - metabolism</subject><subject>Peptides</subject><subject>Spiro Compounds - chemistry</subject><subject>Spiro Compounds - metabolism</subject><subject>Toxins</subject><issn>1433-7851</issn><issn>1521-3773</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNqFkcuP0zAQxiMEYh9w5YgsceGS4kf8yDFES7eiWwQCcbRcZ8K6pHax07L979elS4W47GE0I-v3fdbMVxSvCJ4QjOk74x1MKCYVloJWT4pzwikpmZTsaZ4rxkqpODkrLlJaZV4pLJ4XZ5QzTCtCzgv_3oW09-MtJJdQ6FGe0LUZwg_wZoQO3extGMOd86hJGxeDvR1CdB5QfvkYVg7dhKFDM78Lww4SMqiN-83oLGrWzgfUWNehNvgdxOSCf1E8682Q4OVDvyy-fbj62l6X80_TWdvMS8srWZW8UrWqOM8FFnorrOKqN9QwVXeC1LbDFBvKsagB8n5SLjPGsFpKgzvTscvi7dF3E8OvLaRRr12yMAzGQ9gmTSQ-nE_W1eOoyFdThCqc0Tf_oauwjT4v8ofKMQghMjU5UjaGlCL0ehPd2sS9JlgfftWH0PQptCx4_WC7Xa6hO-F_U8pAfQR-uwH2j9jpZjG7-te8PGpdGuHupDXxpxaSSa6_L6b6y5xO28-i1Qt2Dyo9scs</recordid><startdate>20141201</startdate><enddate>20141201</enddate><creator>Chankhamjon, Pranatchareeya</creator><creator>Boettger-Schmidt, Daniela</creator><creator>Scherlach, Kirstin</creator><creator>Urbansky, Barbara</creator><creator>Lackner, Gerald</creator><creator>Kalb, Daniel</creator><creator>Dahse, Hans-Martin</creator><creator>Hoffmeister, Dirk</creator><creator>Hertweck, Christian</creator><general>WILEY-VCH Verlag</general><general>WILEY‐VCH Verlag</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TM</scope><scope>K9.</scope><scope>7X8</scope><scope>7SR</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope></search><sort><creationdate>20141201</creationdate><title>Biosynthesis of the Halogenated Mycotoxin Aspirochlorine in Koji Mold Involves a Cryptic Amino Acid Conversion</title><author>Chankhamjon, Pranatchareeya ; 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Chem. Int. Ed</addtitle><date>2014-12-01</date><risdate>2014</risdate><volume>53</volume><issue>49</issue><spage>13409</spage><epage>13413</epage><pages>13409-13413</pages><issn>1433-7851</issn><eissn>1521-3773</eissn><coden>ACIEAY</coden><abstract>Aspirochlorine (1) is an epidithiodiketopiperazine (ETP) toxin produced from koji mold (Aspergillus oryzae), which has been used in the oriental cuisine for over two millennia. Considering its potential risk for food safety, we have elucidated the molecular basis of aspirochlorine biosynthesis. By a combination of genetic and chemical analyses we found the acl gene locus and identified the key role of AclH as a chlorinase. Stable isotope labeling, biotransformation, and mutational experiments, analysis of intermediates and an in vitro adenylation domain assay gave totally unexpected insights into the acl pathway: Instead of one Phe and one Gly, two Phe units are assembled by an iterative non‐ribosomal peptide synthetase (NRPS, AclP), followed by halogenation and an unprecedented Phe to Gly amino acid conversion. Biological assays showed that both amino acid transformations are required to confer cytotoxicity and antifungal activity to the mycotoxin.
A delicious riddle: The koji mold Aspergillus oryzae is used for the production of Asian delicacies like soy sauce and sake. The biosynthesis of the toxin aspirochlorine (1) in A. oryzae was elucidated by mutagenesis, in vitro adenylation, and isotope labeling. It was found that its peptide core is not assembled from Phe and Gly, but from two Phe units: one Phe undergoes chlorination and oxygenation whereas the other one is transformed into Gly.</abstract><cop>Weinheim</cop><pub>WILEY-VCH Verlag</pub><pmid>25302411</pmid><doi>10.1002/anie.201407624</doi><tpages>5</tpages><edition>International ed. in English</edition></addata></record> |
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subjects | Amino acids Aspergillus oryzae Aspergillus oryzae - chemistry Aspergillus oryzae - enzymology Aspergillus oryzae - genetics Aspergillus oryzae - metabolism Biosynthesis Biosynthetic Pathways CC cleavage epidithiodiketopiperazine Food Microbiology Genetic Loci halogenases Halogenation Koji Marking Molds Mycotoxins Mycotoxins - chemistry Mycotoxins - genetics Mycotoxins - metabolism Peptide Synthases - chemistry Peptide Synthases - genetics Peptide Synthases - metabolism Peptides Spiro Compounds - chemistry Spiro Compounds - metabolism Toxins |
title | Biosynthesis of the Halogenated Mycotoxin Aspirochlorine in Koji Mold Involves a Cryptic Amino Acid Conversion |
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