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  2. High Level of Spinosad Production in the Heterologous Host Saccharopolyspora erythraea

High Level of Spinosad Production in the Heterologous Host Saccharopolyspora erythraea

  • Appl Environ Microbiol. 2016 Aug 30;82(18):5603-11. doi: 10.1128/AEM.00618-16.
Jun Huang 1 Zhen Yu 2 Mei-Hong Li 2 Ji-Dong Wang 2 Hua Bai 2 Jun Zhou 3 Yu-Guo Zheng 4
Affiliations

Affiliations

  • 1 Institute of Bioengineering, Zhejiang University of Technology, Hangzhou, China Central Research Institute, Zhejiang Hisun Pharmaceutical Co., Ltd., Taizhou, China.
  • 2 Central Research Institute, Zhejiang Hisun Pharmaceutical Co., Ltd., Taizhou, China.
  • 3 Central Research Institute, Zhejiang Hisun Pharmaceutical Co., Ltd., Taizhou, China zhoujun@hisunpharm.com zhengyg@zjut.edu.cn.
  • 4 Institute of Bioengineering, Zhejiang University of Technology, Hangzhou, China zhoujun@hisunpharm.com zhengyg@zjut.edu.cn.
Abstract

Spinosad, a highly effective insecticide, has an excellent environmental and mammalian toxicological profile. Global market demand for spinosad is huge and growing. However, after much effort, there has been almost no improvement in the spinosad yield from the original producer, Saccharopolyspora spinosa Here, we report the heterologous expression of spinosad using Saccharopolyspora erythraea as a host. The native erythromycin polyketide synthase (PKS) genes in S. erythraea were replaced by the assembled spinosad gene cluster through iterative recombination. The production of spinosad could be detected in the recombinant strains containing the whole biosynthesis gene cluster. Both metabolic engineering and UV mutagenesis were applied to further improve the yield of spinosad. The final strain, AT-ES04PS-3007, which could produce spinosad with a titer of 830 mg/liter, has significant potential in industrial applications.

Importance: This work provides an innovative and promising way to improve the industrial production of spinosad. At the same time, it also describes a successful method of heterologous expression for target metabolites of interest by replacing large gene clusters.

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