Rhoads D B, Epstein W
J Gen Physiol. 1978 Sep;72(3):283-95. doi: 10.1085/jgp.72.3.283.
Kinetics of K exchange in the steady state and of net K uptake after osmotic upshock are reported for the four K transport systems of Escherichia coli: Kdp, TrkA, TrkD, and TrkF. Energy requirements for K exchange are reported for the Kdp and TrkA systems. For each system, kinetics of these two modes of K transport differ from those for net K uptake by K-depleted cells (Rhoads, D. B. F.B. Walters, and W. Epstein. 1976. J. Gen. Physiol. 67:325-341). The TrkA and TrkD systems are inhibited by high intracellular K, the TrkF system is stimulated by intracellular K, whereas the Kdp system is inhibited by external K when intracellular K is high. All four systems mediate net K uptake in response to osmotic upshock. Exchange by the Kdp and TrkA systems requires ATP but is not dependent on the protonmotive force. Energy requirements for the Kdp system are thus identical whether measured as net K uptake or K exchange, whereas the TrkA system differs in that it is dependent on the protonmotive force only for net K uptake. We suggest that in both the Kpd and TrkA systems formation of a phosphorylated intermediate is necessary for all K transport, although exchange transport may not consume energy. The protonmotive-force dependence of the TrkA system is interpreted as a regulatory influence, limiting this system to exchange except when the protonmotive force is high.
本文报道了大肠杆菌四种钾转运系统(Kdp、TrkA、TrkD和TrkF)在稳态下的钾交换动力学以及渗透休克后的净钾摄取情况。还报道了Kdp和TrkA系统钾交换的能量需求。对于每个系统,这两种钾转运模式的动力学与低钾细胞的净钾摄取动力学不同(Rhoads, D. B., F. B. Walters, and W. Epstein. 1976. J. Gen. Physiol. 67:325 - 341)。TrkA和TrkD系统受到高细胞内钾的抑制,TrkF系统受到细胞内钾的刺激,而当细胞内钾含量高时,Kdp系统受到外部钾的抑制。所有这四个系统都介导对渗透休克的净钾摄取。Kdp和TrkA系统的交换需要ATP,但不依赖于质子动力。因此,无论以净钾摄取还是钾交换来衡量,Kdp系统的能量需求都是相同的,而TrkA系统的不同之处在于,它仅在净钾摄取时依赖于质子动力。我们认为,在Kdp和TrkA系统中,磷酸化中间体的形成对于所有钾转运都是必要的,尽管交换转运可能不消耗能量。TrkA系统对质子动力的依赖性被解释为一种调节作用,限制该系统仅进行交换,除非质子动力很高。