Tobisch S, Zühlke D, Bernhardt J, Stülke J, Hecker M
Institut für Mikrobiologie und Molekularbiologie, Ernst-Moritz-Arndt-Universität Greifswald, D-17487 Greifswald, Germany.
J Bacteriol. 1999 Nov;181(22):6996-7004. doi: 10.1128/JB.181.22.6996-7004.1999.
The Bacillus subtilis two-dimensional (2D) protein index contains almost all glycolytic and tricarboxylic acid (TCA) cycle enzymes, among them the most abundant housekeeping proteins of growing cells. Therefore, a comprehensive study on the regulation of glycolysis and the TCA cycle was initiated. Whereas expression of genes encoding the upper and lower parts of glycolysis (pgi, pfk, fbaA, and pykA) is not affected by the glucose supply, there is an activation of the glycolytic gap gene and the pgk operon by glucose. This activation seems to be dependent on the global regulator CcpA, as shown by 2D polyacrylamide gel electrophoresis analysis as well as by transcriptional analysis. Furthermore, a high glucose concentration stimulates production and excretion of organic acids (overflow metabolism) in the wild type but not in the ccpA mutant. Finally, CcpA is involved in strong glucose repression of almost all TCA cycle genes. In addition to TCA cycle and glycolytic enzymes, the levels of many other proteins are affected by the ccpA mutation. Our data suggest (i) that ccpA mutants are unable to activate glycolysis or carbon overflow metabolism and (ii) that CcpA might be a key regulator molecule, controlling a superregulon of glucose catabolism.
枯草芽孢杆菌二维(2D)蛋白质索引包含几乎所有糖酵解和三羧酸(TCA)循环酶,其中包括生长细胞中最丰富的管家蛋白。因此,启动了一项关于糖酵解和TCA循环调控的全面研究。虽然编码糖酵解上下游部分(pgi、pfk、fbaA和pykA)的基因表达不受葡萄糖供应的影响,但糖酵解间隙基因和pgk操纵子会被葡萄糖激活。如二维聚丙烯酰胺凝胶电泳分析以及转录分析所示,这种激活似乎依赖于全局调节因子CcpA。此外,高葡萄糖浓度会刺激野生型中有机酸的产生和分泌(溢流代谢),但在ccpA突变体中则不会。最后,CcpA参与了几乎所有TCA循环基因的强烈葡萄糖抑制作用。除了TCA循环和糖酵解酶外,许多其他蛋白质的水平也受到ccpA突变的影响。我们的数据表明:(i)ccpA突变体无法激活糖酵解或碳溢流代谢;(ii)CcpA可能是一个关键的调节分子,控制着葡萄糖分解代谢的一个超级调控子。