Enzymatic formation of an unnatural methylated triketide by plant type III polyketide synthases

被引:15
|
作者
Abe, Tsuyoshi
Noma, Hisashi
Noguchi, Hiroshi
Abe, Ikuro
机构
[1] Univ Shizuoka, Sch Pharmaceut Sci, Shizuoka 4228526, Japan
[2] Univ Shizuoka, 21st Century COE Program, Shizuoka 4228526, Japan
[3] Japan Sci & Technl Agcy, PRESTO, Kawaguchi, Saitama 3320012, Japan
基金
日本科学技术振兴机构;
关键词
type III polyketide synthase; chalcone synthase; octaketide synthase; benzalacetone synthase; methylated triketide pyrone; CHALCONE SYNTHASE; SUBSTRATE-SPECIFICITY; ENGINEERED BIOSYNTHESIS; BENZALACETONE SYNTHASE; STILBENE SYNTHASE; MECHANISM; STARTER; SITE; COA;
D O I
10.1016/j.tetlet.2006.10.012
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Octaketide synthase, a novel plant-specific type III polyketide synthase from Aloe arborescens, efficiently accepted (2RS)-methylmalonyl-CoA as a sole substrate to produce 6-ethyl-4-hydroxy-3,5-dimethyl-2-pyrone. On the other hand, a tetraketide-producing chalcone synthase from Scutellaria baicalensis and a diketide-producing benzalacetone synthase from Rheum palmatum also yielded the unnatural methylated C-9 triketide pyrone as a single product by sequential decarboxylative condensations of three molecules of (2RS)-methylmalonyl-CoA. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:8727 / 8730
页数:4
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