Literature DB >> 23418022

Synthesis of heterocyclic terpenoids by promiscuous squalene-hopene cyclases.

Miriam Seitz1, Per-Olof Syrén, Lisa Steiner, Janosch Klebensberger, Bettina M Nestl, Bernhard Hauer.   

Abstract

PROMISCUOUS ENZYMES: The substrate promiscuity of squalene-hopene cyclases has been explored and applied in the enzyme-catalyzed synthesis of heterocyclic terpenoids. Features of this work include cyclization reactions without pyrophosphate activation, and stereospecific ring closure of substrates of varying chain length and terminal nucleophile. This provides a biocatalytic alternative to traditional chemical catalysts.
Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

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Year:  2013        PMID: 23418022     DOI: 10.1002/cbic.201300018

Source DB:  PubMed          Journal:  Chembiochem        ISSN: 1439-4227            Impact factor:   3.164


  8 in total

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8.  Enantioselective Enzyme-Catalyzed Aziridination Enabled by Active-Site Evolution of a Cytochrome P450.

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  8 in total

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