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Oxygen exchange in relation to carbon assimilation in water-stressed leaves during photosynthesis.

ABSTRACT: In a study on metabolic consumption of photosynthetic electrons and dissipation of excess light energy under water stress, O2 and CO2 gas exchange was measured by mass spectrometry in tomato plants using 18O2 and 13CO2. Under water stress, gross O2 evolution (E(O)), gross O2 uptake (U(O)), net CO2 uptake (PN), gross CO2 uptake (TPS), and gross CO2 evolution (Ec) declined. The ratio P(N)/E(O) fell during stress, while the ratios U(O)/E(O) and E(C)/TPS rose. Mitochondrial respiration in the light, which can be measured directly by 12CO2 evolution during 13CO2 uptake at 3000 microl l(-1) 13CO2, is small in relation to gross CO2 evolution and CO2 release from the glycolate pathway. It is concluded that PSII, the Calvin cycle and mitochondrial respiration are down-regulated under water stress. The percentages of photosynthetic electrons dissipated by CO2 assimilation, photorespiration and the Mehler reaction were calculated: in control leaves more than 50% of the electrons were consumed in CO2 assimilation, 23% in photorespiration and 13% in the Mehler reaction. Under severe stress the percentages of electrons dissipated by CO2 assimilation and the Mehler reaction declined while the percentage of electrons used in photorespiration doubled. The consumption of electrons in photorespiration may reduce the likelihood of damage during water deficit.

SUBMITTER: Haupt-Herting S

PROVIDER: S-EPMC4233798 | biostudies-literature | 2002 Jun

REPOSITORIES: biostudies-literature

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Oxygen exchange in relation to carbon assimilation in water-stressed leaves during photosynthesis.

Haupt-Herting Silke S Fock Heinrich P HP

Annals of botany 20020601

In a study on metabolic consumption of photosynthetic electrons and dissipation of excess light energy under water stress, O2 and CO2 gas exchange was measured by mass spectrometry in tomato plants using 18O2 and 13CO2. Under water stress, gross O2 evolution (E(O)), gross O2 uptake (U(O)), net CO2 uptake (PN), gross CO2 uptake (TPS), and gross CO2 evolution (Ec) declined. The ratio P(N)/E(O) fell during stress, while the ratios U(O)/E(O) and E(C)/TPS rose. Mitochondrial respiration in the light, ...[more]

PMID: 12102511

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Project description:BackgroundWe report a method to estimate carbon assimilation based on isotope ratio-mass spectrometry (IRMS) of 13CO2 labeled plant tissue. Photosynthetic carbon assimilation is the principal experimental observable which integrates important aspects of primary plant metabolism. It is traditionally measured through gas exchange. Despite its centrality in plant research, gas exchange performs poorly with rosette growth habits typical of Arabidopsis thaliana, mutant lines with limited biomass, and accounts poorly for leaf shading.ResultsIRMS-based carbon assimilation values from plants labeled at different light intensities were compared to those obtained by gas exchange, and the two methods yielded similar values. Using this method, we observed a strong correlation between 13C content and labeling time (R2 = 0.999) for 158 wild-type plants labeled for 6 to 42 min. Plants cultivated under different light regimes showed a linear response with respect to carbon assimilation, varying from 7.38 nmol 13C mg-1 leaf tissue min-1 at 80 PAR to 19.27 nmol 13C mg-1 leaf tissue min-1 at 500 PAR. We applied this method to examine the link between inhibition of the 2C-methyl-D-erythritol-4-phosphate (MEP) pathway and suppression of photosynthesis. A significant decrease in carbon assimilation was observed when metabolic activity in the MEP pathway was compromised by mutation or herbicides targeting the MEP pathway. Mutants affected in MEP pathway genes 1-DEOXY-D-XYLULOSE 5-PHOSPHATE SYNTHASE (DXS) or 1-HYDROXY-2-METHYL-2-(E)-BUTENYL 4-DIPHOSPHATE SYNTHASE (HDS) showed assimilation rates 36% and 61% lower than wild type. Similarly, wild type plants treated with the MEP pathway inhibitors clomazone or fosmidomycin showed reductions of 52% and 43%, respectively, while inhibition of the analogous mevalonic acid pathway, which supplies the same isoprenoid intermediates in the cytosol, did not, suggesting inhibition of photosynthesis was specific to disruption of the MEP pathway.ConclusionsThis method provides an alternative to gas exchange that offers several advantages: resilience to differences in leaf overlap, measurements based on tissue mass rather than leaf surface area, and compatibility with mutant Arabidopsis lines which are not amenable to gas exchange measurements due to low biomass and limited leaf surface area. It is suitable for screening large numbers of replicates simultaneously as well as post-hoc analysis of previously labeled plant tissue and is complementary to downstream detection of isotopic label in targeted metabolite pools.

Dataset Information

Oxygen exchange in relation to carbon assimilation in water-stressed leaves during photosynthesis.

Publications

Oxygen exchange in relation to carbon assimilation in water-stressed leaves during photosynthesis.

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