Abstract

BackgroundThe 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.ResultsTo 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.ConclusionsThese 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.

Highlights

  • The polyene macrocyclic compound amphotericin B (AmB) is an important antifungal antibiotic for the clinical treatment of invasive fungal infections

  • Comparative metabolomics analysis was applied on wild-type Streptomyces nodosus and its mutant to investigate the mechanism of amphotericin B overproduction for the first time

  • PH values in the medium showed no significant differences, but AmB could be detected in mutant S. nodosus at 24 h while no AmB was detected in wild-type S. nodosus

Read more

Summary

Introduction

The polyene macrocyclic compound amphotericin B (AmB) is an important antifungal antibiotic for the clinical treatment of invasive fungal infections. The precursors are cyclized under the action of PKS to form the macrolactone core On this basis, the target product AmB is obtained by the oxidation of a methyl branch at ­C41, mycosaminylation at ­C19 [8] and hydroxylation at ­C8 sequentially. Through optimization of fermentation process, changes of α-ketoglutarate, pyruvate and citric acid concentration were identified as the most critical metabolite nodes for AmB biosynthesis [11]. Based on these results, further comparative metabolomics analysis can be useful for metabolic engineering of strain for AmB overproduction. Metabolic engineering has been applied based on analysis of metabolic network in Escherichia coli, Streptomyces and Corynebacterium glutamicum for the industrial production of valuable amino acids and chemicals, such as

Methods
Results
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call