Studies on the induction of chlorophyll fluorescence in isolated barley protoplasts. IV. Resolution of non-photochemical quenching

Abstract Using DCMU addition and light-saturation pulses, chlorophyll fluorescence quenching by isolated barley protoplasts has been examined upon illumination with different light intensities. Total quenching was constant at all intensities, photochemical quenching predominating in low light and non-photochemical quenching becoming increasingly important at higher intensity. The components of non-photochemical quenching were resolved by examination of kinetics of relaxation of quenching upon DCMU addition or darkening. It was found that: (a) energy-dependent quenching saturated with characteristics similar to photosynthesis; (b) a slowly relaxing, NaF-sensitive component attributed to protein phosphorylation saturated in low light and decreased at high light; (c) an irreversible component ascribed to photoinhibition was a major quencher as light levels were increased above saturation; (d) the decreased photochemical quenching at high light was not strictly correlated with alteration in rate of O2 evolution. Analysis of these data showed that the quantum yield of Photosystem II declined as the light intensity was increased from zero to that saturating for photosynthesis and was associated with the presence of energy-dependent quenching. The regulation of excitation dissipation by the thylakoid membrane is discussed.

[1]  G. Krause,et al.  ΔpH‐dependent chlorophyll fluorescence quenching indicating a mechanism of protection against photoinhibition of chloroplasts , 1986 .

[2]  J. Bennett,et al.  Chloroplast phosphoproteins. Evidence for a thylakoid-bound phosphoprotein phosphatase. , 1980, European journal of biochemistry.

[3]  C. Foyer,et al.  An investigation into the ATP requirement for phosphorylation of thylakoid proteins and for the ATP-induced decrease in the yield of chlorophyll fluorescence in chloroplasts at different stages of development , 1984 .

[4]  Peter Horton,et al.  Studies on the induction of chlorophyll fluorescence in barley protoplasts. III. Correlation betweeen changes in the level of glycerate 3-phosphate and the pattern of fluorescence quenching , 1986 .

[5]  C. Foyer,et al.  Increase in the level of thylakoid protein phosphorylation in maize mesophyll chloroplasts by decrease in the transthylakoid pH gradient , 1984 .

[6]  N. Baker,et al.  Analysis of the slow phases of the in vivo chlorophyll fluorescence induction curve. Changes in the redox state of photosystem II electron acceptors and fluorescence emission from photosystems I and II. , 1981, Biochimica et biophysica acta.

[7]  N. Baker,et al.  Evaluation of a technique for the measurement of chlorophyll fluorescence from leaves exposed to continuous white light , 1985 .

[8]  Pam Lee,et al.  Regulation of thylakoid protein phosphorylation by high‐energy‐state quenching , 1987 .

[9]  D. Kyle THE 32000 DALTON QB PROTEIN OF PHOTOSYSTEM II , 1985 .

[10]  Stephen B. Powles,et al.  Photoinhibition of Photosynthesis Induced by Visible Light , 1984 .

[11]  N. Baker,et al.  The kinetics of photoinhibition of the photosynthetic apparatus in pea chloroplasts , 1986 .

[12]  P. Horton,et al.  Regulation of phosphorylation of chloroplast membrane polypeptides by the redox state of plastoquinone , 1981 .

[13]  Joseph A. Berry,et al.  Quantum efficiency of Photosystem II in relation to ‘energy’-dependent quenching of chlorophyll fluorescence , 1987 .

[14]  K. Winter,et al.  Photoinhibition and zeaxanthin formation in intact leaves : a possible role of the xanthophyll cycle in the dissipation of excess light energy. , 1987, Plant physiology.

[15]  J. Briantais,et al.  Photoinduced quenching of chlorophyll fluorescence in intact chloroplasts and algae. Resolution into two components , 1982 .

[16]  P. Horton,et al.  Light-dependent quenching of chlorophyll fluorescence in pea chloroplasts induced by adenosine 5'-triphosphate. , 1981, Biochimica et biophysica acta.