Epstein Wolfgang
Department of Molecular Genetics and Cell Biology, The University of Chicago, Chicago, IL 60637, USA.
Prog Nucleic Acid Res Mol Biol. 2003;75:293-320. doi: 10.1016/s0079-6603(03)75008-9.
Potassium is the major intracellular cation in bacteria as well as in eucaryotic cells. Bacteria accumulate K+ by a number of different transport systems that vary in kinetics, energy coupling, and regulation. The Trk and Kdp systems of enteric organisms have been well studied and are found in many distantly related species. The Ktr system, resembling Trk in many ways, is also found in many bacteria. In most species two or more independent saturable K(+)-transport systems are present. The KefB and KefC type of system that is activated by treatment of cells with toxic electrophiles is the only specific K(+)-efflux system that has been well characterized. Pressure-activated channels of at least three types are found in bacteria; these represent nonspecific paths of efflux when turgor pressure is dangerously high. A close homolog of eucaryotic K+ channels is found in many bacteria, but its role remains obscure. K+ transporters are regulated both by ion concentrations and turgor. A very general property is activation of K+ uptake by an increase in medium osmolarity. This response is modulated by both internal and external concentrations of K+. Kdp is the only K(+)-transport system whose expression is regulated by environmental conditions. Decrease in turgor pressure and/or reduction in external K+ rapidly increase expression of Kdp. The signal created by these changes, inferred to be reduced turgor, is transmitted by the KdpD sensor kinase to the KdpE-response regulator that in turn stimulates transcription of the kdp genes. K+ acts as a cytoplasmic-signaling molecule, activating and/or inducing enzymes and transport systems that allow the cell to adapt to elevated osmolarity. The signal could be ionic strength or specifically K+. This signaling response is probably mediated by a direct sensing of internal ionic strength by each particular system and not by a component or system that coordinates this response by different systems to elevated K+.
钾是细菌以及真核细胞中的主要细胞内阳离子。细菌通过多种不同的转运系统积累钾离子,这些系统在动力学、能量偶联和调节方面各不相同。肠道生物的Trk和Kdp系统已得到充分研究,并且在许多远缘物种中都有发现。Ktr系统在许多方面与Trk相似,也存在于许多细菌中。在大多数物种中,存在两个或更多独立的可饱和钾离子转运系统。KefB和KefC类型的系统在细胞用有毒亲电试剂处理时被激活,是唯一已得到充分表征的特异性钾离子外流系统。细菌中发现了至少三种类型的压力激活通道;当膨压危险地升高时,这些通道代表非特异性的外流途径。在许多细菌中发现了与真核钾离子通道密切同源的蛋白,但其作用仍不清楚。钾离子转运体受离子浓度和膨压的调节。一个非常普遍的特性是培养基渗透压的增加会激活钾离子的摄取。这种反应受到细胞内和细胞外钾离子浓度的调节。Kdp是唯一其表达受环境条件调节的钾离子转运系统。膨压降低和/或细胞外钾离子减少会迅速增加Kdp的表达。由这些变化产生的信号,推测是膨压降低,由KdpD传感器激酶传递给KdpE应答调节因子,后者进而刺激kdp基因的转录。钾离子作为一种细胞质信号分子,激活和/或诱导酶和转运系统,使细胞能够适应渗透压升高。这个信号可能是离子强度或特定的钾离子。这种信号反应可能是由每个特定系统直接感知内部离子强度介导的,而不是由一个协调不同系统对升高的钾离子作出这种反应的成分或系统介导的。