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[大肠杆菌中的H⁺-K⁺离子交换系统]

[Systems of H+ K+ ion exchange in E. coli].

作者信息

Martirosov S M, Trchunian A A, Vartanian A G

出版信息

Biofizika. 1982 Jan-Feb;27(1):48-51.

PMID:7039686
Abstract

Membrane potentials in bacteria E. coli have been estimated by means of electrodes for determination of activity of tetraphenilphosphonium ions in the medium. The strain E. coli K12 (lambda), TK 509, AN 120 and AN 382 indicate the membrane potential (delta psi) of -125 mV in the salt solution without glucose (2 mM KCl, tris-phosphate buffer, pH 7.5). The delta psi of the first three strains include that N,N1--dicyclohexylcarbodiimide (DCCD)--sensitive part (20--25 mV) that has not been detected in the strain AN 382 (F0 is resistant to DCCD). This component of delta psi eliminated by (alpha K+)0 equal to 30 mM or pH 5.0, is assumed to be produced by activity of the channel F0 deprived of its enzyme F1. Addition of glucose in the medium leads to the short-lasting (2--5 min) increase in the delta psi from 125 to 145 mV in E. coli K12 (lambda). This energy-dependent extra potential is actuated only through increasing external osmolarity and does not occur after decreasing that or application of DCCD as well. The extra delta psi was not recognized in the strains TK 509 and AN 120. The results confirm the hypothesis of the energy-dependent potassium accumulation in glycolysing bacteria being not in need of ATP and delta muH+ but requiring in operation of F1 . F0.

摘要

已通过电极对大肠杆菌中的膜电位进行了估算,以测定培养基中四苯基鏻离子的活性。大肠杆菌K12(λ)、TK 509、AN 120和AN 382菌株在不含葡萄糖的盐溶液(2 mM KCl、三磷酸缓冲液,pH 7.5)中显示出-125 mV的膜电位(Δψ)。前三种菌株的Δψ包括N,N'-二环己基碳二亚胺(DCCD)敏感部分(20 - 25 mV),而在菌株AN 382中未检测到该部分(F0对DCCD有抗性)。当(αK +)0等于30 mM或pH为5.0时,这种被消除的Δψ成分被认为是由缺乏酶F1的F0通道活性产生的。向培养基中添加葡萄糖会导致大肠杆菌K12(λ)中的Δψ在短时间内(2 - 5分钟)从125 mV增加到145 mV。这种能量依赖性的额外电位仅通过增加外部渗透压来激活,在降低渗透压或应用DCCD后不会出现。在菌株TK 509和AN 120中未识别到额外的Δψ。结果证实了糖酵解细菌中能量依赖性钾积累的假设,即不需要ATP和ΔμH +,但需要F1.F0的运作。

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