Light-Induced Accumulation and Stability of Chlorophylls and Chlorophyll-Proteins during Chloroplast Development in Radish Seedlings

Abstract

Illumination of 3 day old etiolated radish seedlings with continuous white light results in a progressive accumulation of chlorophyll a and b. Both pigments are bound in a different way to the thylakoid chlorophyll-proteins, which appear parallel to the formation of chlorophylls. By applying the SDS-PAGE method to SDS-digested chloroplasts, it was possible to show that the chloroplasts of radish cotyledons contain the typical chlorophyll proteins LHCP1-3, CPa, CPI and CPIa which have been found in other plants. Between LHCP1 and CPI an additional chlorophyll protein is detected with the spectral properties of a LHCP; it is termed here LHCPy. When the green plants are transferred to continuous darkness, chlorophylls and the chlorophyll-proteins are progressively degraded. At an early stage of greening chlorophyll b is destroyed at a much higher rate in darkness than chlorophyll a, which yields high chlorophyll a/b ratios. This is paralleled by a faster decrease in the level of the corresponding chloro­phyll a/b-protein LHCP3 than of CPI. At a later stage of greening, after the end of the logarithmic chlorophyll accumulation, the chlorophylls a and b and also the LHCP3 and CPI are destroyed in continuous darkness at equal rates; the a/b ratios and the LHCP3/CPI ratios are then little different from the light control. The data indicate that at an early stage of greening the light-harvesting chlorophyll a/b-protein LHCP3 is less stable than the other chlorophyll-proteins (CPI, CPIa, CPa), which contain pre­ dominantly chlorophyll a. The ratio chlorophyll a to β-carotene (a/c ratio) of CPIa, CPI and CPa is about 10, while that of the LHCP1-3 is found to be between 150 to 300. We therefore propose using the a/c ratio to define the chlorophyll-proteins which, besides the absorption spectra, is the most suitable parameter.

Ribulose bisphosphate carboxylase capacity and chlorophyll content in developing seedlings of Chenopodium rubrum L. growing under light of different qualities and fluence rates

“…Changes in Chl a/b ratios during dark periods (Fig. 5) were found under WL-D cycles in Chenopodium [19] and in other developing plants [2,5,31]. During darkness Chl b is degraded more rapidly than Chl a and this effect did not depend on the light quality used.…”

“…During darkness Chl b is degraded more rapidly than Chl a and this effect did not depend on the light quality used. The loss of Chl may be due to an increased turnover of Chl [21], an increased instability or turnover of the light harvesting Chl-protein complex (LHCP) [5,31] or to the reorganisation of the pigment-protein complexes [2]. Reformation of prolamellar bodies (Fig.…”

Chlorophyll-protein and polypeptide composition of Mn-deficient sugar beet thylakoids

“…for two hours (after introduction of all the green material in the stacking gel). Gels were scanned at 663 nm [22] and the relative amount of Chl in each band determined from the area under the curves. Thylakoid solubization with octylglucoside was performed with a detergent/Chl ratio of 10/1 (w/w) in 2 mM Tris-maleate pH 8.0 [10].…”

Regulation of photosynthesis by reversible phosphorylation of the light-harvesting chlorophyll a/b protein

“…The fact that pre-existing LHC is degraded when immature greening pea leaves (Bennett, 1981) or immature radish cotyledons (Lichtenthaler et al, 1981) Fig. 2.…”