4.7 Article

Reconstruction of Secondary Metabolic Pathway to Synthesize Novel Metabolite in Saccharopolyspora erythraea

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fbioe.2021.628569

关键词

CRISPR-Cas9; Saccharopolyspora erythraea; polyketide; Acyl-CoA; heterologous expression; metabolic pathway

资金

  1. National Key Research and Development Program of China [2018YFA0900404]
  2. National Natural Science Foundation of China [31730004]
  3. Shenzhen Key Laboratory of Synthetic Genomics [ZDSYS201802061806209]
  4. Shenzhen Science and Technology Program [KQTD20180413181837372]
  5. Guangdong Provincial Key Laboratory of Synthetic Genomics [2019B030301006]
  6. China Postdoctoral Science Foundation [2020M682974]

向作者/读者索取更多资源

This study created a valuable heterologous host Ab Delta ery by knocking out the erythromycin biosynthesis gene cluster, which showed higher production of heterologous products than the wild type strain.
Natural polyketides play important roles in clinical treatment, agriculture, and animal husbandry. Compared to natural hosts, heterologous chassis (especially Actinomycetes) have many advantages in production of polyketide compounds. As a widely studied model Actinomycete, Saccharopolyspora erythraea is an excellent host to produce valuable heterologous polyketide compounds. However, many host factors affect the expression efficiency of heterologous genes, and it is necessary to modify the host to adapt heterologous production. In this study, the CRISPR-Cas9 system was used to knock out the erythromycin biosynthesis gene cluster of Ab (erythromycin high producing stain). A fragment of 49491 bp in genome (from SACE_0715 to SACE_0733) was deleted, generating the recombinant strain Ab Delta ery in which erythromycin synthesis was blocked and synthetic substrates methylmalonyl-CoA and propionyl-CoA accumulated enormously. Based on Ab Delta ery as heterologous host, three genes, AsCHS, RgTAL, and Sc4CL, driven by strong promoters Pj23119, PermE, and PkasO, respectively, were introduced to produce novel polyketide by L-tyrosine and methylmalonyl-CoA. The product (E)-4-hydroxy-6-(4-hydroxystyryl)-3,5-dimethyl-2H-pyrone was identified in fermentation by LC-MS. High performance liquid chromatography analysis showed that knocking out ery BGC resulted in an increase of methylmalonyl-CoA by 142% and propionyl-CoA by 57.9% in Ab Delta ery compared to WT, and the yield of heterologous product in Ab Delta ery:AsCHS-RgTAL-Sc4CL was higher than WT:AsCHS-RgTAL-Sc4CL. In summary, this study showed that Ab Delta ery could potentially serve as a precious heterologous host to boost the synthesis of other valuable polyketone compounds using methylmalonyl-CoA and propionyl-CoA in the future.

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