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Synthesis of Heterocyclic Terpenoids by Promiscuous Squalene-Hopene Cyclases
Univ Stuttgart, Inst Tech Biochem, Allmandring 31, D-70569 Stuttgart, Germany..
Univ Stuttgart, Inst Tech Biochem, Allmandring 31, D-70569 Stuttgart, Germany..ORCID-id: 0000-0002-4066-2776
Univ Stuttgart, Inst Tech Biochem, Allmandring 31, D-70569 Stuttgart, Germany..
Univ Stuttgart, Inst Tech Biochem, Allmandring 31, D-70569 Stuttgart, Germany..
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2013 (engelsk)Inngår i: ChemBioChem (Print), ISSN 1439-4227, E-ISSN 1439-7633, Vol. 14, nr Copyright (C) 2013 American Chemical Society (ACS). All Rights Reserved., s. 436-439Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

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.

sted, utgiver, år, opplag, sider
Wiley-VCH Verlag GmbH & Co. KGaA , 2013. Vol. 14, nr Copyright (C) 2013 American Chemical Society (ACS). All Rights Reserved., s. 436-439
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URN: urn:nbn:se:kth:diva-185567DOI: 10.1002/cbic.201300018ISI: 000315492200005PubMedID: 23418022Scopus ID: 2-s2.0-84874382156OAI: oai:DiVA.org:kth-185567DiVA, id: diva2:922319
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QC 20160422. QC 20200414

Tilgjengelig fra: 2016-04-22 Laget: 2016-04-22 Sist oppdatert: 2020-04-14bibliografisk kontrollert

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Syrén, Per-Olof

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