Low threshold levels of ultraviolet‐B in a background of photosynthetically active radiation trigger rapid degradation of the D2 protein of photosystem‐II
Author(s) -
Jansen Marcel A.K.,
Gaba Victor,
Greenberg Bruce M.,
Mattoo Autar K.,
Edelman Marvin
Publication year - 1996
Publication title -
the plant journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.058
H-Index - 269
eISSN - 1365-313X
pISSN - 0960-7412
DOI - 10.1046/j.1365-313x.1996.9050693.x
Subject(s) - photosystem ii , photosynthetically active radiation , degradation (telecommunications) , ultraviolet b radiation , ultraviolet , photochemistry , ultraviolet radiation , biophysics , photosynthesis , radiation , chemistry , biology , biochemistry , materials science , optoelectronics , physics , optics , radiochemistry , telecommunications , computer science
Summary The photosystem II reaction centre has at its core a heterodimer made up of two proteins, D1 and D2. The D1 protein is known to be rapidly degraded by photosyn‐thetically active radiation while the D2 protein is relatively stable. This paper reports that when the aquatic higher plant, Spirodela was exposed to ultraviolet‐B radiation, D2 degradation accelerated markedly and half life times approached those of the D1 protein. Moreover, in the presence of an environmentally relevant background of photosynthetically active radiation, low fluxes of ultraviolet‐B (but not ultraviolet‐A) radiation synergistically stimulated degradation of the D2 protein within functional reaction centres. Thus, above a critical threshold, ultraviolet‐B specifically targets the D1–D2 heterodimer for accelerated degradation.
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