Larsen S H, Adler J, Gargus J J, Hogg R W
Proc Natl Acad Sci U S A. 1974 Apr;71(4):1239-43. doi: 10.1073/pnas.71.4.1239.
The source of energy for bacterial motility is the intermediate in oxidative phosphorylation, not ATP directly. For chemotaxis, however, there is an additional requirement, presumably ATP. These conclusions are based on the following findings. (i) Unlike their parents, mutants of Escherichia coli and Salmonella typhimurium that are blocked in the conversion of ATP to the intermediate of oxidative phosphorylation failed to swim anaerobically, even when they produced ATP. When respiration was restored to the mutants, motility was simultaneously restored. (ii) Carbonylcyanide m-chlorophenylhydrazone, which uncouples oxidative phosphorylation, completely inhibited motility even though ATP remained present. (iii) Arsenate did not inhibit motility in the presence of an oxidizable substrate, though it did reduce ATP levels to less than 0.3% (iv) Arsenate completely inhibited chemotaxis under conditions where motility was normal.
细菌运动的能量来源是氧化磷酸化过程中的中间体,而非直接来自ATP。然而,对于趋化作用,可能还需要额外的ATP。这些结论基于以下发现:(i)与它们的亲本不同,大肠杆菌和鼠伤寒沙门氏菌中那些在ATP转化为氧化磷酸化中间体过程中受阻的突变体,即使能产生ATP,也无法在无氧条件下游动。当这些突变体恢复呼吸作用时,运动能力也同时恢复。(ii)羰基氰化物间氯苯腙可使氧化磷酸化解偶联,即使ATP仍然存在,它也能完全抑制运动能力。(iii)在存在可氧化底物的情况下,砷酸盐不会抑制运动能力,尽管它确实能将ATP水平降低至低于0.3%。(iv)在运动能力正常的条件下,砷酸盐能完全抑制趋化作用。