Literature DB >> 18552367

C4 photosynthesis and water stress.

Oula Ghannoum1.   

Abstract

BACKGROUND: In contrast to C(3) photosynthesis, the response of C(4) photosynthesis to water stress has been less-well studied in spite of the significant contribution of C(4) plants to the global carbon budget and food security. The key feature of C(4) photosynthesis is the operation of a CO(2)-concentrating mechanism in the leaves, which serves to saturate photosynthesis and suppress photorespiration in normal air. This article reviews the current state of understanding about the response of C(4) photosynthesis to water stress, including the interaction with elevated CO(2) concentration. Major gaps in our knowledge in this area are identified and further required research is suggested. SCOPE: Evidence indicates that C(4) photosynthesis is highly sensitive to water stress. With declining leaf water status, CO(2) assimilation rate and stomatal conductance decrease rapidly and photosynthesis goes through three successive phases. The initial, mainly stomatal phase, may or may not be detected as a decline in assimilation rates depending on environmental conditions. This is because the CO(2)-concentrating mechanism is capable of saturating C(4) photosynthesis under relatively low intercellular CO(2) concentrations. In addition, photorespired CO(2) is likely to be refixed before escaping the bundle sheath. This is followed by a mixed stomatal and non-stomatal phase and, finally, a mainly non-stomatal phase. The main non-stomatal factors include reduced activity of photosynthetic enzymes; inhibition of nitrate assimilation, induction of early senescence, and changes to the leaf anatomy and ultrastructure. Results from the literature about CO(2) enrichment indicate that when C(4) plants experience drought in their natural environment, elevated CO(2) concentration alleviates the effect of water stress on plant productivity indirectly via improved soil moisture and plant water status as a result of decreased stomatal conductance and reduced leaf transpiration.
CONCLUSIONS: It is suggested that there is a limited capacity for photorespiration or the Mehler reaction to act as significant alternative electron sinks under water stress in C(4) photosynthesis. This may explain why C(4) photosynthesis is equally or even more sensitive to water stress than its C(3) counterpart in spite of the greater capacity and water use efficiency of the C(4) photosynthetic pathway.

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Year:  2008        PMID: 18552367      PMCID: PMC2707343          DOI: 10.1093/aob/mcn093

Source DB:  PubMed          Journal:  Ann Bot        ISSN: 0305-7364            Impact factor:   4.357


  25 in total

1.  Drought-inhibition of photosynthesis in C3 plants: stomatal and non-stomatal limitations revisited.

Authors:  J Flexas; H Medrano
Journal:  Ann Bot       Date:  2002-02       Impact factor: 4.357

Review 2.  Diffusive and metabolic limitations to photosynthesis under drought and salinity in C(3) plants.

Authors:  J Flexas; J Bota; F Loreto; G Cornic; T D Sharkey
Journal:  Plant Biol (Stuttg)       Date:  2004-05       Impact factor: 3.081

3.  Drought constraints on C4 photosynthesis: stomatal and metabolic limitations in C3 and C4 subspecies of Alloteropsis semialata.

Authors:  Brad S Ripley; Matthew E Gilbert; Douglas G Ibrahim; Colin P Osborne
Journal:  J Exp Bot       Date:  2007-02-24       Impact factor: 6.992

4.  Drought-induced effects on nitrate reductase activity and mRNA and on the coordination of nitrogen and carbon metabolism in maize leaves

Authors: 
Journal:  Plant Physiol       Date:  1998-05       Impact factor: 8.340

5.  Photophosphorylation in Attached Leaves of Helianthus annuus at Low Water Potentials.

Authors:  A Ortiz-Lopez; D R Ort; J S Boyer
Journal:  Plant Physiol       Date:  1991-08       Impact factor: 8.340

6.  Short-term changes in leaf carbon isotope discrimination in salt- and water-stressed c(4) grasses.

Authors:  W D Bowman; K T Hubick; S von Caemmerer; G D Farquhar
Journal:  Plant Physiol       Date:  1989-05       Impact factor: 8.340

7.  Mild water stress effects on carbon-reduction-cycle intermediates, ribulose bisphosphate carboxylase activity, and spatial homogeneity of photosynthesis in intact leaves.

Authors:  T D Sharkey; J R Seemann
Journal:  Plant Physiol       Date:  1989-04       Impact factor: 8.340

8.  Photosynthesis, productivity, and yield of maize are not affected by open-air elevation of CO2 concentration in the absence of drought.

Authors:  Andrew D B Leakey; Martin Uribelarrea; Elizabeth A Ainsworth; Shawna L Naidu; Alistair Rogers; Donald R Ort; Stephen P Long
Journal:  Plant Physiol       Date:  2006-01-11       Impact factor: 8.340

9.  Estimation of Bundle Sheath Cell Conductance in C4 Species and O2 Insensitivity of Photosynthesis.

Authors:  R. H. Brown; G. T. Byrd
Journal:  Plant Physiol       Date:  1993-12       Impact factor: 8.340

10.  Photorespiration in C4 grasses remains slow under drought conditions.

Authors:  Ana E Carmo-Silva; Stephen J Powers; Alfred J Keys; Maria Celeste Arrabaça; Martin A J Parry
Journal:  Plant Cell Environ       Date:  2008-03-11       Impact factor: 7.228

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  66 in total

Review 1.  The hidden function of photosynthesis: a sensing system for environmental conditions that regulates plant acclimation responses.

Authors:  Thomas Pfannschmidt; Chunhong Yang
Journal:  Protoplasma       Date:  2012-03-23       Impact factor: 3.356

2.  Musings about the effects of environment on photosynthesis.

Authors:  David W Lawlor
Journal:  Ann Bot       Date:  2009-02       Impact factor: 4.357

Review 3.  Differential positioning of chloroplasts in C4 mesophyll and bundle sheath cells.

Authors:  Eri Maai; Hiroshi Miyake; Mitsutaka Taniguchi
Journal:  Plant Signal Behav       Date:  2011-08-01

4.  C4 photosynthesis and climate through the lens of optimality.

Authors:  Haoran Zhou; Brent R Helliker; Matthew Huber; Ashley Dicks; Erol Akçay
Journal:  Proc Natl Acad Sci U S A       Date:  2018-11-06       Impact factor: 11.205

5.  Evaluating water deficit and glyphosate treatment on the accumulation of phenolic compounds and photosynthesis rate in transgenic Codonopsis lanceolata (Siebold & Zucc.) Trautv. over-expressing γ-tocopherol methyltransferase (γ-tmt) gene.

Authors:  Bimal Kumar Ghimire; Na-Young Son; Seung-Hyun Kim; Chang Yeon Yu; Ill-Min Chung
Journal:  3 Biotech       Date:  2017-06-29       Impact factor: 2.406

6.  A Dynamic Hydro-Mechanical and Biochemical Model of Stomatal Conductance for C4 Photosynthesis.

Authors:  Chandra Bellasio; Joe Quirk; Thomas N Buckley; David J Beerling
Journal:  Plant Physiol       Date:  2017-07-27       Impact factor: 8.340

7.  Transcriptome comparisons shed light on the pre-condition and potential barrier for C4 photosynthesis evolution in eudicots.

Authors:  Yimin Tao; Ming-Ju Amy Lyu; Xin-Guang Zhu
Journal:  Plant Mol Biol       Date:  2016-02-18       Impact factor: 4.076

8.  Rubisco activities, properties, and regulation in three different C4 grasses under drought.

Authors:  A Elizabete Carmo-Silva; Alfred J Keys; P John Andralojc; Stephen J Powers; M Celeste Arrabaça; Martin A J Parry
Journal:  J Exp Bot       Date:  2010-04-02       Impact factor: 6.992

9.  Ectopic expression of Rubisco subunits in maize mesophyll cells does not overcome barriers to cell type-specific accumulation.

Authors:  Katia Wostrikoff; Aimee Clark; Shirley Sato; Tom Clemente; David Stern
Journal:  Plant Physiol       Date:  2012-06-28       Impact factor: 8.340

10.  Role of bundle sheath conductance in sustaining photosynthesis competence in sugarcane plants under nitrogen deficiency.

Authors:  Vanessa R Tofanello; Larissa M Andrade; Denisele N A Flores-Borges; Eduardo Kiyota; Juliana L S Mayer; Silvana Creste; Eduardo C Machado; Xinyou Yin; Paul C Struik; Rafael V Ribeiro
Journal:  Photosynth Res       Date:  2021-06-06       Impact factor: 3.573

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