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. 1995 Jan 10;316(1):421-7.
doi: 10.1006/abbi.1995.1056.

H+/PPi stoichiometry of membrane-bound pyrophosphatase of Rhodospirillum rubrum

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H+/PPi stoichiometry of membrane-bound pyrophosphatase of Rhodospirillum rubrum

A Sosa et al. Arch Biochem Biophys. .

Abstract

Two kinetic methods have been used to measure the H+/PPi stoichiometry in the chromatophores of the photosynthetic bacteria Rhodospirillum rubrum. In the first method, the fluorescent probe acridine orange was employed to infer the proton pump activity at the steady state of the delta pH generation. At this point the translocation of protons by the H(+)-PPiase in one direction is balanced exactly by the leak of protons in the opposite direction. Pyrophosphatase activity was then quickly stopped by adding EDTA, producing a relaxation of delta pH. From the initial rate of this relaxation and the rate of PPi hydrolysis measured under the same condition, the H+/PPi stoichiometry was obtained. In the second method, a mathematical model was used to describe the time course of delta pH formation. In the two methods an apparent H+/PPi stoichiometry of nearly 2 was obtained. The H+/ATP stoichiometry was determined also as an internal control, giving a value of nearly 3.6, which is in agreement with the value in different F-type H(+)-ATPases.

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