4.4 Article

Catalase protects against nonenzymatic decarboxylations during photorespiration in Arabidopsis thaliana

期刊

PLANT DIRECT
卷 5, 期 12, 页码 -

出版社

JOHN WILEY & SONS LTD
DOI: 10.1002/pld3.366

关键词

metabolism; photorespiration; photosynthesis; carbon reactions/Calvin cycle/C3 photosynthesis; redox homeostasis/redox reactions

资金

  1. Deutsche Forschungsgemeinschaft [390686111]
  2. National Science Foundation [2030337, 2015843]
  3. US Department of Energy (Office of Science, Office of Basic Energy Sciences and Energy Efficiency and Renewable Energy, Solar Energy Technology Program) [DE-FG02-91ER20021]
  4. Alexander von Humboldt Foundation
  5. Division Of Integrative Organismal Systems
  6. Direct For Biological Sciences [2030337] Funding Source: National Science Foundation
  7. Div Of Molecular and Cellular Bioscience
  8. Direct For Biological Sciences [2015843] Funding Source: National Science Foundation

向作者/读者索取更多资源

Photorespiration is a crucial carbon recovery process in plants, and catalase in peroxisomes plays a protective role by preventing nonenzymatic decarboxylations between hydrogen peroxide and photorespiratory intermediates. Mutants lacking peroxisomal catalase show increased CO2 release from photorespiration, supporting the hypothesis of excess nonenzymatic decarboxylations, particularly the decarboxylation of hydroxypyruvate.
Photorespiration recovers carbon that would be otherwise lost following the oxygenation reaction of rubisco and production of glycolate. Photorespiration is essential in plants and recycles glycolate into usable metabolic products through reactions spanning the chloroplast, mitochondrion, and peroxisome. Catalase in peroxisomes plays an important role in this process by disproportionating H2O2 resulting from glycolate oxidation into O-2 and water. We hypothesize that catalase in the peroxisome also protects against nonenzymatic decarboxylations between hydrogen peroxide and photorespiratory intermediates (glyoxylate and/or hydroxypyruvate). We test this hypothesis by detailed gas exchange and biochemical analysis of Arabidopsis thaliana mutants lacking peroxisomal catalase. Our results strongly support this hypothesis, with catalase mutants showing gas exchange evidence for an increased stoichiometry of CO2 release from photorespiration, specifically an increase in the CO2 compensation point, a photorespiratory-dependent decrease in the quantum efficiency of CO2 assimilation, increase in the (CO2)-C-12 released in a (CO2)-C-13 background, and an increase in the postillumination CO2 burst. Further metabolic evidence suggests this excess CO2 release occurred via the nonenzymatic decarboxylation of hydroxypyruvate. Specifically, the catalase mutant showed an accumulation of photorespiratory intermediates during a transient increase in rubisco oxygenation consistent with this hypothesis. Additionally, end products of alternative hypotheses explaining this excess release were similar between wild type and catalase mutants. Furthermore, the calculated rate of hydroxypyruvate decarboxylation in catalase mutant is much higher than that of glyoxylate decarboxylation. This work provides evidence that these nonenzymatic decarboxylation reactions, predominately hydroxypyruvate decarboxylation, can occur in vivo when photorespiratory metabolism is genetically disrupted.

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