Inhibition Of Apparent Photosynthesis Research Articles

Immunocytochemical localization of phosphoenolpyruvate carboxylase and photosynthetic gas-exchange characteristics in ears of Triticum durum Desf.

The presence and distribution of phosphoenolpyruvate carboxylase (PEPCase) in the glumes and immature grains of durum wheat (Triticum durum Desf.) were studied by electron-microscopical immunolabeling of PEPCase with polyclonal antibodies followed by protein A-gold. Plants were grown under mediterranean field conditions and samples were obtained two weeks after anthesis. In the kernels, high gold label was associated with the unstained areas of the protein bodies of aleurone cells, whereas labeling in the cytoplasm and chloroplasts of the pericarp was slight, although significantly above the background. In the glumes, high gold label was only located in cytoplasmic granules (vesicles) of the mesophyll cells, although labeling in the cytoplasm and chloroplasts was also significantly above the background. These observations in immature kernels and glumes are in accordance with the anaplerotic role of this enzyme, as evidenced in C3 plants. Measurements of apparent photosynthesis and its O2 dependence and CO2 compensation concentration were made on ears and flag leaves of durum wheat. In addition, an analog of phosphoenolpyruvate, 3,3-dichloro-2-dihydroxy-phosphinoylmethyl-2-propenoate, was used to inhibit PEPCase and, thereby, to assess the contribution of the PEPCase to photosynthesis in detached ears. There was no effect of the inhibitor on the apparent photosynthesis of ears. Whereas inhibition of apparent photosynthesis by 210 mL · L−1 O2 in flag leaves was typical of C3 species, inhibition in ears was even greater. The CO2 compensation concentrations in different ear parts were similar to or higher than in flag leaves and the O2 dependence was also comparable (about 70%). Therefore, gas-exchange data give further support to the assumption that a C4 cycle is absent or limited to very low rates in ears of durum wheat.

Assessing the Degree of C4 Photosynthesis in C3-C4 Species Using an Inhibitor of Phosphoenolpyruvate Carboxylase

An analog of phosphoenolpyruvate, 3,3-dichloro-2-dihydroxyphosphinoylmethyl-2-propenoate (DCDP), was used to inhibit phosphoenolpyruvate carboxylase and, therefore, assess the contribution of the C(4) pathway to photosynthesis in detached leaves of several C(3)-C(4) intermediate species. There was no effect of 4 millimolar DCDP on apparent photosynthesis or on inhibition of apparent photosynthesis by 210 milliliters per liter of O(2) for the C(3)-C(4) species Panicum milioides, Moricandia arvensis, and Neurachne minor or the C(3) species Flaveria pringlei. However, when leaves of Flaveria linearis (C(3)-C(4)), Flaveria brownii (C(4)-like), and Flaveria trinervia (C(4)) were fed 4 millimolar DCDP, photosynthesis was reduced 32, 60, and 90%, respectively. Photosynthetic inhibition by 210 milliliter per liter of O(2) was also significantly increased in 4 millimolar DCDP-fed leaves of F. linearis and F. brownii but not in F. trinervia when compared with control values. These results with DCDP clearly demarcate C(3)-C(4) species into species including Panicum, Moricandia, and Neurachne whose reduced photorespiration occurs without any C(4) photosynthetic involvement and species of Flaveria in which C(4) photosynthesis contributes to CO(2) assimilation.

Transfer of C4 Photosynthetic Characters through Hybridization of Flaveria Species

Transfer of C(4) photosynthetic traits was studied through hybridization of Flaveria trinervia (Spreng.) Mohr (C(4)) and Flaveria brownii A.M. Powell (C(4)-like) with Flaveria linearis Lag. (C(3)-C(4)) and the C(3) species Flaveria pringlei Gandoger (C(3)). Fertility was low, based on irregular chromosome pairing and low pollen stainability, except in F. brownii x F. linearis which had bivalent pairing and 76% stainable pollen. Hybrids had apparent photosynthesis values of 71 to 148% of the midparental means, while the CO(2) compensation concentration was similar to the C(4) or C(4)-like parent, except in hybrids having the C(3) species F. pringlei as a parent. Inhibition of apparent photosynthesis by O(2), and phosphoenolpyruvate carboxylase and NADP-malic enzyme activities and subunit levels in the hybrids were closer to the C(3) or C(3)-C(4) parent. The species F. brownii and F. trinervia were equal in their capacity to transfer reduced O(2) inhibition of AP and CO(2) compensation concentration values to hybrids with F. linearis (C(3)-C(4)), although hybrids with F. trinervia had higher PEPC activity. The O(2) inhibition of AP was correlated with the logarithm of activities of phosphoenolpyruvate carboxylase (r = -0.95) and NADP-malic enzyme (r = -0.87). These results confirm that C(4) traits can be transferred by hybridization of C(3)-C(4) and C(4) or C(4)-like species, with a higher degree of C(4) photosynthesis than exists in C(3)-C(4) species, and at least in F. brownii x F. linearis, fertile progeny are obtained.

Photosynthetic Plasticity in Flaveria brownii

Photosynthesis was examined in leaves of Flaveria brownii A. M. Powell, grown under either 14% or 100% full sunlight. In leaves of high light grown plants, the CO(2) compensation point and the inhibition of photosynthesis by 21% O(2) were significantly lower, while activities of ribulose 1,5-bisphosphate carboxylase/oxygenase and various C(4) cycle enzymes were considerably higher than those in leaves grown in low light. Both the CO(2) compensation point and the degree of O(2) inhibition of apparent photosynthesis were relatively insensitive to the light intensity used during measurements with plants from either growth conditions. Partitioning of atmospheric CO(2) between Rubisco of the C(3) pathway and phosphoenolpyruvate carboxylase of the C(4) cycle was determined by exposing leaves to (14)CO(2) for 3 to 16 seconds, and extrapolating the labeling curves of initial products to zero time. Results indicated that approximately 94% of the CO(2) was fixed by the C(4) cycle in high light grown plants, versus approximately 78% in low light grown plants. Thus, growth of F. brownii in high light increased the expressed level of C(4) photosynthesis. Consistent with the carbon partitioning patterns, photosynthetic enzyme activities (on a chlorophyll basis) in protoplasts from leaves of high light grown plants showed a more C(4)-like pattern of compartmentation. Pyruvate, Pi dikinase and phosphoenolpyruvate carboxylase were more enriched in the mesophyll cells, while NADP-malic enzyme and ribulose 1,5-bisphosphate carboxylase/oxygenase were relatively more abundant in the bundle sheath cells of high light than of low light grown plants. Thus, these results indicate that F. brownii has plasticity in its utilization of different pathways of carbon assimilation, depending on the light conditions during growth.

CO2 Exchange, Cytogenetics, and Leaf Anatomy of Hybrids between Photosynthetically Distinct Flaveria Species

Hybrids between the C(4)-like species, Flaveria brownii, A. M. Powell and the C(3)-C(4) intermediate species Flaveria linearis Lag., Flaveria floridana Johnston, and Flaveria oppositifolia (DC.) Rydb. exhibited bivalent chromosome pairing during meiosis and stainability of pollen was high, ranging from 51 to 95%. An F(2) population produced from an F. brownii x F. linearis F(1) hybrid, exhibited bivalent chromosome pairing and high pollen stainability indicating a high degree of fertility in the hybrid. Oxygen inhibition of apparent photosynthesis averaged 6.8% for F. brownii and 22.2% for the C(3)-C(4) species (in two experiments), and F(1) hybrids exhibited inhibitions which were intermediate to their parents. Values of carbon dioxide compensation concentration determined at low irradiance were 4.0, 34.0, and 6.5 microliters per liter for F. brownii, F. linearis and their F(1) hybrid, respectively. The mean value at low irradiance for 33 F(1) plants was 6.8 microliters per liter, and individual values ranged only from 3.7 to 11.7 microliters per liter. Anatomical characteristics for the F(1) hybrid leaves were intermediate to those of the parents, and there was considerable variation among F(2) plants derived from F. brownii x F. linearis. In the F(2) population delta(13)C values ranged from -27 per thousand to -20 per thousand. The expression of more C(4)-like characteristics by the F(1) hybrids in this study and their apparent high fertility make them promising specimens for producing segregating populations for use in C(4) inheritance studies.

Photosynthesis of F1 Hybrids between C4 and C3-C4 Species of Flaveria

Photosynthetic characteristics were studied in several F(1) hybrids between C(4) and C(3)-C(4) species of Flaveria. Stable carbon isotope ratios, O(2) inhibition of apparent photosynthesis, and phosphoenolpyruvate carboxylase activities in the hybrids were similar to the means for the parents. Values of CO(2) compensation concentrations were nearer to those of the C(4) parent and apparent photosynthesis was below that of both parents, being only 60 and 74% of that of the lowest (C(3)-C(4)) parent in two experiments. Reductions of CO(2) compensation concentration and O(2) inhibition of apparent photosynthesis as well as increases in carbon isotope ratios and phosphoenolpyruvate carboxylase activities compared to values in C(3)-C(4) species suggest transfer of a limited degree of C(4) photosynthesis to the F(1) hybrids. However, the lower apparent photosynthesis of the hybrids suggests that transfer of C(4) characteristics to non-C(4) species is detrimental unless characteristics associated with C(4) photosynthesis are fully developed. There was a highly significant negative correlation (r = -0.90) between CO(2) compensation concentration and the logarithm of phosphoenolpyruvate carboxylase activity in the parents and hybrids, suggesting involvement of this enzyme in controlling the CO(2) compensation concentration. Although bundle-sheath cells were more developed in leaves of hybrids than in C(3)-C(4) parents, they appeared to contain lower quantities of organelles than those of the C(4) parent. Reduced quantities of organelles in bundle-sheath cells could indicate incomplete compartmentation of partial pathways of the C(4) cycle in the hybrids. This may mean that the reduction of CO(2) compensation and O(2) inhibition of apparent photosynthesis relative to the C(3)-C(4) parents is less dependent on fully developed Kranz anatomy than is increased apparent photosynthesis.

Effect of aminoacetonitrile on the CO2 exchange rate in rice leaves.

Aminoacetonitrile (AAN), a specific inhibitor of glycine oxidation in the photorespiratory glycolate pathway, did not inhibit photosynthetic CO2 fixation, but inhibited the apparent photosynthesis of rice leaves under high photosynthetic conditions. However, under such low photosynthetic conditions as low light intensity or senescent leaves, the apparent photosynthesis was not inhibited by AAN. The application of AAN to the leaves led to a greater accumulation of glycine under a high photosynthetic condition like strong light intensity.From these results, it can be postulated that the inhibition of apparent photosynthesis by AAN was due to the accumulation of intermediate metabolites in the photorespiratory glycolate pathway which was induced by AAN treatment.

Photosynthesis of Grass Species Differing in Carbon Dioxide Fixation Pathways

Reduced photorespiration has been reported in Panicum milioides on the basis of lower CO(2) compensation concentrations than in C(3) species, lower CO(2) evolution in the light, and less response of apparent photosynthesis to O(2) concentration. The lower response to O(2) in P. milioides could be due to reduced O(2) competition with CO(2) for reaction with ribulose 1,5-bisphosphate, to a reduced loss of CO(2), or to an initial fixation of CO(2) by phosphoenolpyruvate carboxylase. Experiments were carried out with Panicum maximum Jacq., a C(4) species having no apparent photorespiration; tall fescue (Festuca arundinacea Schreb.), a C(3) species; P. milioides Nees ex Trin.; and Panicum schenckii Hack. The latter two species are closely related and have low photorespiration rates. CO(2) exchange was measured at five CO(2) concentrations ranging from 0 to 260 microliters per liter at both 2 and 21% O(2). Mesophyll conductance or carboxylation efficiency was estimated by plotting substomatal CO(2) concentrations against apparent photosynthesis. In the C(4) species P. maximum, mesophyll conductance was 0.96 centimeters per second and was unaffected by O(2) concentration. At 21% O(2) mesophyll conductance of tall fescue was decreased 32% below the value at 2% O(2). Decreases in mesophyll conductance at 21% O(2) for P. milioides and P. schenckii were similar to that for tall fescue. On the other hand, loss of CO(2) in CO(2)-free air, estimated by extrapolating the CO(2) response curve to zero CO(2), was increased from 1.8 to 6.5 milligrams per square decimeter per hour in tall fescue as O(2) was raised from 2-21%. Loss of CO(2) was less than 1 milligram per square decimeter per hour for P. milioides and P. schenckii and was unaffected by O(2). The results suggest that the reduced O(2) response in P. milioides and P. schenckii is due to a lower loss of CO(2) in the light rather than less inhibition of carboxylation by O(2), since the decrease in carboxylation efficiency at 21% O(2) was similar for P. milioides, P. schenckii, and tall fescue. The inhibition of apparent photosynthesis by 21% O(2) in these three species at low light intensities was similar at 31 to 36% which also indicates similar O(2) effects on carboxylation. Apparent photosynthesis at high light intensity was inhibited less by 21% O(2) in P. milioides (16.8%) and P. schenckii (23.8%) than in tall fescue (28.4%). This lower inhibition in the Panicum species may have been due to a higher degree of recycling of photorespired CO(2) in these species than in tall fescue.

Inhibition of Apparent Photosynthesis by Air Pollutants

AbstractThe reversible effects of hydrogen fluoride, sulfur dioxide, and chlorine exposures on net carbon dioxide absorption rates (apparent photosynthesis) of alfalfa (Medicago sativa L.) and barley (Hordeum vulgare L.) plants were studied. Pollutant exposures required (i) to reversibly depress CO2 uptake rates and (ii) to cause cellular necrosis in the leaves were appraised. Plant responses to these air pollutants were compared with responses observed from previous equivalent studies with ozone, nitric oxide, and nitrogen dioxide. The experimental data show that CO2 uptake could be reversibly suppressed by exposure dosages of these pollutants which did not cause cellular destruction in the leaves. However, except for the nitrogen oxides, some necrosis resulted from treatments which depressed CO2 uptake rates more than 25–60% (depending upon the pollutant) by the end of 2‐hour fumigation trials.The six air pollutants can be ranked in the following order according to the relative amounts that plant CO2 uptake rates were depressed by the end of 2 hours of pollutant exposure: HF > 03 ≥ Cl2 > SO2 > NO2 > NO. Carbon monoxide was also tested but did not measurably reduce plant CO2 uptake when applied in concentrations ranging up to 80 ppm. The phytotoxicants ranked in essentially the reverse order when compared on the basis of the rapidity that CO2 uptake was suppressed as a function of exposure time. Nitric oxide treatments caused very rapid reductions in the plant CO2 uptake rates during the first hour of exposure. By this time, plant uptake rates had attained new (depressed) steady‐state equilibrium levels which were then maintained over the remainder of the expo,sure periods. Hydrogen fluoride treatment induced much more gradual reductions in plant CO2 uptake rates throughout the test periods. Plant responses to the other pollutants, SO2, NO2, Cl2, and O3, were intermediate between those caused by NO and HF.The experimental plants were fumigated after steady‐state CO2 exchange rates were established and the percent reduction in the CO2 uptake (along with the rates of recovery) were determined. The investigations were conducted in two identical internalrecirculating environmental chambers (control and treatment chambers) designed to precisely control and continuously monitor light, temperature, wind parameters, relative humidity, and gas exchange rates.

Inhibition of apparent photosynthesis by nitrogen oxides

Inhibition of apparent photosynthesis by nitrogen oxides

Inhibition of apparent photosynthesis by nitrogen oxides

The nitrogen oxides (NO 2 and NO) inhibited apparent photosynthesis of oats and alfalfa at concentrations below those required to cause visible injury. There appeared to be a threshold concentration of about 0.6 ppm for each pollutant. An additive effect in depressing apparent photosynthesis occurred when the plants were exposed to a mixture of NO and NO 2. Although NO produced a more rapid effect on the plants, lower concentrations of NO 2 were required to cause a given inhibition after 2 hr of exposure. Inhibition by nitric oxide was more closely related to its partial pressure than was inhibition by NO 2.

Effect of Temperature, CO2 Concentration, and Light Intensity on Oxygen Inhibition of Photosynthesis in Wheat Leaves

The effect of 21% O(2) and 3% O(2) on the CO(2) exchange of detached wheat leaves was measured in a closed system with an infrared carbon dioxide analyzer. Temperature was varied between 2 degrees and 43 degrees , CO(2) concentration between 0.000% and 0.050% and light intensity between 40 ft-c and 1000 ft-c. In most conditions, the apparent rate of photosynthesis was inhibited in 21% O(2) compared to 3% O(2). The degree of inhibition increased with increasing temperature and decreasing CO(2) concentration. Light intensity did not alter the effect of O(2) except at light intensities or CO(2) concentrations near the compensation point. At high CO(2) concentrations and low temperature, O(2) inhibition of apparent photosynthesis was absent. At 3% O(2), wheat resembled tropical grasses in possessing a high rate of photosynthesis, a temperature optimum for photosynthesis above 30 degrees , and a CO(2) compensation point of less than 0.0005% CO(2). The effect of O(2) on apparent photosynthesis could be ascribed to a combination of stimulation of CO(2) production during photosynthesis, and inhibition of photosynthesis itself.