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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...
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Published in: | Applied and environmental microbiology 2016-02, Vol.82 (4), p.1196-1204 |
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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. |
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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. 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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 |
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