Peterkofsky A
Adv Cyclic Nucleotide Res. 1981;14:215-28.
Adenylate cyclase of E. coli is a membrane-bound enzyme the function of which is to synthesize a cofactor for processes that are important in metabolic transitions. The depletion from the environment of a supply of a preferred carbon source dictates the requirement for initiating the synthesis of a new metabolic system; this synthesis will require cAMP. After the adaptation period, the requirement for a high level of synthesis diminishes, resulting in a diminished requirement for cAMP. A mechanism for regulating the activity of adenylate cyclase accomplishes the variation in the required cellular cAMP concentrations. In the absence of a transportable carbon source, adenylate cyclase activity is activated by cellular regulators; when carbon sources are transported, the cellular activators are dissipated, resulting in inhibition of adenylate cyclase activity. This scheme is summarized in Fig. 6. Sugar transport systems fall into two categories: one in which the energy for the process comes from PEP (the PTS) and one in which the energy comes from the proton electrochemical gradient. Adenylate cyclase communicates with both of these systems by interacting with intermediates on the pathway to energy generation for driving these two transport processes. Adenylate cyclase couples indirectly to a large array of sugar-specific transport systems by interacting with intermediates common to all the processes. The net result of this regulatory mechanism is that, without physically communicating with the extracellular environment by spanning the membrane, adenylate cyclase effectively senses the presence of external sugars that interact with cells that have become competent to transport them.
大肠杆菌的腺苷酸环化酶是一种膜结合酶,其功能是合成一种对代谢转变中重要过程起作用的辅助因子。环境中首选碳源供应的耗尽决定了启动新代谢系统合成的需求;这种合成需要环磷酸腺苷(cAMP)。在适应期之后,对高水平合成的需求减少,导致对cAMP的需求减少。一种调节腺苷酸环化酶活性的机制实现了所需细胞cAMP浓度的变化。在没有可转运碳源的情况下,腺苷酸环化酶活性被细胞调节因子激活;当碳源被转运时,细胞激活剂消散,导致腺苷酸环化酶活性受到抑制。该方案总结于图6中。糖转运系统分为两类:一类过程的能量来自磷酸烯醇式丙酮酸(PTS),另一类能量来自质子电化学梯度。腺苷酸环化酶通过与驱动这两种转运过程的能量产生途径上的中间体相互作用,与这两种系统进行通信。腺苷酸环化酶通过与所有过程共有的中间体相互作用,间接与大量糖特异性转运系统偶联。这种调节机制的最终结果是,腺苷酸环化酶无需通过跨越膜与细胞外环境进行物理通信,就能有效地感知与有能力转运它们的细胞相互作用的外部糖的存在。