Lengeler J, Steinberger H
Mol Gen Genet. 1978 Nov 16;167(1):75-82. doi: 10.1007/BF00270323.
The transport systems (enzymeII-complexes of the PEP-dependent sugar:phosphotransferase system) coded for in the mtl and in the gut (srl) operon of E. coli K12 have been shown to be the pacemaker enzymes in the catabolism of the two hexitols D-mannitol and D-glucitol, respectively. As for other pacemaker enzymes their activity is regulated in a complex way: (i) via competitive inhibition by analogues. (ii) via non-competitive (feedback) inhibition by the simultaneous, rapid uptake of a number of structurally related or non-related carbohydrates, regardless if these are transported by group translocation, active transport or facilitated diffusion. This type of inhibition is strongly reinforced, if the inhibitory carbohydrates are converted efficiently into hexose-phosphates at the same time. Among these, predominantly D-fructose-6-P seems to act as a feedback inhibitor for the hexitol specific enzymeII-complexes: (iii) inhibition of hixitol-phosphate accumulation by D-glucose-6-P. The influence of additional parameters (PEP level, P approximately HPr level) and indications for the existence of further mechanisms controlling the activity of hexitol and other carbohydrate transport systems will be discussed, as will be the part the inhibitory mechanisms described above play in the phenomena of transient repression and inducer exclusion.
大肠杆菌K12的mtl操纵子和肠道(srl)操纵子中编码的转运系统(磷酸烯醇式丙酮酸依赖性糖:磷酸转移酶系统的酶II复合物)已被证明分别是两种己糖醇D-甘露醇和D-葡糖醇分解代谢中的限速酶。与其他限速酶一样,它们的活性受到复杂的调节:(i)通过类似物的竞争性抑制。(ii)通过同时快速摄取多种结构相关或不相关的碳水化合物进行非竞争性(反馈)抑制,无论这些碳水化合物是通过基团转位、主动运输还是易化扩散进行转运。如果抑制性碳水化合物同时有效地转化为己糖磷酸,则这种抑制类型会大大增强。其中,主要是D-果糖-6-P似乎作为己糖醇特异性酶II复合物的反馈抑制剂:(iii)D-葡萄糖-6-P对己糖醇磷酸积累的抑制。将讨论其他参数(磷酸烯醇式丙酮酸水平、P~HPr水平)的影响以及控制己糖醇和其他碳水化合物转运系统活性的其他机制存在的迹象,以及上述抑制机制在瞬时阻遏和诱导物排除现象中所起的作用。