Mutated variants of squalene-hopene cyclase: enzymatic syntheses of triterpenes bearing oxygen-bridged monocycles and a new 6,6,6,6,6-fusded pentacyclic scaffold, named neogammacerane, from 2,3-oxidosqualene
Author:
Affiliation:
1. Graduate School of Science and Technology and Department of Applied Biological Chemistry
2. Faculty of Agriculture
3. Niigata University
4. Niigata 950-2181
5. Japan
Abstract
First enzymatic syntheses of triterpenes bearing a 7-oxabicyclo[2.2.1]heptane moiety and a novel scaffold, named neogammacerane, by the mutated cyclases.
Funder
Japan Society for the Promotion of Science
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2018/OB/C8OB02009D
Reference57 articles.
1. Zur Kenntnis der Triterpene. 190. Mitteilung. Eine stereochemische Interpretation der biogenetischen Isoprenregel bei den Triterpenen
2. Enzyme Mechanisms for Polycyclic Triterpene Formation
3. Squalene–hopene cyclase: catalytic mechanism and substrate recognition
4. A Case Study in Biomimetic Total Synthesis: Polyolefin Carbocyclizations to Terpenes and Steroids
5. Mutagenesis approaches to deduce structure–function relationships in terpene synthases
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