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Methylation at the C-2 position of hopanoids increases rigidity in native bacterial membranes
Sedimentary rocks host a vast reservoir of organic carbon, such as 2-methylhopane biomarkers, whose evolutionary significance we poorly understand. Our ability to interpret this molecular fossil record is constrained by ignorance of the function of their molecular antecedents. To gain insight into t...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4337730/ https://www.ncbi.nlm.nih.gov/pubmed/25599566 http://dx.doi.org/10.7554/eLife.05663 |
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author | Wu, Chia-Hung Bialecka-Fornal, Maja Newman, Dianne K |
author_facet | Wu, Chia-Hung Bialecka-Fornal, Maja Newman, Dianne K |
author_sort | Wu, Chia-Hung |
collection | PubMed |
description | Sedimentary rocks host a vast reservoir of organic carbon, such as 2-methylhopane biomarkers, whose evolutionary significance we poorly understand. Our ability to interpret this molecular fossil record is constrained by ignorance of the function of their molecular antecedents. To gain insight into the meaning of 2-methylhopanes, we quantified the dominant (des)methylated hopanoid species in the membranes of the model hopanoid-producing bacterium Rhodopseudomonas palustris TIE-1. Fluorescence polarization studies of small unilamellar vesicles revealed that hopanoid 2-methylation specifically renders native bacterial membranes more rigid at concentrations that are relevant in vivo. That hopanoids differentially modify native membrane rigidity as a function of their methylation state indicates that methylation itself promotes fitness under stress. Moreover, knowing the in vivo (2Me)-hopanoid concentration range in different cell membranes, and appreciating that (2Me)-hopanoids' biophysical effects are tuned by the lipid environment, permits the design of more relevant in vitro experiments to study their physiological functions. DOI: http://dx.doi.org/10.7554/eLife.05663.001 |
format | Online Article Text |
id | pubmed-4337730 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-43377302015-03-04 Methylation at the C-2 position of hopanoids increases rigidity in native bacterial membranes Wu, Chia-Hung Bialecka-Fornal, Maja Newman, Dianne K eLife Biophysics and Structural Biology Sedimentary rocks host a vast reservoir of organic carbon, such as 2-methylhopane biomarkers, whose evolutionary significance we poorly understand. Our ability to interpret this molecular fossil record is constrained by ignorance of the function of their molecular antecedents. To gain insight into the meaning of 2-methylhopanes, we quantified the dominant (des)methylated hopanoid species in the membranes of the model hopanoid-producing bacterium Rhodopseudomonas palustris TIE-1. Fluorescence polarization studies of small unilamellar vesicles revealed that hopanoid 2-methylation specifically renders native bacterial membranes more rigid at concentrations that are relevant in vivo. That hopanoids differentially modify native membrane rigidity as a function of their methylation state indicates that methylation itself promotes fitness under stress. Moreover, knowing the in vivo (2Me)-hopanoid concentration range in different cell membranes, and appreciating that (2Me)-hopanoids' biophysical effects are tuned by the lipid environment, permits the design of more relevant in vitro experiments to study their physiological functions. DOI: http://dx.doi.org/10.7554/eLife.05663.001 eLife Sciences Publications, Ltd 2015-01-19 /pmc/articles/PMC4337730/ /pubmed/25599566 http://dx.doi.org/10.7554/eLife.05663 Text en © 2015, Wu et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Biophysics and Structural Biology Wu, Chia-Hung Bialecka-Fornal, Maja Newman, Dianne K Methylation at the C-2 position of hopanoids increases rigidity in native bacterial membranes |
title | Methylation at the C-2 position of hopanoids increases rigidity in native bacterial membranes |
title_full | Methylation at the C-2 position of hopanoids increases rigidity in native bacterial membranes |
title_fullStr | Methylation at the C-2 position of hopanoids increases rigidity in native bacterial membranes |
title_full_unstemmed | Methylation at the C-2 position of hopanoids increases rigidity in native bacterial membranes |
title_short | Methylation at the C-2 position of hopanoids increases rigidity in native bacterial membranes |
title_sort | methylation at the c-2 position of hopanoids increases rigidity in native bacterial membranes |
topic | Biophysics and Structural Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4337730/ https://www.ncbi.nlm.nih.gov/pubmed/25599566 http://dx.doi.org/10.7554/eLife.05663 |
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