Characterization of a LanC-free pathway for the formation of an ll-MeLan residue and an alloAviMeCys residue in the newly identified class V lanthipeptide triantimycins

Author:

Ding Weizhong1,Wang Xiaofeng12,Yin Yu3,Tao Jiang4,Xue Yanqing1ORCID,Liu Wen1

Affiliation:

1. State Key Laboratory of Chemical Biology, Shanghai Institute of Organic Chemistry, University of Chinese Academy of Sciences, Chinese Academy of Sciences, 345 Lingling Road, Shanghai 200032, China

2. School of Chemistry and Materials Science, Hangzhou Institute for Advanced Study, University of Chinese Academy of Sciences, 1 Sublane Xiangshan, Hangzhou 310024, China

3. Shanghai Jiao Tong University, Shanghai 200240, China

4. Department of General Dentistry, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, College of Stomatology, Shanghai Jiao Tong University, National Center for Stomatology, National Clinical Research Center for Oral Diseases, Shanghai Key Laboratory of Stomatology, Shanghai Research Institute of Stomatology, Research Unit of Oral and Maxillofacial Regenerative Medicine, Chinese Academy of Medical Science, No. 639 Zhizaoju Road, Shanghai 200011, China

Abstract

The cyclization step of lanthionines is typically catalyzed by a LanC cyclase or a cyclase domain. Here, we report a LanC-free pathway for the formation of an ll-MeLan residue and a stereochemically diverse alloAviMeCys residue in triantimycins.

Funder

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

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