Abstract
Xylose reductase (XR), which requires NADPH as a co-substrate, catalyzes the reduction of d-xylose to xylitol, which is the first step in the metabolism of d - xylose. The detailed three-dimensional structure of XR will provide a better understanding of the biological significance of XR in the efficient production of xylitol from biomass. XR of molecular mass 36.6 kDa from Candida tropicalis was crystallized using the hanging-drop vapour-diffusion method. According to X-ray diffraction data from C. tropicalis XR crystals at 2.91 Å resolution, the unit cell belongs to space group P31 or P32. Preliminary analysis indicated the presence of four XR molecules in the asymmetric unit, with 68.0% solvent content. © 2009 International Union of Crystallography All rights reserved.
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Chen, L. C., Huang, S. C., Chuankhayan, P., Chen, C. D., Huang, Y. C., Jeyakanthan, J., … Chen, C. J. (2009). Purification, crystallization and preliminary X-ray crystallographic analysis of xylose reductase from candida tropicalis. Acta Crystallographica Section F: Structural Biology and Crystallization Communications, 65(4), 419–421. https://doi.org/10.1107/S1744309109008719
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