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Biochim Biophys Acta ; 1468(1-2): 1-5, 2000 Sep 29.
Article in English | MEDLINE | ID: mdl-11018644

ABSTRACT

The high potential, ascorbate-reducible b-type cytochrome of plant plasma membranes, named cytochrome b-561, has been purified to homogeneity from etiolated bean hypocotyls. The pure protein migrated in denaturing electrophoresis as a broad band of approximately 55 kDa, and was found to be glycosylated. Optical redox titrations of partially purified cytochrome b-561 indicated that it contains two hemes with similar spectral features, but distinct midpoint redox potentials (E(m7)+135 mV and +206 mV, respectively). The presence of two heme centers in cytochrome b-561 is consistent with its role in electron transfer across plant plasma membranes.


Subject(s)
Cytochrome b Group/isolation & purification , Fabaceae/chemistry , Plants, Medicinal , Cell Membrane/chemistry , Chromatography, Ion Exchange , Cytochrome b Group/chemistry , Electrophoresis, Polyacrylamide Gel , Heme/chemistry , Hypocotyl/chemistry , Potentiometry , Spectrophotometry
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