Loading…

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...

Full description

Saved in:
Bibliographic Details
Published in:Angewandte Chemie International Edition 2014-12, Vol.53 (49), p.13409-13413
Main Authors: Chankhamjon, Pranatchareeya, Boettger-Schmidt, Daniela, Scherlach, Kirstin, Urbansky, Barbara, Lackner, Gerald, Kalb, Daniel, Dahse, Hans-Martin, Hoffmeister, Dirk, Hertweck, Christian
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c5474-54898455845ecefc6c858fa2a389d619cd020a25069ee85177bcef308b7a0dad3
cites cdi_FETCH-LOGICAL-c5474-54898455845ecefc6c858fa2a389d619cd020a25069ee85177bcef308b7a0dad3
container_end_page 13413
container_issue 49
container_start_page 13409
container_title Angewandte Chemie International Edition
container_volume 53
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.
doi_str_mv 10.1002/anie.201407624
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1701002794</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>3508857451</sourcerecordid><originalsourceid>FETCH-LOGICAL-c5474-54898455845ecefc6c858fa2a389d619cd020a25069ee85177bcef308b7a0dad3</originalsourceid><addsrcrecordid>eNqFkcuP0zAQxiMEYh9w5YgsceGS4kf8yDFES7eiWwQCcbRcZ8K6pHax07L979elS4W47GE0I-v3fdbMVxSvCJ4QjOk74x1MKCYVloJWT4pzwikpmZTsaZ4rxkqpODkrLlJaZV4pLJ4XZ5QzTCtCzgv_3oW09-MtJJdQ6FGe0LUZwg_wZoQO3extGMOd86hJGxeDvR1CdB5QfvkYVg7dhKFDM78Lww4SMqiN-83oLGrWzgfUWNehNvgdxOSCf1E8682Q4OVDvyy-fbj62l6X80_TWdvMS8srWZW8UrWqOM8FFnorrOKqN9QwVXeC1LbDFBvKsagB8n5SLjPGsFpKgzvTscvi7dF3E8OvLaRRr12yMAzGQ9gmTSQ-nE_W1eOoyFdThCqc0Tf_oauwjT4v8ofKMQghMjU5UjaGlCL0ehPd2sS9JlgfftWH0PQptCx4_WC7Xa6hO-F_U8pAfQR-uwH2j9jpZjG7-te8PGpdGuHupDXxpxaSSa6_L6b6y5xO28-i1Qt2Dyo9scs</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1628201666</pqid></control><display><type>article</type><title>Biosynthesis of the Halogenated Mycotoxin Aspirochlorine in Koji Mold Involves a Cryptic Amino Acid Conversion</title><source>Wiley</source><creator>Chankhamjon, Pranatchareeya ; Boettger-Schmidt, Daniela ; Scherlach, Kirstin ; Urbansky, Barbara ; Lackner, Gerald ; Kalb, Daniel ; Dahse, Hans-Martin ; Hoffmeister, Dirk ; Hertweck, Christian</creator><creatorcontrib>Chankhamjon, Pranatchareeya ; Boettger-Schmidt, Daniela ; Scherlach, Kirstin ; Urbansky, Barbara ; Lackner, Gerald ; Kalb, Daniel ; Dahse, Hans-Martin ; Hoffmeister, Dirk ; Hertweck, Christian</creatorcontrib><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><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 ; CC 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 &amp; Co. KGaA, Weinheim</rights><rights>2014 WILEY-VCH Verlag GmbH &amp; Co. KGaA, Weinheim.</rights><rights>2014 WILEY-VCH Verlag GmbH &amp; 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>CC 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 ; Boettger-Schmidt, Daniela ; Scherlach, Kirstin ; Urbansky, Barbara ; Lackner, Gerald ; Kalb, Daniel ; Dahse, Hans-Martin ; Hoffmeister, Dirk ; Hertweck, Christian</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5474-54898455845ecefc6c858fa2a389d619cd020a25069ee85177bcef308b7a0dad3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Amino acids</topic><topic>Aspergillus oryzae</topic><topic>Aspergillus oryzae - chemistry</topic><topic>Aspergillus oryzae - enzymology</topic><topic>Aspergillus oryzae - genetics</topic><topic>Aspergillus oryzae - metabolism</topic><topic>Biosynthesis</topic><topic>Biosynthetic Pathways</topic><topic>CC cleavage</topic><topic>epidithiodiketopiperazine</topic><topic>Food Microbiology</topic><topic>Genetic Loci</topic><topic>halogenases</topic><topic>Halogenation</topic><topic>Koji</topic><topic>Marking</topic><topic>Molds</topic><topic>Mycotoxins</topic><topic>Mycotoxins - chemistry</topic><topic>Mycotoxins - genetics</topic><topic>Mycotoxins - metabolism</topic><topic>Peptide Synthases - chemistry</topic><topic>Peptide Synthases - genetics</topic><topic>Peptide Synthases - metabolism</topic><topic>Peptides</topic><topic>Spiro Compounds - chemistry</topic><topic>Spiro Compounds - metabolism</topic><topic>Toxins</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><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><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Nucleic Acids Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><collection>Engineered Materials Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><jtitle>Angewandte Chemie International Edition</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chankhamjon, Pranatchareeya</au><au>Boettger-Schmidt, Daniela</au><au>Scherlach, Kirstin</au><au>Urbansky, Barbara</au><au>Lackner, Gerald</au><au>Kalb, Daniel</au><au>Dahse, Hans-Martin</au><au>Hoffmeister, Dirk</au><au>Hertweck, Christian</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Biosynthesis of the Halogenated Mycotoxin Aspirochlorine in Koji Mold Involves a Cryptic Amino Acid Conversion</atitle><jtitle>Angewandte Chemie International Edition</jtitle><addtitle>Angew. 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>
fulltext fulltext
identifier ISSN: 1433-7851
ispartof Angewandte Chemie International Edition, 2014-12, Vol.53 (49), p.13409-13413
issn 1433-7851
1521-3773
language eng
recordid cdi_proquest_miscellaneous_1701002794
source Wiley
subjects Amino acids
Aspergillus oryzae
Aspergillus oryzae - chemistry
Aspergillus oryzae - enzymology
Aspergillus oryzae - genetics
Aspergillus oryzae - metabolism
Biosynthesis
Biosynthetic Pathways
CC 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
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-20T20%3A59%3A44IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Biosynthesis%20of%20the%20Halogenated%20Mycotoxin%20Aspirochlorine%20in%20Koji%20Mold%20Involves%20a%20Cryptic%20Amino%20Acid%20Conversion&rft.jtitle=Angewandte%20Chemie%20International%20Edition&rft.au=Chankhamjon,%20Pranatchareeya&rft.date=2014-12-01&rft.volume=53&rft.issue=49&rft.spage=13409&rft.epage=13413&rft.pages=13409-13413&rft.issn=1433-7851&rft.eissn=1521-3773&rft.coden=ACIEAY&rft_id=info:doi/10.1002/anie.201407624&rft_dat=%3Cproquest_cross%3E3508857451%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c5474-54898455845ecefc6c858fa2a389d619cd020a25069ee85177bcef308b7a0dad3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1628201666&rft_id=info:pmid/25302411&rfr_iscdi=true