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  • Chlorophyll fluorescence  (2)
  • NADP-malate dehydrogenase  (2)
  • Oxygen  (2)
  • 1
    ISSN: 1432-2048
    Keywords: Key words: C4 plant ; Chlorophyll fluorescence ; Mehler reaction ; Oxygen ; Photorespiration ; Photosynthesis (C4)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract. The photosynthetic linear electron transport rate in excess of that used for CO2 reduction was evaluated in Sorghum bicolor Moench. [NADP-malic enzyme (ME)-type C4 plant], Amaranthus cruentus L. (NAD-ME-type C4 plant) and Helianthus annuus L. (C3 plant) leaves at different CO2 and O2 concentrations. The electron transport rate (J F) was calculated from fluorescence using the light partitioning factor (relative PSII cross-section) determined under conditions where excess electron transport was assumed to be negligible: low light intensities, 500 μmol CO2 · mol−1 and 2% O2. Under high light intensities there was a large excess of J F/4 at 10–100% O2 in the C3 plant due to photorespiration, but very little in sorghum and somewhat more in amaranth, showing that photorespiration is suppressed, more in the NADP-ME- and less in the NAD-ME-type species. It is concluded that when C4 photosynthesis is limited by supply of atmospheric CO2 to the C4 cycle, the C3 cycle becomes limited by regeneration of ribulose 1,5-bisphosphate (RuBP) which in turn limits RuBP oxygenase activity and photorespiration. The rate of excess electron transport over that consumed for CO2 fixation in C4 plants was very sensitive to the presence of O2 in the gas phase, rapidly increasing between 0.01 and 0.1% O2, and at 2% O2 it was about two-thirds of that at 21% O2. This shows the importance of the Mehler O2 reduction as an electron sink, compared with photorespiration in C4 plants. However, the rate of the Mehler reaction is still too low to fully account for the extra ATP which is needed in C4 photosynthesis.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-2048
    Keywords: Chlorophyll fluorescence ; Flaveria ; Oxygen ; Photosynthesis ; Photorespiration
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Two major indicators were used to access the degree of photorespiration in various photosynthetic types of Flaveria species (C3, C3-C4, C4-like, and C4): the O2 inhibition of photosynthesis measured above the O2 partial pressure which gives a maximum rate, and O2- and light-dependent whole-chain electron flow measured at the CO2 compensation point (Γ). The optimum level of O2 for maximum photosynthetic rates under atmospheric levels of CO2 (34 Pa) was lower in C3 and C3-C4 species (ca. 2 kPa) than in C4-like and C4 species (ca. 9 kPa). Increasing O2 partial pressures from the optimum for photosynthesis up to normal atmospheric levels (ca. 20 kPa) caused an inhibition of photosynthesis which was more severe under lower CO2. This inhibition was calculated as the O2 inhibition index (ΘA, the percentage inhibition of photosynthesis per kPa increase in O2). From measurements of 18 Flaveria species at atmospheric CO2, the ΘA values decreased from C3 (1.9–2.1) to C3-C4 (1.2–1.6), C4-like (0.6–0.8) and C4 species (0.3–0.4), indicating a progressive decrease in apparent photorespiration in this series. With increasing irradiance at Γ under atmospheric levels of O2, and increasing O2 partial pressure at 300 μmol quanta·m−2·s−1, there was a similar increase in the rate of O2 evolution associated with whole-chain electron flow (Jo 2, calculated from chlorophyll fluorescence analysis) in the C3 and C3-C4 species compared to a much lower rate in the C4-like and C4 species. The results indicate that there is substantial O2-dependent electron flow in C3 and C3-C4 species, reflecting a high level of photorespiration compared to that in C4-like and C4 species. Consistent with these results, there was a significant decrease in Γ from C3 (6–6.2 Pa) to C3-C4 (1.0–3.0 Pa), to C4-like and C4 species (0.3–0.8 Pa), indicating a progressive decrease in apparent photorespiration. However, C3 and C3-C4 species examined had high intrinsic levels of photorespiration with the latter maintaining low apparent rates of photorespiration and lower Γ values, primarily by refixing photorespired CO2. The C4-like and C4 Flaveria species had low, but measurable, levels of photorespiration via selective localization of ribulose-1,5-bisphosphate carboxylase in bundle sheath cells and operation of a CO2 pump via the C4 pathway.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Photosynthesis research 14 (1987), S. 113-124 
    ISSN: 1573-5079
    Keywords: NADP-malate dehydrogenase ; glutathione
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract NADP-malate dehydrogenase extracted from darkened leaves of the C3 plants pea, barley, wheat and spinach was activated by reduced glutathione, a monothiol, as well as by dithiothreitol (DTT). However, in the C4 plants maize and Flaveria trinervia, only dithiothreitol could effectively activate the enzyme. There was no activation of the maize enzyme and little or no activation of the F. trinervia enzyme by glutathione. The failure of glutathione to activate NADP-MDH in leaf extracts of maize and F. trinervia may indicate there is some difference in disulfide groups of the protein compared to the C3 plant enzyme. Both DTT and glutathione could activate NADP-malate dehydrogenase in a partially purified enzyme preparation from pea leaves with or without addition of partially purified thioredoxin. However, the required concentration of reductant was lower with addition of thioredoxin than in its absence. In extracts of C3 species and the partially purified pea enzyme the level of activation after 40 to 60 min under aerobic conditions was higher (up to twofold) with DTT than with glutathione. Under anaerobic conditions, the initial rate of activation was about twice as high with DTT as with glutathione, but the total activation after 40 to 60 min was similar. Ascorbate was totally ineffective as a reducing agent in activating NADP-MDH from C3 or C4 plants, possibly due to its more positive redox potential.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Photosynthesis research 14 (1987), S. 125-135 
    ISSN: 1573-5079
    Keywords: NADP-malate dehydrogenase ; leaf development ; C3 species ; nitrate assimilation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The activity of NADP-malate dehydrogenase (NADP-MDH) was determined in the developing first leaf of the C3 plants wheat, barley and pea. Light dependent activation of the enzyme was observed in all three species following rapid extraction and immediate assay. Maximum activity was obtained following extraction from preilluminated leaves and incubation on ice for 45 min in the presence of dithiothreitol. In all three species, maximum activity was obtained in the young leaf 4 days after emergence of the seedling (about 2.5 to 3 μmoles per milligram chlorophyll per min in wheat and barley, and 6 μmoles per milligram chlorophyll per min in pea). On a chlorophyll basis there was an approximate five-fold decrease in NADP-MDH activity as the leaf matured. A similar pattern was found for phospho-enolpyruvate carboxylase and NADP-malic enzyme which had maximum activity in younger leaf tissue. Similarly, the activity of nitrate reductase in wheat and barley was high in the young leaf and it rapidly declined as the leaf matured. In contrast, the capacity for photosynthesis was relatively low in the young leaf, reaching a maximum 6 to 8 days after seedling emergence. The pattern of change in activity of phosphoribulokinase, an enzyme of the reductive pentose phosphate pathway, was similar to that of photosynthesis. The results suggest NADP-MDH and phospho-enolpyruvate carboxylase have important function(s) in the young leaf, which are not directly linked to C3 photosynthesis, and which, in part, may be linked to nitrate assimilation and provision of malate to mitochondria.
    Type of Medium: Electronic Resource
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