Acetyl-coenzyme A synthetase (AMP forming)

被引:189
作者
Starai, VJ [1 ]
Escalante-Semerena, JC [1 ]
机构
[1] Univ Wisconsin, Dept Bacteriol, Enzyme Inst 264, Madison, WI 53726 USA
关键词
two-carbon metabolism; acetyl-coenzyme A; acetate : CoA ligase; lifespan; gene expression; sirtuins; chromosome stability; gene silencing;
D O I
10.1007/s00018-004-3448-x
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
Acetyl-coenzyme A synthetase (AMP forming; Acs) is an enzyme whose activity is central to the metabolism of prokaryotic and eukaryotic cells. The physiological role of this enzyme is to activate acetate to acetyl-coenzyme A (Ac-CoA). The importance of Acs has been recognized for decades, since it provides the cell the two-carbon metabolite used in many anabolic and energy generation processes. In the last decade researchers have learned how carefully the cell monitors the synthesis and activity of this enzyme. In eukaryotes and prokaryotes, complex regulatory systems control acs gene expression as a function carbon flux, with a second layer of regulation exerted posttranslationally by the NAD(+)/sirtuin-dependent protein acetylation/deacetylation system. Recent structural work provides snapshots of the dramatic conformational changes Acs undergoes during catalysis. Future work on the regulation of acs gene expression will expand our understanding of metabolic integration, while structure/function studies will reveal more details of the function of this splendid molecular machine.
引用
收藏
页码:2020 / 2030
页数:11
相关论文
共 106 条
[1]   Twelve species of the nucleoid-associated protein from Escherichia coli -: Sequence recognition specificity and DNA binding affinity [J].
Azam, TA ;
Ishihama, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (46) :33105-33113
[2]   DRAMATIC CHANGES IN FIS LEVELS UPON NUTRIENT UPSHIFT IN ESCHERICHIA-COLI [J].
BALL, CA ;
OSUNA, R ;
FERGUSON, KC ;
JOHNSON, RC .
JOURNAL OF BACTERIOLOGY, 1992, 174 (24) :8043-8056
[3]   DIETARY CHANGES OF CYTOPLASMIC ACETYL-COA SYNTHETASE IN DIFFERENT RAT TISSUES [J].
BARTH, C ;
SLADEK, M ;
DECKER, K .
BIOCHIMICA ET BIOPHYSICA ACTA, 1972, 260 (01) :1-&
[4]   Cyclic AMP receptor protein-dependent activation of the Escherichia coli acsP2 promoter by a synergistic class III mechanism [J].
Beatty, CM ;
Browning, DF ;
Busby, SJW ;
Wolfe, AJ .
JOURNAL OF BACTERIOLOGY, 2003, 185 (17) :5148-5157
[5]   From 'reactive C2 units' to acetyl coenzyme A:: a long trail with an acetyl phosphate detour [J].
Bentley, R .
TRENDS IN BIOCHEMICAL SCIENCES, 2000, 25 (06) :302-305
[6]   Inhibition of silencing and accelerated aging by nicotinamide, a putative negative regulator of yeast Sir2 and human SIRT1 [J].
Bitterman, KJ ;
Anderson, RM ;
Cohen, HY ;
Latorre-Esteves, M ;
Sinclair, DA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (47) :45099-45107
[7]   Acid- and base-induced proteins during aerobic and anaerobic growth of Escherichia coli revealed by two-dimensional gel electrophoresis [J].
Blankenhorn, D ;
Phillips, J ;
Slonczewski, JL .
JOURNAL OF BACTERIOLOGY, 1999, 181 (07) :2209-2216
[8]   THE SIR2 GENE FAMILY, CONSERVED FROM BACTERIA TO HUMANS, FUNCTIONS IN SILENCING, CELL-CYCLE PROGRESSION, AND CHROMOSOME STABILITY [J].
BRACHMANN, CB ;
SHERMAN, JM ;
DEVINE, SE ;
CAMERON, EE ;
PILLUS, L ;
BOEKE, JD .
GENES & DEVELOPMENT, 1995, 9 (23) :2888-2902
[9]   The role of lysine 529, a conserved residue of the acyl-adenylate-forming enzyme superfamily, in firefly luciferase [J].
Branchini, BR ;
Murtiashaw, MH ;
Magyar, RA ;
Anderson, SM .
BIOCHEMISTRY, 2000, 39 (18) :5433-5440
[10]   ENZYMIC INTERCONVERSION OF ACETATE AND ACETYL-COENZYME-A IN ESCHERICHIA-COLI [J].
BROWN, TDK ;
JONESMORTIMER, MC ;
KORNBERG, HL .
JOURNAL OF GENERAL MICROBIOLOGY, 1977, 102 (OCT) :327-336