Promoting Butenyl-spinosyn Production Based on Omics Research and Metabolic Network Construction in Saccharopolyspora pogona
Metabolic pathway
Gene cluster
Metabolic Engineering
DOI:
10.1021/acs.jafc.2c00285
Publication Date:
2022-03-04T18:53:37Z
AUTHORS (12)
ABSTRACT
Understanding the metabolism of Saccharopolyspora pogona on a global scale is essential for manipulating its metabolic capabilities to improve butenyl-spinosyn biosynthesis. Here, we combined multiomics analysis parse S. genomic information, construct network, and mine important functional genes that affect This research not only elucidated relationship between biosynthesis primary pathway but also showed low expression level continuous downregulation bus cluster competitive utilization acetyl-CoA were main reasons reduced production. Our framework identified 148 related significantly differentially expressed, confirming polyketide synthase (PKS) succinic semialdehyde dehydrogenase (GabD) play an role in regulating Combined modification these increased overall production by 6.38-fold 154.1 ± 10.98 mg/L. results provide strategy further promoting titer.
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