| Literature DB >> 24915093 |
Hackwon Do1, Il-Sup Kim2, Young-Saeng Kim2, Sun-Young Shin2, Jin-Ju Kim2, Ji-Eun Mok2, Seong-Im Park2, Ah Ram Wi1, Hyun Park1, Han-Woo Kim1, Ho-Sung Yoon2, Jun Hyuck Lee1.
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 P2₁ with unit-cell parameters a=47.03, b=48.38, c=51.83 Å, β=107.41°.Entities:
Keywords: Oryza sativa L. japonica; ascorbate; dehydroascorbate reductase
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Year: 2014 PMID: 24915093 PMCID: PMC4051537 DOI: 10.1107/S2053230X14009133
Source DB: PubMed Journal: Acta Crystallogr F Struct Biol Commun ISSN: 2053-230X Impact factor: 1.056