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Molecular genetic and physical analysis of gas vesicles in buoyant enterobacteria
Different modes of bacterial taxis play important roles in environmental adaptation, survival, colonization and dissemination of disease. One mode of taxis is flotation due to the production of gas vesicles. Gas vesicles are proteinaceous intracellular organelles, permeable only to gas, that enable...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4982088/ https://www.ncbi.nlm.nih.gov/pubmed/26743231 http://dx.doi.org/10.1111/1462-2920.13203 |
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author | Tashiro, Yosuke Monson, Rita E. Ramsay, Joshua P. Salmond, George P. C. |
author_facet | Tashiro, Yosuke Monson, Rita E. Ramsay, Joshua P. Salmond, George P. C. |
author_sort | Tashiro, Yosuke |
collection | PubMed |
description | Different modes of bacterial taxis play important roles in environmental adaptation, survival, colonization and dissemination of disease. One mode of taxis is flotation due to the production of gas vesicles. Gas vesicles are proteinaceous intracellular organelles, permeable only to gas, that enable flotation in aquatic niches. Gene clusters for gas vesicle biosynthesis are partially conserved in various archaea, cyanobacteria, and some proteobacteria, such as the enterobacterium, S erratia sp. ATCC 39006 (S39006). Here we present the first systematic analysis of the genes required to produce gas vesicles in S39006, identifying how this differs from the archaeon H alobacterium salinarum. We define 11 proteins essential for gas vesicle production. Mutation of gvpN or gvpV produced small bicone gas vesicles, suggesting that the cognate proteins are involved in the morphogenetic assembly pathway from bicones to mature cylindrical forms. Using volumetric compression, gas vesicles were shown to comprise 17% of S39006 cells, whereas in E scherichia coli heterologously expressing the gas vesicle cluster in a deregulated environment, gas vesicles can occupy around half of cellular volume. Gas vesicle production in S39006 and E . coli was exploited to calculate the instantaneous turgor pressure within cultured bacterial cells; the first time this has been performed in either strain. |
format | Online Article Text |
id | pubmed-4982088 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-49820882016-08-26 Molecular genetic and physical analysis of gas vesicles in buoyant enterobacteria Tashiro, Yosuke Monson, Rita E. Ramsay, Joshua P. Salmond, George P. C. Environ Microbiol Research Articles Different modes of bacterial taxis play important roles in environmental adaptation, survival, colonization and dissemination of disease. One mode of taxis is flotation due to the production of gas vesicles. Gas vesicles are proteinaceous intracellular organelles, permeable only to gas, that enable flotation in aquatic niches. Gene clusters for gas vesicle biosynthesis are partially conserved in various archaea, cyanobacteria, and some proteobacteria, such as the enterobacterium, S erratia sp. ATCC 39006 (S39006). Here we present the first systematic analysis of the genes required to produce gas vesicles in S39006, identifying how this differs from the archaeon H alobacterium salinarum. We define 11 proteins essential for gas vesicle production. Mutation of gvpN or gvpV produced small bicone gas vesicles, suggesting that the cognate proteins are involved in the morphogenetic assembly pathway from bicones to mature cylindrical forms. Using volumetric compression, gas vesicles were shown to comprise 17% of S39006 cells, whereas in E scherichia coli heterologously expressing the gas vesicle cluster in a deregulated environment, gas vesicles can occupy around half of cellular volume. Gas vesicle production in S39006 and E . coli was exploited to calculate the instantaneous turgor pressure within cultured bacterial cells; the first time this has been performed in either strain. John Wiley and Sons Inc. 2016-02-15 2016-04 /pmc/articles/PMC4982088/ /pubmed/26743231 http://dx.doi.org/10.1111/1462-2920.13203 Text en © 2016 The Authors. Environmental Microbiology published by Society for Applied Microbiology and John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Tashiro, Yosuke Monson, Rita E. Ramsay, Joshua P. Salmond, George P. C. Molecular genetic and physical analysis of gas vesicles in buoyant enterobacteria |
title | Molecular genetic and physical analysis of gas vesicles in buoyant enterobacteria |
title_full | Molecular genetic and physical analysis of gas vesicles in buoyant enterobacteria |
title_fullStr | Molecular genetic and physical analysis of gas vesicles in buoyant enterobacteria |
title_full_unstemmed | Molecular genetic and physical analysis of gas vesicles in buoyant enterobacteria |
title_short | Molecular genetic and physical analysis of gas vesicles in buoyant enterobacteria |
title_sort | molecular genetic and physical analysis of gas vesicles in buoyant enterobacteria |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4982088/ https://www.ncbi.nlm.nih.gov/pubmed/26743231 http://dx.doi.org/10.1111/1462-2920.13203 |
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