Abstract

Rifampicin resistance (Rifr) mutations in the RNA polymerase β subunit (rpoB) gene exhibit pleiotropic phenotypes as a result of their effects on the transcription machinery in prokaryotes. However, the differences in the effects of the mutations on the physiology and metabolism of the bacteria remain unknown. In this study, we isolated seven Rifr mutations in rpoB, including six single point mutations (H485Y, H485C, H485D, H485R, Q472R, and S490L) and one double point mutation (S490L/S617F) from vegetative cells of an endophytic strain, Bacillus velezensis CC09. Compared to the wild-type (WT) strain (CC09), the H485R and H485D mutants exhibited a higher degree of inhibition of Aspergillus niger spore germination, while the H485Y, S490L, Q472R, and S490L/S617F mutants exhibited a lower degree of inhibition due to their lower production of the antibiotic iturin A. These mutants all exhibited defective phenotypes in terms of pellicle formation, sporulation, and swarming motility. A hierarchical clustering analysis of the observed phenotypes indicated that the four mutations involving amino acid substitutions at H485 in RpoB belonged to the same cluster. In contrast, the S490L and Q472R mutations, as well as the WT strain, were in another cluster, indicating a functional connection between the mutations in B. velezensis and phenotypic changes. Our data suggest that Rifr mutations cannot only be used to study transcriptional regulation mechanisms, but can also serve as a tool to increase the production of bioactive metabolites in B. velezensis.

Highlights

  • DNA-dependent RNA polymerase (RNAP) is an enzyme that is essential to life

  • These Rifampicin resistance (Rifr) mutations have been described in other bacteria, such as E. coli (Jin et al, 1988b), S. lividans (Hu et al, 2002), B. subtilis (Ingham and Furneaux, 2000), M. tuberculosis (Mokrousov et al, 2003), and S. aureus (Wichelhaus et al, 1999)

  • These Rifr mutations in B. velezensis influence a wide range of processes, including cell growth, pellicle formation, swarming motility, sporulation, and iturin A production, which might be a result of the regulation of related genes

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Summary

Introduction

DNA-dependent RNA polymerase (RNAP) is an enzyme that is essential to life. The core of the bacterial RNAP consists of five subunits (α2ββ ω). The RNAP associates with the transcription initiation factor, σ, to form the RNAP holoenzyme (Ebright, 2000). The antibiotic rifampicin, which is used to treat multiple types of bacterial infections, exerts its effect by inhibiting RNAP. The crystal structure and genetic and biochemical data suggest that rifampicin binds to RNAP at a site adjacent to its active center, thereby physically blocking the formation of phosphodiester bonds in the RNA backbone. Rifampicin inhibits any RNA extension greater than two or three nucleotides (Campbell and Holt, 2001)

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