Enzymatic formation of an aromatic dodecaketide by engineered plant polyketide synthase

被引:18
作者
Wanibuchi, Kiyofumi [1 ,2 ,3 ]
Morita, Hiroyuki [1 ]
Noguchi, Hiroshi [2 ,3 ]
Abe, Ikuro [1 ]
机构
[1] Univ Tokyo, Grad Sch Pharmaceut Sci, Bunkyo Ku, Tokyo 1130033, Japan
[2] Univ Shizuoka, Sch Pharmaceut Sci, Shizuoka 4228526, Japan
[3] Global COE Program, Shizuoka 4228526, Japan
关键词
Octaketide synthase; Pentaketide chromone synthase; Chalcone synthase; Polyketide synthase; CHAIN-LENGTH CONTROL; PENTAKETIDE CHROMONE; BIOSYNTHESIS; SPECIFICITY; CHALCONE;
D O I
10.1016/j.bmcl.2011.01.135
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Octaketide synthase (OKS) from Aloe arborescens is a plant-specific type III polyketide synthase (PKS) that catalyzes iterative condensations of eight molecules of malonyl-CoA to produce the C-16 aromatic octaketides SEK4 and SEK4b. On the basis of the crystal structures of OKS, the F66L/N222G double mutant was constructed and shown to produce an unnatural dodecaketide TW95a by sequential condensations of 12 molecules of malonyl-CoA. The C-24 naphthophenone TW95a is a product of the minimal type II PKS (whiE from Streptomyces coelicolor), and is structurally related to the C-20 decaketide benzophenone SEK15, the product of the OKS N222G point mutant. The C-24 dodecaketide naphthophenone TW95a is the first and the longest polyketide scaffold generated by a structurally simple type III PKS. A homology model predicted that the active-site cavity volume of the F66L/N222G mutant is increasedo 748 angstrom(3), from 652 angstrom(3) of the wild-type OKS. The structure-based engine tering thus greatly expanded the catalytic repertoire of the simple type III PKS to further produce larger and more complex polyketide molecules. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2083 / 2086
页数:4
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