Reversible inactivation of photosystem II reaction centers in cation-depleted chloroplast membranes

Salil Bose, Charles J. Arntzen

Research output: Contribution to journalArticlepeer-review

22 Scopus citations

Abstract

Isolated pea chloroplasts were washed once in 10 mm NaCl and were then suspended in "low-salt" medium. Approximately one-half of the photosystem II reaction centers of these salt-depleted membranes were found to be photochemically inactive. These units became active in the presence of low concentrations of divalent cations (5-10 mm Mg2+) or high concentrations of monovalent cations (150-200 mm Na+), as evidenced by a twofold increase in the steady-state flash yield of oxygen evolution under short (~10-μs) saturating repetitive flashes (two per second). The half-maximal increase in flash yield occurred at ~2 mM Mg2+ or ~75 mm Na+. The flash yield of hydroxylamine oxidation in these low-salt chloroplasts increased twofold after Mg2+ addition, indicating that the cation action was close to the reaction-center chlorophyll complex. The relation between flash yield and dark time between flashes was not changed significantly by Mg2+, indicating that the rate-limiting step of the overall electron transport (H20 -→ ferricyanide) was not affected significantly. When the rate-limiting step was bypassed using silicomolybdate as the photosystem II electron acceptor (in the presence of diuron), the reduction rate doubled in the presence of Mg2+, even under continuous, saturating light. In glutaraldehyde-fixed chloroplasts, Mg2+ did not increase the flash yield of O2 evolution; this suggests that protein conformational changes in the chloroplast membranes were involved in Mg2+ activation of photosystem II centers.

Original languageEnglish (US)
Pages (from-to)567-575
Number of pages9
JournalArchives of Biochemistry and Biophysics
Volume185
Issue number2
DOIs
StatePublished - Jan 30 1978
Externally publishedYes

ASJC Scopus subject areas

  • Biophysics
  • Biochemistry
  • Molecular Biology

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