Reductase of Mutanobactin Synthetase Triggers Sequential C-C Macrocyclization, C-S Bond Formation, and C-C Bond Cleavage

被引:8
|
作者
Wang, Min [1 ,2 ,3 ]
Xie, Zhoujie [1 ]
Tang, Shoubin [3 ]
Chang, Ee Ling [3 ]
Tang, Yue [1 ,2 ,3 ]
Guo, Zhengyan [2 ]
Cui, Yinglu [1 ]
Wu, Bian [1 ,2 ]
Ye, Tao [3 ]
Chen, Yihua [1 ,2 ]
机构
[1] Chinese Acad Sci, Inst Microbiol, Beijing, Peoples R China
[2] Univ Chinese Acad Sci, Beijing, Peoples R China
[3] Tsinghua Univ, Shenzhen Int Grad Sch, Peking Univ, Shenzhen Grad Sch, Shenzhen, Peoples R China
关键词
BIOSYNTHESIS; POLYKETIDE; CYCLIZATION; INHIBITORS; MECHANISM;
D O I
10.1021/acs.orglett.9b04501
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Mutanobactins (MUBs) and their congeners that contain a macrocycle and/or a thiazepane ring are lipopeptides from Streptococcus mutans, a major causative agent of dental caries. Here we show that the C-terminal reductase domain of MubD releases the lipohexapeptide intermediates in an aldehyde form, which enables a spontaneous C-C macrocyclization. In the presence of a thiol group, the macrocyclized MUBs can further undergo spontaneous C-S bond formation and C-C bond cleavage to generate diverse MUB congeners.
引用
收藏
页码:960 / 964
页数:5
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