Light-dependent reversal of dark-chilling induced changes in chloroplast structure and arrangement of chlorophyll-protein complexes in bean thylakoid membranes

被引:27
|
作者
Garstka, M
Drozak, A
Rosiak, M
Venema, JH
Kierdaszuk, B
Simeonova, E
van Hasselt, PR
Dobrucki, J
Mostowska, A
机构
[1] Warsaw Univ, Inst Biochem, Dept Metab Regulat, PL-02096 Warsaw, Poland
[2] Univ Groningen, Dept Plant Physiol, NL-9750 AA Haren, Netherlands
[3] Warsaw Univ, Dept Biophys, Inst Expt Phys, Fac Phys, PL-02089 Warsaw, Poland
[4] Warsaw Univ, Inst Plant Expt Biol, Dept Plant & Cell Anat, Fac Biol, PL-02096 Warsaw, Poland
[5] Jagiellonian Univ, Lab Confocal Microscopy, Dept Biophys, Fac Biotechnol, PL-30387 Krakow, Poland
来源
基金
英国惠康基金;
关键词
bean; chloroplast and thylakoid structure; chlorophyll a fluorescence; confocal laser scanning microscopy; dark-chilling stress; LHCI-PSI; LHCII-PSII;
D O I
10.1016/j.bbabio.2005.08.006
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Changes in chloroplast structure and rearrangement of chlorophyll-protein (CP) complexes were investigated in detached leaves of bean (Phaseolus vulgaris L. cv. Eureka), a chilling-sensitive plant, during 5-day dark-chilling at 1 degrees C and subsequent 3-h photoactivation under white light (200 mu mol photons m(-2) s(-1)) at 22 degrees C. Although, no change in chlorophyll (Chl) content and Chl a/b ratio in all samples was observed, overall fluorescence intensity of fluorescence emission and excitation spectra of thylakoid membranes isolated from dark-chilled leaves decreased to about 50%, and remained after photoactivation at 70% of that of the control sample. Concomitantly, the ratio between fluorescence intensities of PSI and PSII (F736/ F681) at 120 K increased 1.5-fold upon chilling, and was fully reversed after photoactivation. Moreover, chilling stress seems to induce a decrease of the relative contribution of LHCII fluorescence to the thylakoid emission spectra at 120 K, and an increase of that from LHCI and PSI, correlated with a decrease of stability of LHCI-PSI and LHCII trimers, shown by mild-denaturing electrophoresis. These effects were reversed to a large extent after photoactivation, with the exception of LHCII, which remained partly in the aggregated form. In view of these data, it is likely that dark-chilling stress induces partial disassembly of CP complexes, not completely restorable upon photoactivation. These data are further supported by confocal laser scanning fluorescence microscopy, which showed that regular grana arrangement observed in chloroplasts isolated from control leaves was destroyed by dark-chilling stress, and was partially reconstructed after photoactivation. In line with this, Chl a fluorescence spectra of leaf discs demonstrated that dark-chilling caused a decrease of the quantum yield PSII photochemistry (F-v/F-m) by almost 40% in 5 days. Complete restoration of the photochemical activity of PSII required 9 h post-chilling photoactivation, while only 3 h were needed to reconstruct thylakoid membrane organization and chloroplast structure. The latter demonstrated that the long-term dark-chilled bean leaves started to suffer from photoinhibition after transfer to moderate irradiance and temperature conditions, delaying the recovery of PSII photochemistry, independently of photo-induced reconstruction of PSII complexes. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:13 / 23
页数:11
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