Photoadaptation of two members of the Chlorophyta ( Scenedesmus and Chlorella ) in laboratory and outdoor cultures: changes in chlorophyll fluorescence quenching and the xanthophyll cycle

Planta ◽  
1999 ◽  
Vol 209 (1) ◽  
pp. 126-135 ◽  
Author(s):  
Jiří Masojídek ◽  
Giuseppe Torzillo ◽  
Michal Koblížek ◽  
Jiří Kopecký ◽  
Paola Bernardini ◽  
...  
Keyword(s):  
Chlorophyll Fluorescence ◽  
Fluorescence Quenching ◽  
Xanthophyll Cycle ◽  
Chlorophyll Fluorescence Quenching ◽  
Outdoor Cultures

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

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