Abstract

Streptomyces chartreusis NRRL 3882 produces the polyether ionophore calcimycin and a variety of analogs, which originate from the same biosynthetic gene cluster. The role of calcimycin and its analogs for the producer is unknown, but calcimycin has strong antibacterial activity. Feeding experiments were performed in chemically defined medium systematically supplemented with proteinogenic amino acids to analyze their individual effects on calcimycin synthesis. In the culture supernatants, in addition to known calcimycin analogs, eight so far unknown analogs were detected using LC-MS/MS. Under most conditions cezomycin was the compound produced in highest amounts. The highest production of calcimycin was detected upon feeding with glutamine. Supplementation of the medium with glutamic acid resulted in a decrease in calcimycin production, and supplementation of other amino acids such as tryptophan, lysine, and valine resulted in the decrease in the synthesis of calcimycin and of the known intermediates of the biosynthetic pathway. We demonstrated that the production of calcimycin and its analogs is strongly dependent on amino acid supply. Utilization of amino acids as precursors and as nitrogen sources seem to critically influence calcimycin synthesis. Even amino acids not serving as direct precursors resulted in a different product profile regarding the stoichiometry of calcimycin analogs. Only slight changes in cultivation conditions can lead to major changes in the metabolic output, which highlights the hidden potential of biosynthetic gene clusters. We emphasize the need to further study the extent of this potential to understand the ecological role of metabolite diversity originating from single biosynthetic gene clusters.

Highlights

  • Published: 19 August 2021The polyether ionophore calcimycin (A23187) produced by S. chartreusis NRRL 3882 acts as antibiotic and is a well-known biochemical tool with broad use in pharmacological and toxicological studies [1]

  • Amino Acid Supplementation Leads to the Detection of New Calcimycin Analogs

  • To analyze the influence of the medium composition on the biosynthesis of calcimycin and its analogs we conducted a cultivation experiment in which S. chartreusis was grown in chemically defined medium supplemented with the different proteinogenic amino acids

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Summary

Introduction

Published: 19 August 2021The polyether ionophore calcimycin (A23187) produced by S. chartreusis NRRL 3882 acts as antibiotic and is a well-known biochemical tool with broad use in pharmacological and toxicological studies [1]. The biosynthetic pathway of calcimycin is not yet fully understood. Calcimycin is composed of a pyrrole, a polyketide, and a benzoxazole moiety, and this complex structure is the product of a sophisticated multistep biosynthesis [7]. A multi-domain enzyme synthesizes a polyketide chain from propionate and acetate. This chain reacts with 3-hydroxyanthranilic acid, derived from glucose via a shikimate-type pathway, in a hitherto unknown manner to yield the benzoxazole ring system. The emerging intermediate cezomycin is aminated at the benzoxazole moiety to give N-demethyl calcimycin, which is further methylated at Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations

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