Correlations between the temperature dependence of chlorophyll fluorescence and the fluidity of thylakoid membranes

2012 ◽  
Vol 147 (4) ◽  
pp. 409-416 ◽  
Author(s):  
Altanzaya Tovuu ◽  
Ismayil S. Zulfugarov ◽  
Choon-Hwan Lee
Nitric Oxide ◽  
2011 ◽  
Vol 24 (2) ◽  
pp. 84-90 ◽  
Author(s):  
Radka Vladkova ◽  
Anelia G. Dobrikova ◽  
Ranjeet Singh ◽  
Amarendra N. Misra ◽  
Emilia Apostolova

1996 ◽  
Vol 23 (6) ◽  
pp. 669 ◽  
Author(s):  
WW Iii Adams ◽  
B Demmig-Adams ◽  
DH Barker ◽  
S Kiley

Acclimation of the leaves or stems of four succulent species to different light environments and to the light gradient across high light-acclimated tissues was examined through measurements of chlorophyll fluorescence and characterisation of the pigment composition of the thylakoid membranes. Whereas the total amounts of light striking the upper (sun-exposed) and lower (self-shaded) surfaces were quite different, resulting in a much smaller pool of the xanthophyll cycle carotenoids in the lower halves of high light-acclimated tissues, the conversion state of the xanthophyll cycle (the degree to which violaxanthin is converted to antheraxanthin and zeaxanthin) was similar throughout the tissues during exposure to natural sunlight. Under full sunlight, less than 25% of the light absorbed by the upper surface was utilised through photosynthesis, with the majority of the remaining excitation energy being dissipated thermally. In contrast, a considerably greater fraction of the light absorbed by the lower surface was utilised in photosynthesis, ranging from one-third to more than two-thirds of the total energy absorbed.


1995 ◽  
Vol 22 (2) ◽  
pp. 239 ◽  
Author(s):  
N Mohanty ◽  
AM Gilmore ◽  
HY Yamamoto

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.


2003 ◽  
Vol 70 (2) ◽  
pp. 75-80 ◽  
Author(s):  
Emilia Apostolova ◽  
Tzvetelina Markova ◽  
Tzvetanka Filipova ◽  
Maria T Molina ◽  
Stefka G Taneva

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