Redox and acid-base characterization of cytochrome b-559 in photosystem II particles

Eur J Biochem. 1988 Feb 1;171(3):449-55. doi: 10.1111/j.1432-1033.1988.tb13810.x.

Abstract

The redox and acid/base states and midpoint potentials of cytochrome b-559 have been determined in oxygen-evolving photosystem II (PS II) particles at room temperature in the pH range from 6.5 to 8.5. At pH 7.5 the fresh PS II particles present about 2/3 of their cytochrome b-559 in its reduced and protonated (non-auto-oxidizable) high-potential form and about 1/3 in its oxidized and non-protonated low-potential form. Potentiometric reductive titration shows that the protonated high-potential couple is pH-independent (E'0, + 380 mV), whereas the low-potential couple is non-protonated and pH-independent above pH 7.6 (E'0, pH greater than 7.6, + 140 mV), but becomes pH-dependent below this pH, with a slope of -72 mV/pH unit. Moreover, evidence is presented that in PS II particles cytochrome b-559 can cycle, according to its established redox and acid/base properties, as an energy transducer at two alternate midpoint potentials and at two alternate pKa values. Red light absorbed by PS II induces reduction of cytochrome b-559 in these particles at room temperature, the reaction being completely blocked by dichlorophenyldimethylurea.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Chlorophyll / analysis*
  • Cytochrome b Group / analysis*
  • Energy Transfer
  • Hydrogen-Ion Concentration
  • Light
  • Light-Harvesting Protein Complexes
  • Oxidation-Reduction
  • Photosynthetic Reaction Center Complex Proteins
  • Photosystem II Protein Complex*
  • Plant Proteins / analysis*
  • Temperature

Substances

  • Cytochrome b Group
  • Light-Harvesting Protein Complexes
  • Photosynthetic Reaction Center Complex Proteins
  • Photosystem II Protein Complex
  • Plant Proteins
  • Chlorophyll
  • cytochrome b559