[HTML][HTML] Modulation of photosynthetic electron transport in the absence of terminal electron acceptors: characterization of the rbcL deletion mutant of tobacco

Y Allahverdiyeva, F Mamedov, P Mäenpää… - … et Biophysica Acta (BBA …, 2005 - Elsevier
Biochimica et Biophysica Acta (BBA)-Bioenergetics, 2005Elsevier
Tobacco rbcL deletion mutant, which lacks the key enzyme Rubisco for photosynthetic
carbon assimilation, was characterized with respect to thylakoid functional properties and
protein composition. The ΔrbcL plants showed an enhanced capacity for dissipation of light
energy by non-photochemical quenching which was accompanied by low photochemical
quenching and low overall photosynthetic electron transport rate. Flash-induced
fluorescence relaxation and thermoluminescence measurements revealed a slow electron …
Tobacco rbcL deletion mutant, which lacks the key enzyme Rubisco for photosynthetic carbon assimilation, was characterized with respect to thylakoid functional properties and protein composition. The ΔrbcL plants showed an enhanced capacity for dissipation of light energy by non-photochemical quenching which was accompanied by low photochemical quenching and low overall photosynthetic electron transport rate. Flash-induced fluorescence relaxation and thermoluminescence measurements revealed a slow electron transfer and decreased redox gap between QA and QB, whereas the donor side function of the Photosystem II (PSII) complex was not affected. The 77 K fluorescence emission spectrum of ΔrbcL plant thylakoids implied a presence of free light harvesting complexes. Mutant plants also had a low amount of photooxidisible P700 and an increased ratio of PSII to Photosystem I (PSI). On the other hand, an elevated level of plastid terminal oxidase and the lack of F0 ‘dark rise’ in fluorescence measurements suggest an enhanced plastid terminal oxidase-mediated electron flow to O2 in ΔrbcL thylakoids. Modified electron transfer routes together with flexible dissipation of excitation energy through PSII probably have a crucial role in protection of PSI from irreversible protein damage in the ΔrbcL mutant under growth conditions. This protective capacity was rapidly exceeded in ΔrbcL mutant when the light level was elevated resulting in severe degradation of PSI complexes.
Elsevier
以上显示的是最相近的搜索结果。 查看全部搜索结果