4.4 Article

Bursts in biosynthetic gene cluster transcription are accompanied by surges of natural compound production in the myxobacterium Sorangium sp.

Journal

MICROBIAL BIOTECHNOLOGY
Volume 16, Issue 5, Pages 1054-1068

Publisher

WILEY
DOI: 10.1111/1751-7915.14246

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A better understanding of the genetic regulation of microbial compound biosynthesis can accelerate the discovery and production of new biologically active molecules. This study investigated the transcriptional dynamics of biosynthetic gene clusters (BGCs) in the myxobacterium Sorangium sp. So ce836, revealing that BGC transcription is associated with the production of natural compounds. The findings challenge the commonly held belief of preferential BGC expression under nutrient-limited conditions and highlight the need for genetic engineering tools to enhance compound yields from myxobacterial strains.
A better understanding of the genetic regulation of the biosynthesis of microbial compounds could accelerate the discovery of new biologically active molecules and facilitate their production. To this end, we have investigated the time course of genome-wide transcription in the myxobacterium Sorangium sp. So ce836 in relation to its production of natural compounds. Time-resolved RNA sequencing revealed that core biosynthesis genes from 48 biosynthetic gene clusters (BGCs; 92% of all BGCs encoded in the genome) were actively transcribed at specific time points in a batch culture. The majority (80%) of polyketide synthase and non-ribosomal peptide synthetase genes displayed distinct peaks of transcription during exponential bacterial growth. Strikingly, these bursts in BGC transcriptional activity were associated with surges in the net production rates of known natural compounds, indicating that their biosynthesis was critically regulated at the transcriptional level. In contrast, BGC read counts from single time points had limited predictive value about biosynthetic activity, since transcription levels varied >100-fold among BGCs with detected natural products. Taken together, our time-course data provide unique insights into the dynamics of natural compound biosynthesis and its regulation in a wild-type myxobacterium, challenging the commonly cited notion of preferential BGC expression under nutrient-limited conditions. The close association observed between BGC transcription and compound production warrants additional efforts to develop genetic engineering tools for boosting compound yields from myxobacterial producer strains.

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