Influence of carbon monoxide on metabolite formation in Methanosarcina acetivorans

被引:21
作者
Oelgeschlaeger, Ellen [1 ]
Rother, Michael [1 ]
机构
[1] Univ Frankfurt, Inst Mol Biowissensch, D-60438 Frankfurt, Germany
关键词
Methanosarcina acetivorans; carbon monoxide; methanogenesis; acetogenesis; formate; methyl-sulfide; COENZYME-M METHYLTRANSFERASE; METHANOGENIC ARCHAEA; METHANE FORMATION; BARKERI; BACTERIA; GROWTH; ENERGY; NA+; FORMALDEHYDE; REDUCTION;
D O I
10.1111/j.1574-6968.2009.01492.x
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Methanogenic archaea conserve energy for growth by reducing some one- and two-carbon compounds to methane and concomitantly generating an ion motive force. Growth of Methanosarcina acetivorans on carbon monoxide (CO) is peculiar as it involves formation of, besides methane, formate, acetate and methylated thiols. It has been argued that methane formation is partially inhibited under carboxidotrophic conditions and that the other products result from either detoxification of CO or from bypassing methanogenesis with other pathways for energy conservation. To gain a deeper understanding of the CO-dependent physiology of M. acetivorans we analyzed metabolite formation in resting cells. The initial rates of methane, acetate, formate, and dimethylsulfide formation increased differentially with increasing CO concentrations but were maximal already at the same moderate CO partial pressure. Strikingly, further increase of the amount of CO was not inhibitory. The maximal rate of methane formation from CO was approximately fivefold lower than that from methanol, consistent with the previously observed significant downregulation of the energy converting sodium-dependent methyltransferase. The rate of dimethylsulfide formation from CO was only 1-2% of that of methane formation under any conditions tested. Implications of the data presented for previously proposed pathways of CO utilization are discussed.
引用
收藏
页码:254 / 260
页数:7
相关论文
共 26 条
[1]   N-5-METHYL-TETRAHYDROMETHANOPTERIN - COENZYME-M METHYLTRANSFERASE OF METHANOSARCINA STRAIN GO1 IS AN NA+-TRANSLOCATING MEMBRANE-PROTEIN [J].
BECHER, B ;
MULLER, V ;
GOTTSCHALK, G .
JOURNAL OF BACTERIOLOGY, 1992, 174 (23) :7656-7660
[2]  
Deppenmeier Uwe, 2008, V45, P123, DOI 10.1007/400_2006_026
[3]   FERREDOXIN-DEPENDENT METHANE FORMATION FROM ACETATE IN CELL-EXTRACTS OF METHANOSARCINA-BARKERI (STRAIN MS) [J].
FISCHER, R ;
THAUER, RK .
FEBS LETTERS, 1990, 269 (02) :368-372
[4]   The genome of M-acetivorans reveals extensive metabolic and physiological diversity [J].
Galagan, JE ;
Nusbaum, C ;
Roy, A ;
Endrizzi, MG ;
Macdonald, P ;
FitzHugh, W ;
Calvo, S ;
Engels, R ;
Smirnov, S ;
Atnoor, D ;
Brown, A ;
Allen, N ;
Naylor, J ;
Stange-Thomann, N ;
DeArellano, K ;
Johnson, R ;
Linton, L ;
McEwan, P ;
McKernan, K ;
Talamas, J ;
Tirrell, A ;
Ye, WJ ;
Zimmer, A ;
Barber, RD ;
Cann, I ;
Graham, DE ;
Grahame, DA ;
Guss, AM ;
Hedderich, R ;
Ingram-Smith, C ;
Kuettner, HC ;
Krzycki, JA ;
Leigh, JA ;
Li, WX ;
Liu, JF ;
Mukhopadhyay, B ;
Reeve, JN ;
Smith, K ;
Springer, TA ;
Umayam, LA ;
White, O ;
White, RH ;
de Macario, EC ;
Ferry, JG ;
Jarrell, KF ;
Jing, H ;
Macario, AJL ;
Paulsen, I ;
Pritchett, M ;
Sowers, KR .
GENOME RESEARCH, 2002, 12 (04) :532-542
[5]   PURIFICATION AND PROPERTIES OF N(5)-METHYLTETRAHYDROMETHANOPTERIN COENZYME-M METHYLTRANSFERASE FROM METHANOBACTERIUM-THERMOAUTOTROPHICUM [J].
GARTNER, P ;
ECKER, A ;
FISCHER, R ;
LINDER, D ;
FUCHS, G ;
THAUER, RK .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1993, 213 (01) :537-545
[6]   Genetic analysis of mch mutants in two Methanosarcina species demonstrates multiple roles for the methanopterin-dependent C-1 oxidation/reduction pathway and differences in H2 metabolism between closely related species [J].
Guss, AM ;
Mukhopadhyay, B ;
Zhang, JK ;
Metcalf, WW .
MOLECULAR MICROBIOLOGY, 2005, 55 (06) :1671-1680
[7]   THE SODIUM CYCLE IN METHANOGENESIS - CO2 REDUCTION TO THE FORMALDEHYDE LEVEL IN METHANOGENIC BACTERIA IS DRIVEN BY A PRIMARY ELECTROCHEMICAL POTENTIAL OF NA+ GENERATED BY FORMALDEHYDE REDUCTION TO CH4 [J].
KAESLER, B ;
SCHONHEIT, P .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1989, 186 (1-2) :309-316
[8]   An unconventional pathway for reduction of CO2 to methane in CO-grown Methanosarcina acetivorans revealed by proteomics [J].
Lessner, Daniel J. ;
Li, Lingyun ;
Li, Qingbo ;
Rejtar, Tomas ;
Andreev, Victor P. ;
Reichlen, Matthew ;
Hill, Kevin ;
Moran, James J. ;
Karger, Barry L. ;
Ferry, James G. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (47) :17921-17926
[9]   PRODUCTION AND CONSUMPTION OF H-2 DURING GROWTH OF METHANOSARCINA SPP ON ACETATE [J].
LOVLEY, DR ;
FERRY, JG .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1985, 49 (01) :247-249
[10]   Molecular, genetic, and biochemical characterization of the serC gene of Methanosarcina barkeri fusaro [J].
Metcalf, WW ;
Zhang, JK ;
Shi, X ;
Wolfe, RS .
JOURNAL OF BACTERIOLOGY, 1996, 178 (19) :5797-5802