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Bacterial Stationary Phase Transition and Stress Adaptation: A Matter of Survival?

A special issue of International Journal of Molecular Sciences (ISSN 1422-0067). This special issue belongs to the section "Molecular Microbiology".

Deadline for manuscript submissions: closed (30 November 2020) | Viewed by 7973

Special Issue Editors


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Guest Editor
Tasmanian Institute of Agriculture, University of Tasmania, Hobart, TAS 7005, Australia
Interests: bacterial response to stress; lactic acid bacteria; degradation of toxic pollutants; Actinobacteria; Corynebacteriales; cell surface biology; probiotics

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Co-Guest Editor
Merieux Nutrisciences, Australia
Interests: proteomics; probiotics; bio-nanotechnology; food safety; microbial physiology; biochemistry; microbiology

Special Issue Information

Dear Colleagues,

The bacterial stationary phase is often regarded as a less active period of the growth cycle, which is associated with the transition into a dormant state in which the population’s numbers do not increase and in which cell division is balanced by cell death. However, this is far from the biochemical and regulatory reality of this phase of bacterial life, as cells close down pathways that are linked with logarithmic growth and induce a suite of new pathways that support survival or movement towards cell death for some members of the population. The associated mechanisms may include cell differentiation, modification of cell structures, and sporulation or entry into viable, non-culturable states. The stationary phase is often triggered by nutrient starvation, particularly lack of availability of essential carbon and nitrogen sources, accumulation of toxic end-products, or exposure to stressors, which inhibit further cell division and prematurely induce the onset of the stationary phase. While laboratory culture media provide all nutrients for growth, in natural ecosystems, bacteria are often in nutrient-poor environments where competition for essential nutrients occurs, together with exposure to assaults from anti-microbial agents produced by organisms sharing the same ecosystem or from host cells in the case of pathogenesis.

There is a long history of studies on the idiophase (the period of transition from log growth to the stationary phase, when cells switch from primary to secondary metabolite biosynthesis) in Actinobacteria, Escherichia coli, and Bacillus species, particularly due to the biotechnological importance of secondary metabolites and storage polymers synthesized during the stationary phase. These products include (for example) the following: antibiotics, anti-cancer drugs, and other bioactive compounds; triacylglycerols, polyhydroxyalkanoates, and other feedstocks for biofuels; and enzymes important in food manufacture and industrial processing. Alterations in surface polymers influence biofilm formation, which impacts the survival of microbial communities and resistance to antibiotics and chemical descaling agents in manufacturing processes, as well as in bacterial diseases. Furthermore, the ability to survive for long periods in a ‘quiescent’ state is medically important, as exemplified by the intracellular survival of mycobacterial species during long-term infections. Understanding the genetics, biochemistry, and regulation of the transition into the stationary phase and long-term survival in non-growing states can assist in identifying novel antimicrobials, targets for vaccine development, and antimicrobials for recalcitrant infections, as well as underpinning our understanding of sustainability in complex microbial ecosystems where populations are largely uncultured species.

With the rapid increase in the number of bacterial genomes sequenced and bioinformatic analytical tools, new knowledge of how cells survive in adverse environments is also rapidly emerging.

The aim of this Special Issue is to provide a useful reference tool on the mechanisms underpinning the transition into the stationary phase across bacterial genera to summarize the common and divergent strategies used by bacteria from diverse environments and how this knowledge can be exploited for biotechnological and medical benefit.

Dedication: I would like to honor Dr Wilkinson for his outstanding reputation as a teacher—we so often honor researchers but forget that training and encouraging the next innovators in microbiology is equally important (and often has a more pervasive impact). He had an outstanding mind but circumstances at UniMelb meant he took up a large teaching load to free up other staff to undertake research. He was a lovely person, which counts for a lot in life.

Prof. Margaret L. Britz
Guest Editor

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Keywords

  • stationary phase
  • idiophase
  • stress responses
  • biofilms
  • secondary metabolites
  • cell survival

Published Papers (2 papers)

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18 pages, 762 KiB  
Article
Transcriptome-Wide Analysis of Stationary Phase Small ncRNAs in E. coli
by Nicole Raad, Hannes Luidalepp, Michel Fasnacht and Norbert Polacek
Int. J. Mol. Sci. 2021, 22(4), 1703; https://doi.org/10.3390/ijms22041703 - 08 Feb 2021
Cited by 11 | Viewed by 3266
Abstract
Almost two-thirds of the microbiome’s biomass has been predicted to be in a non-proliferating, and thus dormant, growth state. It is assumed that dormancy goes hand in hand with global downregulation of gene expression. However, it remains largely unknown how bacteria manage to [...] Read more.
Almost two-thirds of the microbiome’s biomass has been predicted to be in a non-proliferating, and thus dormant, growth state. It is assumed that dormancy goes hand in hand with global downregulation of gene expression. However, it remains largely unknown how bacteria manage to establish this resting phenotype at the molecular level. Recently small non-protein-coding RNAs (sRNAs or ncRNAs) have been suggested to be involved in establishing the non-proliferating state in bacteria. Here, we have deep sequenced the small transcriptome of Escherichia coli in the exponential and stationary phases and analyzed the resulting reads by a novel biocomputational pipeline STARPA (Stable RNA Processing Product Analyzer). Our analysis reveals over 12,000 small transcripts enriched during both growth stages. Differential expression analysis reveals distinct sRNAs enriched in the stationary phase that originate from various genomic regions, including transfer RNA (tRNA) fragments. Furthermore, expression profiling by Northern blot and RT-qPCR analyses confirms the growth phase-dependent expression of several enriched sRNAs. Our study adds to the existing repertoire of bacterial sRNAs and suggests a role for some of these small molecules in establishing and maintaining stationary phase as well as the bacterial stress response. Functional characterization of these detected sRNAs has the potential of unraveling novel regulatory networks central for stationary phase biology. Full article
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19 pages, 2632 KiB  
Article
Application of Thin-Layer Chromatography-Flame Ionization Detection (TLC-FID) to Total Lipid Quantitation in Mycolic-Acid Synthesizing Rhodococcus and Williamsia Species
by Akhikun Nahar, Anthony L. Baker, David S. Nichols, John P. Bowman and Margaret L. Britz
Int. J. Mol. Sci. 2020, 21(5), 1670; https://doi.org/10.3390/ijms21051670 - 29 Feb 2020
Cited by 8 | Viewed by 3877
Abstract
In addition to cell membrane phospholipids, Actinobacteria in the order Corynebacteriales possess a waxy cell envelope containing mycolic acids (MA). In optimized culture condition, some species can also accumulate high concentrations of intracellular triacylglycerols (TAG), which are a potential source of biodiesel. Bacterial [...] Read more.
In addition to cell membrane phospholipids, Actinobacteria in the order Corynebacteriales possess a waxy cell envelope containing mycolic acids (MA). In optimized culture condition, some species can also accumulate high concentrations of intracellular triacylglycerols (TAG), which are a potential source of biodiesel. Bacterial lipid classes and composition alter in response to environmental stresses, including nutrient availability, thus understanding carbon flow into different lipid classes is important when optimizing TAG synthesis. Quantitative and qualitative analysis of lipid classes normally requires combinations of different extraction, derivatization, chromatographic and detection methods. In this study, a single-step thin-layer chromatography-flame ionization detection (TLC-FID) technique was applied to quantify lipid classes in six sub-Antarctic Corynebacteriales strains identified as Rhodococcus and Williamsia species. A hexane:diethyl-ether:acetic acid solvent system separated the total cellular lipids extracted from cells lysed by bead beating, which released more bound and unbound MA than sonication. Typical profiles included a major broad non-polar lipid peak, TAG and phospholipids, although trehalose dimycolates, when present, co-eluted with phospholipids. Ultra-performance liquid chromatography-tandem mass-spectrometry and nuclear magnetic resonance spectroscopy detected MA signatures in the non-polar lipid peak and indicated that these lipids were likely bound, at least in part, to sugars from cell wall arabinogalactan. Waxy esters were not detected. The single-solvent TLC-FID procedure provides a useful platform for the quantitation and preliminary screening of cellular lipid classes when testing the impacts of growth conditions on TAG synthesis. Full article
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