The effect of high-energy-state excitation quenching on maximum and dark level chlorophyll fluorescence yield

1990 ◽  
Vol 25 (3) ◽  
pp. 199-211 ◽  
Author(s):  
D. Rees ◽  
G. D. Noctor ◽  
P. Horton
1976 ◽  
Vol 31 (11-12) ◽  
pp. 722-729 ◽  
Author(s):  
Bernd Schmidt ◽  
Hans Rurainski

Abstract The chlorophyll fluorescence of isolated chloroplasts in the presence of phenazine methosulfate (PMS) and 3-(3,4-dichlorophenyl)-1,1-dimethylurea (DCMU) can be quenched in a light-dependent reaction. This phenomenan has been studied and the following observations were made: 1. Quenching occurs under non-phosphorylating conditions and is stimulated by Mg2+ ions. 2. Under the same conditions, a light-dependent, Mg2+ stimulated transient decrease of absorp­ tion at 388 nm is observed which shows the spectral characteristics of PMS. 3. PMS is reversibly bound to chloroplasts. Under the experimental conditions used, binding amounts to as much as 0.5 mol PMS/mol chlorophyll. 4. Some uncouplers of photophosphorylation such as carbonylcyanide-m-chlorophenylhydrazon (CCCP) and atebrin analog abolish quenching, transient absorption change and binding of PMS. Others, such as methylamine, ammonia, gramicidin and nigericin do not. It is suggested that fluorescence quenching, transient absorption change and binding of PMS are causally related. The concept, postulated by others, that a high-energy state of the chloroplast membrane is involved in the fluorescence lowering is questioned.


1992 ◽  
Vol 188 (3-4) ◽  
pp. 359-367 ◽  
Author(s):  
Steven L. Mielke ◽  
Ronald S. Friedman ◽  
Donald G. Truhlar ◽  
David W. Schwenke

2018 ◽  
Vol 11 (11) ◽  
pp. 112702 ◽  
Author(s):  
Tsung-Tse Lin ◽  
Li Wang ◽  
Ke Wang ◽  
Thomas Grange ◽  
Hideki Hirayama

Author(s):  
A. R. Crofts ◽  
J. B. Jackson ◽  
E. H. Evans ◽  
R. J. Cogdell

2019 ◽  
Vol 55 (54) ◽  
pp. 7836-7839 ◽  
Author(s):  
Shenfei Zhao ◽  
Zhuanzhuan Shi ◽  
Chun Xian Guo ◽  
Chang Ming Li

A high-energy-state biomimetic enzyme for the superoxide anion is presented by inducing surface oxygen defects in MnTiO3 nanodiscs.


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