Literature DB >> 24193849

Decreased ribulose-1,5-bisphosphate carboxylase-oxygenase in transgenic tobacco transformed with 'antisense' rbcS : II. Flux-control coefficients for photosynthesis in varying light, CO2, and air humidity.

M Stitt1, W P Quick, U Schurr, E D Schulze, S R Rodermel, L Bogorad.   

Abstract

Transgenic tobacco (Nicotiana tabacum L.) plants transformed with 'antisense' rbcS to produce a series of plants with a progressive decrease in the amount of ribulose-1,5-bisphosphate carboxylase/oxygenase (Rubisco) have been used to investigate the contribution of Rubsico to the control of photosynthesis at different irradiance, CO2 concentrations and vapour-pressure deficits. Assimilation rates, transpiration, the internal CO2 concentration and chlorophyll fluorescence were measured in each plant. (i) The flux-control coefficient of Rubisco was estimated from the slope of the plot of Rubisco content versus assimilation rate. The flux-control coefficient had a value of 0.8 or more in high irradiance, (1050 μmol·m(-2)·s(-1)), low-vapour pressure deficit (4 mbar) and ambient CO2 (350 μbar). Control was marginal in enhanced CO2 (450 μbar) or low light (310 μmol·m(-2)·s(-1)) and was also decreased at high vapour-pressure deficit (17 mbar). No control was exerted in 5% CO2. (ii) The flux-control coefficients of Rubisco were compared with the fractional demand placed on the calculated available Rubisco capacity. Only a marginal control on photosynthetic flux is exerted by Rubisco until over 50% of the available capacity is being used. Control increases as utilisation rises to 80%, and approaches unity (i.e. strict limitation) when more than 80% of the available capacity is being used. (iii) In low light, plants with reduced Rubisco have very high energy-dependent quenching of chlorophyll fluorescence (qE) and a decreased apparent quantum yield. It is argued that Rubisco still exerts marginal control in these conditions because decreased Rubisco leads to increased thylakoid energisation and high-energy dependent dissipation of light energy, and lower light-harvesting efficiency. (iv) The flux-control coefficient of stomata for photosynthesis was calculated from the flux-control coefficient of Rubisco and the internal CO2 concentration, by applying the connectivity theorem. Control by the stomata varies between zero and about 0.25. It is increased by increased irradiance, decreased CO2 or decreased vapour-pressure deficit. (v) Photosynthetic oscillations in saturating irradiance and CO2 are suppressed in decreased-activity transformants before the steady-state rate of photosynthesis is affected. This provides direct evidence that these oscillations reveal the presence of "excess" Rubisco. (vi) Comparison of the flux-control coefficients of Rubisco with mechanistic models of photosynthesis provides direct support for the reliability of these models in conditions where Rubisco has a flux-control coefficient approach unity (i.e. "limits" photosynthesis), but also indicates that these models are less useful in conditions where control is shared between Rubisco and other components of the photosynthetic apparatus.

Entities:  

Year:  1991        PMID: 24193849     DOI: 10.1007/BF00194277

Source DB:  PubMed          Journal:  Planta        ISSN: 0032-0935            Impact factor:   4.116


  7 in total

1.  Fractional control of photosynthesis by the QB protein, the cytochrome f/b 6 complex and other components of the photosynthesic apparatus.

Authors:  U Heber; S Neimanis; K J Dietz
Journal:  Planta       Date:  1988-02       Impact factor: 4.116

2.  Nuclear-organelle interactions: nuclear antisense gene inhibits ribulose bisphosphate carboxylase enzyme levels in transformed tobacco plants.

Authors:  S R Rodermel; M S Abbott; L Bogorad
Journal:  Cell       Date:  1988-11-18       Impact factor: 41.582

3.  Limitation of Photosynthesis by Carbon Metabolism : I. Evidence for Excess Electron Transport Capacity in Leaves Carrying Out Photosynthesis in Saturating Light and CO(2).

Authors:  M Stitt
Journal:  Plant Physiol       Date:  1986-08       Impact factor: 8.340

4.  Nitrogen and Photosynthesis in the Flag Leaf of Wheat (Triticum aestivum L.).

Authors:  J R Evans
Journal:  Plant Physiol       Date:  1983-06       Impact factor: 8.340

5.  Stimulation of photosynthesis by 2% oxygen at low temperatures is restored by phosphate.

Authors:  R C Leegood; R T Furbank
Journal:  Planta       Date:  1986-05       Impact factor: 4.116

6.  Control analysis of photosynthate partitioning : Impact of reduced activity of ADP-glucose pyrophosphorylase or plastid phosphoglucomutase on the fluxes to starch and sucrose inArabidopsis thaliana (L.) Heynh.

Authors:  H Ekkehard Neuhaus; M Stitt
Journal:  Planta       Date:  1990-10       Impact factor: 4.116

7.  Decreased ribulose-1,5-bisphosphate carboxylase-oxygenase in transgenic tobacco transformed with "antisense" rbcS : I. Impact on photosynthesis in ambient growth conditions.

Authors:  W P Quick; U Schurr; R Scheibe; E D Schulze; S R Rodermel; L Bogorad; M Stitt
Journal:  Planta       Date:  1991-03       Impact factor: 4.116

  7 in total
  26 in total

1.  Targeted inactivation of the plastid ndhB gene in tobacco results in an enhanced sensitivity of photosynthesis to moderate stomatal closure.

Authors:  E M Horváth; S O Peter; T Joët; D Rumeau; L Cournac; G V Horváth; T A Kavanagh; C Schäfer; G Peltier; P Medgyesy
Journal:  Plant Physiol       Date:  2000-08       Impact factor: 8.340

2.  Evaluation of light regulatory potential of Calvin cycle steps based on large-scale gene expression profiling data.

Authors:  Ning Sun; Ligeng Ma; Deyun Pan; Hongyu Zhao; Xing Wang Deng
Journal:  Plant Mol Biol       Date:  2003-11       Impact factor: 4.076

3.  The Calvin cycle revisited.

Authors:  Christine A Raines
Journal:  Photosynth Res       Date:  2003       Impact factor: 3.573

4.  A brief history of systems biology. "Every object that biology studies is a system of systems." Francois Jacob (1974).

Authors:  Anthony Trewavas
Journal:  Plant Cell       Date:  2006-10       Impact factor: 11.277

5.  Discoveries in Rubisco (Ribulose 1,5-bisphosphate carboxylase/oxygenase): a historical perspective.

Authors:  Archie R Portis; Martin A J Parry
Journal:  Photosynth Res       Date:  2007-07-31       Impact factor: 3.573

6.  Decreased ribulose-1,5-bisphosphate carboxylase-oxygenase in transgenic tobacco transformed with "antisense" rbcS : IV. Impact on photosynthesis in conditions of altered nitrogen supply.

Authors:  W P Quick; K Fichtner; E D Schulze; R Wendler; R C Leegood; H Mooney; S R Rodermel; L Bogorad; M Stitt
Journal:  Planta       Date:  1992-11       Impact factor: 4.116

7.  Systems-level engineering of nonfermentative metabolism in yeast.

Authors:  Caleb J Kennedy; Patrick M Boyle; Zeev Waks; Pamela A Silver
Journal:  Genetics       Date:  2009-06-29       Impact factor: 4.562

8.  Manipulating photosynthesis.

Authors:  J S Knight; F Madueño; S A Barnes; J C Gray
Journal:  Mol Biotechnol       Date:  1996-12       Impact factor: 2.695

Review 9.  Opinion: the red-light response of stomatal movement is sensed by the redox state of the photosynthetic electron transport chain.

Authors:  Florian A Busch
Journal:  Photosynth Res       Date:  2013-03-13       Impact factor: 3.573

10.  Rubisco in planta kcat is regulated in balance with photosynthetic electron transport.

Authors:  H Eichelmann; E Talts; V Oja; E Padu; A Laisk
Journal:  J Exp Bot       Date:  2009-08-06       Impact factor: 6.992

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