Simons J A, Teixeira de Mattos M J, Neijssel O M
Department of Microbiology, Biotechnology Centre, University of Amsterdam, The Netherlands.
J Gen Microbiol. 1991 Jul;137(7):1479-83. doi: 10.1099/00221287-137-7-1479.
Klebsiella pneumoniae NCTC 418 is able to convert 2-ketogluconate intracellularly to 6-phosphogluconate by the combined action of an NADPH-dependent 2-ketogluconate reductase and gluconate kinase. Synthesis of the former enzyme was maximal under 2-ketogluconate-limited growth conditions. An instantaneous transition to a 2-ketogluconate-excess condition resulted in an acceleration of catabolism of this carbon source, accompanied by complete inhibition of biosynthesis. It is suggested that the cause of this inhibition resides in depletion of the NADPH pool due to the high rate at which NADPH is oxidized by 2-ketogluconate reductase.
肺炎克雷伯菌NCTC 418能够通过NADPH依赖性2-酮葡萄糖酸还原酶和葡萄糖酸激酶的联合作用,在细胞内将2-酮葡萄糖酸转化为6-磷酸葡萄糖酸。在前一种酶的合成在2-酮葡萄糖酸限制的生长条件下达到最大值。瞬间转变为2-酮葡萄糖酸过量的条件会导致这种碳源分解代谢的加速,同时伴随着生物合成的完全抑制。有人认为这种抑制的原因在于由于NADPH被2-酮葡萄糖酸还原酶氧化的速率很高,导致NADPH库的耗尽。