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Possible mechanisms of light‐induced chlorophyll degradation in senescing leaves of Hydrilla verticillata
Author(s) -
Kar R. K.,
Choudhuri M. A.
Publication year - 1987
Publication title -
physiologia plantarum
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.351
H-Index - 146
eISSN - 1399-3054
pISSN - 0031-9317
DOI - 10.1111/j.1399-3054.1987.tb04331.x
Subject(s) - hydrilla , spinacia , darkness , chlorophyll , spinach , cycloheximide , peroxidase , botany , biology , light intensity , horticulture , chemistry , chloroplast , biochemistry , protein biosynthesis , aquatic plant , enzyme , ecology , physics , macrophyte , gene , optics
Light treatment markedly accelerated the chlorophyll loss in senescing leaves of Hydrilla verticillata [(L.f.) Royle] as compared to dark treatment, whereas such acceleration could not be observed in senescing spinach ( Spinacia oleracea L.) leaves. The light‐induced cholorophyll loss in Hydrilla was retarded slightly by chloramphenicol and markedly by cycloheximide. Catalase (EC 1.11.1.6) activity did not change appreciably in Hydrilla leaves either in light or in darkness, while in spinach it declined markedly in the dark, and light retarded such decline. Peroxidase activity in Hydrilla showed faster increase in light than in darkness, while in spinach it increased only in light during senescence. The activity of phenol(pyrogallol)‐specific peroxidase increased markedly in light, and that of ascorbate‐specific peroxidase decreased slightly both in light and darkness during senescence of Hydrilla leaves. This rise in phenolspecific peroxidase activity was prevented by cycloheximide treatment. Pretreatment of Hydrilla leaves with monophenol (2,4‐dichlorophenol) and o‐diphenol (hydroquinone) accelerated and retarded, respectively, the light‐induced cholorophyll loss. Pretreatment of Hydrilla leaves with H 2 O 2 augmented the chlorophyll loss more markedly in light than in darkness. The endogenous level of H 2 O 2 increased more in light than in dark during senescence of Hydrilla leaves. Treatment of Hydrilla leaves with 3‐(3.4‐dichlorophenyl)‐l,l‐dimethylurea. a photosystem II inhibitor, prevented both light‐induced rise in H 2 O: level and chlorophyll loss, but it was without effect in the dark. Retardation of light‐induced chlorophyll loss occurred during senescence of Hydrilla leaves when light was given in different photoperiods in a 24‐h daily cycle for 6 days instead of as continuous irradiance. There was a negative correlation between the length of the photoperiod and the extent of cholorophyll loss.