Crystallization and X-ray diffraction analysis of an l-arabinonate dehydratase from Rhizobium leguminosarum bv. trifolii and a d-xylonate dehydratase from Caulobacter crescentus
- 1. University of Eastern Finland, Joensuu Campus, PO Box 111, FIN-80101 Joensuu (Finland)
- 2. VTT Technical Research Centre of Finland Ltd, PO Box 1000, FIN-02044 VTT Espoo (Finland)
Description
l-Arabinonate dehydratase and d-xylonate dehydratase from the IlvD/EDD family were crystallized by the vapour-diffusion method. Diffraction data sets were collected to resolutions of 2.40 and 2.66 Å from crystals of l-arabinonate dehydratase and d-xylonate dehydratase, respectively. l-Arabinonate dehydratase (EC 4.2.1.25) and d-xylonate dehydratase (EC 4.2.1.82) are two enzymes that are involved in a nonphosphorylative oxidation pathway of pentose sugars. l-Arabinonate dehydratase converts l-arabinonate into 2-dehydro-3-deoxy-l-arabinonate, and d-xylonate dehydratase catalyzes the dehydration of d-xylonate to 2-dehydro-3-deoxy-d-xylonate. l-Arabinonate and d-xylonate dehydratases belong to the IlvD/EDD family, together with 6-phosphogluconate dehydratases and dihydroxyacid dehydratases. No crystal structure of any l-arabinonate or d-xylonate dehydratase is available in the PDB. In this study, recombinant l-arabinonate dehydratase from Rhizobium leguminosarum bv. trifolii (RlArDHT) and d-xylonate dehydratase from Caulobacter crescentus (CcXyDHT) were heterologously expressed in Escherichia coli and purified by the use of affinity chromatography followed by gel-filtration chromatography. The purified proteins were crystallized using the hanging-drop vapour-diffusion method at 293 K. Crystals of RlArDHT that diffracted to 2.40 Å resolution were obtained using sodium formate as a precipitating agent. They belonged to space group P21, with unit-cell parameters a = 106.07, b = 208.61, c = 147.09 Å, β = 90.43°. Eight RlArDHT molecules (two tetramers) in the asymmetric unit give a VM value of 3.2 Å3 Da−1 and a solvent content of 62%. Crystals of CcXyDHT that diffracted to 2.66 Å resolution were obtained using sodium formate and polyethylene glycol 3350. They belonged to space group C2, with unit-cell parameters a = 270.42, b = 236.13, c = 65.17 Å, β = 97.38°. Four CcXyDHT molecules (a tetramer) in the asymmetric unit give a VM value of 4.0 Å3 Da−1 and a solvent content of 69%
Availability note (English)
Available from http://dx.doi.org/10.1107/S2053230X16010311; Available from http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4973301Additional details
Identifiers
Publishing Information
- Journal Title
- Acta Crystallographica. Section F, Structural Biology Communications
- Journal Volume
- 72
- Journal Issue
- Pt 8
- Journal Page Range
- p. 604-608
- ISSN
- 2053-230X
- CODEN
- ACSFEN
INIS
- Country of Publication
- United States
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 47102080
- Subject category
- S75: CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND SUPERFLUIDITY;
- Descriptors DEI
- CRYSTALLIZATION; CRYSTALS; ESCHERICHIA COLI; MONOCLINIC LATTICES; PRECIPITATION; RESOLUTION; SPACE GROUPS; X-RAY DIFFRACTION
- Descriptors DEC
- BACTERIA; COHERENT SCATTERING; CRYSTAL LATTICES; CRYSTAL STRUCTURE; DIFFRACTION; MICROORGANISMS; PHASE TRANSFORMATIONS; SCATTERING; SEPARATION PROCESSES; SYMMETRY GROUPS; THREE-DIMENSIONAL LATTICES
Optional Information
- Copyright
- Copyright (c) Rahman et al. 2016
- Notes
- PMCID: PMC4973301; PMID: 27487924; PUBLISHER-ID: nj5256; PUBLISHER-ID: S2053230X16010311; OAI: oai:pubmedcentral.nih.gov:4973301; This is an open-access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.