Unknown

Dataset Information

0

Crystallization and preliminary X-ray crystallographic studies of dehydroascorbate reductase (DHAR) from Oryza sativa L. japonica.


ABSTRACT: Dehydroascorbate reductase from Oryza sativa L. japonica (OsDHAR), a key enzyme in the regeneration of vitamin C, maintains reduced pools of ascorbic acid to detoxify reactive oxygen species. In previous studies, the overexpression of OsDHAR in transgenic rice increased grain yield and biomass as well as the amount of ascorbate, suggesting that ascorbate levels are directly associated with crop production in rice. Hence, it has been speculated that the increased level of antioxidants generated by OsDHAR protects rice from oxidative damage and increases the yield of rice grains. However, the crystal structure and detailed mechanisms of this important enzyme need to be further elucidated. In this study, recombinant OsDHAR protein was purified and crystallized using the sitting-drop vapour-diffusion method at pH 8.0 and 298?K. Plate-shaped crystals were obtained using 0.15?M potassium bromide, 30%(w/v) PEG MME 2000 as a precipitant, and the crystals diffracted to a resolution of 1.9?Å on beamline 5C at the Pohang Accelerator Laboratory. The X-ray diffraction data indicated that the crystal contained one OsDHAR molecule in the asymmetric unit and belonged to space group P2? with unit-cell parameters a=47.03, b=48.38, c=51.83?Å, ?=107.41°.

SUBMITTER: Do H 

PROVIDER: S-EPMC4051537 | BioStudies | 2014-01-01

REPOSITORIES: biostudies

Similar Datasets

2016-01-01 | S-EPMC4726096 | BioStudies
1000-01-01 | S-EPMC4687524 | BioStudies
1000-01-01 | S-EPMC5616140 | BioStudies
2013-01-01 | S-EPMC3887988 | BioStudies
1983-01-01 | S-EPMC1154305 | BioStudies
2017-01-01 | S-EPMC5307357 | BioStudies
1994-01-01 | S-EPMC1137105 | BioStudies
2000-01-01 | S-EPMC1221163 | BioStudies
2013-01-01 | S-EPMC3688944 | BioStudies
2013-01-01 | S-EPMC3818054 | BioStudies