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Incorporation of nonmethyl branches by isoprenoid-like logic: multiple beta-alkylation events in the biosynthesis of myxovirescin A1.

Incorporation of nonmethyl branches by isoprenoid-like logic: multiple beta-alkylation events in the biosynthesis of myxovirescin A1. Research Abstract Details 

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  • Incorporation of nonmethyl branches by isoprenoid-like logic: multiple beta-alkylation events in the biosynthesis of myxovirescin A1. Abstract Text:

    christopher t calderoneChristopher T Calderone,david f iwigDavid F Iwig,pieter c dorresteinPieter C Dorrestein,neil l kelleherNeil L Kelleher,christopher t walshChristopher T Walsh,christopher t calderoneChristopher T Calderone,david f iwigDavid F Iwig,pieter c dorresteinPieter C Dorrestein,neil l kelleherNeil L Kelleher,christopher t walshChristopher T Walsh,

    Several polyketide secondary metabolites are predicted to undergo isoprenoid-like beta-alkylations during biosynthesis. One such secondary metabolite is myxovirescin A1, produced by Myxococcus xanthus. Myxovirescin is of special interest in that it appears to undergo two distinct beta-alkylations. Additionally, the myxovirescin biosynthetic gene cluster lacks tandem thiolation domains required in the synthesis of other beta-branched secondary metabolites. To probe the origins of the beta-branches in myxovirescin, we heterologously overexpressed the proteins predicted to be responsible for myxovirescin beta-alkylation and reconstituted their activities in vitro on model substrates. Our results confirm that myxovirescin undergoes two isoprenoid-like beta-alkylations during its biosynthesis, including an unprecedented beta-ethylation. The study of its biosynthesis should shed light on the scope and requirements for isoprenoid-like biosynthetic logic in a polyketide context.

    Incorporation of nonmethyl branches by isoprenoid-like logic: multiple beta-alkylation events in the biosynthesis of myxovirescin A1. Publishing Authors By Initials

    ct calderoneCT Calderone,df iwigDF Iwig,pc dorresteinPC Dorrestein,nl kelleherNL Kelleher,ct walshCT Walsh,ct calderoneCT Calderone,df iwigDF Iwig,pc dorresteinPC Dorrestein,nl kelleherNL Kelleher,ct walshCT Walsh,

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    PUBMED ID PMID:

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    Incorporation of nonmethyl branches by isoprenoid-like logic: multiple beta-alkylation events in the biosynthesis of myxovirescin A1. Journal Published:

    PUBLICATION TYPE: Research Support, Non-U.S. Gov

    Journal: Chemistry & biology

    VOLUME: 14

    Page Numbers: 835-46

    Journal Abbreviation: Chem. Biol.

    ISSN: 1074-5521

    DAY: 27

    MONTH: Jul

    YEAR: 2007

    Incorporation of nonmethyl branches by isoprenoid-like logic: multiple beta-alkylation events in the biosynthesis of myxovirescin A1. Information

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    LANGUAGE: eng

    NlmUniqueID: 9500160

    Incorporation of nonmethyl branches by isoprenoid-like logic: multiple beta-alkylation events in the biosynthesis of myxovirescin A1. Keywords Mesh Terms:

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    Grant and Affiliation Information for Incorporation of nonmethyl branches by isoprenoid-like logic: multiple beta-alkylation events in the biosynthesis of myxovirescin A1.

    AFFILIATION: Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, MA 02115, USA.

    Country: England

    England Research PublicationEngland Research Publication

    AGENCY: United States NIGMS

    GRANT: GM081743

    ACRONYM: GM

    MEDLINETA: Chem Biol

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