Assaying for the 3-hydroxypropionate cycle of carbon fixation

被引:11
作者
Hügler, M [1 ]
Fuchs, G [1 ]
机构
[1] Univ Freiburg, Fac Biol, D-79104 Freiburg, Germany
来源
ENVIRONMENTAL MICROBIOLOGY | 2005年 / 397卷
关键词
D O I
10.1016/S0076-6879(05)97012-2
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The 3-hydroxypropionate cycle is a novel pathway for autotrophic CO(2) fixation, which has been demonstrated in the thermophilic phototrophic bacterium Chloroflexus aurantiacus; a yet to be defined variant of this pathway occurs in autotrophic members of the Sulfolobales (Crenarchaeota). The 3-hydroxypropionate cycle consists of the conversion of acetyl-CoA to succinyl-CoA, via malonyl-CoA, 3-hydroxypropionate, propionyl-CoA, and methylmalonyl-CoA. Carboxylation of acetyl-CoA and propionyl-CoA by acetyl-CoA/propionyl-CoA carboxylase are the CO(2) fixation reactions. Succinyl-CoA serves as a precursor of cell carbon and also as a precursor of the starting compound acetyl-CoA. In C. aurantiacus, the cycle is completed by converting succinyl-CoA to malyl-CoA and cleaving malyl-CoA to acetyl-CoA and glyoxylate. Glyoxylate is then converted in a second cyclic pathway to pyruvate, which serves as a universal cell carbon precursor. The fate of succinyl-CoA in Sulfolobales is at issue. Assays used to study the characteristic enzymes of this novel pathway in C aurantiacus are reported.
引用
收藏
页码:212 / 221
页数:10
相关论文
共 22 条
[1]   Propionyl-coenzyme A synthase from Chloroflexus aurantiacus, a key enzyme of the 3-hydroxypropionate cycle for autotrophic CO2 fixation [J].
Alber, BE ;
Fuchs, G .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (14) :12137-12143
[2]   Carboxylase genes of Sulfolobus metallicus [J].
Burton, NP ;
Williams, TD ;
Norris, PR .
ARCHIVES OF MICROBIOLOGY, 1999, 172 (06) :349-353
[3]   Characterization of a bifunctional archaeal acyl coenzyme A carboxylase [J].
Chuakrut, S ;
Arai, H ;
Ishii, M ;
Igarashi, Y .
JOURNAL OF BACTERIOLOGY, 2003, 185 (03) :938-947
[4]  
EGGERER H, 1964, BIOCHEM Z, V229, P436
[5]   RETROBIOSYNTHETIC ANALYSIS OF CARBON FIXATION IN THE PHOTOTROPHIC EUBACTERIUM CHLOROFLEXUS-AURANTIACUS [J].
EISENREICH, W ;
STRAUSS, G ;
WERZ, U ;
FUCHS, G ;
BACHER, A .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1993, 215 (03) :619-632
[6]   A bicyclic autotrophic CO2 fixation pathway in Chloroflexus aurantiacus. [J].
Herter, S ;
Fuchs, G ;
Bacher, A ;
Eisenreich, W .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (23) :20277-20283
[7]   Autotrophic CO2 fixation by Chloroflexus aurantiacus:: Study of glyoxylate formation and assimilation via the 3-hydroxypropionate cycle [J].
Herter, S ;
Farfsing, J ;
Gad'on, N ;
Rieder, C ;
Eisenreich, W ;
Bacher, A ;
Fuchs, G .
JOURNAL OF BACTERIOLOGY, 2001, 183 (14) :4305-4316
[8]   L-malyl-coenzyme A Lyase/β-methylmalyl-coenzyme A lyase from Chloroflexus aurantiacus, a bifunctional enzyme involved in autotrophic CO2 fixation [J].
Herter, S ;
Busch, A ;
Fuchs, G .
JOURNAL OF BACTERIOLOGY, 2002, 184 (21) :5999-6006
[9]   AUTOTROPHIC GROWTH AND CO2 FIXATION OF CHLOROFLEXUS-AURANTIACUS [J].
HOLO, H ;
SIREVAG, R .
ARCHIVES OF MICROBIOLOGY, 1986, 145 (02) :173-180
[10]   CHLOROFLEXUS-AURANTIACUS SECRETES 3-HYDROXYPROPIONATE, A POSSIBLE INTERMEDIATE IN THE ASSIMILATION OF CO-2 AND ACETATE [J].
HOLO, H .
ARCHIVES OF MICROBIOLOGY, 1989, 151 (03) :252-256