Giuseppe
Emeritus
Rapid Acquisition of Gigapascal-High-Pressure Resistance by Escherichia coli (mBio, abstract, edited)
[Source: mBio, full text: <cite cite="http://mbio.asm.org/content/2/1/e00130-10.short?rss=1">Rapid Acquisition of Gigapascal-High-Pressure Resistance by Escherichia coli ? mBio</cite>. Abstract, edited.]
Rapid Acquisition of Gigapascal-High-Pressure Resistance by Escherichia coli
1. Dietrich Vanlint a, 2. Rachael Mitchell b, 3. Edward Bailey b, 4. Filip Meersman b,c, 5. Paul F. McMillan b, 6. Chris W. Michiels a, and 7. Abram Aertsen a
Author Affiliations
1. Laboratory of Food Microbiology and Leuven Food Science and Nutrition Research Centre (LFoRCe), Department of Microbial and Molecular Systems (M?S), Faculty of Bioscience Engineering, Katholieke Universiteit Leuven, Leuven, Belgium (a);
2. University College London, Department of Chemistry, Christopher Ingold Laboratories, London, United Kingdom (b); and
3. Department of Chemistry, Katholieke Universiteit Leuven, Leuven, Belgium (c)
1. Address correspondence to Abram Aertsen, abram.aertsen@biw.kuleuven.be.
1. Editor Sankar Adhya, National Cancer Institute
ABSTRACT
Pressure and temperature are important environmental variables that influence living systems. However, while they vary over a considerable range on Earth and other planets, it has hardly been addressed how straightforwardly and to what extent cellular life can acquire resistance to extremes of these parameters within a defined genomic context and a limited number of generations. Nevertheless, this is a very pertinent question with respect to the penetration of life in allegedly inhospitable environments. In this study, directed evolution was used to reveal the potential of the nonsporulating and mesophilic model bacterium Escherichia coli to develop the ability to survive exposure to high temperature or pressure. While heat resistance could only marginally be increased, our data show that piezoresistance could readily and reproducibly be extended into the GPa range, thereby greatly exceeding the currently recognized maximum for growth or survival.
IMPORTANCE
While extremophilic microorganisms generally serve as the reference for microbial survival capacities in inhospitable environments, we set out to examine how readily a mesophilic model bacterium such as Escherichia coli could build up resistance to extremes of temperature or pressure within a very short evolutionary time scale. Both heat and high pressure constitute ecologically important physical stresses that are able to irrevocably penetrate the entire cell. Our results for the first time establish that cellular life can acquire resistance to pressures extending into the GPa range.
Footnotes
* Citation Vanlint, D., R. Mitchell, E. Bailey, F. Meersman, P. F. McMillan, et al. 2011. Rapid acquisition of gigapascal-high-pressure resistance by Escherichia coli. mBio 2(1):e00130-10. doi:10.1128/mBio.00130-10.
* Received 3 December 2010
* Accepted 29 December 2010
* Published 25 January 2011
* Copyright ? 2011 Vanlint et al.
This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported License, which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original author and source are credited.
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[Source: mBio, full text: <cite cite="http://mbio.asm.org/content/2/1/e00130-10.short?rss=1">Rapid Acquisition of Gigapascal-High-Pressure Resistance by Escherichia coli ? mBio</cite>. Abstract, edited.]
Rapid Acquisition of Gigapascal-High-Pressure Resistance by Escherichia coli
1. Dietrich Vanlint a, 2. Rachael Mitchell b, 3. Edward Bailey b, 4. Filip Meersman b,c, 5. Paul F. McMillan b, 6. Chris W. Michiels a, and 7. Abram Aertsen a
Author Affiliations
1. Laboratory of Food Microbiology and Leuven Food Science and Nutrition Research Centre (LFoRCe), Department of Microbial and Molecular Systems (M?S), Faculty of Bioscience Engineering, Katholieke Universiteit Leuven, Leuven, Belgium (a);
2. University College London, Department of Chemistry, Christopher Ingold Laboratories, London, United Kingdom (b); and
3. Department of Chemistry, Katholieke Universiteit Leuven, Leuven, Belgium (c)
1. Address correspondence to Abram Aertsen, abram.aertsen@biw.kuleuven.be.
1. Editor Sankar Adhya, National Cancer Institute
ABSTRACT
Pressure and temperature are important environmental variables that influence living systems. However, while they vary over a considerable range on Earth and other planets, it has hardly been addressed how straightforwardly and to what extent cellular life can acquire resistance to extremes of these parameters within a defined genomic context and a limited number of generations. Nevertheless, this is a very pertinent question with respect to the penetration of life in allegedly inhospitable environments. In this study, directed evolution was used to reveal the potential of the nonsporulating and mesophilic model bacterium Escherichia coli to develop the ability to survive exposure to high temperature or pressure. While heat resistance could only marginally be increased, our data show that piezoresistance could readily and reproducibly be extended into the GPa range, thereby greatly exceeding the currently recognized maximum for growth or survival.
IMPORTANCE
While extremophilic microorganisms generally serve as the reference for microbial survival capacities in inhospitable environments, we set out to examine how readily a mesophilic model bacterium such as Escherichia coli could build up resistance to extremes of temperature or pressure within a very short evolutionary time scale. Both heat and high pressure constitute ecologically important physical stresses that are able to irrevocably penetrate the entire cell. Our results for the first time establish that cellular life can acquire resistance to pressures extending into the GPa range.
Footnotes
* Citation Vanlint, D., R. Mitchell, E. Bailey, F. Meersman, P. F. McMillan, et al. 2011. Rapid acquisition of gigapascal-high-pressure resistance by Escherichia coli. mBio 2(1):e00130-10. doi:10.1128/mBio.00130-10.
* Received 3 December 2010
* Accepted 29 December 2010
* Published 25 January 2011
* Copyright ? 2011 Vanlint et al.
This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported License, which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original author and source are credited.
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