CHANNELING OF TCA CYCLE INTERMEDIATES IN CULTURED SACCHAROMYCES-CEREVISIAE

被引:74
作者
SUMEGI, B
SHERRY, AD
MALLOY, CR
机构
[1] UNIV TEXAS, SW MED CTR, DEPT INTERNAL MED, DALLAS, TX 75235 USA
[2] UNIV TEXAS, SW MED CTR, DEPT RADIOL, DALLAS, TX 75235 USA
关键词
D O I
10.1021/bi00491a002
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
Oxidation of [3-13C]propionate was studied in cultured yeast cells, and the distribution of label in the 2-and 3-positions of alanine was detected by 13C NMR. [3-13C]Propionate forms [2-13C]succinyl-CoA in the mitochondria which then enters the citric acid cycle and forms malate through two symmetrical intermediates, succinate and fumarate. If these symmetrical intermediates randomly diffuse from one enzyme to the next in mitochondria as is normally assumed, then 13C labeling in malate C2 and C3 must be equal. However, any direct transfer of metabolites from site to site between succinate thiokinase, succinate dehydrogenase, and fumarase would result in an uneven distribution of 13C in malate C2 and C3 and any molecules derived from malate. Since pyruvate may be derived from malate via the malic enzyme and subsequently converted into alanine by transamination, any 13C asymmetry in alanine C2 and C3 must directly reflect the 13C distribution in the malate pool. During oxidation of [3-13C] propionate, we detect a significant quantity of labeled alanine, where 13C enrichment in C3 is significantly higher than that in C2. Inhibition of succinate dehydrogenase with malonate or creating conditions that increase the chances of a back-reaction (from malate to fumarate) result in a significant decrease in the asymmetric labeling of alanine. Ubiquinone-deficient yeast cells (having only 10% of the oxidative capacity of wild-type cells) could slowly oxidize propionate, but in this case the 13C labeling was equal in the C2 and C3 of alanine, showing that isotope randomization had occurred. Addition of ubiquinone restores the respiratory activity of this cell line, and the asymmetry in alanine is once again clearly evident. These data show that actively respiring yeast cells can directly transfer intermediates between succinate thiokinase, succinate dehydrogenase, and fumarase under in vivo conditions. © 1990, American Chemical Society. All rights reserved.
引用
收藏
页码:9106 / 9110
页数:5
相关论文
共 39 条
[1]  
AJL SJ, 1951, J BIOL CHEM, V189, P845
[2]  
AKITT JW, 1987, MULTINUCLEAR NMR, P449
[3]  
BEECKMANS S, 1981, EUR J BIOCHEM, V117, P527
[4]   THE VISUALIZATION BY AFFINITY ELECTROPHORESIS OF A SPECIFIC ASSOCIATION BETWEEN THE CONSECUTIVE CITRIC-ACID CYCLE ENZYMES FUMARASE AND MALATE-DEHYDROGENASE [J].
BEECKMANS, S ;
VANDRIESSCHE, E ;
KANAREK, L .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1989, 183 (02) :449-454
[5]  
Bergmeyer HI., 1974, METHODS ENZYMATIC AN
[6]   THE MECHANISM OF SUCCINATE OR FUMARATE TRANSFER IN THE TRICARBOXYLIC-ACID CYCLE ALLOWS MOLECULAR ROTATION OF THE INTERMEDIATE [J].
BERNHARD, SA ;
TOMPA, P .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1990, 276 (01) :191-198
[7]  
COHEN NS, 1987, J BIOL CHEM, V262, P203
[8]  
DSOUZA SF, 1983, J BIOL CHEM, V258, P4706
[9]  
EHRENSVARD G, 1951, J BIOL CHEM, V189, P93
[10]   COMPLEXES BETWEEN MITOCHONDRIAL-ENZYMES AND EITHER CITRATE SYNTHASE OR GLUTAMATE-DEHYDROGENASE [J].
FAHIEN, LA ;
KMIOTEK, E .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1983, 220 (02) :386-397