Two yellow rice mutants VG28-1 and VG30-5 were obtained during the tissue culture process from a rice plant (cv. Zhonghua No.11 japonica) with inserted maize Ds transposon element. Absorption spectra and pigment composition showed that two mutants had no chlorophyll (Chl) b and lower Chl a content in comparison to the wild type (WT). Net photosynthetic rate (PN), total electron transport rate (JF), photochemical quenching (qp), quantum yield of PS2 dependent non-cyclic electron transport (ΦPS2), fraction of Prate, and leaf area were lower but Fv/Fm and apparent quantum yield (AQY) remained at similar levels as in the WT plant. Xanthophyll cycle pool size (V+A+Z) on a Chl basis, and de-epoxidation state were enhanced in the mutants. The mutants had larger amounts of soluble protein and ribulose-1,5-bisphosphate carboxylase/oxygenase (RuBPCO), especially the small subunit of RuBPCO, than WT. The characteristics of two rice mutants differed somewhat from the other common Chl b-less mutants originating from mutagenic agent treatments. and Zhi-Fang Li ... [et al.].
Two stress imposing systems were used: a rapid stress developed by allowing excised leaves to loose water by transpiration, and a slow stress developed by withholding watering of potted plants. Carboxylating enzymes reacted differently on both types of stress. Rapid stress increased ribulose-1,5-bisphosphate carboxylase/oxygenase (RuBPCO) activation, but both activities (initial and total) showed little variation with stress. Under slow stress the activation did not change, although both activities decreased much under stress. Phosphoenolpyruvate carboxylase (PEPC) showed a deep decrease of activity under rapid stress, nevertheless, a certain recovery was found under extreme stress. On the other hand, under slow stress the activity of PEPC showed a linear increase with decreasing relative water content. The ratio between physiological and maximal activity increased slightly under both types of stress. The activity of malic enzyme did not change under rapid stress, and decreased linearly under slow stress. and J. Marques da Silva, M. C. Arrabaça.
Plant growth, chlorophyll (Chl) content, photosynthetic gas exchange, ribulose-1,5-bisphosphate carboxylase (RuBPCO) enzyme activity, and Chl fluorescence in radish (Raphanus sativus var. longipinnatus) plants were examined after turnip mosaic virus (TuMV) infection. Plant fresh mass, dry mass, Chl content, net photosynthetic rate (PN), transpiration rate (E), stomatal conductance (gs), and RuBPCO activity were significantly lower in infected plants after 5 weeks of virus infection as compared to healthy plants. The 5-week virus infection did not induce significant differences in intercellular CO2 concentration (Ci, photochemical efficiency of photosystem 2, PS2 (Fv/Fm), excitation capture efficiency of open PS2 reaction centres (Fv'/Fm'), effective quantum efficiency of photosystem 2 (ΔF/Fm'), and photochemical quenching (qP), but non-photochemical quenching (qN) and alternative electron sink (AES) were significantly enhanced. Thus the decreased plant biomass of TuMV-infected plants might be associated with the decreased photosynthetic activity mainly due to reduced RuBPCO activity. and Y.-P. Guo ... [et al.].
At the whole plant level, the effect of stress is usually perceived as a decrease in photosynthesis and growth. That is why this review is focused mainly on the effect of drought on photosynthesis, its injury, and mechanisms of adaptation. The analysed literature shows that plants have evolved a number of adaptive mechanisms that allow the photochemical and biochemical systems to cope with negative changes in environment, including increased water deficit. In addition, the acquisition of tolerance to drought includes both phenotypic and genotypic changes. The approaches were made to identify those metabolic steps that are most sensitive to drought. Some studies also examined the mechanisms controlling gene expression and putative regulatory pathways. and I. Yordanov, V. Velikova, T. Tsonev.
Net photosynthetic rate (PN) measured at elevated CO2 concentration (Ce), ribulose-1,5-bisphosphate carboxylase/oxygenase (Rubisco), and nitrogen (N) content in rice leaves decreased significantly after exposure to long term Ce. The reduction in PN, Rubisco, and leaf N at Ce was similar for the last fully expanded leaf blade (LFELB) and expanding leaf blade (ELB). Spatial leaf N content in the ELB was highest in the zone of cell division, sharply declined as cell expansion progressed and gradually increased with cell maturation. Maximum reduction in spatial leaf N and Rubisco content was found at Ce only within cell expansion and maturation zones. The spatial leaf N content correlated well with the amount of Rubisco synthesized during leaf expansion, suggesting that N deposition into the expanding leaf blade may be the key for Rubisco synthesis and possibly photosynthetic acclimation to Ce. and S. Seneweera.
10-5 M methyl jasmonate (JA-Me) treatment itself did not considerably change the 14CO2 fixation, parameters of room temperature chlorophyll fluorescence induction, proline content, and Na+ as well as Cl- accumulation. Salt stress (30 mM NaCl) lead to a decrease of both 14CO2 fixation and relative water content, and to an increase of proline content. Immediate nonvariable fluorescence (F0) also increased and the variable to maximal fluorescence ratio (Fv/Fm) decreased. Pretreatment with JA-Me for 3 d before salt treatment diminished the inhibitory effect of NaCl on the rate of 14CO2 fixation, protein content, and activity and content of ribulose-1,5-bisophosphate carboxylase/oxygenase. The Na+ and Cl- contents in leaves decreased in JA-Me pretreated plants. The JA-Me pretreatment prevented the increase of F0 level and restored the values of Fv/Fm. and M. Velitchkova, I. Fedina.
Five-year-old plants of two olive cultivars (Frantoio and Moraiolo) grown in large pots were exposed for 7 to 8 months to ambient (AC) or elevated (EC) CO2 concentration in a free-air CO2 enrichment (FACE) facility. Exposure to EC enhanced net photosynthetic rate (PN) and decreased stomatal conductance, leading to greater instantaneous transpiration efficiency. Stomata density also decreased under EC, while the ratio of intercellular (Ci) to atmospheric CO2 concentration and chlorophyll content did not differ, except for the cv. Moraiolo after seven months of exposure to EC. Analysis of the relationship between photosynthesis and Ci indicated no significant change in carboxylation efficiency of ribulose-1,5-bisphosphate carboxylase/oxygenase after five months of exposure to EC. Based on estimates derived from the PN-Ci relationship, there were no apparent treatment differences in daytime respiration, CO2 compensation concentration, CO2-saturated photosynthetic rate, or photosynthetic rate at the mean Ci, but there was a reduction in stomata limitation to PN at EC. Thus 5-year-old olive trees did not exhibit down regulation of leaf-level photosynthesis in their response to EC, though some indication of adjustment was evident for the cv. Frantoio with respect to the cv. Moraiolo. and R. Tognetti ... [et al.].
Twelve-year-old Norway spruce (Picea abies [L.] Karst.) trees were exposed to ambient (AC) or elevated (EC) [ambient + 350 µmol(CO2) mol-1] CO2 concentrations in open-top-chamber (OTC) experiment under the field conditions of a mountain stand. Short-term (4 weeks, beginning of the vegetation season) and long-term (4 growing seasons, end of the vegetation season) effects of this treatment on biochemical parameters of CO2 assimilation were evaluated. A combination of gas exchange, fluorescence of chlorophyll a, and application of a mathematical model of ribulose-1,5-bisphosphate carboxylase/oxygenase (RuBPCO) activity was used. The analysis showed that the depression of photosynthetic activity by long-term impact of elevated CO2 was mainly caused by decreased RuBPCO carboxylation rate. The electron transport rate as well as the rate of ribulose-1,5-bisphosphate (RuBP) formation were also modified. These modifications to photosynthetic assimilation depended on time during the growing season. Changes in the spring were caused mainly by local deficiency of nitrogen in the assimilating tissue. However, the strong depression of assimilation observed in the autumn months was the result of insufficient carbon sink capacity. and O. Urban, M. V. Marek.
In spring and winter cultivars of oilseed rape (Brassica napus var. oleifera), acclimation of photosynthetic apparatus to cold was connected with the increase in activities of ribulose-1,5-bisphosphate carboxylase/oxygenase (RuBPCO) and sucrose-phosphate synthase (SPS). Conversely, cold de-acclimation entailed the decline of RuBPCO and SPS activities. The rate of this photosynthetic de-acclimation might depend on day temperature. On the other hand, temperature rise during de-acclimation (identical during the day and night) resulted in the improvement of photosynthetic activity measured by means of chlorophyll fluorescence. An increase in SPS activity (and even transitory increase in RuBPCO activity) was observed when the elongation growth rate (EGR) accelerated during de-acclimation. Throughout re-acclimation, plants with high EGR were unable to maintain or recover higher photosynthetic capacity, despite the fact that SPS activity remained high or even increased during re-acclimation. and M. Rapacz, K. Hura.
Midday measurements of single leaf gas exchange rates of upper canopy leaves of soybeans grown in the field at 350 (AC) and 700 (EC) µmol(CO2) mol-1 in open topped chambers sometimes indicated up to 50 % higher net photosynthetic rates (PN) measured at EC in plants grown at AC compared to EC. On other days mean PN were nearly identical in the two growth [CO2] treatments. There was no seasonal pattern to the variable photosynthetic responses of soybean to growth [CO2]. Even on days with significantly lower PN in the plants grown at EC, there was no reduction in ribulose-1,5-bisphosphate carboxylase/oxygenase, chlorophyll, or soluble protein contents per unit of leaf area. Over three years, gas exchange evidence of acclimation occurred on days when either soil was dry or the water vapor pressure deficit was high (n = 12 d) and did not occur on days after rain or on days with low water vapor pressure deficit (n = 9 d). On days when photosynthetic acclimation was evident, midday leaf water potentials were consistently 0.2 to 0.3 MPa lower for the plants grown at EC than at AC. This suggested that greater susceptibility to water stress in plants grown at EC cause the apparent photosynthetic acclimation. In other experiments, plants were grown in well-watered pots in field chambers and removed to the laboratory early in the morning for gas exchange measurements. In these experiments, the amount of photosynthetic acclimation evident in the gas exchange measurements increased with the maximum water vapor pressure deficit on the day prior to the measurements, indicating a lag in the recovery of photosynthesis from water stress. The apparent increase in susceptibility to water stress in soybean plants grown at EC is opposite to that observed in some other species, where photosynthetic acclimation was evident under wet but not dry conditions, and may be related to the observation that hydraulic conductance is reduced in soybeans when grown at EC. The day-to-day variation in photosynthetic acclimation observed here may account for some of the conflicting results in the literature concerning the existence of acclimation to EC in field-grown plants. and J. A. Bunce, R. C. Sicher.