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Comparative genomic analysis of Streptomyces rapamycinicus NRRL 5491 and its mutant overproducing rapamycin

Streptomyces rapamycinicus NRRL 5491 is a well-known producer of rapamycin, a secondary metabolite with useful bioactivities, including antifungal, antitumor, and immunosuppressive functions. For the enhanced rapamycin production, a rapamycin-overproducing strain SRMK07 was previously obtained as a...

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Autores principales: Jo, Hee-Geun, Adidjaja, Joshua Julio, Kim, Do-Kyung, Park, Bu-Soo, Lee, Namil, Cho, Byung-Kwan, Kim, Hyun Uk, Oh, Min-Kyu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9206652/
https://www.ncbi.nlm.nih.gov/pubmed/35717543
http://dx.doi.org/10.1038/s41598-022-14199-6
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author Jo, Hee-Geun
Adidjaja, Joshua Julio
Kim, Do-Kyung
Park, Bu-Soo
Lee, Namil
Cho, Byung-Kwan
Kim, Hyun Uk
Oh, Min-Kyu
author_facet Jo, Hee-Geun
Adidjaja, Joshua Julio
Kim, Do-Kyung
Park, Bu-Soo
Lee, Namil
Cho, Byung-Kwan
Kim, Hyun Uk
Oh, Min-Kyu
author_sort Jo, Hee-Geun
collection PubMed
description Streptomyces rapamycinicus NRRL 5491 is a well-known producer of rapamycin, a secondary metabolite with useful bioactivities, including antifungal, antitumor, and immunosuppressive functions. For the enhanced rapamycin production, a rapamycin-overproducing strain SRMK07 was previously obtained as a result of random mutagenesis. To identify genomic changes that allowed the SRMK07 strain’s enhanced rapamycin production, genomes of the NRRL 5491 and SRMK07 strains were newly sequenced in this study. The resulting genome sequences of the wild-type and SRMK07 strains showed the size of 12.47 Mbp and 9.56 Mbp, respectively. Large deletions were observed at both end regions of the SRMK07 strain’s genome, which cover 17 biosynthetic gene clusters (BGCs) encoding secondary metabolites. Also, genes in a genomic region containing the rapamycin BGC were shown to be duplicated. Finally, comparative metabolic network analysis using these two strains’ genome-scale metabolic models revealed biochemical reactions with different metabolic fluxes, which were all associated with NADPH generation. Taken together, the genomic and computational approaches undertaken in this study suggest biological clues for the enhanced rapamycin production of the SRMK07 strain. These clues can also serve as a basis for systematic engineering of a production host for further enhanced rapamycin production.
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spelling pubmed-92066522022-06-20 Comparative genomic analysis of Streptomyces rapamycinicus NRRL 5491 and its mutant overproducing rapamycin Jo, Hee-Geun Adidjaja, Joshua Julio Kim, Do-Kyung Park, Bu-Soo Lee, Namil Cho, Byung-Kwan Kim, Hyun Uk Oh, Min-Kyu Sci Rep Article Streptomyces rapamycinicus NRRL 5491 is a well-known producer of rapamycin, a secondary metabolite with useful bioactivities, including antifungal, antitumor, and immunosuppressive functions. For the enhanced rapamycin production, a rapamycin-overproducing strain SRMK07 was previously obtained as a result of random mutagenesis. To identify genomic changes that allowed the SRMK07 strain’s enhanced rapamycin production, genomes of the NRRL 5491 and SRMK07 strains were newly sequenced in this study. The resulting genome sequences of the wild-type and SRMK07 strains showed the size of 12.47 Mbp and 9.56 Mbp, respectively. Large deletions were observed at both end regions of the SRMK07 strain’s genome, which cover 17 biosynthetic gene clusters (BGCs) encoding secondary metabolites. Also, genes in a genomic region containing the rapamycin BGC were shown to be duplicated. Finally, comparative metabolic network analysis using these two strains’ genome-scale metabolic models revealed biochemical reactions with different metabolic fluxes, which were all associated with NADPH generation. Taken together, the genomic and computational approaches undertaken in this study suggest biological clues for the enhanced rapamycin production of the SRMK07 strain. These clues can also serve as a basis for systematic engineering of a production host for further enhanced rapamycin production. Nature Publishing Group UK 2022-06-18 /pmc/articles/PMC9206652/ /pubmed/35717543 http://dx.doi.org/10.1038/s41598-022-14199-6 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Jo, Hee-Geun
Adidjaja, Joshua Julio
Kim, Do-Kyung
Park, Bu-Soo
Lee, Namil
Cho, Byung-Kwan
Kim, Hyun Uk
Oh, Min-Kyu
Comparative genomic analysis of Streptomyces rapamycinicus NRRL 5491 and its mutant overproducing rapamycin
title Comparative genomic analysis of Streptomyces rapamycinicus NRRL 5491 and its mutant overproducing rapamycin
title_full Comparative genomic analysis of Streptomyces rapamycinicus NRRL 5491 and its mutant overproducing rapamycin
title_fullStr Comparative genomic analysis of Streptomyces rapamycinicus NRRL 5491 and its mutant overproducing rapamycin
title_full_unstemmed Comparative genomic analysis of Streptomyces rapamycinicus NRRL 5491 and its mutant overproducing rapamycin
title_short Comparative genomic analysis of Streptomyces rapamycinicus NRRL 5491 and its mutant overproducing rapamycin
title_sort comparative genomic analysis of streptomyces rapamycinicus nrrl 5491 and its mutant overproducing rapamycin
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9206652/
https://www.ncbi.nlm.nih.gov/pubmed/35717543
http://dx.doi.org/10.1038/s41598-022-14199-6
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