Xanthophyll cycle and energy-dependent fluorescence quenching in leaves from pea plants grown under intermittent light

Planta ◽  
1994 ◽  
Vol 192 (2) ◽  
pp. 176-182 ◽  
Author(s):  
Peter Jahns ◽  
G. Heinrich Krause
Keyword(s):  
Fluorescence Quenching ◽  
Xanthophyll Cycle ◽  
Intermittent Light ◽  
Energy Dependent

Mechanism of Non-Photochemical Chlorophyll Fluorescence Quenching. I. The Role of De-Epoxidised Xanthophylls and Sequestered Thylakoid Membrane Protons as Probed by Dibucaine

1995 ◽  
Vol 22 (2) ◽  
pp. 231 ◽  
Author(s):  
N Mohanty ◽  
HY Yamamoto
Keyword(s):  
Chlorophyll Fluorescence ◽  
Fluorescence Quenching ◽  
Xanthophyll Cycle ◽  
Thylakoid Membranes ◽  
Photochemical Quenching ◽  
Chlorophyll Fluorescence Quenching ◽  
Mechanism Of Inhibition ◽  
Non Photochemical Quenching ◽  
Energy Dependent

Dibucaine reportedly inhibits the light-induced transthylakoid proton gradient of chloroplasts without inhibiting energy-dependent non-photochemical chlorophyll fluorescence quenching (Laasch, H. and Weis, E. (1989). Photosynthesis Research 22, 137-146). We show that dibucaine can inhibit fluorescence quenching, depending on the de-epoxidation state of the xanthophyll cycle. Whereas dibucaine (20-40 μM) had little effect on fluorescence quenching in pre-illuminated-type thylakoids (loaded with zeaxanthin and antheraxanthin), it strongly inhibited quenching in dark-adapted-type thylakoids (no preinduction of de-epoxidation). Dibucaine inhibited lumen acidification similarly in both types of thylakoids and also the induction of violaxanthin de-epoxidation in dark-adapted thylakoids. Thus dark-adapted and pre-illuminated thylakoids differed in de-epoxidation states and their suspectibility to dibucaine inhibition of fluorescence quenching corresponded to this difference. The mechanism of inhibition of de-epoxidation by dibucaine is unclear. It could be due to the inhibition of lumen acidification but an inhibition of the violaxanthin available for de-epoxidation is not excluded. High dibucaine concentrations inhibited de-epoxidase activity directly. Dibucaine inhibition of fluorescence quenching, however, is not limited to the inhibition of de-epoxidation. Small but clear effects on fluorescence quenching were present in thylakoids even with de-epoxidation preinduced. Moreover, thylakoids with preinduced de-epoxidation were more resistant to dibucaine inhibition of fluorescene quenching when poised by salt treatments for proton partitioning into membrane-sequestered domains than when poised for proton partitioning into delocalised domains. We conclude that non-photochemical quenching of chlorophyll fluorescence depends on both de-epoxidised xanthophylls and sequestered proton domains in the thylakoid membranes

Mechanism of Non-Photochemical Chlorophyll Fluorescence Quenching. II. Resolution of Rapidly Reversible Absorbance Changes at 530 Nm and Fluorescence Quenching by the Effects of Antimycin, Dibucaine and Cation Exchanger, A23187

1995 ◽  
Vol 22 (2) ◽  
pp. 239 ◽  
Author(s):  
N Mohanty ◽  
AM Gilmore ◽  
HY Yamamoto
Keyword(s):  
Chlorophyll Fluorescence ◽  
Fluorescence Quenching ◽  
Cation Exchanger ◽  
Thylakoid Membranes ◽  
Chlorophyll Fluorescence Quenching ◽  
Absorbance Changes ◽  
Energy Dependent ◽  
The Relationship ◽  
Effect Of Inhibitors ◽  
Exchange Properties

The putative relationship between the light-induced absorbance increase at 530 nm (ΔA530), the so-called light-scattering change, and non-photochemical chlorophyll fluorescence quenching (NPQ) was examined by the effect of inhibitors. Antimycin at a low concentration (350 nM) completely inhibited fluorescence quenching while only partially inhibiting A530. This effect was independent of the mode of thylakoid energisation and preinduction of violaxanthin de-epoxidation. Dibucaine at 20 FM abolished NPQ but had little effect on ΔA530. Moreover, the light-induced ΔA530 signal was present even in the absence of de-epoxidised xanthophylls. The cation exchanger A23187 blocked the development of NPQ as well as relaxed fluorescence quenching at steady state without involving a major portion of ΔA530. Thus, the relationship between energy-dependent A530 changes and fluorescence quenching was non-linear under all conditions tested. The light-induced absorbance increase at 530 nm, therefore, is insufficient for NPQ. The differential effects of inhibitors are explained schematically, depicting three phases for NPQ: (a) formation of zeaxanthin and antheraxanthin by the xanthophyll cycle; (b) formation of a state reflected by A530 that is induced by the transthylakoid ApH, possibly involving aggregation of LHCII; and (c) fluorescence quenching by the combined effect of both steps and by the H+-cation exchange properties of thylakoid membranes.

Energy-Dependent Chlorophyll Fluorescence Quenching in Chloroplasts Correlated with Quantum Yield of Photosynthesis

1987 ◽  
Vol 42 (5) ◽  
pp. 581-584 ◽  
Author(s):  
G. Heinrich Krause ◽  
Henrik Laasch
Keyword(s):  
Chlorophyll Fluorescence ◽  
Quantum Yield ◽  
Fluorescence Quenching ◽  
Dynamic Property ◽  
Energy Requirement ◽  
Photosynthetic Pigment ◽  
Thermal Dissipation ◽  
Chlorophyll Fluorescence Quenching ◽  
Pigment System ◽  
Energy Dependent

Abstract Chlorophyll a fluorescence quenching was studied in intact, CO2 fixing chloroplasts isolated from spinach. Energy-dependent quenching (qᴇ), which is correlated with the light-induced pro­ ton gradient across the thylakoid membrane presumably reflects an increase in the rate-constant of thermal dissipation of excitation energy in the photosynthetic pigment system . The extent of qᴇ was found to be linearly related to the decrease of quantum yield of photosynthesis. We suggest that this relationship indicates a dynamic property of the membrane to adjust thermal dissipation of absorbed light energy to the energy requirement of photosynthesis.

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