Comparative metabolomics analysis of amphotericin B high-yield mechanism for metabolic engineering View Full Text


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Article Info

DATE

2021-03-09

AUTHORS

Bo Zhang, Yu Chen, Sheng-Xian Jiang, Xue Cai, Kai Huang, Zhi-Qiang Liu, Yu-Guo Zheng

ABSTRACT

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. More... »

PAGES

66

Identifiers

URI

http://scigraph.springernature.com/pub.10.1186/s12934-021-01552-z

DOI

http://dx.doi.org/10.1186/s12934-021-01552-z

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https://app.dimensions.ai/details/publication/pub.1136256927

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/33750383


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