Induction of Nonphotochemical Energy Dissipation and Absorbance Changes in Leaves (Evidence for Changes in the State of the Light-Harvesting System of Photosystem II in Vivo)

Simultaneous measurements of nonphotochemical quenching of chlorophyll fluorescence and absorbance changes in the 400- to 560-nm region have been made following illumination of dark-adapted leaves of the epiphytic bromeliad Guzmania monostachia. During the first illumination, an absorbance change at 505 nm occurred with a half-time of 45 s as the leaf zeaxanthin content rose to 14% of total leaf carotenoid. Selective light scattering at 535 nm occurred with a half-time of 30 s. During a second illumination, following a 5-min dark period, quenching and the 535-nm absorbance change occurred more rapidly, reaching a maximum extent within 30 s. Nonphotochemical quenching of chlorophyll fluorescence was found to be linearly correlated to the 535-nm absorbance change throughout. Examination of the spectra of chlorophyll fluorescence emission at 77 K for leaves sampled at intervals during this regime showed selective quenching in the light-harvesting complexes of photosystem II (LHCII). The quenching spectrum of the reversible component of quenching had a maximum at 700 nm, indicating quenching in aggregated LHCII, whereas the irreversible component represented a quenching of 680-nm fluorescence from unaggregated LHCII. It is suggested that this latter process, which is associated with the 505-nm absorbance change and zeaxanthin formation, is indicating a change in state of the LHCII complexes that is necessary to amplify or activate reversible pH-dependent energy dissipation, which is monitored by the 535-nm absorbance change. Both of the major forms of nonphotochemical energy dissipation in vivo are therefore part of the same physiological photoprotective process and both result from alterations in the LHCII system.

[1]  A. Gilmore,et al.  Zeaxanthin Formation and Energy-Dependent Fluorescence Quenching in Pea Chloroplasts under Artificially Mediated Linear and Cyclic Electron Transport. , 1991, Plant physiology.

[2]  Peter Horton,et al.  Studies on the induction of chlorophyll fluorescence in isolated barley protoplasts. IV. Resolution of non-photochemical quenching , 1988 .

[3]  C. Mullineaux,et al.  Excitation-energy quenching in aggregates of the LHC II chlorophyll-protein complex: a time-resolved fluorescence study , 1993 .

[4]  U. Heber,et al.  Conformational changes of chloroplasts induced by illumination of leaves in vivo. , 1969, Biochimica et biophysica acta.

[5]  G. Krause,et al.  Chlorophyll Fluorescence and Photosynthesis: The Basics , 1991 .

[6]  J. Sutherland,et al.  ORGANIZATION OF PIGMENT‐PROTEIN COMPLEXES INTO MACRODOMAINS IN THE THYLAKOID MEMBRANES OF WILD‐TYPE and CHLOROPHYLL fo‐LESS MUTANT OF BARLEY AS REVEALED BY CIRCULAR DICHROISM , 1991 .

[7]  G. Krause,et al.  Photoinhibition of photosynthesis. An evaluation of damaging and protective mechanisms , 1988 .

[8]  G. Britton,et al.  Enhancement of the ΔpH‐dependent dissipation of excitation energy in spinach chloroplasts by light‐activation: correlation with the synthesis of zeaxanthin , 1989 .

[9]  G. Noctor,et al.  Long-wavelength chlorophyll species are associated with amplification of high-energy-state excitation quenching in higher plants , 1991 .

[10]  P. Horton,et al.  The mechanisms of changes in Photosystem II efficiency in spinach thylakoids , 1990 .

[11]  J. A. Smith,et al.  Comparative ecophysiology of CAM and C3 bromeliads. III. Environmental influences on CO2 assimilation and transpiration , 1986 .

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

[13]  A. Ruban,et al.  Mechanism of ΔpH-dependent dissipation of absorbed excitation energy by photosynthetic membranes. II. The relationship between LHCII aggregation in vitro and qE in isolated thylakoids , 1992 .

[14]  J. Sutherland,et al.  Macroorganization of Chlorophyll a/b light-harvesting complex in thylakoids and aggregates: information from circular differential scattering , 1988 .

[15]  H. Griffiths,et al.  Photoinhibitory responses of the epiphytic bromeliad Guzmania monostachia during the dry season in Trinidad maintain photochemical integrity under adverse conditions , 1992 .

[16]  G. Krause The high-energy state of the thylakoid system as indicated by chlorophyll fluorescence and chloroplast shrinkage. , 1973, Biochimica et biophysica acta.

[17]  N. Geacintov,et al.  Domain sizes in chloroplasts and chlorophyll-protein complexes probed by fluorescence yield quenching induced by singlet-triplet exciton annihilation , 1985 .

[18]  D. Deamer,et al.  Mechanisms of light-induced structural change in chloroplasts II. The role of ion movements in volume changes , 1967 .

[19]  W. W. Adams,et al.  Relative contributions of zeaxanthin-related and zeaxanthin-unrelated types of ;high-energy-state' quenching of chlorophyll fluorescence in spinach leaves exposed to various environmental conditions. , 1990, Plant physiology.

[20]  R. Bassi,et al.  A supramolecular light-harvesting complex from chloroplast photosystem-II membranes. , 1992, European journal of biochemistry.

[21]  G. Noctor,et al.  Control of the light‐harvesting function of chloroplast membranes by aggregation of the LHCII chlorophyll—protein complex , 1991, FEBS letters.

[22]  W. Bilger,et al.  Light-induced spectral absorbance changes in relation to photosynthesis and the epoxidation state of xanthophyll cycle components in cotton leaves. , 1989, Plant physiology.

[23]  J. Briantais,et al.  A quantitative study of the slow decline of chlorophyll a fluorescence in isolated chloroplasts. , 1979, Biochimica et biophysica acta.

[24]  G. Peter,et al.  Biochemical composition and organization of higher plant photosystem II light-harvesting pigment-proteins. , 1991, The Journal of biological chemistry.

[25]  G. Noctor,et al.  The relationship between zeaxanthin, energy-dependent quenching of chlorophyll fluorescence, and trans-thylakoid pH gradient in isolated chloroplasts , 1991 .

[26]  H. Yamamoto,et al.  An Ascorbate-induced Absorbance Change in Chloroplasts from Violaxanthin De-epoxidation. , 1972, Plant physiology.

[27]  P. Horton,et al.  The molecular mechanism of the control of excitation energy dissipation in chloroplast membranes Inhibition of ΔpH‐dependent quenching of chlorophyll fluorescence by dicyclohexylcarbodiimide , 1992, FEBS letters.

[28]  I. Moya,et al.  Energy-dependent quenching of chlorophyll a fluorescence: effect of pH on stationary fluorescence and picosecond-relaxation kinetics in thylakoid membranes and Photosystem II preparations , 1992 .

[29]  E. Weis,et al.  Fluorescence analysis during steady-state photosynthesis , 1989 .

[30]  W. Junge,et al.  The photosynthetic water oxidase: its proton pumping activity is short‐circuited within the protein by DCCD , 1988, The EMBO journal.

[31]  B. Demmig‐Adams,et al.  Photoprotection and Other Responses of Plants to High Light Stress , 1992 .

[32]  W. L. Butler,et al.  Quenching of chlorophyll fluorescence and primary photochemistry in chloroplasts by dibromothymoquinone. , 1975, Biochimica et biophysica acta.

[33]  G. Britton,et al.  Photodestruction of Pigments in Higher Plants by Herbicide Action I. THE EFFECT OF DCMU (DIURON) ON ISOLATED CHLOROPLASTS , 1990 .

[34]  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.