Author
Listed:
- Pengwei Li
(Chinese Academy of Sciences)
- Meng Chen
(Chinese Academy of Sciences
University of Chinese Academy of Sciences)
- Wei Tang
(Chinese Academy of Sciences
University of Chinese Academy of Sciences)
- Zhengyan Guo
(Chinese Academy of Sciences)
- Yuwei Zhang
(Chinese Academy of Sciences
University of Chinese Academy of Sciences)
- Min Wang
(Chinese Academy of Sciences
University of Chinese Academy of Sciences
Wuyi University)
- Geoff P. Horsman
(Wilfrid Laurier University)
- Jin Zhong
(Chinese Academy of Sciences)
- Zhaoxin Lu
(Nanjing Agriculture University)
- Yihua Chen
(Chinese Academy of Sciences
University of Chinese Academy of Sciences)
Abstract
Aurantinins (ARTs) are antibacterial polyketides featuring a unique 6/7/8/5-fused tetracyclic ring system and a triene side chain with a carboxyl terminus. Here we identify the art gene cluster and dissect ART’s C-methyl incorporation patterns to study its biosynthesis. During this process, an apparently redundant methyltransferase Art28 was characterized as a malonyl-acyl carrier protein O-methyltransferase, which represents an unusual on-line methyl esterification initiation strategy for polyketide biosynthesis. The methyl ester bond introduced by Art28 is kept until the last step of ART biosynthesis, in which it is hydrolyzed by Art9 to convert inactive ART 9B to active ART B. The cryptic reactions catalyzed by Art28 and Art9 represent a protecting group biosynthetic logic to render the ART carboxyl terminus inert to unwanted side reactions and to protect producing organisms from toxic ART intermediates. Further analyses revealed a wide distribution of this initiation strategy for polyketide biosynthesis in various bacteria.
Suggested Citation
Pengwei Li & Meng Chen & Wei Tang & Zhengyan Guo & Yuwei Zhang & Min Wang & Geoff P. Horsman & Jin Zhong & Zhaoxin Lu & Yihua Chen, 2021.
"Initiating polyketide biosynthesis by on-line methyl esterification,"
Nature Communications, Nature, vol. 12(1), pages 1-12, December.
Handle:
RePEc:nat:natcom:v:12:y:2021:i:1:d:10.1038_s41467-021-24846-7
DOI: 10.1038/s41467-021-24846-7
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