Delta subunit of chloroplast coupling factor 1 inhibits proton leakage through coupling factor O
- PMID: 2902083
Delta subunit of chloroplast coupling factor 1 inhibits proton leakage through coupling factor O
Abstract
The ATP synthase of chloroplasts consists of a proton-conducting portion, CF0, and a catalytic portion, CF1. The smaller subunits of CF1, in particular delta, may play a key role in the coupling of proton transport to ATP synthesis. Purified subunit delta, when added to partially CF1-depleted thylakoid membranes, can restore photophosphorylation (Engelbrecht, S., and Junge, W. (1987) Eur. J. Biochem. 172, 213-218). We report here that it does so by blocking proton conduction through CF0. Thylakoids were CF1-depleted by incubation in hypoosmolar NaCl/EDTA solutions. Variation of the NaCl concentrations and of the incubation times not only changed the overall degree of CF1 depletion but also the subunit composition of solubilized CF1, namely CF1 containing delta and CF1(-delta). This was quantified by immunoelectrophoresis and by fast protein liquid chromatography. Proton conduction was measured by flash spectrophotometry by using standard electrochromic and pH-indicating absorption changes. The removal of integral CF1 was correlated with high electric conductance of thylakoid membranes, an increased extent of rapid proton leakage, and loss of ATP synthesis activity, which exceeded the percentual loss of CF1. The removal of predominantly CF1(-delta) resulted in comparatively lesser effects on the loss of ATP synthesis and on the extent and velocity of proton leakage. On the same line, addition of integral CF1 and of purified delta diminished the electric leak in CF1-depleted thylakoids. Both approaches, the controlled removal of CF1 and CF1(-delta), respectively, and addition of delta and CF1 showed that delta can act as a "stopcock" to the exposed proton channel CF0.
Similar articles
-
Purified subunit delta of chloroplast coupling factor CF1 reconstitutes photophosphorylation in partially CF1-depleted membranes.Eur J Biochem. 1988 Feb 15;172(1):213-8. doi: 10.1111/j.1432-1033.1988.tb13875.x. Eur J Biochem. 1988. PMID: 2894310
-
CF0, the proton channel of chloroplast ATP synthase. After removal of CF1 it appears in two forms with highly different proton conductance.Eur J Biochem. 1989 Feb 1;179(2):459-67. doi: 10.1111/j.1432-1033.1989.tb14575.x. Eur J Biochem. 1989. PMID: 2465153
-
Reconstitution of CF1-depleted thylakoid membranes with complete and fragmented chloroplast ATPase. The role of the delta subunit for proton conduction through CF0.Eur J Biochem. 1986 Nov 3;160(3):635-43. doi: 10.1111/j.1432-1033.1986.tb10085.x. Eur J Biochem. 1986. PMID: 2877879
-
Subunit delta of H(+)-ATPases: at the interface between proton flow and ATP synthesis.Biochim Biophys Acta. 1990 Feb 22;1015(3):379-90. doi: 10.1016/0005-2728(90)90072-c. Biochim Biophys Acta. 1990. PMID: 2154253 Review.
-
Recent developments on structural and functional aspects of the F1 sector of H+-linked ATPases.Mol Cell Biochem. 1984;60(1):33-71. doi: 10.1007/BF00226299. Mol Cell Biochem. 1984. PMID: 6231469 Review.
Cited by
-
Purification and reconstitution into proteoliposomes of the F1F0 ATP synthase from the obligately anaerobic gram-positive bacterium Clostridium thermoautotrophicum.J Bacteriol. 1997 Mar;179(5):1714-20. doi: 10.1128/jb.179.5.1714-1720.1997. J Bacteriol. 1997. PMID: 9045833 Free PMC article.
-
Effect of the delta subunit on assembly and proton permeability of the F0 proton channel of Escherichia coli F1F0 ATPase.J Bacteriol. 1991 Jan;173(1):407-11. doi: 10.1128/jb.173.1.407-411.1991. J Bacteriol. 1991. PMID: 1702783 Free PMC article.
-
Protons, proteins and ATP.Photosynth Res. 2004;80(1-3):197-221. doi: 10.1023/B:PRES.0000030677.98474.74. Photosynth Res. 2004. PMID: 16328822
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources