Literature DB >> 12231705

Temperature Dependence of the Linkage of Quantum Yield of Photosystem II to CO2 Fixation in C4 and C3 Plants.

W. Oberhuber1, G. E. Edwards.   

Abstract

The temperature dependence of quantum yields of electron transport from photosystem II (PSII) ([phi]II, determined from chlorophyll a fluorescence) and CO2 assimilation ([phi]CO2, apparent quantum yield for CO2 assimilation) were determined simultaneously in vivo. With C4 species representing NADP-malic enzyme, NAD-malic enzyme, and phosphoenolpyruvate carboxykinase subgroups, the ratio of [phi]II/[phi]CO2 was constant over the temperature range from 15 to 40[deg]C at high light intensity (1100 [mu]mol quanta m-2 s-1). A similar response was obtained at low light intensity (300 [mu]mol quanta m-2 s-1), except the ratio of [phi]II/[phi]CO2 increased at high temperature. When the true quantum yield for CO2 fixation ([phi]CO2*) was calculated by correcting for respiration in the light (estimated from temperature dependence of dark respiration), the ratio of [phi]II/[phi]C02* remained constant with varying temperature and under both light intensities in all C4 species examined. Because the [phi]II/[phi]CO2* ratio was the same in C4 monocots representing the three subgroups, the ratio was not affected by differences in the bio-chemical mechanism of concentrating CO2 in the bundle sheath cells. The results suggest that PSII activity is closely linked to the true rate of CO2 fixation in C4 plants. The close relationship between [phi]II and [phi]CO2* in C4 species under varying temperature and light intensity conditions is apparently due to a common low level of photorespiration and a primary requirement for reductive power in the C3 pathway. In contrast, in a C3 plant the [phi] II/[phi]CO2* ratio is higher under normal atmospheric conditions than under nonphotorespiratory conditions and it increases with rising temperature. This decrease in efficiency in utilizing energy derived from PSII for CO2 fixation is due to an increase in photorespiration. In both the C3 and C4 species, photochemistry is limited under low temperature, and thus excess energy must be dissipated by nonphotochemical means.

Entities:  

Year:  1993        PMID: 12231705      PMCID: PMC160598          DOI: 10.1104/pp.101.2.507

Source DB:  PubMed          Journal:  Plant Physiol        ISSN: 0032-0889            Impact factor:   8.340


  5 in total

1.  Variation in Quantum Yield for CO(2) Uptake among C(3) and C(4) Plants.

Authors:  J Ehleringer; R W Pearcy
Journal:  Plant Physiol       Date:  1983-11       Impact factor: 8.340

2.  Kok effect and the quantum yield of photosynthesis : light partially inhibits dark respiration.

Authors:  R E Sharp; M A Matthews; J S Boyer
Journal:  Plant Physiol       Date:  1984-05       Impact factor: 8.340

3.  Partitioning of Noncyclic Photosynthetic Electron Transport to O(2)-Dependent Dissipative Processes as Probed by Fluorescence and CO(2) Exchange.

Authors:  R B Peterson
Journal:  Plant Physiol       Date:  1989-08       Impact factor: 8.340

4.  Regulation of Ribulose-1,5-Bisphosphate Carboxylase Activity in Alocasia macrorrhiza in Response to Step Changes in Irradiance.

Authors:  J R Seemann; M U Kirschbaum; T D Sharkey; R W Pearcy
Journal:  Plant Physiol       Date:  1988-09       Impact factor: 8.340

5.  Quantum Yields for CO(2) Uptake in C(3) and C(4) Plants: Dependence on Temperature, CO(2), and O(2) Concentration.

Authors:  J Ehleringer; O Björkman
Journal:  Plant Physiol       Date:  1977-01       Impact factor: 8.340

  5 in total
  19 in total

1.  C4 photosynthesis at low temperature. A study using transgenic plants with reduced amounts of Rubisco.

Authors:  David S Kubien; Susanne von Caemmerer; Robert T Furbank; Rowan F Sage
Journal:  Plant Physiol       Date:  2003-07       Impact factor: 8.340

2.  The C(4) pathway: an efficient CO(2) pump.

Authors:  Susanne von Caemmerer; Robert T Furbank
Journal:  Photosynth Res       Date:  2003       Impact factor: 3.573

Review 3.  Temperature response of photosynthesis in C3, C4, and CAM plants: temperature acclimation and temperature adaptation.

Authors:  Wataru Yamori; Kouki Hikosaka; Danielle A Way
Journal:  Photosynth Res       Date:  2013-06-26       Impact factor: 3.573

Review 4.  C4 photosynthesis and water stress.

Authors:  Oula Ghannoum
Journal:  Ann Bot       Date:  2008-06-13       Impact factor: 4.357

5.  A novel mechanistic interpretation of instantaneous temperature responses of leaf net photosynthesis.

Authors:  Jörg Kruse; Saleh Alfarraj; Heinz Rennenberg; Mark Adams
Journal:  Photosynth Res       Date:  2016-05-24       Impact factor: 3.573

6.  Effects of Growth Temperature on the Responses of Ribulose-1,5-Biphosphate Carboxylase, Electron Transport Components, and Sucrose Synthesis Enzymes to Leaf Nitrogen in Rice, and Their Relationships to Photosynthesis.

Authors:  A. Makino; H. Nakano; T. Mae
Journal:  Plant Physiol       Date:  1994-08       Impact factor: 8.340

7.  C4 Photosynthesis (The Effects of Leaf Development on the CO2-Concentrating Mechanism and Photorespiration in Maize).

Authors:  Z. Dai; MSB. Ku; G. E. Edwards
Journal:  Plant Physiol       Date:  1995-03       Impact factor: 8.340

8.  Effect of High Temperature on Photosynthesis in Beans (I. Oxygen Evolution and Chlorophyll Fluorescence).

Authors:  C. Pastenes; P. Horton
Journal:  Plant Physiol       Date:  1996-11       Impact factor: 8.340

9.  The Effect of Leaf Temperature and Photorespiratory Conditions on Export of Sugars during Steady-State Photosynthesis in Salvia splendens.

Authors:  J. Jiao; B. Grodzinski
Journal:  Plant Physiol       Date:  1996-05       Impact factor: 8.340

10.  Rapid Chlorophyll a Fluorescence Light Response Curves Mechanistically Inform Photosynthesis Modeling.

Authors:  Jonathan R Pleban; Carmela R Guadagno; David S Mackay; Cynthia Weinig; Brent E Ewers
Journal:  Plant Physiol       Date:  2020-03-09       Impact factor: 8.340

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