5yn3
From Proteopedia
Crystal structure of xylose isomerase from Piromyces sp. E2
Structural highlights
FunctionPublication Abstract from PubMedBiofuel production using lignocellulosic biomass is gaining attention because it can be substituted for fossil fuels without competing with edible resources. However, because Saccharomyces cerevisiae does not have a D-xylose metabolic pathway, oxidoreductase or isomerase pathways must be introduced to utilize D-xylose from lignocellulosic biomass in S. cerevisiae. To elucidate the biochemical properties of xylose isomerase (XI) from Piromyces sp. E2 (PsXI), we determine its crystal structure in complex with substrate mimic glycerol. An amino acid sequence comparison with other reported XIs and the relative activity measurements using five kinds of divalent metal ions confirmed that PsXI belongs to class II XI. Moreover kinetic analysis of PsXI was also performed using Mn(2)(+), the preferred divalent metal ion for PsXI. In addition, the substrate-binding mode of PsXI could be predicted with the substrate mimic glycerol bound to the active site. These studies may provide structural information to enhance D-xylose utilization for biofuel production. Crystal Structure and Biochemical Characterization of Xylose Isomerase from Piromyces sp. E2.,Son H, Lee SM, Kim KJ J Microbiol Biotechnol. 2018 Apr 28;28(4):571-578. doi: 10.4014/jmb.1711.11026. PMID:29385668[1] From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine. References
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