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Concentration and Function of Membrane-Bound Cytochromes in Cyanobacterial Heterocysts ¹

Biology Department, Brookhaven National Laboratory, Upton, New York 11973

Membranes isolated from heterocysts and vegetative cells of Anabaena 7120 were assayed for content of cytochrome f, cytochrome b-563, cytochrome b-559_HP, cytochrome b-559_LP, and cytochrome aa₃ by use of reduced-minus-oxidized difference spectra. The level of cytochrome aa₃ in heterocyst membranes was 4 to 100 times higher than that in vegetative cells of Anabaena 7120 or other species of cyanobacteria. Heterocyst membranes lack cytochrome b-559_HP but contain cytochrome b-559_LP (E_m7.5 = +77 millivolts, n = 1) at approximately the same concentration as cytochrome f. The role of cytochrome b-559_LP in the hydrogenase-dependent electron transfer pathway was investigated with the inhibitor 2-(n-heptyl)-4-hydroxyquinoline N-oxide which blocks electron flow from hydrogenase to acceptors reacting with the plastoquinone pool. Addition of inhibitor elicited no change in the reduction level of cytochrome b-559_LP indicating that this cytochrome is not directly involved in this pathway.

¹ Supported by the Competitive Research Grants Office of the United States Department of Agriculture, Science and Education Administration. It was carried out at Brookhaven National Laboratory under the auspices of, and with additional support from, the United States Department of Energy.