Influence of Oxygen and Temperature on the Dark Inactivation of Pyruvate, Orthophosphate Dikinase and NADP-Malate Dehydrogenase in Maize
- PMID: 16662868
- PMCID: PMC1066079
- DOI: 10.1104/pp.71.3.568
Influence of Oxygen and Temperature on the Dark Inactivation of Pyruvate, Orthophosphate Dikinase and NADP-Malate Dehydrogenase in Maize
Abstract
The influence of oxygen and temperature on the inactivation of pyruvate, Pi dikinase and NADP-malate dehydrogenase was studied in Zea mays. O(2) was required for inactivation of both pyruvate, Pi dikinase and NADP-malate dehydrogenase in the dark in vivo. The rate of inactivation under 2% O(2) was only slightly lower than that at 21% O(2). The in vitro inactivation of pyruvate, Pi dikinase, while dependent on adenine nucleotides (ADP + ATP), did not require O(2).The postillumination inactivation of pyruvate, Pi dikinase in leaves was strongly dependent on temperature. As temperature was decreased in the dark, there was a lag period of increasing length (e.g. at 17 degrees C there was a lag of about 25 minutes) before inactivation proceeded. Following the lag period, the rate of inactivation decreased with decreasing temperature. The half-time for dark inactivation was about 7 minutes at 32 degrees C and 45 minutes at 17 degrees C. The inactivation of pyruvate, Pi dikinase in vitro following extraction from illuminated leaves was also strongly dependent on temperature, but occurred without a lag period. In contrast, NADP-malate dehydrogenase was rapidly inactivated in leaves (half-time of approximately 3 minutes) during the postillumination period without a lag, and there was little effect of temperature between 10 and 32 degrees C. The results are discussed in relation to known differences in the mechanism of activation/inactivation of the two enzymes.
Similar articles
-
Light and temperature dependence of the rate and degree of activation of pyruvate, Pi dikinase in vivo in maize.Photosynth Res. 1980 Sep;1(3):199-207. doi: 10.1007/BF00020599. Photosynth Res. 1980. PMID: 24470084
-
Plants under Climatic Stress: VI. Chilling and Light Effects on Photosynthetic Enzymes of Sorghum and Maize.Plant Physiol. 1974 Nov;54(5):696-701. doi: 10.1104/pp.54.5.696. Plant Physiol. 1974. PMID: 16658954 Free PMC article.
-
Activation of NADP-Malate Dehydrogenase, Pyruvate,Pi Dikinase, and Fructose 1,6-Bisphosphatase in Relation to Photosynthetic Rate in Maize.Plant Physiol. 1984 Sep;76(1):238-43. doi: 10.1104/pp.76.1.238. Plant Physiol. 1984. PMID: 16663806 Free PMC article.
-
Molecular and biochemical mechanisms in maize endosperm development: the role of pyruvate-Pi-dikinase and Opaque-2 in the control of C/N ratio.C R Biol. 2008 Oct;331(10):772-9. doi: 10.1016/j.crvi.2008.07.019. Epub 2008 Sep 4. C R Biol. 2008. PMID: 18926491 Review.
-
Regulation of enzymes in C4 photosynthesis.Curr Top Cell Regul. 1978;14:1-27. Curr Top Cell Regul. 1978. PMID: 32012 Review. No abstract available.
Cited by
-
Experimental evidence of phosphoenolpyruvate resynthesis from pyruvate in illuminated leaves.Plant Physiol. 2011 Sep;157(1):86-95. doi: 10.1104/pp.111.180711. Epub 2011 Jul 5. Plant Physiol. 2011. PMID: 21730197 Free PMC article.
-
Pyruvate,orthophosphate dikinase in leaves and chloroplasts of C(3) plants undergoes light-/dark-induced reversible phosphorylation.Plant Physiol. 2002 Apr;128(4):1368-78. doi: 10.1104/pp.010806. Plant Physiol. 2002. PMID: 11950985 Free PMC article.
-
Pyruvate, phosphate dikinase regulatory protein impacts light response of C4 photosynthesis in Setaria viridis.Plant Physiol. 2022 Sep 28;190(2):1117-1133. doi: 10.1093/plphys/kiac333. Plant Physiol. 2022. PMID: 35876823 Free PMC article.
-
Energetic aspects of the light activation of two chloroplast enzymes: fructose-1,6-bisphosphatase and NADP-malate dehydrogenase.Photosynth Res. 1985 Sep;6(3):201-13. doi: 10.1007/BF00049276. Photosynth Res. 1985. PMID: 24442918
-
Carbon metabolism and gas exchange in leaves of Zea mays L. : Interaction between the C3 and C 4 pathways during photosynthetic induction.Planta. 1984 Nov;162(5):457-62. doi: 10.1007/BF00393459. Planta. 1984. PMID: 24253228
References
LinkOut - more resources
Full Text Sources
Research Materials
Miscellaneous