Abstract

Streptomyces spp. are a rich source for natural products with recognized industrial value, explaining the high interest to improve and streamline the performance of in these microbes. Here, we studied the production of pamamycins, macrodiolide homologs with a high activity against multiresistant pathogenic microbes, using recombinant Streptomyces albus J1074/R2. Talc particles (hydrous magnesium silicate, 3MgO·4SiO2 ·H2 O) of micrometer size, added to submerged cultures of the recombinant strain, tripled pamamycin production up to 50 mg/L. Furthermore, they strongly affected morphology, reduced the size of cell pellets formed by the filamentous microbe during the process up to sixfold, and shifted the pamamycin spectrum to larger derivatives. Integrated analysis of transcriptome and precursor (CoA thioester) supply of particle-enhanced and control cultures provided detailed insights into the underlying molecular changes. The microparticles affected the expression of 3,341 genes (56% of all genes), revealing a global and fundamental impact on metabolism. Morphology-associated genes, encoding major regulators such as SsgA, RelA, EshA, Factor C, as well as chaplins and rodlins, were found massively upregulated, indicating that the particles caused a substantially accelerated morphogenesis. In line, the pamamycin cluster was strongly upregulated (up to 1,024-fold). Furthermore, the microparticles perturbed genes encoding for CoA-ester metabolism, which were mainly activated. The altered expression resulted in changes in the availability of intracellular CoA-esters, the building blocks of pamamycin. Notably, the ratio between methylmalonyl CoA and malonyl-CoA was increased fourfold. Both metabolites compete for incorporation into pamamycin so that the altered availability explained the pronounced preference for larger derivatives in the microparticle-enhanced process. The novel insights into the behavior of S. albus in response to talc appears of general relevance to further explore and upgrade the concept of microparticle enhanced cultivation, widely used for filamentous microbes.

Highlights

  • Streptomycetes are an important source of natural products for pharmaceutical, medical, agricultural, and nutraceutical application, including more than two‐third of all known antibiotics of microbial origin (Bibb, 2013)

  • Members of the genus are well known for a complex morphology linked to their multicellular life cycle, which starts with the germination of a single spore that grows into a vegetative mycelium by linear tip extension and hyphae branching (Chater & Losick, 1997; van Dissel, Claessen, & van Wezel, 2014), forms an aerial mycelium, and differentiates into uninucleoid cells that further develop again into spores (Angert, 2005)

  • We studied the use of talc microparticles for the production of pamamycins (Figure 1), a family of 16 macrodiolide homologs that are highly active against multiresistant pathogenic microbes, using recombinant Streptomyces albus J1074/R2 (Rebets et al, 2015)

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Summary

| INTRODUCTION

Streptomycetes are an important source of natural products for pharmaceutical, medical, agricultural, and nutraceutical application, including more than two‐third of all known antibiotics of microbial origin (Bibb, 2013). Other studies aimed to influence morphology on the process level, including the modification of agitation speed (Belmar‐Beiny & Thomas, 1991; Xia, Lin, Xia, Cong, & Zhong, 2014), medium viscosity (O'Cleirigh, Casey, Walsh, & O'Shea, 2005), pH value (Glazebrook, Vining, & White, 1992), the addition of specific nutrients (Jonsbu, McIntyre, & Nielsen, 2002), and even subinhibitory antibiotic concentrations (Wang, Zhao, & Ding, 2017). These studies, have revealed a mixed outcome and largely remained on a trial and error level. Transcriptome and intracellular CoA thioester analyses provided insights into the cellular response of S. albus and provided a systems‐level picture on how the particles reprogrammed morphogenesis and streamlined metabolism for enhanced production and a notable shift toward heavier pamamycin homologs

| MATERIALS AND METHODS
| RESULTS
| DISCUSSION
Findings
| CONCLUSIONS
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