QUENCHING OF A ROOM-TEMPERATURE FLUORESCENCE BAND AT 693-NM DURING PHOTOACTIVATION OF THE WATER-SPLITTING SYSTEM OF PHOTOSYSTEM-II IN FLASHED BARLEY LEAVES
Franck, Fabrice; Dujardin, E.
1992 • In Photosynthesis Research, 31 (1), p. 41-47
[en] The modifications of the room temperature fluorescence spectrum during the photoactivation of the water-splitting system by continuous illumination were investigated in flashed barley leaves. A blue shift of the chlorophyll fluorescence band was detected during the first 2 min of illumination. During this shift, a decrease of the fluorescence intensity around 693 nm could be demonstrated in difference spectra and in second derivative spectra. This decrease is interpreted as a quenching of PS II fluorescence during the photoactivation. A relative fluorescence increase around 672 nm also occurred during the same period and is thought to reflect rapid light-induced chlorophyll formation. The flashed leaves contained small amounts of photoactive photochlorophyllide which could be removed by a short flash of intense white light given before continuous illumination. The fact that such flash had only weak effect on the 693 nm fluorescence decrease, whereas it strongly reduced the amplitude of the 672 nm fluorescence increase, favours the above interpretations.
QUENCHING OF A ROOM-TEMPERATURE FLUORESCENCE BAND AT 693-NM DURING PHOTOACTIVATION OF THE WATER-SPLITTING SYSTEM OF PHOTOSYSTEM-II IN FLASHED BARLEY LEAVES
Akoyunoglou G., Argyroudi-Akoyunoglou J.H., Michel-Wolwertz, Sironval C. (1966) Effect of intermittent and continuous light on chlorophyll formation in etiolated plants. Physiologia Plantarum 19:1101-1104.
Bricker T.M. (1990) The structure and function of CPa-1 and CPa-2 in Photosystem II. Photosynth Res 24:1-13.
Cheniae G.M., Martin I.F. (1973) Absence of oxygen evolving capacity in dark-grown Chlorella: The photoactivation of oxygen-evolving centers. Photochem Photobiol 17:441-459.
Franzén L.G., Styring S., Etienne A.L., Hansson O., Vernotte C. (1986) Spectroscopic and functional characterization of a highly oxygen evolving Photosystem II reaction center complex from spinach. Photobiochem Photobiophys 13:15-28.
Inoue Y. (1975) Multiple-flash activation of the water-photolysis system in wheat leaves as observed by delayed emission. Biochim Biophys Acta 396:402-413.
Inoue Y., Furuta S., Oku T., Shibata K. (1976) Light-dependent development of thermoluminescence, delayed emission and fluorescence variation in dark-grown spruce leaves. Biochim Biophys Acta 449:357-367.
Inoue Y., Kobayashi Y., Sakamoto E., Shibata K. (1974) Action spectrum for photoactivation of the water-splitting system in plastids of intermittently illuminated leaves. Physiologia Plantarum 32:228-232.
Krey A., Govindjee (1964) Fluorescence changes in Porphyridium exposed to green light of different intensity: A new emission band at 693 nm and its significance in photosynthesis. Proceedings of the National Academy of Sciences 52:1568-1572.
Krey A., Govindjee (1966) Fluorescence studies on a red alga, Porphyridium cruentum. Biochim Biophys Acta 120:1-18.
Miyao M., Inoue Y. (1991) An improved procedure for photoactivation of photosynthetic oxygen evolution: Effect of artificial electron acceptors on the photoactivation yield of NH2OH-treated wheat Photosystem II membranes. Biochim Biophys Acta 1056:47-56.
Nakatani N.Y., Ke B., Dolan E., Arntzen C.J. (1984) Identity of the Photosystem II reaction center polypeptide. Biochim Biophys Acta 765:347-352.
.
Ono T., Inoue Y. (1982) Photoactivation of the water-oxidation system in isolated intact chloroplasts prepared from wheat leaves grown under intermittent flash illumination. PLANT PHYSIOLOGY 69:1418-1422.
Ono T., Kajikawa H., Inoue Y. (1986) Changes in protein composition and Mn abundance in Photosystem II particles on photoactivation of the latent O2-evolving system in flash-grown wheat leaves. PLANT PHYSIOLOGY 80:85-90.
Rémy R. (1973) Appearance and development of photosynthetic activities in wheat etioplasts greened under continuous or intermittent light-evidence for water-side Photosystem II deficiency after greening under intermittent light. Photochemistry and Photobiology 18:409-416.
Rémy R., Phung Nhu Hung S., Moyse A. (1972) La différentiation fonctionnelle et structurale au cours du verdissement des étioplastes. Quelques aperçus sur la mise en place des deux systèmes photochimiques. Physiol Vég 10:269-290.
Shibata K. (1957) Spectroscopic studies on chlorophyll formation in intact leaves. J Biochem 44:147-173.
Sironval C., Brouers M., Michel J.M., Kuyper Y. (1968) The reduction of photochlorophyllide into chlorophyllide. I: The kinetics of the P657–647→P688–676 phototransformation. Photosynthetica 2:268-287.
Sironval C., Franck F., Gysembergh R., Bereza B., Dujardin E. (1984) The Franck-Inoue Chlorophyllide microcycle II in vivo and in vitro. Photochlorophyllide Reduction and Greening , C., Sironval, M., Brouers, Nijhoff Junk, The Hague; 197-222.
Strasser R.J. (1973) Uber das Vorhandensein eines lichtabhängigen Mechanismus, welcher die photosyntetische Sauerstoffentwkcklung induziert und reguliert. Ber Schweiz Bot Ges 83:1-13.
Strasser R.J., Butler L. (1977) Fluorescence emission spectra of Photosystem I, Photosystem II and the light-harvesting chlorphyll a/b complex of higher plants. Biochim Biophys Acta 462:307-313.
Strasser R.J., Sironval C. (1974) Correlation between the induction of oxygen evolution and of variable fluorescence in flashed bean leaves. Plant Sci Lett 3:135-141.
Tamura N., Cheniae (1987) Photoactivation of the water-oxidizing complex in Photosystem II membranes depleted of Mn and extrinsic proteins I. Biochemical and kinetic characterization. Biochim Biophys Acta 890:179-194.
Thorne S.W. (1971) The greening of etiolated bean leaves. I: The initial photoconversion process. Biochim Biophys Acta 226:113-127.