Mitsumori F, Rees D, Brindle K M, Radda G K, Campbell I D
Department of Biochemistry, University of Oxford, U.K.
Biochim Biophys Acta. 1988 Apr 25;969(2):185-93. doi: 10.1016/0167-4889(88)90074-2.
31P-NMR measurements of saturation transfer have been used to measure the flux between Pi and ATP in Escherichia coli cells respiring on an endogenous carbon source. Measurements were made in the wild type and in cells genetically modified to give a 5-fold higher concentration of the F1F0-ATP synthase. The flux in the two cell types was not significantly different. This, together with studies using inhibitors specific for the glycolytic enzyme, glyceraldehyde-3-phosphate dehydrogenase and the ATP synthase, suggests that the observed flux arises predominantly from glycolytic rather than ATP synthase activity. Although this conclusion is in disagreement with previous experiments on E. coli, it is in agreement with recent experiments on yeast.
利用31P-核磁共振饱和转移测量法,测定了以内源性碳源进行呼吸作用的大肠杆菌细胞中磷酸(Pi)与三磷酸腺苷(ATP)之间的通量。在野生型细胞以及经过基因改造、F1F0-ATP合酶浓度提高5倍的细胞中进行了测量。两种细胞类型中的通量没有显著差异。这一点,再加上使用对糖酵解酶、甘油醛-3-磷酸脱氢酶和ATP合酶具有特异性的抑制剂所做的研究,表明观察到的通量主要源于糖酵解而非ATP合酶的活性。尽管这一结论与之前对大肠杆菌所做的实验不一致,但与最近对酵母所做的实验相符。