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Engineering lithoheterotrophy in an obligate chemolithoautotrophic Fe(II) oxidizing bacterium

Neutrophilic Fe(II) oxidizing bacteria like Mariprofundus ferrooxydans are obligate chemolithoautotrophic bacteria that play an important role in the biogeochemical cycling of iron and other elements in multiple environments. These bacteria generally exhibit a singular metabolic mode of growth which...

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Autores principales: Jain, Abhiney, Gralnick, Jeffrey A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7835226/
https://www.ncbi.nlm.nih.gov/pubmed/33495498
http://dx.doi.org/10.1038/s41598-021-81412-3
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author Jain, Abhiney
Gralnick, Jeffrey A.
author_facet Jain, Abhiney
Gralnick, Jeffrey A.
author_sort Jain, Abhiney
collection PubMed
description Neutrophilic Fe(II) oxidizing bacteria like Mariprofundus ferrooxydans are obligate chemolithoautotrophic bacteria that play an important role in the biogeochemical cycling of iron and other elements in multiple environments. These bacteria generally exhibit a singular metabolic mode of growth which prohibits comparative “omics” studies. Furthermore, these bacteria are considered non-amenable to classical genetic methods due to low cell densities, the inability to form colonies on solid medium, and production of copious amounts of insoluble iron oxyhydroxides as their metabolic byproduct. Consequently, the molecular and biochemical understanding of these bacteria remains speculative despite the availability of substantial genomic information. Here we develop the first genetic system in neutrophilic Fe(II) oxidizing bacterium and use it to engineer lithoheterotrophy in M. ferrooxydans, a metabolism that has been speculated but not experimentally validated. This synthetic biology approach could be extended to gain physiological understanding and domesticate other bacteria that grow using a single metabolic mode.
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spelling pubmed-78352262021-01-27 Engineering lithoheterotrophy in an obligate chemolithoautotrophic Fe(II) oxidizing bacterium Jain, Abhiney Gralnick, Jeffrey A. Sci Rep Article Neutrophilic Fe(II) oxidizing bacteria like Mariprofundus ferrooxydans are obligate chemolithoautotrophic bacteria that play an important role in the biogeochemical cycling of iron and other elements in multiple environments. These bacteria generally exhibit a singular metabolic mode of growth which prohibits comparative “omics” studies. Furthermore, these bacteria are considered non-amenable to classical genetic methods due to low cell densities, the inability to form colonies on solid medium, and production of copious amounts of insoluble iron oxyhydroxides as their metabolic byproduct. Consequently, the molecular and biochemical understanding of these bacteria remains speculative despite the availability of substantial genomic information. Here we develop the first genetic system in neutrophilic Fe(II) oxidizing bacterium and use it to engineer lithoheterotrophy in M. ferrooxydans, a metabolism that has been speculated but not experimentally validated. This synthetic biology approach could be extended to gain physiological understanding and domesticate other bacteria that grow using a single metabolic mode. Nature Publishing Group UK 2021-01-25 /pmc/articles/PMC7835226/ /pubmed/33495498 http://dx.doi.org/10.1038/s41598-021-81412-3 Text en © The Author(s) 2021 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Jain, Abhiney
Gralnick, Jeffrey A.
Engineering lithoheterotrophy in an obligate chemolithoautotrophic Fe(II) oxidizing bacterium
title Engineering lithoheterotrophy in an obligate chemolithoautotrophic Fe(II) oxidizing bacterium
title_full Engineering lithoheterotrophy in an obligate chemolithoautotrophic Fe(II) oxidizing bacterium
title_fullStr Engineering lithoheterotrophy in an obligate chemolithoautotrophic Fe(II) oxidizing bacterium
title_full_unstemmed Engineering lithoheterotrophy in an obligate chemolithoautotrophic Fe(II) oxidizing bacterium
title_short Engineering lithoheterotrophy in an obligate chemolithoautotrophic Fe(II) oxidizing bacterium
title_sort engineering lithoheterotrophy in an obligate chemolithoautotrophic fe(ii) oxidizing bacterium
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7835226/
https://www.ncbi.nlm.nih.gov/pubmed/33495498
http://dx.doi.org/10.1038/s41598-021-81412-3
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