Cargando…

Core Metabolism Shifts during Growth on Methanol versus Methane in the Methanotroph Methylomicrobium buryatense 5GB1

Methylomicrobium buryatense 5GB1 is an obligate methylotroph which grows on methane or methanol with similar growth rates. It has long been assumed that the core metabolic pathways must be similar on the two substrates, but recent studies of methane metabolism in this bacterium suggest that growth o...

Descripción completa

Detalles Bibliográficos
Autores principales: Fu, Yanfen, He, Lian, Reeve, Jennifer, Beck, David A. C., Lidstrom, Mary E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6456754/
https://www.ncbi.nlm.nih.gov/pubmed/30967465
http://dx.doi.org/10.1128/mBio.00406-19
_version_ 1783409802884415488
author Fu, Yanfen
He, Lian
Reeve, Jennifer
Beck, David A. C.
Lidstrom, Mary E.
author_facet Fu, Yanfen
He, Lian
Reeve, Jennifer
Beck, David A. C.
Lidstrom, Mary E.
author_sort Fu, Yanfen
collection PubMed
description Methylomicrobium buryatense 5GB1 is an obligate methylotroph which grows on methane or methanol with similar growth rates. It has long been assumed that the core metabolic pathways must be similar on the two substrates, but recent studies of methane metabolism in this bacterium suggest that growth on methanol might have significant differences from growth on methane. In this study, both a targeted metabolomics approach and a (13)C tracer approach were taken to understand core carbon metabolism in M. buryatense 5GB1 during growth on methanol and to determine whether such differences occur. Our results suggest a systematic shift of active core metabolism in which increased flux occurred through both the Entner-Doudoroff (ED) pathway and the partial serine cycle, while the tricarboxylic acid (TCA) cycle was incomplete, in contrast to growth on methane. Using the experimental results as constraints, we applied flux balance analysis to determine the metabolic flux phenotype of M. buryatense 5GB1 growing on methanol, and the results are consistent with predictions based on ATP and NADH changes. Transcriptomics analysis suggested that the changes in fluxes and metabolite levels represented results of posttranscriptional regulation. The combination of flux balance analysis of the genome-scale model and the flux ratio from (13)C data changed the solution space for a better prediction of cell behavior and demonstrated the significant differences in physiology between growth on methane and growth on methanol.
format Online
Article
Text
id pubmed-6456754
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher American Society for Microbiology
record_format MEDLINE/PubMed
spelling pubmed-64567542019-04-12 Core Metabolism Shifts during Growth on Methanol versus Methane in the Methanotroph Methylomicrobium buryatense 5GB1 Fu, Yanfen He, Lian Reeve, Jennifer Beck, David A. C. Lidstrom, Mary E. mBio Research Article Methylomicrobium buryatense 5GB1 is an obligate methylotroph which grows on methane or methanol with similar growth rates. It has long been assumed that the core metabolic pathways must be similar on the two substrates, but recent studies of methane metabolism in this bacterium suggest that growth on methanol might have significant differences from growth on methane. In this study, both a targeted metabolomics approach and a (13)C tracer approach were taken to understand core carbon metabolism in M. buryatense 5GB1 during growth on methanol and to determine whether such differences occur. Our results suggest a systematic shift of active core metabolism in which increased flux occurred through both the Entner-Doudoroff (ED) pathway and the partial serine cycle, while the tricarboxylic acid (TCA) cycle was incomplete, in contrast to growth on methane. Using the experimental results as constraints, we applied flux balance analysis to determine the metabolic flux phenotype of M. buryatense 5GB1 growing on methanol, and the results are consistent with predictions based on ATP and NADH changes. Transcriptomics analysis suggested that the changes in fluxes and metabolite levels represented results of posttranscriptional regulation. The combination of flux balance analysis of the genome-scale model and the flux ratio from (13)C data changed the solution space for a better prediction of cell behavior and demonstrated the significant differences in physiology between growth on methane and growth on methanol. American Society for Microbiology 2019-04-09 /pmc/articles/PMC6456754/ /pubmed/30967465 http://dx.doi.org/10.1128/mBio.00406-19 Text en Copyright © 2019 Fu et al. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Fu, Yanfen
He, Lian
Reeve, Jennifer
Beck, David A. C.
Lidstrom, Mary E.
Core Metabolism Shifts during Growth on Methanol versus Methane in the Methanotroph Methylomicrobium buryatense 5GB1
title Core Metabolism Shifts during Growth on Methanol versus Methane in the Methanotroph Methylomicrobium buryatense 5GB1
title_full Core Metabolism Shifts during Growth on Methanol versus Methane in the Methanotroph Methylomicrobium buryatense 5GB1
title_fullStr Core Metabolism Shifts during Growth on Methanol versus Methane in the Methanotroph Methylomicrobium buryatense 5GB1
title_full_unstemmed Core Metabolism Shifts during Growth on Methanol versus Methane in the Methanotroph Methylomicrobium buryatense 5GB1
title_short Core Metabolism Shifts during Growth on Methanol versus Methane in the Methanotroph Methylomicrobium buryatense 5GB1
title_sort core metabolism shifts during growth on methanol versus methane in the methanotroph methylomicrobium buryatense 5gb1
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6456754/
https://www.ncbi.nlm.nih.gov/pubmed/30967465
http://dx.doi.org/10.1128/mBio.00406-19
work_keys_str_mv AT fuyanfen coremetabolismshiftsduringgrowthonmethanolversusmethaneinthemethanotrophmethylomicrobiumburyatense5gb1
AT helian coremetabolismshiftsduringgrowthonmethanolversusmethaneinthemethanotrophmethylomicrobiumburyatense5gb1
AT reevejennifer coremetabolismshiftsduringgrowthonmethanolversusmethaneinthemethanotrophmethylomicrobiumburyatense5gb1
AT beckdavidac coremetabolismshiftsduringgrowthonmethanolversusmethaneinthemethanotrophmethylomicrobiumburyatense5gb1
AT lidstrommarye coremetabolismshiftsduringgrowthonmethanolversusmethaneinthemethanotrophmethylomicrobiumburyatense5gb1