Regulation of Antimycin Biosynthesis Is Controlled by the ClpXP Protease

Author:

Bilyk Bohdan1,Kim Sora2,Fazal Asif1,Baker Tania A.23,Seipke Ryan F.1ORCID

Affiliation:

1. Astbury Centre for Structural Molecular Biology, Faculty of Biological Sciences, University of Leeds, Leeds, United Kingdom

2. Department of Biology, Massachusetts Institute of Technology, Cambridge, Massachusetts, USA

3. Howard Hughes Medical Institute, Chevy Chase, Maryland, USA

Abstract

Natural products produced by Streptomyces species underpin many industrially and medically important compounds. However, the majority of the ∼30 biosynthetic pathways harbored by an average species are not expressed in the laboratory. This unrevealed biochemical diversity is believed to comprise an untapped resource for natural product drug discovery. Major roadblocks preventing the exploitation of unexpressed biosynthetic pathways are a lack of insight into their regulation and limited technology for activating their expression. Our findings reveal that the abundance of σ AntA , which is the cluster-situated regulator of antimycin biosynthesis, is controlled by the ClpXP protease. These data link proteolysis to the regulation of natural product biosynthesis for the first time to our knowledge, and we anticipate that this will emerge as a major strategy by which actinobacteria regulate production of their natural products. Further study of this process will advance understanding of how expression of secondary metabolism is controlled and will aid pursuit of activating unexpressed biosynthetic pathways.

Funder

National Science Foundation

Howard Hughes Medical Institute

University of Leeds

UKRI | Biotechnology and Biological Sciences Research Council

Publisher

American Society for Microbiology

Subject

Molecular Biology,Microbiology

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