Targeted accumulation of selective anticancer depsipeptides by reconstructing the precursor supply in the neoantimycin biosynthetic pathway

Lin Zhou , Yaoyao Shen , Nannan Chen , Wanlu Li , Hou-wen Lin , Yongjun Zhou

Bioresources and Bioprocessing ›› 2021, Vol. 8 ›› Issue (1) : 43

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Bioresources and Bioprocessing ›› 2021, Vol. 8 ›› Issue (1) : 43 DOI: 10.1186/s40643-021-00397-z
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Targeted accumulation of selective anticancer depsipeptides by reconstructing the precursor supply in the neoantimycin biosynthetic pathway

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Abstract

Background

Neoantimycins are a group of 15-membered ring depsipeptides isolated from Streptomycetes with a broad-spectrum of anticancer activities. Neoantimycin biosynthesis is directed by the hybrid multimodular megaenzymes of non-ribosomal peptide synthetase and polyketide synthase. We previously discovered a new neoantimycin analogue unantimycin B, which was demonstrated to have selective anticancer activities and was produced from the neoantimycin biosynthetic pathway with a starter unit of 3-hydroxybenzoate, instead of the 3-formamidosalicylate unit that is common for neoantimycins. However, the low fermentation titre and tough isolation procedure have hindered in-depth pharmacological investigation of unantimycin B as an anticancer agent.

Results

In this work, we genetically constructed two unantimycin B producer strains and inhibited neoantimycins production by removing natO and natJ-L genes essential for 3-formamidosalicylate biosynthesis, therefore facilitating chromatographic separation of unantimycin B from the complex fermentation extract. Based on the ΔnatO mutant, we improved unantimycin B production twofold, reaching approximately 12.8 mg/L, by feeding 3-hydroxybenzoate during fermentation. Furthermore, the production was improved more than sixfold, reaching approximately 40.0 mg/L, in the ΔnatO strain introduced with a chorismatase gene highly expressed under a strong promoter for endogenously over-producing 3-hydroxybenzoate.

Conclusion

This work provides a case of targeting accumulation and significant production improvement of medicinally interesting natural products via genetic manipulation of precursor biosynthesis in Streptomycetes, the talented producers of pharmaceutical molecules.

Keywords

Anticancer / Depsipeptides / Natural product biosynthesis / 3-Hydroxybenzoate / 3-Formamidosalicylate / Chorismic acid

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Lin Zhou, Yaoyao Shen, Nannan Chen, Wanlu Li, Hou-wen Lin, Yongjun Zhou. Targeted accumulation of selective anticancer depsipeptides by reconstructing the precursor supply in the neoantimycin biosynthetic pathway. Bioresources and Bioprocessing, 2021, 8(1): 43 DOI:10.1186/s40643-021-00397-z

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Zhou Y, Lin X, Williams SR, Liu L, Shen Y, Wang SP, Sun F, Xu S, Deng H, Leadlay PF, Lin HW. Directed accumulation of anticancer depsipeptides by characterization of neoantimycins biosynthetic pathway and an NADPH-dependent reductase. ACS Chem Biol, 2018, 13(8): 2153-2160.

Funding

National Natural Science Foundation of China(31670096)

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