Affiliation:
1. Institute of Bioengineering, Zhejiang University of Technology, Hangzhou, China
2. Central Research Institute, Zhejiang Hisun Pharmaceutical Co., Ltd., Taizhou, China
Abstract
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.
Publisher
American Society for Microbiology
Subject
Ecology,Applied Microbiology and Biotechnology,Food Science,Biotechnology
Cited by
23 articles.
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