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Reversing methanogenesis to capture methane for liquid biofuel precursors

BACKGROUND: Energy from remote methane reserves is transformative; however, unintended release of this potent greenhouse gas makes it imperative to convert methane efficiently into more readily transported biofuels. No pure microbial culture that grows on methane anaerobically has been isolated, des...

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Autores principales: Soo, Valerie W. C., McAnulty, Michael J., Tripathi, Arti, Zhu, Fayin, Zhang, Limin, Hatzakis, Emmanuel, Smith, Philip B., Agrawal, Saumya, Nazem-Bokaee, Hadi, Gopalakrishnan, Saratram, Salis, Howard M., Ferry, James G., Maranas, Costas D., Patterson, Andrew D., Wood, Thomas K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4714516/
https://www.ncbi.nlm.nih.gov/pubmed/26767617
http://dx.doi.org/10.1186/s12934-015-0397-z
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author Soo, Valerie W. C.
McAnulty, Michael J.
Tripathi, Arti
Zhu, Fayin
Zhang, Limin
Hatzakis, Emmanuel
Smith, Philip B.
Agrawal, Saumya
Nazem-Bokaee, Hadi
Gopalakrishnan, Saratram
Salis, Howard M.
Ferry, James G.
Maranas, Costas D.
Patterson, Andrew D.
Wood, Thomas K.
author_facet Soo, Valerie W. C.
McAnulty, Michael J.
Tripathi, Arti
Zhu, Fayin
Zhang, Limin
Hatzakis, Emmanuel
Smith, Philip B.
Agrawal, Saumya
Nazem-Bokaee, Hadi
Gopalakrishnan, Saratram
Salis, Howard M.
Ferry, James G.
Maranas, Costas D.
Patterson, Andrew D.
Wood, Thomas K.
author_sort Soo, Valerie W. C.
collection PubMed
description BACKGROUND: Energy from remote methane reserves is transformative; however, unintended release of this potent greenhouse gas makes it imperative to convert methane efficiently into more readily transported biofuels. No pure microbial culture that grows on methane anaerobically has been isolated, despite that methane capture through anaerobic processes is more efficient than aerobic ones. RESULTS: Here we engineered the archaeal methanogen Methanosarcina acetivorans to grow anaerobically on methane as a pure culture and to convert methane into the biofuel precursor acetate. To capture methane, we cloned the enzyme methyl-coenzyme M reductase (Mcr) from an unculturable organism, anaerobic methanotrophic archaeal population 1 (ANME-1) from a Black Sea mat, into M. acetivorans to effectively run methanogenesis in reverse. Starting with low-density inocula, M. acetivorans cells producing ANME-1 Mcr consumed up to 9 ± 1 % of methane (corresponding to 109 ± 12 µmol of methane) after 6 weeks of anaerobic growth on methane and utilized 10 mM FeCl(3) as an electron acceptor. Accordingly, increases in cell density and total protein were observed as cells grew on methane in a biofilm on solid FeCl(3). When incubated on methane for 5 days, high-densities of ANME-1 Mcr-producing M. acetivorans cells consumed 15 ± 2 % methane (corresponding to 143 ± 16 µmol of methane), and produced 10.3 ± 0.8 mM acetate (corresponding to 52 ± 4 µmol of acetate). We further confirmed the growth on methane and acetate production using (13)C isotopic labeling of methane and bicarbonate coupled with nuclear magnetic resonance and gas chromatography/mass spectroscopy, as well as RNA sequencing. CONCLUSIONS: We anticipate that our metabolically-engineered strain will provide insights into how methane is cycled in the environment by Archaea as well as will possibly be utilized to convert remote sources of methane into more easily transported biofuels via acetate. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12934-015-0397-z) contains supplementary material, which is available to authorized users.
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spelling pubmed-47145162016-01-16 Reversing methanogenesis to capture methane for liquid biofuel precursors Soo, Valerie W. C. McAnulty, Michael J. Tripathi, Arti Zhu, Fayin Zhang, Limin Hatzakis, Emmanuel Smith, Philip B. Agrawal, Saumya Nazem-Bokaee, Hadi Gopalakrishnan, Saratram Salis, Howard M. Ferry, James G. Maranas, Costas D. Patterson, Andrew D. Wood, Thomas K. Microb Cell Fact Research BACKGROUND: Energy from remote methane reserves is transformative; however, unintended release of this potent greenhouse gas makes it imperative to convert methane efficiently into more readily transported biofuels. No pure microbial culture that grows on methane anaerobically has been isolated, despite that methane capture through anaerobic processes is more efficient than aerobic ones. RESULTS: Here we engineered the archaeal methanogen Methanosarcina acetivorans to grow anaerobically on methane as a pure culture and to convert methane into the biofuel precursor acetate. To capture methane, we cloned the enzyme methyl-coenzyme M reductase (Mcr) from an unculturable organism, anaerobic methanotrophic archaeal population 1 (ANME-1) from a Black Sea mat, into M. acetivorans to effectively run methanogenesis in reverse. Starting with low-density inocula, M. acetivorans cells producing ANME-1 Mcr consumed up to 9 ± 1 % of methane (corresponding to 109 ± 12 µmol of methane) after 6 weeks of anaerobic growth on methane and utilized 10 mM FeCl(3) as an electron acceptor. Accordingly, increases in cell density and total protein were observed as cells grew on methane in a biofilm on solid FeCl(3). When incubated on methane for 5 days, high-densities of ANME-1 Mcr-producing M. acetivorans cells consumed 15 ± 2 % methane (corresponding to 143 ± 16 µmol of methane), and produced 10.3 ± 0.8 mM acetate (corresponding to 52 ± 4 µmol of acetate). We further confirmed the growth on methane and acetate production using (13)C isotopic labeling of methane and bicarbonate coupled with nuclear magnetic resonance and gas chromatography/mass spectroscopy, as well as RNA sequencing. CONCLUSIONS: We anticipate that our metabolically-engineered strain will provide insights into how methane is cycled in the environment by Archaea as well as will possibly be utilized to convert remote sources of methane into more easily transported biofuels via acetate. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12934-015-0397-z) contains supplementary material, which is available to authorized users. BioMed Central 2016-01-14 /pmc/articles/PMC4714516/ /pubmed/26767617 http://dx.doi.org/10.1186/s12934-015-0397-z Text en © Soo et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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.
spellingShingle Research
Soo, Valerie W. C.
McAnulty, Michael J.
Tripathi, Arti
Zhu, Fayin
Zhang, Limin
Hatzakis, Emmanuel
Smith, Philip B.
Agrawal, Saumya
Nazem-Bokaee, Hadi
Gopalakrishnan, Saratram
Salis, Howard M.
Ferry, James G.
Maranas, Costas D.
Patterson, Andrew D.
Wood, Thomas K.
Reversing methanogenesis to capture methane for liquid biofuel precursors
title Reversing methanogenesis to capture methane for liquid biofuel precursors
title_full Reversing methanogenesis to capture methane for liquid biofuel precursors
title_fullStr Reversing methanogenesis to capture methane for liquid biofuel precursors
title_full_unstemmed Reversing methanogenesis to capture methane for liquid biofuel precursors
title_short Reversing methanogenesis to capture methane for liquid biofuel precursors
title_sort reversing methanogenesis to capture methane for liquid biofuel precursors
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4714516/
https://www.ncbi.nlm.nih.gov/pubmed/26767617
http://dx.doi.org/10.1186/s12934-015-0397-z
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