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An unconventional pathway for reduction of CO2 to methane in CO-grown Methanosarcina acetivorans revealed by proteomics.

An unconventional pathway for reduction of CO2 to methane in CO-grown Methanosarcina acetivorans revealed by proteomics. Research Abstract Details 

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  • An unconventional pathway for reduction of CO2 to methane in CO-grown Methanosarcina acetivorans revealed by proteomics. Abstract Text:

    daniel j lessnerDaniel J Lessner,lingyun liLingyun Li,qingbo liQingbo Li,tomas rejtarTomas Rejtar,victor p andreevVictor P Andreev,matthew reichlenMatthew Reichlen,kevin hillKevin Hill,james j moranJames J Moran,barry l kargerBarry L Karger,james g ferryJames G Ferry,

    Methanosarcina acetivorans produces acetate, formate, and methane when cultured with CO as the growth substrate [Rother M, Metcalf WW (2004) Proc Natl Acad Sci USA 101:], which suggests novel features of CO metabolism. Here we present a genome-wide proteomic approach to identify and quantify proteins differentially abundant in response to growth on CO versus methanol or acetate. The results indicate that oxidation of CO to CO2 supplies electrons for reduction of CO2 to a methyl group by steps and enzymes of the pathway for CO2 reduction determined for other methane-producing species. However, proteomic and quantitative RT-PCR results suggest that reduction of the methyl group to methane involves novel methyltransferases and a coenzyme F420H2:heterodisulfide oxidoreductase system that generates a proton gradient for ATP synthesis not previously described for pathways reducing CO2 to methane. Biochemical assays support a role for the oxidoreductase, and transcriptional mapping identified an unusual operon structure encoding the oxidoreductase. The proteomic results further indicate that acetate is synthesized from the methyl group and CO by a reversal of initial steps in the pathway for conversion of acetate to methane that yields ATP by substrate level phosphorylation. The results indicate that M. acetivorans utilizes a pathway distinct from all known CO2 reduction pathways for methane formation that reflects an adaptation to the marine environment. Finally, the pathway supports the basis for a recently proposed primitive CO-dependent energy-conservation cycle that drove and directed the early evolution of life on Earth.

    An unconventional pathway for reduction of CO2 to methane in CO-grown Methanosarcina acetivorans revealed by proteomics. Publishing Authors By Initials

    dj lessnerDJ Lessner,l liL Li,q liQ Li,t rejtarT Rejtar,vp andreevVP Andreev,m reichlenM Reichlen,k hillK Hill,jj moranJJ Moran,bl kargerBL Karger,jg ferryJG Ferry,

    For similar biological sciences: biochemistry: proteomics research abstracts see: biological sciences: biochemistry: proteomics research

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    An unconventional pathway for reduction of CO2 to methane in CO-grown Methanosarcina acetivorans revealed by proteomics. Journal Published:

    PUBLICATION TYPE: Research Support, U.S. Gov't,

    Journal: Proceedings of the National Academy of Sciences of

    VOLUME: 103

    Page Numbers: 17921-6

    Journal Abbreviation: Proc. Natl. Acad. Sci. U.S.A.

    ISSN: 0027-8424

    DAY: 13

    MONTH: 11

    YEAR: 2006

    An unconventional pathway for reduction of CO2 to methane in CO-grown Methanosarcina acetivorans revealed by proteomics. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 7505876

    An unconventional pathway for reduction of CO2 to methane in CO-grown Methanosarcina acetivorans revealed by proteomics. Keywords Mesh Terms:

    KEYWORDS: Proteomics

    MESH TERMS: metabolism

    Chemical & Substance for Abstract: An unconventional pathway for reduction of CO2 to methane in CO-grown Methanosarcina acetivorans revealed by proteomics. Information

    Substance Name: coenzyme F420 hydrogenase

    Registry Number: EC 1.12.99.1

    Grant and Affiliation Information for An unconventional pathway for reduction of CO2 to methane in CO-grown Methanosarcina acetivorans revealed by proteomics.

    AFFILIATION: Department of Biochemistry and Molecular Biology and Center for Microbial Structural Biology, Pennsylvania State University, University Park, PA 16802, USA.

    Country: United States

    United States Research PublicationUnited States Research Publication

    AGENCY: United States NIGMS

    GRANT: GM15847

    ACRONYM: GM

    MEDLINETA: Proc Natl Acad Sci U S A

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