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  2. Divergent Biosynthesis of C-Nucleoside Minimycin and Indigoidine in Bacteria

Divergent Biosynthesis of C-Nucleoside Minimycin and Indigoidine in Bacteria

  • iScience. 2019 Dec 20:22:430-440. doi: 10.1016/j.isci.2019.11.037.
Liyuan Kong 1 Gudan Xu 1 Xiaoqin Liu 1 Jingwen Wang 1 Zenglin Tang 1 You-Sheng Cai 1 Kun Shen 1 Weixin Tao 1 Yu Zheng 2 Zixin Deng 1 Neil P J Price 3 Wenqing Chen 4
Affiliations

Affiliations

  • 1 Key Laboratory of Combinatorial Biosynthesis and Drug Discovery, Ministry of Education, and School of Pharmaceutical Sciences, Wuhan University, Wuhan 430071, China.
  • 2 State Key Laboratory of Food Nutrition and Safety, Tianjin Engineering Research Center of Microbial Metabolism and Fermentation Process Control, and College of Biotechnology, Tianjin University of Science & Technology, Tianjin 300457, China.
  • 3 Agricultural Research Service, US Department of Agriculture, National Center for Agricultural Utilization Research, Peoria, IL, USA.
  • 4 Key Laboratory of Combinatorial Biosynthesis and Drug Discovery, Ministry of Education, and School of Pharmaceutical Sciences, Wuhan University, Wuhan 430071, China. Electronic address: wqchen@whu.edu.cn.
Abstract

Minimycin (MIN) is a C-nucleoside Antibiotic structurally related to pseudouridine, and indigoidine is a naturally occurring blue pigment produced by diverse bacteria. Although MIN and indigoidine have been known for decades, the logic underlying the divergent biosynthesis of these interesting molecules has been obscure. Here, we report the identification of a minimal 5-gene cluster (min) essential for MIN biosynthesis. We demonstrated that a non-ribosomal peptide synthetase (MinA) governs "the switch" for the divergent biosynthesis of MIN and the cryptic indigoidine. We also demonstrated that MinCN (the N-terminal Phosphatase domain of MinC), MinD (uracil phosphoribosyltransferase), and MinT (transporter) function together as the safeguard Enzymes, which collaboratively constitute an unusual self-resistance system. Finally, we provided evidence that MinD, utilizing an unprecedented substrate-competition strategy for self-resistance of the producer cell, maintains competition advantage over the active molecule MIN-5'-monophosphate by increasing the UMP pool in vivo. These findings greatly expand our knowledge regarding natural product biosynthesis.

Keywords

Biotechnology; Microbial Biotechnology; Systems Biology.

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