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Exploring the onset of B(12) ‐based mutualisms using a recently evolved Chlamydomonas auxotroph and B(12) ‐producing bacteria
Cobalamin (vitamin B(12)) is a cofactor for essential metabolic reactions in multiple eukaryotic taxa, including major primary producers such as algae, and yet only prokaryotes can produce it. Many bacteria can colonize the algal phycosphere, forming stable communities that gain preferential access...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9545926/ https://www.ncbi.nlm.nih.gov/pubmed/35593514 http://dx.doi.org/10.1111/1462-2920.16035 |
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author | Bunbury, Freddy Deery, Evelyne Sayer, Andrew P. Bhardwaj, Vaibhav Harrison, Ellen L. Warren, Martin J. Smith, Alison G. |
author_facet | Bunbury, Freddy Deery, Evelyne Sayer, Andrew P. Bhardwaj, Vaibhav Harrison, Ellen L. Warren, Martin J. Smith, Alison G. |
author_sort | Bunbury, Freddy |
collection | PubMed |
description | Cobalamin (vitamin B(12)) is a cofactor for essential metabolic reactions in multiple eukaryotic taxa, including major primary producers such as algae, and yet only prokaryotes can produce it. Many bacteria can colonize the algal phycosphere, forming stable communities that gain preferential access to photosynthate and in return provide compounds such as B(12). Extended coexistence can then drive gene loss, leading to greater algal–bacterial interdependence. In this study, we investigate how a recently evolved B(12)‐dependent strain of Chlamydomonas reinhardtii, metE7, forms a mutualism with certain bacteria, including the rhizobium Mesorhizobium loti and even a strain of the gut bacterium E. coli engineered to produce cobalamin. Although metE7 was supported by B(12) producers, its growth in co‐culture was slower than the B(12)‐independent wild‐type, suggesting that high bacterial B(12) provision may be necessary to favour B(12) auxotrophs and their evolution. Moreover, we found that an E. coli strain that releases more B(12) makes a better mutualistic partner, and although this trait may be more costly in isolation, greater B(12) release provided an advantage in co‐cultures. We hypothesize that, given the right conditions, bacteria that release more B(12) may be selected for, particularly if they form close interactions with B(12)‐dependent algae. |
format | Online Article Text |
id | pubmed-9545926 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley & Sons, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-95459262022-10-14 Exploring the onset of B(12) ‐based mutualisms using a recently evolved Chlamydomonas auxotroph and B(12) ‐producing bacteria Bunbury, Freddy Deery, Evelyne Sayer, Andrew P. Bhardwaj, Vaibhav Harrison, Ellen L. Warren, Martin J. Smith, Alison G. Environ Microbiol Research Articles Cobalamin (vitamin B(12)) is a cofactor for essential metabolic reactions in multiple eukaryotic taxa, including major primary producers such as algae, and yet only prokaryotes can produce it. Many bacteria can colonize the algal phycosphere, forming stable communities that gain preferential access to photosynthate and in return provide compounds such as B(12). Extended coexistence can then drive gene loss, leading to greater algal–bacterial interdependence. In this study, we investigate how a recently evolved B(12)‐dependent strain of Chlamydomonas reinhardtii, metE7, forms a mutualism with certain bacteria, including the rhizobium Mesorhizobium loti and even a strain of the gut bacterium E. coli engineered to produce cobalamin. Although metE7 was supported by B(12) producers, its growth in co‐culture was slower than the B(12)‐independent wild‐type, suggesting that high bacterial B(12) provision may be necessary to favour B(12) auxotrophs and their evolution. Moreover, we found that an E. coli strain that releases more B(12) makes a better mutualistic partner, and although this trait may be more costly in isolation, greater B(12) release provided an advantage in co‐cultures. We hypothesize that, given the right conditions, bacteria that release more B(12) may be selected for, particularly if they form close interactions with B(12)‐dependent algae. John Wiley & Sons, Inc. 2022-05-20 2022-07 /pmc/articles/PMC9545926/ /pubmed/35593514 http://dx.doi.org/10.1111/1462-2920.16035 Text en © 2022 The Authors. Environmental Microbiology published by Society for Applied Microbiology and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://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 Bunbury, Freddy Deery, Evelyne Sayer, Andrew P. Bhardwaj, Vaibhav Harrison, Ellen L. Warren, Martin J. Smith, Alison G. Exploring the onset of B(12) ‐based mutualisms using a recently evolved Chlamydomonas auxotroph and B(12) ‐producing bacteria |
title | Exploring the onset of B(12)
‐based mutualisms using a recently evolved
Chlamydomonas
auxotroph and B(12)
‐producing bacteria |
title_full | Exploring the onset of B(12)
‐based mutualisms using a recently evolved
Chlamydomonas
auxotroph and B(12)
‐producing bacteria |
title_fullStr | Exploring the onset of B(12)
‐based mutualisms using a recently evolved
Chlamydomonas
auxotroph and B(12)
‐producing bacteria |
title_full_unstemmed | Exploring the onset of B(12)
‐based mutualisms using a recently evolved
Chlamydomonas
auxotroph and B(12)
‐producing bacteria |
title_short | Exploring the onset of B(12)
‐based mutualisms using a recently evolved
Chlamydomonas
auxotroph and B(12)
‐producing bacteria |
title_sort | exploring the onset of b(12)
‐based mutualisms using a recently evolved
chlamydomonas
auxotroph and b(12)
‐producing bacteria |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9545926/ https://www.ncbi.nlm.nih.gov/pubmed/35593514 http://dx.doi.org/10.1111/1462-2920.16035 |
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