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Methane utilization in Methylomicrobium alcaliphilum 20Z(R): a systems approach

Biological methane utilization, one of the main sinks of the greenhouse gas in nature, represents an attractive platform for production of fuels and value-added chemicals. Despite the progress made in our understanding of the individual parts of methane utilization, our knowledge of how the whole-ce...

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Detalles Bibliográficos
Autores principales: Akberdin, Ilya R., Thompson, Merlin, Hamilton, Richard, Desai, Nalini, Alexander, Danny, Henard, Calvin A., Guarnieri, Michael T., Kalyuzhnaya, Marina G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5802761/
https://www.ncbi.nlm.nih.gov/pubmed/29410419
http://dx.doi.org/10.1038/s41598-018-20574-z
Descripción
Sumario:Biological methane utilization, one of the main sinks of the greenhouse gas in nature, represents an attractive platform for production of fuels and value-added chemicals. Despite the progress made in our understanding of the individual parts of methane utilization, our knowledge of how the whole-cell metabolic network is organized and coordinated is limited. Attractive growth and methane-conversion rates, a complete and expert-annotated genome sequence, as well as large enzymatic, (13)C-labeling, and transcriptomic datasets make Methylomicrobium alcaliphilum 20Z(R) an exceptional model system for investigating methane utilization networks. Here we present a comprehensive metabolic framework of methane and methanol utilization in M. alcaliphilum 20Z(R). A set of novel metabolic reactions governing carbon distribution across central pathways in methanotrophic bacteria was predicted by in-silico simulations and confirmed by global non-targeted metabolomics and enzymatic evidences. Our data highlight the importance of substitution of ATP-linked steps with PPi-dependent reactions and support the presence of a carbon shunt from acetyl-CoA to the pentose-phosphate pathway and highly branched TCA cycle. The diverged TCA reactions promote balance between anabolic reactions and redox demands. The computational framework of C(1)-metabolism in methanotrophic bacteria can represent an efficient tool for metabolic engineering or ecosystem modeling.