Journal of Microbiology and Biotechnology

  • 제32권7호
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  • Pages.911-917
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  • 2022
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  • 1017-7825(pISSN)
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  • 1738-8872(eISSN)
한국미생물·생명공학회 (The Korean Society for Microbiology and Biotechnology)
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Streptomyces BAC Cloning of a Large-Sized Biosynthetic Gene Cluster of NPP B1, a Potential SARS-CoV-2 RdRp Inhibitor

  • Park, Ji-Hee (Department of Biological Sciences and Bioengineering, Inha University) ;
  • Park, Heung-Soon (Department of Biological Sciences and Bioengineering, Inha University) ;
  • Nah, Hee-Ju (Department of Biological Sciences and Bioengineering, Inha University) ;
  • Kang, Seung-Hoon (Department of Biological Sciences and Bioengineering, Inha University) ;
  • Choi, Si-Sun (Department of Biological Sciences and Bioengineering, Inha University) ;
  • Kim, Eung-Soo (Department of Biological Sciences and Bioengineering, Inha University)
  • 투고 : 2022.05.22
  • 심사 : 2022.06.06
  • 발행 : 2022.07.28
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초록

As valuable antibiotics, microbial natural products have been in use for decades in various fields. Among them are polyene compounds including nystatin, amphotericin, and nystatin-like Pseudonocardia polyenes (NPPs). Polyene macrolides are known to possess various biological effects, such as antifungal and antiviral activities. NPP A1, which is produced by Pseudonocardia autotrophica, contains a unique disaccharide moiety in the tetraene macrolide backbone. NPP B1, with a heptane structure and improved antifungal activity, was then developed via genetic manipulation of the NPP A1 biosynthetic gene cluster (BGC). Here, we generated a Streptomyces artificial chromosomal DNA library to isolate a large-sized NPP B1 BGC. The NPP B1 BGC was successfully isolated from P. autotrophica chromosome through the construction and screening of a bacterial artificial chromosome (BAC) library, even though the isolated 140-kb BAC clone (named pNPPB1s) lacked approximately 8 kb of the right-end portion of the NPP B1 BGC. The additional introduction of the pNPPB1s as well as co-expression of the 32-kb portion including the missing 8 kb led to a 7.3-fold increase in the production level of NPP B1 in P. autotrophica. The qRT-PCR confirmed that the transcription level of NPP B1 BGC was significantly increased in the P. autotrophica strain containing two copies of the NPP B1 BGCs. Interestingly, the NPP B1 exhibited a previously unidentified SARS-CoV-2 RNA-dependent RNA polymerase (RdRp) inhibition activity in vitro. These results suggest that the Streptomyces BAC cloning of a large-sized, natural product BGC is a valuable approach for titer improvement and biological activity screening of natural products in actinomycetes.

키워드

과제정보

The authors appreciate the BAC-associated technical support provided by Bio S&T Inc. (Quebec, Canada). This work was funded by the National Research Foundation of Korea (Project No. NRF-2021R1A2C2012203).

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