Changes in chloroplast ultrastructure and total content of endogenous cytokinins (CK) were studied during different phases of plant development in transgenic Pssu-ipt tobacco (Nicotiana tabacum L. cv. Petit Havana SR1). Permanent overproduction of CK was found in both rooted (SE) and grafted (G) Pssu-ipt plants in all phases of plant development with the peak in vegetative and flowering phase in the latter ones. No such a correlation was observed in SE on the contrary to control non-transgenic plants (SR1) and grafts (SRG), which showed also CK increase at juvenile and flowering phases. No significant differences in parameters of chloroplast ultrastructure, such as length of chloroplast, starch content, granum width, and number of thylakoids per granum, were proved between chloroplasts from young mature leaves of control and transgenic tobacco during plant ontogeny. Nevertheless, several anomalies in the ultrastructure of cell organelles were found in Pssu-ipt tobacco. Amoeboid shape of chloroplasts was often observed in connection with "tubular clusters" resembling peripheral reticulum. The distinct crystalline structures located in chloroplasts might be formed by LHC protein aggregates. Smaller crystals of unknown composition were found also in mitochondria. Numerous crystalline cores were present in peroxisomes. The alterations might be the result of imbalance of phytohormone content, degradation effect of CK overproduction, or the example of acclimation to permanent stress. and H. Synková, R. Pechová, R. Valcke.
Violaxanthin de-epoxidase (VDE) is localised in the thylakoid lumen of chloroplasts and catalyses de-epoxidation of violaxanthin into antheraxanthin and zeaxanthin. Tobacco vde gene was inserted into a binary vector pCAMBIA1301 with the hygromycin resistant gene for selection in antisense and overexpressed ways. Two constructs with antisense and overexpressed vde gene were introduced in tobacco (Nicotiana tabacum L.) using Agrobacterium tumefaciens strain LBA4404, PCR and Southern blot analyses demonstrated that the exogenous gene was integrated into genome of tobacco plants. VDE activity assay and HPLC analysis of pigments showed that the vde gene was expressed in the overexpressed transformants, whereas suppressed in the antisense ones. The chlorophyll fluorescence measurements proved that the contents of VDE in transgenic plants have a significant function in non-photochemical quenching. and Ying Deng ... [et al.].
Tobacco (Nicotiana tabacum L.) has been transformed to accumulate different compatible solutes (proline, fructans, or glycine betaine) in order to improve its tolerance to abiotic stress. Photosynthetic activity of wild Type (wt) and transformed tobacco plants before and after freezing stress was studied by measuring chlorophyll (Chl) fluorescence. The JIP test of Chl fluorescence induction was used to analyze in details the functional activity of photosystem 2. No significant differences were found among wild Type and transgenic plants after 12 h of freezing. Both plant Types maintained the same values of the measured parameters [FV/FM, PI(CSM), ABS/RC, TR0/RC, ET/RC] after recovery of stress. The studied Chl fluorescence parameters decreased only for the wild Type plants, stressed for 24 h at -2 °C. The strong inhibition of photosynthetic reactions in the wt plant after 24 h of freezing could not be restored. The evaluated parameters of transgenic plants did not change significantly after 24 h at -2 °C and successfully survived freezing stress. and D. Parvanova ... [et al.].
We developed transgenic rice plants (Oryza sativa L. cv. Daeribbyeo) overproducing cytosolic glutathione reductase (GR) using a GR gene from Brassica campestris and studied their response to photo-oxidative stress in the presence of methyl viologen (MV, 10 and 50 μM concentrations) under room (25 °C) and moderately elevated (35 °C) temperature by analysis of chlorophyll (Chl) a fluorescence parameters (FV/FM, qN, and qP) and of Chl content. Elevated temperature enhanced and accelerated the photo-oxidative damage to photosynthetic apparatus expressed mainly by a fast decrease of qN. Higher temperature supported the protective reaction in transformed rice plants for lower MV concentration (10 μM) and eliminated the enhanced tolerance of photosystem 2 photochemistry to photooxidative stress for higher (50 μM) MV concentration. Different mechanisms and temperature dependence of oxidative and protective reactions explain the results. and R. Kouřil ... [et al.].
High level of phosphoenolpyruvate carboxylase (PEPC) gene was stably inherited and transferred from the male parent, PEPC transgenic rice, into a female parent, japonica rice cv. 9516. Relative to the female parent, the produced JAAS45 pollen lines exhibited high PEPC activity (17-fold increase) and also higher photosynthetic rates (about 36 %-fold increase). The JAAS45 pollen lines were more tolerant to photoinhibition and to photo-oxidative stress. Furthermore, JAAS45 pollen lines, as well as their male parent, were tested to exhibit a limiting C4 cycle by feeding with exogenous C4 primary products such as oxaloacetate (OAA). Thus the PEPC gene and photosynthetic characteristics of PEPC transgenic rice could be stably transferred to the hybrid progenies, which might open a new breeding approach to the integration of conventional hybridization and biological technology. and L. Ling, B. J. Zhang, D. M. Jiao.
Thermoluminescence (TL) in green plants arises from charge recombination of charged molecules in the reaction centre (RC) of photosystem 2 (PS2) in chloroplasts. The TL technique is used for detection of alterations in the architecture of PS2 RCs. The donor side 'S-states' and the acceptor side quinone molecules (QA and QB) are involved the charge recombination processes of PS2. High temperature (70-75 °C) glow peaks are also used to detect non-photosynthetic peroxidation processes in thylakoid membranes. The TL peaks with their characteristic charge recombination can be utilised for the study of chloroplast development, ageing, chemical, biotic, and abiotic stress induced alterations in the PS2 RC and for the study of the primary photochemical events of photosynthesis. The technique has been used successfully in the characterisation of transgenic plants in the study of genetically engineered organisms. and A. N. Misra ... [et al.].
Characterization of different component processes of photosynthesis is useful to understand the growth status of plants and to discover possible unintended effects of genetic modification on photosynthesis in transgenic plants. We focused on the changes in photosynthetic gas-exchange properties, reflectance spectra, and plant growth traits among groups of different transgenic barley T1 (TolT1) and its isogenic controls (TolNT1), TolT1, and group of its own transgenic progenies T2 (TolT2), TolNT1 and its wild type (WT), respectively. Gas-exchange measurements showed that only the net photosynthetic rate (P N) and the light-use efficiency (LUE) differed significantly between TolT1 and TolT2 with no obvious changes of other characteristics. Reflectance measurements indicated that the reflectance ratio was sensitive to identify the differences between two barley groups. Differences in reflectance expressed on an index basis depended on barley groups. The relationship between LUE and the photochemical reflectance index (PRI) at a leaf level among different barley groups of WT, TolNT1, TolT1 and TolT2 did not changed obviously. The differences in the total leaf area per plant (LA) between WT and TolNT1 as well as between TolT1 and TolT2 were significant. This study finally provided a plausible complex explanation for the unintended effects of genetic transformation on photosynthesis-related properties in barley at different levels. Furthermore, it was concluded that the photosynthesis-related properties of transgenic plants based on gas exchange, leaf reflectance, and plant growth measurements responded to the same environment in a more different way between two subsequent generations than to the processes of the gene insertion by Agrobacterium and associated tissue culture., C. X. Sun ... [et al. ]., and Obsahuje bibliografii