Skip to main content
Plant Physiology logoLink to Plant Physiology
. 1972 May;49(5):769–774. doi: 10.1104/pp.49.5.769

Extraction and Reconstitution of Photosystem II

S Okayama a,1, W L Butler a,2
PMCID: PMC366049  PMID: 16658045

Abstract

Hill activity (oxygen evolution with ferricyanide as the electron acceptor), light-induced absorbance changes at liquid nitrogen temperature associated with the primary activity of photosystem II, and fluorescence yield changes at both low temperature and room temperature were measured with lyophilized spinach chloroplasts before and after extraction with hexane and reconstitution with β-carotene and plastoquinone A. Extraction eliminated the Hill activity, and both β-carotene and plastoquinone A were required for maximal restoration of activity to the reconstituted chloroplasts.

Extraction also eliminated the light-induced absorbance changes at −196 C due to the photoreduction of C-550 and photooxidation of cytochrome b559, and reconstitution with β-carotene and plastoquinone A restored the low temperature photoreactions. However, only β-carotene was essential for the restoration of the photoreactions. Cytochrome b559 was modified, as a result of the extraction, to a lower redox potential, autooxidizable form and remained as such after reconstitution with β-carotene. The β-carotene-restored chloroplasts showed the photoreduction of C-550 but not the photooxidation of cytochrome b559 because the cytochrome was already oxidized. When β-carotene-reconstituted chloroplasts were suspended in buffer containing ascorbate prior to freezing, the cytochrome b559 was reduced and could be photooxidized by irradiation at low temperature. After reconstitution with β-carotene plus plastoquinone A the cytochrome b559 was partially restored to its original high potential form and was in the reduced state so that both the photoreduction of C-550 and the photooxidation of cytochrome b559 occurred on irradiation of the β-carotene plus plastoquinone A-reconstituted chloroplasts. Reconstitution with plastoquinone A alone had essentially no effect on restoring the photoreactions.

The fluorescence yield of dark-adapted lyophilized chloroplasts at −196 C showed an irreversible increase of about 2.5-fold during irradiation. After extraction the fluorescence yield of the chloroplasts was high (at the maximal light-induced level of the lyophilized control chloroplasts) and showed very little change in the light. Reconstitution with β-carotene alone restored some fluorescence quenching which was relieved by irradiation at low temperature. Reconstitution with plastoquinone A alone restored a high degree of quenching, but this quenching was not relieved by light at low temperature. Fluorescence emission spectra at −196 C showed that the fluorescence of variable yield in the lyophilized and β-carotene-reconstituted chloroplasts involved only the 680 and 695 nm emission bands but not the larger 730 nm emission band, whereas the irreversible quenching in plastoquinone A-reconstituted chloroplasts involved all wavelengths of emission. Extraction of the chloroplasts also eliminated the sharp 695 nm emission band at low temperature, and reconstitution with β-carotene partially restored it.

The fluorescence yield changes at room temperature differed from the low temperature measurements in that the strong fluorescence quenching restored to the plastoquinone A-reconstituted chloroplasts was relieved by light and reappeared in the dark. Thus plastoquinone A appeared to be much more effective than β-carotene in restoring the fluorescence of variable yield in room temperature measurements. However, it is argued from the results at low temperature that the quenching in plastoquinone A-reconstituted chloroplasts, which is probably due to the oxidized form of the quinone, is nonspecific and a different quenching mechanism from that which obtains in normal chloroplasts.

The results suggest that extraction with hexane removes plastoquinone A, which interrupts electron transport, and β-carotene, which disrupts the primary photochemical activity of photosystem II. Reconstitution of the extracted chloroplasts with β-carotene alone restores C-550 and the primary photochemical activity of photosystem II, and when the photosystem II reaction centers are restored the additional requirement of plastoquinone A for the Hill reaction can be demonstrated.

Full text

PDF
769

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Amesz J., Fork D. C. Quenching of chlorophyll fluorescence by quinones in algae and chloroplasts. Biochim Biophys Acta. 1967 Jul 5;143(1):97–107. doi: 10.1016/0005-2728(67)90114-4. [DOI] [PubMed] [Google Scholar]
  2. Barr R., Henninger M. D., Crane F. L. Comparative Studies on Plastoquinone II. Analysis for Plastoquinones A, B, C, and D. Plant Physiol. 1967 Sep;42(9):1246–1254. doi: 10.1104/pp.42.9.1246. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Bishop N. I. THE REACTIVITY OF A NATURALLY OCCURRING QUINONE (Q-255) IN PHOTOCHEMICAL REACTIONS OF ISOLATED CHLOROPLASTS. Proc Natl Acad Sci U S A. 1959 Dec;45(12):1696–1702. doi: 10.1073/pnas.45.12.1696. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Butler W. L., Okayama S. The photoreduction of C-550 in chloroplasts and its inhibition by lipase. Biochim Biophys Acta. 1971 Aug 6;245(1):237–239. doi: 10.1016/0005-2728(71)90028-4. [DOI] [PubMed] [Google Scholar]
  5. Erixon K., Butler W. L. The relationship between Q, C- 550 and cytochrome b 559 in photoreactions at -196 degrees in chloroplasts. Biochim Biophys Acta. 1971 Jun 15;234(3):381–389. doi: 10.1016/0005-2728(71)90205-2. [DOI] [PubMed] [Google Scholar]
  6. Govindjee R., Govindjee, Lavorel J., Briantais J. M. Fluorescence characteristics of lyophilized maize chloroplasts suspended in buffer. Biochim Biophys Acta. 1970 Jun 30;205(3):361–370. doi: 10.1016/0005-2728(70)90102-7. [DOI] [PubMed] [Google Scholar]
  7. KROGMANN D. W., OLIVERO E. The specificity of plastoquinone as a cofactor for photophosphorylation. J Biol Chem. 1962 Oct;237:3292–3295. [PubMed] [Google Scholar]
  8. Knaff D. B., Arnon D. I. LIGHT-INDUCED OXIDATION OF A CHLOROPLAST B-TYPE CYTOCHROME AT -189 degrees C. Proc Natl Acad Sci U S A. 1969 Jul;63(3):956–962. doi: 10.1073/pnas.63.3.956. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. LYNCH V. H., FRENCH C. S. Beta-carotene, an active component of chloroplasts. Arch Biochem Biophys. 1957 Aug;70(2):382–391. doi: 10.1016/0003-9861(57)90125-x. [DOI] [PubMed] [Google Scholar]
  10. Murata N. Fluorescence of chlorophyll in photosynthetic systems. IV. Induction of various emissions at low temperatures. Biochim Biophys Acta. 1968 Jul 16;162(1):106–121. doi: 10.1016/0005-2728(68)90219-3. [DOI] [PubMed] [Google Scholar]
  11. NISHIMURA M., TAKAMATSU K. A carotene-protein complex isolated from green leaves. Nature. 1957 Oct 5;180(4588):699–700. doi: 10.1038/180699a0. [DOI] [PubMed] [Google Scholar]
  12. Stiehl H. H., Witt H. T. Quantitative treatment of the function of plastoquinone in phostosynthesis. Z Naturforsch B. 1969 Dec;24(12):1588–1598. doi: 10.1515/znb-1969-1219. [DOI] [PubMed] [Google Scholar]
  13. Wood P. M., Bhagavan H. N., Crane F. L. Requirement for plastoquinone a in the hill reaction of isolated chloroplasts. Plant Physiol. 1966 Apr;41(4):633–640. doi: 10.1104/pp.41.4.633. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Yamashita T., Butler W. L. Photoreduction and photophosphorylation with tris-washed chloroplasts. Plant Physiol. 1968 Dec;43(12):1978–1986. doi: 10.1104/pp.43.12.1978. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Plant Physiology are provided here courtesy of Oxford University Press

RESOURCES