Beyond Toxin Transport: Novel Role of ABC Transporter for Enzymatic Machinery of Cereulide NRPS Assembly Line

Author:

Gacek-Matthews A.1ORCID,Chromiková Z.12,Sulyok M.3,Lücking G.4,Barák I.2,Ehling-Schulz M.1ORCID

Affiliation:

1. Institute of Microbiology, Vetmeduni Vienna, Vienna, Austria

2. Institute of Molecular Biology, Slovak Academy of Sciences, Bratislava, Slovakia

3. Institute for Bioanalytics and Agro-Metabolomics, Department IFA-Tulln, University of Natural Resources and Life Sciences Vienna (BOKU), Vienna, Austria

4. ZIEL Institute for Food and Health, Technische Universität München, Freising, Germany

Abstract

This study revealed a novel, potentially conserved mechanism involved in the biosynthesis of microbial natural products, exemplified by the mitochondrial active depsipeptide cereulide. Similar to other bioactive substances, such as the last-resort antibiotics vancomycin and daptomycin, the antitumor drug cryptophycin or the cholesterol-lowering agent lovastatin, cereulide is synthesized nonribosomally by multienzyme machinery, requiring the concerted actions of multiple proteins to ensure correct product assembly. Given the importance of microbial secondary metabolites in human and veterinary medicine, it is critical to understand how these processes are orchestrated within the host cells. By revealing that tethering of a biosynthetic enzyme to the cell membrane by an ABC transporter is essential for nonribosomal peptide production, our study provides novel insights into synthesis of microbial secondary metabolites, which could contribute to isolation of novel compounds from cryptic secondary metabolite clusters or improve the yield of produced pharmaceuticals.

Funder

University of Veterinary Medicine Vienna

Slovak Academy of Science

Slovak Research and Development Agency

Publisher

American Society for Microbiology

Subject

Virology,Microbiology

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