We provide here a general introduction on chlorophyll (Chl) a fluorescence, then we present our measurements on fast (< 1 s) induction curves (the so-called OJIP transients) on dark-adapted intact leaves of Arabidopsis thaliana, under five different light intensities [in the range of ~ 500 to ~ 3,000 µmol(photons) m‒2 s‒1] using two different instruments: Handy PEA (Hansatech Instruments, UK; excitation light, 650 nm) and FluorPen (model FP-110; Photon Systems Instruments, The Czech Republic; excitation light, 470 nm). We then discuss the observed differences in the OJIP curves, as well as in Fo (F20μs, F50μs, or the extrapolated Ft→0), FP (the peak), and the ratios FP/Fo, and Fv (= FP ‒ Fo)/FP in terms of differences in excitation light intensity and absorptance (or absorbance) of the excitation light by the leaves, and other factors, as well as the data available in the literature. We suggest that such measurements be accompanied, in the future, by parallel measurements on Chl a fluorescence imaging, an area pioneered by Hartmut K. Lichtenthaler., B. Padhi, G. Chauhan, D. Kandoi, A. Stirbet, B. C. Tripathy, G. Govindjee., and Obsahuje bibliografické odkazy
RNA editing is post-transcriptional modification to RNA molecules. In plants, RNA editing primarily occurs to two energy-producing organelles: plastids and mitochondria. Organelle RNA editing is often viewed as a mechanism of correction to compensate for defects or mutations in haploid organelle genomes. A common type of organelle RNA editing is deamination from cytidine to uridine. Cytidine-to-uridine plastid RNA editing is carried out by the RNA editing complex which consists of at least four types of proteins: pentatricopeptide repeat proteins, RNA editing interacting proteins/multiple organellar RNA editing factors, organelle RNA recognition motif proteins, and organelle zinc-finger proteins. The four types of RNA editing factors work together to carry out RNA editing site recognition, zinc cofactor binding, and cytidine-to-uridine deamination. In addition, three other types of proteins have been found to be important for plastid RNA editing. These additional proteins may play a regulatory or stabilizing role in the RNA editing complex., Y. Lu., and Obsahuje bibliografické odkazy
Ascorbate is an important antioxidant involved in both enzymatic and nonenzymatic reactions in plant cells. To reveal the function of ascorbate associated with defense against photo-oxidative damage, responses of the ascorbate-deficient mutant vtc2-1 of Arabidopsis thaliana to high-light stress were investigated. After high-light treatment at 1,600 μmol(photon) m-2 s-1 for 8 h, the vtc2-1 mutant exhibited visible photo-oxidative damage. The total ascorbate content was lower, whereas accumulation of H2O2 was higher in the vtc2-1 mutant than that in the wild type. The chlorophyll (Chl) content and PSII Chl fluorescence parameters, such as maximal quantum yield of PSII photochemistry, yield, and electron transport rate, in vtc2-1 mutant decreased more than that in the wild type, whereas the nonphotochemical quenching coefficient increased more in the wild type than that in vtc2-1 mutant. Therefore, the vtc2-1 mutant was more sensitive to high-light stress than the wild type. Accumulation of reactive oxygen species was mainly responsible for the damage of PSII in the vtc2-1 mutant under high light. The results indicate that ascorbate plays a critical role in maintaining normal photosynthetic function in plants under high-light stress., L.-D. Zeng, M. Li, W. S. Chow, C.-L. Peng., and Obsahuje bibliografické odkazy