Loading…

A Fivefold Parallelized Biosynthetic Process Secures Chlorination of Armillaria mellea (Honey Mushroom) Toxins

The basidiomycetous tree pathogen Armillaria mellea (honey mushroom) produces a large variety of structurally related antibiotically active and phytotoxic natural products, referred to as the melleolides. During their biosynthesis, some members of the melleolide family of compounds undergo monochlor...

Full description

Saved in:
Bibliographic Details
Published in:Applied and environmental microbiology 2016-02, Vol.82 (4), p.1196-1204
Main Authors: Wick, Jonas, Heine, Daniel, Lackner, Gerald, Misiek, Mathias, Tauber, James, Jagusch, Hans, Hertweck, Christian, Hoffmeister, Dirk
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-c511t-1436851b7823363aa439b4fde66c3b76cf23446fc13e7b8a6cdd19f3f34c5a273
cites cdi_FETCH-LOGICAL-c511t-1436851b7823363aa439b4fde66c3b76cf23446fc13e7b8a6cdd19f3f34c5a273
container_end_page 1204
container_issue 4
container_start_page 1196
container_title Applied and environmental microbiology
container_volume 82
creator Wick, Jonas
Heine, Daniel
Lackner, Gerald
Misiek, Mathias
Tauber, James
Jagusch, Hans
Hertweck, Christian
Hoffmeister, Dirk
description The basidiomycetous tree pathogen Armillaria mellea (honey mushroom) produces a large variety of structurally related antibiotically active and phytotoxic natural products, referred to as the melleolides. During their biosynthesis, some members of the melleolide family of compounds undergo monochlorination of the aromatic moiety, whose biochemical and genetic basis was not known previously. This first study on basidiomycete halogenases presents the biochemical in vitro characterization of five flavin-dependent A. mellea enzymes (ArmH1 to ArmH5) that were heterologously produced in Escherichia coli. We demonstrate that all five enzymes transfer a single chlorine atom to the melleolide backbone. A 5-fold, secured biosynthetic step during natural product assembly is unprecedented. Typically, flavin-dependent halogenases are categorized into enzymes acting on free compounds as opposed to those requiring a carrier-protein-bound acceptor substrate. The enzymes characterized in this study clearly turned over free substrates. Phylogenetic clades of halogenases suggest that all fungal enzymes share an ancestor and reflect a clear divergence between ascomycetes and basidiomycetes.
doi_str_mv 10.1128/AEM.03168-15
format article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4751827</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1762965824</sourcerecordid><originalsourceid>FETCH-LOGICAL-c511t-1436851b7823363aa439b4fde66c3b76cf23446fc13e7b8a6cdd19f3f34c5a273</originalsourceid><addsrcrecordid>eNqNkU1rFTEUhoMo9lrduZaAmwpOzfdkNsL10lqhxYJ1HTKZE2_KTFKTmeL115t-WNSVq7M4Dw_nPS9CLyk5pJTpd-ujs0PCqdINlY_QipJON5Jz9RitCOm6hjFB9tCzUi4JIYIo_RTtMaWkbBVbobjGx-EafBoHfG6zHUcYw08Y8IeQyi7OW5iDw-c5OSgFfwG3ZCh4sx1TDtHOIUWcPF7nKYyjzcHiCarC4oOTFGGHz5ayzSlNb_BF-hFieY6eeDsWeHE_99HX46OLzUlz-vnjp836tHGS0rmhgistad9qVpNwawXveuEHUMrxvlXOMy6E8o5yaHttlRsG2nnuuXDSspbvo_d33quln2BwEOeazVzlMNm8M8kG8_cmhq35lq6NaCXVt4KDe0FO3xcos5lCcTWbjZCWYmhbD9SaSfU_KOuU1ExU9PU_6GVacqyfuKGUJkoIUqm3d5TLqZQM_uFuSsxN56Z2bm47N1RW_NWfWR_g3yXzXyblp6Q</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1766806440</pqid></control><display><type>article</type><title>A Fivefold Parallelized Biosynthetic Process Secures Chlorination of Armillaria mellea (Honey Mushroom) Toxins</title><source>American Society for Microbiology</source><source>PubMed Central</source><creator>Wick, Jonas ; Heine, Daniel ; Lackner, Gerald ; Misiek, Mathias ; Tauber, James ; Jagusch, Hans ; Hertweck, Christian ; Hoffmeister, Dirk</creator><contributor>Cullen, D.</contributor><creatorcontrib>Wick, Jonas ; Heine, Daniel ; Lackner, Gerald ; Misiek, Mathias ; Tauber, James ; Jagusch, Hans ; Hertweck, Christian ; Hoffmeister, Dirk ; Cullen, D.</creatorcontrib><description>The basidiomycetous tree pathogen Armillaria mellea (honey mushroom) produces a large variety of structurally related antibiotically active and phytotoxic natural products, referred to as the melleolides. During their biosynthesis, some members of the melleolide family of compounds undergo monochlorination of the aromatic moiety, whose biochemical and genetic basis was not known previously. This first study on basidiomycete halogenases presents the biochemical in vitro characterization of five flavin-dependent A. mellea enzymes (ArmH1 to ArmH5) that were heterologously produced in Escherichia coli. We demonstrate that all five enzymes transfer a single chlorine atom to the melleolide backbone. A 5-fold, secured biosynthetic step during natural product assembly is unprecedented. Typically, flavin-dependent halogenases are categorized into enzymes acting on free compounds as opposed to those requiring a carrier-protein-bound acceptor substrate. The enzymes characterized in this study clearly turned over free substrates. Phylogenetic clades of halogenases suggest that all fungal enzymes share an ancestor and reflect a clear divergence between ascomycetes and basidiomycetes.</description><identifier>ISSN: 0099-2240</identifier><identifier>EISSN: 1098-5336</identifier><identifier>DOI: 10.1128/AEM.03168-15</identifier><identifier>PMID: 26655762</identifier><identifier>CODEN: AEMIDF</identifier><language>eng</language><publisher>United States: American Society for Microbiology</publisher><subject>Armillaria - enzymology ; Armillaria - genetics ; Armillaria - metabolism ; Armillaria mellea ; Ascomycetes ; Basidiomycetes ; Biosynthesis ; Chlorine ; E coli ; Enzymes ; Enzymology and Protein Engineering ; Escherichia coli ; Escherichia coli - genetics ; Escherichia coli - metabolism ; Gene Expression ; Halogenation ; Mushrooms ; Mycotoxins - metabolism ; Oxidoreductases - genetics ; Oxidoreductases - metabolism ; Phylogenetics ; Sesquiterpenes - metabolism</subject><ispartof>Applied and environmental microbiology, 2016-02, Vol.82 (4), p.1196-1204</ispartof><rights>Copyright © 2016, American Society for Microbiology. All Rights Reserved.</rights><rights>Copyright American Society for Microbiology Feb 2016</rights><rights>Copyright © 2016, American Society for Microbiology. All Rights Reserved. 2016 American Society for Microbiology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c511t-1436851b7823363aa439b4fde66c3b76cf23446fc13e7b8a6cdd19f3f34c5a273</citedby><cites>FETCH-LOGICAL-c511t-1436851b7823363aa439b4fde66c3b76cf23446fc13e7b8a6cdd19f3f34c5a273</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4751827/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4751827/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,3186,27923,27924,53790,53792</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26655762$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Cullen, D.</contributor><creatorcontrib>Wick, Jonas</creatorcontrib><creatorcontrib>Heine, Daniel</creatorcontrib><creatorcontrib>Lackner, Gerald</creatorcontrib><creatorcontrib>Misiek, Mathias</creatorcontrib><creatorcontrib>Tauber, James</creatorcontrib><creatorcontrib>Jagusch, Hans</creatorcontrib><creatorcontrib>Hertweck, Christian</creatorcontrib><creatorcontrib>Hoffmeister, Dirk</creatorcontrib><title>A Fivefold Parallelized Biosynthetic Process Secures Chlorination of Armillaria mellea (Honey Mushroom) Toxins</title><title>Applied and environmental microbiology</title><addtitle>Appl Environ Microbiol</addtitle><description>The basidiomycetous tree pathogen Armillaria mellea (honey mushroom) produces a large variety of structurally related antibiotically active and phytotoxic natural products, referred to as the melleolides. During their biosynthesis, some members of the melleolide family of compounds undergo monochlorination of the aromatic moiety, whose biochemical and genetic basis was not known previously. This first study on basidiomycete halogenases presents the biochemical in vitro characterization of five flavin-dependent A. mellea enzymes (ArmH1 to ArmH5) that were heterologously produced in Escherichia coli. We demonstrate that all five enzymes transfer a single chlorine atom to the melleolide backbone. A 5-fold, secured biosynthetic step during natural product assembly is unprecedented. Typically, flavin-dependent halogenases are categorized into enzymes acting on free compounds as opposed to those requiring a carrier-protein-bound acceptor substrate. The enzymes characterized in this study clearly turned over free substrates. Phylogenetic clades of halogenases suggest that all fungal enzymes share an ancestor and reflect a clear divergence between ascomycetes and basidiomycetes.</description><subject>Armillaria - enzymology</subject><subject>Armillaria - genetics</subject><subject>Armillaria - metabolism</subject><subject>Armillaria mellea</subject><subject>Ascomycetes</subject><subject>Basidiomycetes</subject><subject>Biosynthesis</subject><subject>Chlorine</subject><subject>E coli</subject><subject>Enzymes</subject><subject>Enzymology and Protein Engineering</subject><subject>Escherichia coli</subject><subject>Escherichia coli - genetics</subject><subject>Escherichia coli - metabolism</subject><subject>Gene Expression</subject><subject>Halogenation</subject><subject>Mushrooms</subject><subject>Mycotoxins - metabolism</subject><subject>Oxidoreductases - genetics</subject><subject>Oxidoreductases - metabolism</subject><subject>Phylogenetics</subject><subject>Sesquiterpenes - metabolism</subject><issn>0099-2240</issn><issn>1098-5336</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNqNkU1rFTEUhoMo9lrduZaAmwpOzfdkNsL10lqhxYJ1HTKZE2_KTFKTmeL115t-WNSVq7M4Dw_nPS9CLyk5pJTpd-ujs0PCqdINlY_QipJON5Jz9RitCOm6hjFB9tCzUi4JIYIo_RTtMaWkbBVbobjGx-EafBoHfG6zHUcYw08Y8IeQyi7OW5iDw-c5OSgFfwG3ZCh4sx1TDtHOIUWcPF7nKYyjzcHiCarC4oOTFGGHz5ayzSlNb_BF-hFieY6eeDsWeHE_99HX46OLzUlz-vnjp836tHGS0rmhgistad9qVpNwawXveuEHUMrxvlXOMy6E8o5yaHttlRsG2nnuuXDSspbvo_d33quln2BwEOeazVzlMNm8M8kG8_cmhq35lq6NaCXVt4KDe0FO3xcos5lCcTWbjZCWYmhbD9SaSfU_KOuU1ExU9PU_6GVacqyfuKGUJkoIUqm3d5TLqZQM_uFuSsxN56Z2bm47N1RW_NWfWR_g3yXzXyblp6Q</recordid><startdate>20160215</startdate><enddate>20160215</enddate><creator>Wick, Jonas</creator><creator>Heine, Daniel</creator><creator>Lackner, Gerald</creator><creator>Misiek, Mathias</creator><creator>Tauber, James</creator><creator>Jagusch, Hans</creator><creator>Hertweck, Christian</creator><creator>Hoffmeister, Dirk</creator><general>American Society for Microbiology</general><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>7QL</scope><scope>7QO</scope><scope>7SN</scope><scope>7SS</scope><scope>7ST</scope><scope>7T7</scope><scope>7TM</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>SOI</scope><scope>7X8</scope><scope>7U7</scope><scope>5PM</scope></search><sort><creationdate>20160215</creationdate><title>A Fivefold Parallelized Biosynthetic Process Secures Chlorination of Armillaria mellea (Honey Mushroom) Toxins</title><author>Wick, Jonas ; Heine, Daniel ; Lackner, Gerald ; Misiek, Mathias ; Tauber, James ; Jagusch, Hans ; Hertweck, Christian ; Hoffmeister, Dirk</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c511t-1436851b7823363aa439b4fde66c3b76cf23446fc13e7b8a6cdd19f3f34c5a273</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Armillaria - enzymology</topic><topic>Armillaria - genetics</topic><topic>Armillaria - metabolism</topic><topic>Armillaria mellea</topic><topic>Ascomycetes</topic><topic>Basidiomycetes</topic><topic>Biosynthesis</topic><topic>Chlorine</topic><topic>E coli</topic><topic>Enzymes</topic><topic>Enzymology and Protein Engineering</topic><topic>Escherichia coli</topic><topic>Escherichia coli - genetics</topic><topic>Escherichia coli - metabolism</topic><topic>Gene Expression</topic><topic>Halogenation</topic><topic>Mushrooms</topic><topic>Mycotoxins - metabolism</topic><topic>Oxidoreductases - genetics</topic><topic>Oxidoreductases - metabolism</topic><topic>Phylogenetics</topic><topic>Sesquiterpenes - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wick, Jonas</creatorcontrib><creatorcontrib>Heine, Daniel</creatorcontrib><creatorcontrib>Lackner, Gerald</creatorcontrib><creatorcontrib>Misiek, Mathias</creatorcontrib><creatorcontrib>Tauber, James</creatorcontrib><creatorcontrib>Jagusch, Hans</creatorcontrib><creatorcontrib>Hertweck, Christian</creatorcontrib><creatorcontrib>Hoffmeister, Dirk</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Environment Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>Environment Abstracts</collection><collection>MEDLINE - Academic</collection><collection>Toxicology Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Applied and environmental microbiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wick, Jonas</au><au>Heine, Daniel</au><au>Lackner, Gerald</au><au>Misiek, Mathias</au><au>Tauber, James</au><au>Jagusch, Hans</au><au>Hertweck, Christian</au><au>Hoffmeister, Dirk</au><au>Cullen, D.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A Fivefold Parallelized Biosynthetic Process Secures Chlorination of Armillaria mellea (Honey Mushroom) Toxins</atitle><jtitle>Applied and environmental microbiology</jtitle><addtitle>Appl Environ Microbiol</addtitle><date>2016-02-15</date><risdate>2016</risdate><volume>82</volume><issue>4</issue><spage>1196</spage><epage>1204</epage><pages>1196-1204</pages><issn>0099-2240</issn><eissn>1098-5336</eissn><coden>AEMIDF</coden><abstract>The basidiomycetous tree pathogen Armillaria mellea (honey mushroom) produces a large variety of structurally related antibiotically active and phytotoxic natural products, referred to as the melleolides. During their biosynthesis, some members of the melleolide family of compounds undergo monochlorination of the aromatic moiety, whose biochemical and genetic basis was not known previously. This first study on basidiomycete halogenases presents the biochemical in vitro characterization of five flavin-dependent A. mellea enzymes (ArmH1 to ArmH5) that were heterologously produced in Escherichia coli. We demonstrate that all five enzymes transfer a single chlorine atom to the melleolide backbone. A 5-fold, secured biosynthetic step during natural product assembly is unprecedented. Typically, flavin-dependent halogenases are categorized into enzymes acting on free compounds as opposed to those requiring a carrier-protein-bound acceptor substrate. The enzymes characterized in this study clearly turned over free substrates. Phylogenetic clades of halogenases suggest that all fungal enzymes share an ancestor and reflect a clear divergence between ascomycetes and basidiomycetes.</abstract><cop>United States</cop><pub>American Society for Microbiology</pub><pmid>26655762</pmid><doi>10.1128/AEM.03168-15</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0099-2240
ispartof Applied and environmental microbiology, 2016-02, Vol.82 (4), p.1196-1204
issn 0099-2240
1098-5336
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4751827
source American Society for Microbiology; PubMed Central
subjects Armillaria - enzymology
Armillaria - genetics
Armillaria - metabolism
Armillaria mellea
Ascomycetes
Basidiomycetes
Biosynthesis
Chlorine
E coli
Enzymes
Enzymology and Protein Engineering
Escherichia coli
Escherichia coli - genetics
Escherichia coli - metabolism
Gene Expression
Halogenation
Mushrooms
Mycotoxins - metabolism
Oxidoreductases - genetics
Oxidoreductases - metabolism
Phylogenetics
Sesquiterpenes - metabolism
title A Fivefold Parallelized Biosynthetic Process Secures Chlorination of Armillaria mellea (Honey Mushroom) Toxins
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-12T01%3A38%3A01IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=A%20Fivefold%20Parallelized%20Biosynthetic%20Process%20Secures%20Chlorination%20of%20Armillaria%20mellea%20(Honey%20Mushroom)%20Toxins&rft.jtitle=Applied%20and%20environmental%20microbiology&rft.au=Wick,%20Jonas&rft.date=2016-02-15&rft.volume=82&rft.issue=4&rft.spage=1196&rft.epage=1204&rft.pages=1196-1204&rft.issn=0099-2240&rft.eissn=1098-5336&rft.coden=AEMIDF&rft_id=info:doi/10.1128/AEM.03168-15&rft_dat=%3Cproquest_pubme%3E1762965824%3C/proquest_pubme%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c511t-1436851b7823363aa439b4fde66c3b76cf23446fc13e7b8a6cdd19f3f34c5a273%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1766806440&rft_id=info:pmid/26655762&rfr_iscdi=true