Literature DB >> 25994388

Twofold polyketide branching by a stereoselective enzymatic Michael addition.

Daniel Heine1, Srividhya Sundaram, Tom Bretschneider, Christian Hertweck.   

Abstract

The versatility of the branching module of the rhizoxin polyketide synthase was tested in an in vitro enzyme assay with a polyketide mimic and branched (di)methylmalonyl-CoA extender units. Comparison of the products with synthetic reference compounds revealed that the module is able to stereoselectively introduce two branches in one step by a Michael addition-lactonisation sequence, thus expanding the scope of previously studied PKS systems.

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Year:  2015        PMID: 25994388     DOI: 10.1039/c5cc03085d

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  3 in total

1.  Polyketide synthase chimeras reveal key role of ketosynthase domain in chain branching.

Authors:  Srividhya Sundaram; Daniel Heine; Christian Hertweck
Journal:  Nat Chem Biol       Date:  2015-10-19       Impact factor: 15.040

Review 2.  Biosynthesis of oxygen and nitrogen-containing heterocycles in polyketides.

Authors:  Franziska Hemmerling; Frank Hahn
Journal:  Beilstein J Org Chem       Date:  2016-07-20       Impact factor: 2.883

3.  A widespread bacterial phenazine forms S-conjugates with biogenic thiols and crosslinks proteins.

Authors:  D Heine; S Sundaram; Matthias Beudert; K Martin; C Hertweck
Journal:  Chem Sci       Date:  2016-04-14       Impact factor: 9.825

  3 in total

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