Cozzone A J
Institut de Biologie et Chimie des Protéines, Université de Lyon, France.
Annu Rev Microbiol. 1998;52:127-64. doi: 10.1146/annurev.micro.52.1.127.
Growth of enteric bacteria on acetate as the sole source of carbon and energy requires operation of a particular anaplerotic pathway known as the glyoxylate bypass. In this pathway, two specific enzymes, isocitrate lyase and malate synthase, are activated to divert isocitrate from the tricarboxylic acid cycle and prevent the quantitative loss of acetate carbons as carbon dioxide. Bacteria are thus supplied with the metabolic intermediates they need for synthesizing their cellular components. The channeling of isocitrate through the glyoxylate bypass is regulated via the phosphorylation/dephosphorylation of isocitrate dehydrogenase, the enzyme of the tricarboxylic acid cycle which competes for a common substrate with isocitrate lyase. When bacteria are grown on acetate, isocitrate dehydrogenase is phosphorylated and, concomitantly, its activity declines drastically. Conversely, when cells are cultured on a preferred carbon source, such as glucose, the enzyme is dephosphorylated and recovers full activity. Such reversible phosphorylation is mediated by an unusual bifunctional enzyme, isocitrate dehydrogenase kinase/phosphatase, which contains both modifying and demodifying activities on the same polypeptide. The genes coding for malate synthase, isocitrate lyase, and isocitrate dehydrogenase kinase/phosphatase are located in the same operon. Their expression is controlled by a complex dual mechanism that involves several transcriptional repressors and activators. Recent developments have brought new insights into the nature and mode of action of these different regulators. Also, significant advances have been made lately in our understanding of the control of enzyme activity by reversible phosphorylation. In general, analyzing the physiological behavior of bacteria on acetate provides a valuable approach for deciphering at the molecular level the mechanisms of cell adaptation to the environment.
肠道细菌以乙酸盐作为唯一碳源和能源进行生长时,需要一种特殊的回补途径——乙醛酸循环支路发挥作用。在该途径中,两种特定的酶,即异柠檬酸裂解酶和苹果酸合酶被激活,从而使异柠檬酸从三羧酸循环中分流出来,防止乙酸盐碳以二氧化碳的形式定量损失。这样细菌就能获得合成其细胞成分所需的代谢中间体。通过乙醛酸循环支路对异柠檬酸的分流是通过异柠檬酸脱氢酶的磷酸化/去磷酸化来调节的,异柠檬酸脱氢酶是三羧酸循环中的一种酶,它与异柠檬酸裂解酶竞争共同底物。当细菌在乙酸盐上生长时,异柠檬酸脱氢酶被磷酸化,其活性随之急剧下降。相反,当细胞在葡萄糖等优质碳源上培养时,该酶会去磷酸化并恢复全部活性。这种可逆磷酸化由一种特殊的双功能酶——异柠檬酸脱氢酶激酶/磷酸酶介导,它在同一多肽上同时具有修饰和去修饰活性。编码苹果酸合酶、异柠檬酸裂解酶和异柠檬酸脱氢酶激酶/磷酸酶的基因位于同一个操纵子中。它们的表达受一种复杂的双重机制控制,该机制涉及多种转录抑制因子和激活因子。最近的研究进展为这些不同调节因子的性质和作用方式带来了新的见解。此外,最近我们对可逆磷酸化对酶活性的控制的理解也取得了重大进展。总体而言,分析细菌在乙酸盐上的生理行为为在分子水平上解读细胞适应环境的机制提供了一种有价值的方法。