Literature DB >> 2160968

Steady-state measurements of Escherichia coli sodium and proton potentials at alkaline pH support the hypothesis of electrogenic antiport.

J W Pan1, R M Macnab.   

Abstract

31P and 23Na NMR spectroscopy was applied to the measurement of proton and sodium potentials in endogenously respiring Escherichia coli cells over an external pH (pHex) range from mildly acidic (6.4) to fairly alkaline (8.4). Stable maintenance of alkaline pHex in the face of metabolic acidification was achieved by use of a perfusion system. In the acidic to neutral pHex range, the sodium chemical potential followed the proton chemical potential quite closely, although always exceeding it slightly, as has been reported previously (Castle, A. M., Macnab, R. M., and Shulman, R. G. (1986) J. Biol. Chem. 261, 7797-7806). Above pHex 7.4, the sodium potential changed abruptly from a decreasing to an increasing function of pHex, whereas the proton potential continued to decrease. As a consequence, the apparent stoichiometry (i.e. the ratio between the sodium and proton electrochemical potentials) took on progressively higher values, increasing from approximately 1.1 at pH 7.4 to approximately 1.3 at pH 7.8. Thereafter, the sodium chemical potential started to decrease again; however, since the decrease was less steep than that of the proton potential, the apparent stoichiometry continued to increase. At the highest pHex examined (8.4), it had reached a value of approximately 1.4. These results strongly support the hypothesis of an electroneutral (1:1) H+/Na+ antiporter operating virtually alone under acidic to neutral conditions and then being supplemented to an ever increasing degree by an electrogenic (for example, 2:1) antiporter under more alkaline conditions.

Entities:  

Mesh:

Substances:

Year:  1990        PMID: 2160968

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  6 in total

1.  Na+-induced transcription of nhaA, which encodes an Na+/H+ antiporter in Escherichia coli, is positively regulated by nhaR and affected by hns.

Authors:  N Dover; C F Higgins; O Carmel; A Rimon; E Pinner; E Padan
Journal:  J Bacteriol       Date:  1996-11       Impact factor: 3.490

2.  The Na+-specific interaction between the LysR-type regulator, NhaR, and the nhaA gene encoding the Na+/H+ antiporter of Escherichia coli.

Authors:  O Carmel; O Rahav-Manor; N Dover; B Shaanan; E Padan
Journal:  EMBO J       Date:  1997-10-01       Impact factor: 11.598

Review 3.  Na+/H+ antiporters, molecular devices that couple the Na+ and H+ circulation in cells.

Authors:  E Padan; S Schuldiner
Journal:  J Bioenerg Biomembr       Date:  1993-12       Impact factor: 2.945

4.  Ion transport and methane production in Methanobacterium thermoautotrophicum.

Authors:  F D Sauer; B A Blackwell; J K Kramer
Journal:  Proc Natl Acad Sci U S A       Date:  1994-05-10       Impact factor: 11.205

5.  pH dependence and gene structure of inaA in Escherichia coli.

Authors:  S White; F E Tuttle; D Blankenhorn; D C Dosch; J L Slonczewski
Journal:  J Bacteriol       Date:  1992-03       Impact factor: 3.490

6.  A single amino acid substitution (Glu134-->Ala) in NhaR1 increases the inducibility by Na+ of the product of nhaA, a Na+/H+ antiporter gene in Escherichia coli.

Authors:  O Carmel; N Dover; O Rahav-Manor; P Dibrov; D Kirsch; R Karpel; S Schuldiner; E Padan
Journal:  EMBO J       Date:  1994-04-15       Impact factor: 11.598

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.