Management of Osmoprotectant Uptake Hierarchy in Bacillus subtilis via a SigB-Dependent Antisense RNA
Under hyperosmotic conditions, bacteria accumulate compatible solutes through synthesis or import. imports a large set of osmostress protectants via five osmotically controlled transport systems (OpuA to OpuE). Biosynthesis of the particularly effective osmoprotectant glycine betaine requires the ex...
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Veröffentlicht in: | Frontiers in microbiology 2020-04, Vol.11, p.622-622 |
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Sprache: | eng |
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Zusammenfassung: | Under hyperosmotic conditions, bacteria accumulate compatible solutes through synthesis or import.
imports a large set of osmostress protectants via five osmotically controlled transport systems (OpuA to OpuE). Biosynthesis of the particularly effective osmoprotectant glycine betaine requires the exogenous supply of choline. While OpuB is rather specific for choline, OpuC imports a broad spectrum of compatible solutes, including choline and glycine betaine. One previously mapped antisense RNA of
, S1290, exhibits strong and transient expression in response to a suddenly imposed salt stress. It covers the coding region of the
operon and is expressed from a strictly SigB-dependent promoter. By inactivation of this promoter and analysis of
and
transcript levels, we discovered a time-delayed osmotic induction of
that crucially depends on the S1290 antisense RNA and on the degree of the imposed osmotic stress. Time-delayed osmotic induction of
is apparently caused by transcriptional interference of RNA-polymerase complexes driving synthesis of the converging
and S1290 mRNAs. When our data are viewed in an ecophysiological framework, it appears that during the early adjustment phase of
to acute osmotic stress, the cell prefers to initially rely on the transport activity of the promiscuous OpuC system and only subsequently fully induces
. Our data also reveal an integration of osmostress-specific adjustment systems with the SigB-controlled general stress response at a deeper level than previously appreciated. |
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ISSN: | 1664-302X 1664-302X |
DOI: | 10.3389/fmicb.2020.00622 |