The ins and outs of Na+ bioenergetics in Acetobacterium woodii

被引:48
作者
Schmidt, Silke [1 ]
Biegel, Eva [1 ]
Mueller, Volker [1 ]
机构
[1] Univ Frankfurt, Inst Mol Biosci, Frankfurt, Germany
来源
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS | 2009年 / 1787卷 / 06期
关键词
Acetogen; Acetobacterium woodii; Energy conservation; Caffeate respiration; Rnf; ATP synthase; POTENTIAL COUPLING SITE; ATP SYNTHASE; VIBRIO-ALGINOLYTICUS; CLOSTRIDIUM-THERMOACETICUM; TRANSLOCATING F1F0-ATPASE; ENERGY-CONSERVATION; CAFFEATE REDUCTION; ANAEROBIC-BACTERIA; ESCHERICHIA-COLI; ROTOR RING;
D O I
10.1016/j.bbabio.2008.12.015
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The acetogenic bacterium Acetobacterium woodii uses a transmembrane electrochemical sodium ion potential for bioenergetic reactions. A primary sodium ion potential is established during carbonate (acetogenesis) as well as caffeate respiration. The electrogenic Na+ pump connected to the Wood-Ljungdahl pathway (acetogenesis) still remains to be identified. The pathway of caffeate reduction with hydrogen as electron donor was investigated and the only membrane-bound activity was found to be a ferredoxin-dependent NAD(+) reduction. This exergonic electron transfer reaction may be catalyzed by the membrane-bound Rnf complex that was discovered recently and is suggested to couple exergonic electron transfer from ferredoxin to NAD(+) to the vectorial transport of Na+ across the cytoplasmic membrane. Rnf may also be involved in acetogenesis. The electrochemical sodium ion potential thus generated is used to drive endergonic reactions such as flagellar rotation and ATP synthesis. The ATP synthase is a member of the F1FO class of enzymes but has an unusual and exceptional feature. Its membrane-embedded rotor is a hybrid made of F-O and V-O-like subunits in a stoichiometry of 9:1. This stoichiometry is apparently not variable with the growth conditions. The structure and function of the Rnf complex and the Na+ F1FO ATP synthase as key elements of the Na+ cycle in A. woodii are discussed. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:691 / 696
页数:6
相关论文
共 71 条
[21]   An intermediate step in the evolution of ATPases -: a hybrid F0-V0 rotor in a bacterial Na+F1F0 ATP synthase [J].
Fritz, Michael ;
Klyszejko, Adriana L. ;
Morgner, Nina ;
Vonck, Janet ;
Brutschy, Bernd ;
Muller, Daniel J. ;
Meier, Thomas ;
Mueller, Volker .
FEBS JOURNAL, 2008, 275 (09) :1999-2007
[22]   An intermediate step in the evolution of ATPases -: the F1F0-ATPase from Acetobacterium woodii contains F-type and V-type rotor subunits and is capable of ATP synthesis [J].
Fritz, Michael ;
Mueller, Volker .
FEBS JOURNAL, 2007, 274 (13) :3421-3428
[23]   The Na+-translocating methyltransferase complex from methanogenic archaea [J].
Gottschalk, G ;
Thauer, RK .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS, 2001, 1505 (01) :28-36
[24]   ATP FORMATION COUPLED TO CAFFEATE REDUCTION BY H-2 IN ACETOBACTERIUM-WOODII NZVA16 [J].
HANSEN, B ;
BOKRANZ, M ;
SCHONHEIT, P ;
KROGER, A .
ARCHIVES OF MICROBIOLOGY, 1988, 150 (05) :447-451
[25]   Energy conservation via electron-transferring flavoprotein in anaerobic bacteria [J].
Herrmann, Gloria ;
Jayamani, Elamparithi ;
Mai, Galina ;
Buckel, Wolfgang .
JOURNAL OF BACTERIOLOGY, 2008, 190 (03) :784-791
[26]   Chemiosmotic energy conservation with Na+ as the coupling ion during hydrogen-dependent caffeate reduction by Acetobacterium woodii [J].
Imkamp, F ;
Müller, V .
JOURNAL OF BACTERIOLOGY, 2002, 184 (07) :1947-1951
[27]   Dissection of the caffeate respiratory chain in the acetogen Acetobactetium woodii:: Identification of an rnf-type NADH dehydrogenase as a potential coupling site [J].
Imkamp, Frank ;
Biegel, Eva ;
Jayamami, Elamparithi ;
Buckel, Wolfgang ;
Mueller, Volker .
JOURNAL OF BACTERIOLOGY, 2007, 189 (22) :8145-8153
[28]   PURIFICATION AND CHARACTERIZATION OF THE F1-ATPASE FROM CLOSTRIDIUM-THERMOACETICUM [J].
IVEY, DM ;
LJUNGDAHL, LG .
JOURNAL OF BACTERIOLOGY, 1986, 165 (01) :252-257
[29]   Mutations in single hairpin units of genetically fused subunit c provide support for a rotary catalytic mechanism in F0F1 ATP synthase [J].
Jones, PC ;
Hermolin, J ;
Fillingame, RH .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (15) :11355-11360
[30]   Arrangement of the multicopy H+-translocating subunit c in the membrane sector of the Escherichia coli F1F0 ATP synthase [J].
Jones, PC ;
Jiang, WP ;
Fillingame, RH .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (27) :17178-17185