Taylor N F, Louie L Y
Can J Biochem. 1977 Aug;55(8):911-5. doi: 10.1139/o77-135.
The uptake of 4-deoxy-4-fluoro-D-glucose (4FG), without subsequent catabolism, by resting cells of Escherichia coli (ATCC 11775) is 0.06 mg/mg dry weight. In frozen-thawed cells of this organism, 4FG is a substrate for the phosphoenolpyruvate phosphotransferase system with a rate of phosphorylation twice that found for the isomeric 3-deoxy-3-fluoro-D-glucose. 4FG is not a carbon source for growth of this organism and it inhibits the extent of growth of cells in the presence of glucose. The inhibition of growth of E. coli K12 on lactose by 4FG is also observed and this is considered to be consistent with the fact that 4FG is an uncompetitive inhibitor of beta-galactosidase (EC 3.2.1.23) activity and that 4FG or 4-deoxy-4-fluoro-D-glucose-6 phosphate repress beta-galactosidase synthesis. These results support the view that catabolite repression may be produced by compounds which are not necessarily metabolised further than hexose-6-phosphates.
大肠杆菌(ATCC 11775)的静止细胞对4-脱氧-4-氟-D-葡萄糖(4FG)的摄取(无后续分解代谢)为0.06毫克/毫克干重。在该生物体的冻融细胞中,4FG是磷酸烯醇丙酮酸磷酸转移酶系统的底物,其磷酸化速率是同分异构体3-脱氧-3-氟-D-葡萄糖的两倍。4FG不是该生物体生长的碳源,并且在有葡萄糖存在时它会抑制细胞的生长程度。还观察到4FG对大肠杆菌K12利用乳糖生长的抑制作用,这被认为与以下事实一致:4FG是β-半乳糖苷酶(EC 3.2.1.23)活性的非竞争性抑制剂,并且4FG或4-脱氧-4-氟-D-葡萄糖-6-磷酸会抑制β-半乳糖苷酶的合成。这些结果支持这样一种观点,即分解代谢物阻遏可能由不一定比己糖-6-磷酸进一步代谢的化合物产生。