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Comparative metabolomics analysis of amphotericin B high-yield mechanism for metabolic engineering
BACKGROUND: The polyene macrocyclic compound amphotericin B (AmB) is an important antifungal antibiotic for the clinical treatment of invasive fungal infections. To rationally guide the improvement of AmB production in the main producing strain Streptomyces nodosus, comparative metabolomics analysis...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7945361/ https://www.ncbi.nlm.nih.gov/pubmed/33750383 http://dx.doi.org/10.1186/s12934-021-01552-z |
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author | Zhang, Bo Chen, Yu Jiang, Sheng-Xian Cai, Xue Huang, Kai Liu, Zhi-Qiang Zheng, Yu-Guo |
author_facet | Zhang, Bo Chen, Yu Jiang, Sheng-Xian Cai, Xue Huang, Kai Liu, Zhi-Qiang Zheng, Yu-Guo |
author_sort | Zhang, Bo |
collection | PubMed |
description | BACKGROUND: The polyene macrocyclic compound amphotericin B (AmB) is an important antifungal antibiotic for the clinical treatment of invasive fungal infections. To rationally guide the improvement of AmB production in the main producing strain Streptomyces nodosus, comparative metabolomics analysis was performed to investigate the intracellular metabolic changes in wild-type S. nodosus ZJB20140315 with low-yield AmB production and mutant S. nodosus ZJB2016050 with high-yield AmB production, the latter of which reached industrial criteria on a pilot scale. RESULTS: To investigate the relationship of intracellular metabolites, 7758 metabolites were identified in mutant S. nodosus and wildtype S. nodosus via LC–MS. Through analysis of metabolism, the level of 26 key metabolites that involved in carbon metabolism, fatty acids metabolism, amino acids metabolism, purine metabolism, folate biosynthesis and one carbon pool by folate were much higher in mutant S. nodosus. The enrichment of relevant metabolic pathways by gene overexpression strategy confirmed that one carbon pool by folate was the key metabolic pathway. Meanwhile, a recombinant strain with gene metH (methionine synthase) overexpressed showed 5.03 g/L AmB production within 120 h fermentation, which is 26.4% higher than that of the mutant strain. CONCLUSIONS: These results demonstrated that comparative metabolomics analysis was an effective approach for the improvement of AmB production and could be applied for other industrially or clinically important compounds as well. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12934-021-01552-z. |
format | Online Article Text |
id | pubmed-7945361 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-79453612021-03-10 Comparative metabolomics analysis of amphotericin B high-yield mechanism for metabolic engineering Zhang, Bo Chen, Yu Jiang, Sheng-Xian Cai, Xue Huang, Kai Liu, Zhi-Qiang Zheng, Yu-Guo Microb Cell Fact Research BACKGROUND: The polyene macrocyclic compound amphotericin B (AmB) is an important antifungal antibiotic for the clinical treatment of invasive fungal infections. To rationally guide the improvement of AmB production in the main producing strain Streptomyces nodosus, comparative metabolomics analysis was performed to investigate the intracellular metabolic changes in wild-type S. nodosus ZJB20140315 with low-yield AmB production and mutant S. nodosus ZJB2016050 with high-yield AmB production, the latter of which reached industrial criteria on a pilot scale. RESULTS: To investigate the relationship of intracellular metabolites, 7758 metabolites were identified in mutant S. nodosus and wildtype S. nodosus via LC–MS. Through analysis of metabolism, the level of 26 key metabolites that involved in carbon metabolism, fatty acids metabolism, amino acids metabolism, purine metabolism, folate biosynthesis and one carbon pool by folate were much higher in mutant S. nodosus. The enrichment of relevant metabolic pathways by gene overexpression strategy confirmed that one carbon pool by folate was the key metabolic pathway. Meanwhile, a recombinant strain with gene metH (methionine synthase) overexpressed showed 5.03 g/L AmB production within 120 h fermentation, which is 26.4% higher than that of the mutant strain. CONCLUSIONS: These results demonstrated that comparative metabolomics analysis was an effective approach for the improvement of AmB production and could be applied for other industrially or clinically important compounds as well. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12934-021-01552-z. BioMed Central 2021-03-09 /pmc/articles/PMC7945361/ /pubmed/33750383 http://dx.doi.org/10.1186/s12934-021-01552-z Text en © The Author(s) 2021 Open AccessThis 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/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Zhang, Bo Chen, Yu Jiang, Sheng-Xian Cai, Xue Huang, Kai Liu, Zhi-Qiang Zheng, Yu-Guo Comparative metabolomics analysis of amphotericin B high-yield mechanism for metabolic engineering |
title | Comparative metabolomics analysis of amphotericin B high-yield mechanism for metabolic engineering |
title_full | Comparative metabolomics analysis of amphotericin B high-yield mechanism for metabolic engineering |
title_fullStr | Comparative metabolomics analysis of amphotericin B high-yield mechanism for metabolic engineering |
title_full_unstemmed | Comparative metabolomics analysis of amphotericin B high-yield mechanism for metabolic engineering |
title_short | Comparative metabolomics analysis of amphotericin B high-yield mechanism for metabolic engineering |
title_sort | comparative metabolomics analysis of amphotericin b high-yield mechanism for metabolic engineering |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7945361/ https://www.ncbi.nlm.nih.gov/pubmed/33750383 http://dx.doi.org/10.1186/s12934-021-01552-z |
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