28
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Ecology of cold environments: new insights of bacterial metabolic adaptation through an integrated genomic-phenomic approach

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Cold environments dominate Earth’s biosphere, hosting complex microbial communities with the ability to thrive at low temperatures. However, the underlying molecular mechanisms and the metabolic pathways involved in bacterial cold-adaptation mechanisms are still not fully understood. Herein, we assessed the metabolic features of the Antarctic bacterium Pseudoalteromonas haloplanktis TAC125 (PhTAC125), a model organism for cold-adaptation, at both 4 °C and 15 °C, by integrating genomic and phenomic (high-throughput phenotyping) data and comparing the obtained results to the taxonomically related Antarctic bacterium Pseudoalteromonas sp. TB41 (PspTB41). Although the genome size of PspTB41 is considerably larger than PhTAC125, the higher number of genes did not reflect any higher metabolic versatility at 4 °C as compared to PhTAC125. Remarkably, protein S-thiolation regulated by glutathione and glutathionylspermidine appeared to be a new possible mechanism for cold adaptation in PhTAC125. More in general, this study represents an example of how ‘multi-omic’ information might potentially contribute in filling the gap between genotypic and phenotypic features related to cold-adaptation mechanisms in bacteria.

          Related collections

          Most cited references52

          • Record: found
          • Abstract: found
          • Article: not found

          The impact of next-generation sequencing technology on genetics.

          If one accepts that the fundamental pursuit of genetics is to determine the genotypes that explain phenotypes, the meteoric increase of DNA sequence information applied toward that pursuit has nowhere to go but up. The recent introduction of instruments capable of producing millions of DNA sequence reads in a single run is rapidly changing the landscape of genetics, providing the ability to answer questions with heretofore unimaginable speed. These technologies will provide an inexpensive, genome-wide sequence readout as an endpoint to applications ranging from chromatin immunoprecipitation, mutation mapping and polymorphism discovery to noncoding RNA discovery. Here I survey next-generation sequencing technologies and consider how they can provide a more complete picture of how the genome shapes the organism.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Psychrophilic microorganisms: challenges for life.

            The ability of psychrophiles to survive and proliferate at low temperatures implies that they have overcome key barriers inherent to permanently cold environments. These challenges include: reduced enzyme activity; decreased membrane fluidity; altered transport of nutrients and waste products; decreased rates of transcription, translation and cell division; protein cold-denaturation; inappropriate protein folding; and intracellular ice formation. Cold-adapted organisms have successfully evolved features, genotypic and/or phenotypic, to surmount the negative effects of low temperatures and to enable growth in these extreme environments. In this review, we discuss the current knowledge of these adaptations as gained from extensive biochemical and biophysical studies and also from genomics and proteomics.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Physiological and genetic responses of bacteria to osmotic stress.

              L N Csonka (1989)
              The capacity of organisms to respond to fluctuations in their osmotic environments is an important physiological process that determines their abilities to thrive in a variety of habitats. The primary response of bacteria to exposure to a high osmotic environment is the accumulation of certain solutes, K+, glutamate, trehalose, proline, and glycinebetaine, at concentrations that are proportional to the osmolarity of the medium. The supposed function of these solutes is to maintain the osmolarity of the cytoplasm at a value greater than the osmolarity of the medium and thus provide turgor pressure within the cells. Accumulation of these metabolites is accomplished by de novo synthesis or by uptake from the medium. Production of proteins that mediate accumulation or uptake of these metabolites is under osmotic control. This review is an account of the processes that mediate adaptation of bacteria to changes in their osmotic environment.
                Bookmark

                Author and article information

                Contributors
                stefano.mocali@crea.gov.it
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                12 April 2017
                12 April 2017
                2017
                : 7
                : 839
                Affiliations
                [1 ]Consiglio per la ricerca in agricoltura e l’analisi dell’economia agraria – Centro di Ricerca per l’Agrobiologia e la Pedologia (CREA-ABP), via di Lanciola 12/A, 50125 Firenze, Italy
                [2 ]GRID grid.428966.7, , Institute of Protein Biochemistry, CNR, ; Via Pietro Castellino 111, 80131 Naples, Italy
                [3 ]Department of Chemical Sciences, University of Naples ‘Federico II’, Complesso Universitario, Monte Sant’Angelo, Via Cinthia 4, 80126 Naples, Italy
                [4 ]GRID grid.8404.8, Department of Biology, LEMM, Laboratory of Microbial and Molecular Evolution Florence, , University of Florence, ; I-50019 Sesto Fiorentino (FI), Italy
                [5 ]GRID grid.5326.2, Institute for the Coastal Marine Environment, , National Research Council (IAMC-CNR), ; Spianata San Raineri 86, 98122 Messina, Italy
                [6 ]GRID grid.10438.3e, Department of Chemical, Biological, Pharmaceutical and Environmental Sciences, , University of Messina, ; Viale F. Stagno d’Alcontrès 31, 98166 Messina, Italy
                Author information
                http://orcid.org/0000-0002-1173-7206
                Article
                876
                10.1038/s41598-017-00876-4
                5429795
                28404986
                4877a44b-a8c6-439d-a418-382c6d7f53de
                © The Author(s) 2017

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 13 January 2017
                : 1 March 2017
                Categories
                Article
                Custom metadata
                © The Author(s) 2017

                Uncategorized
                Uncategorized

                Comments

                Comment on this article