Cargando…
Genome Scale Metabolic Model of the versatile methanotroph Methylocella silvestris
BACKGROUND: Methylocella silvestris is a facultative aerobic methanotrophic bacterium which uses not only methane, but also other alkanes such as ethane and propane, as carbon and energy sources. Its high metabolic versatility, together with the availability of tools for its genetic engineering, mak...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7364539/ https://www.ncbi.nlm.nih.gov/pubmed/32677952 http://dx.doi.org/10.1186/s12934-020-01395-0 |
_version_ | 1783559849891594240 |
---|---|
author | Bordel, Sergio Crombie, Andrew T. Muñoz, Raúl Murrell, J. Colin |
author_facet | Bordel, Sergio Crombie, Andrew T. Muñoz, Raúl Murrell, J. Colin |
author_sort | Bordel, Sergio |
collection | PubMed |
description | BACKGROUND: Methylocella silvestris is a facultative aerobic methanotrophic bacterium which uses not only methane, but also other alkanes such as ethane and propane, as carbon and energy sources. Its high metabolic versatility, together with the availability of tools for its genetic engineering, make it a very promising platform for metabolic engineering and industrial biotechnology using natural gas as substrate. RESULTS: The first Genome Scale Metabolic Model for M. silvestris is presented. The model has been used to predict the ability of M. silvestris to grow on 12 different substrates, the growth phenotype of two deletion mutants (ΔICL and ΔMS), and biomass yield on methane and ethanol. The model, together with phenotypic characterization of the deletion mutants, revealed that M. silvestris uses the glyoxylate shuttle for the assimilation of C1 and C2 substrates, which is unique in contrast to published reports of other methanotrophs. Two alternative pathways for propane metabolism have been identified and validated experimentally using enzyme activity tests and constructing a deletion mutant (Δ1641), which enabled the identification of acetol as one of the intermediates of propane assimilation via 2-propanol. The model was also used to integrate proteomic data and to identify key enzymes responsible for the adaptation of M. silvestris to different substrates. CONCLUSIONS: The model has been used to elucidate key metabolic features of M. silvestris, such as its use of the glyoxylate shuttle for the assimilation of one and two carbon compounds and the existence of two parallel metabolic pathways for propane assimilation. This model, together with the fact that tools for its genetic engineering already exist, paves the way for the use of M. silvestris as a platform for metabolic engineering and industrial exploitation of methanotrophs. |
format | Online Article Text |
id | pubmed-7364539 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-73645392020-07-20 Genome Scale Metabolic Model of the versatile methanotroph Methylocella silvestris Bordel, Sergio Crombie, Andrew T. Muñoz, Raúl Murrell, J. Colin Microb Cell Fact Research BACKGROUND: Methylocella silvestris is a facultative aerobic methanotrophic bacterium which uses not only methane, but also other alkanes such as ethane and propane, as carbon and energy sources. Its high metabolic versatility, together with the availability of tools for its genetic engineering, make it a very promising platform for metabolic engineering and industrial biotechnology using natural gas as substrate. RESULTS: The first Genome Scale Metabolic Model for M. silvestris is presented. The model has been used to predict the ability of M. silvestris to grow on 12 different substrates, the growth phenotype of two deletion mutants (ΔICL and ΔMS), and biomass yield on methane and ethanol. The model, together with phenotypic characterization of the deletion mutants, revealed that M. silvestris uses the glyoxylate shuttle for the assimilation of C1 and C2 substrates, which is unique in contrast to published reports of other methanotrophs. Two alternative pathways for propane metabolism have been identified and validated experimentally using enzyme activity tests and constructing a deletion mutant (Δ1641), which enabled the identification of acetol as one of the intermediates of propane assimilation via 2-propanol. The model was also used to integrate proteomic data and to identify key enzymes responsible for the adaptation of M. silvestris to different substrates. CONCLUSIONS: The model has been used to elucidate key metabolic features of M. silvestris, such as its use of the glyoxylate shuttle for the assimilation of one and two carbon compounds and the existence of two parallel metabolic pathways for propane assimilation. This model, together with the fact that tools for its genetic engineering already exist, paves the way for the use of M. silvestris as a platform for metabolic engineering and industrial exploitation of methanotrophs. BioMed Central 2020-07-16 /pmc/articles/PMC7364539/ /pubmed/32677952 http://dx.doi.org/10.1186/s12934-020-01395-0 Text en © The Author(s) 2020 Open AccessThis 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/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Bordel, Sergio Crombie, Andrew T. Muñoz, Raúl Murrell, J. Colin Genome Scale Metabolic Model of the versatile methanotroph Methylocella silvestris |
title | Genome Scale Metabolic Model of the versatile methanotroph Methylocella silvestris |
title_full | Genome Scale Metabolic Model of the versatile methanotroph Methylocella silvestris |
title_fullStr | Genome Scale Metabolic Model of the versatile methanotroph Methylocella silvestris |
title_full_unstemmed | Genome Scale Metabolic Model of the versatile methanotroph Methylocella silvestris |
title_short | Genome Scale Metabolic Model of the versatile methanotroph Methylocella silvestris |
title_sort | genome scale metabolic model of the versatile methanotroph methylocella silvestris |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7364539/ https://www.ncbi.nlm.nih.gov/pubmed/32677952 http://dx.doi.org/10.1186/s12934-020-01395-0 |
work_keys_str_mv | AT bordelsergio genomescalemetabolicmodeloftheversatilemethanotrophmethylocellasilvestris AT crombieandrewt genomescalemetabolicmodeloftheversatilemethanotrophmethylocellasilvestris AT munozraul genomescalemetabolicmodeloftheversatilemethanotrophmethylocellasilvestris AT murrelljcolin genomescalemetabolicmodeloftheversatilemethanotrophmethylocellasilvestris |