Cloning, expression, purification, crystallization and X-ray crystallographic analysis of glucuronic acid dehydrogenase from Chromohalobacter salexigens

Jae Woo Ahn, Shin Youp Lee, Sangwoo Kim, Sun Ja Cho, Sun Bok Lee, Kyung Jin Kim

Research output: Contribution to journalArticlepeer-review

5 Scopus citations

Abstract

Glucuronic acid dehydrogenase (GluUADH), the product of the Csal-2474 gene from the halophilic bacterium Chromohalobacter salexigens DSM 3043, is an enzyme with potential use in the conversion of glucuronic acid in seaweed biomass to fuels and chemicals. GluUADH is an enzyme that catalyzes the oxidation of glucuronic acid (GluUA) and galacturonic acid (GalUA) and has a preference for NAD+ rather than NADP+ as a cofactor. Recombinant GluUADH was crystallized in the presence of 0.2 M calcium acetate, 0.1 M Tris-HCl pH 7.0 and 20% PEG 3000 at 295 K. X-ray diffraction data were collected to a maximum resolution of 2.1 Å. The GluUADH crystal belonged to space group P63, with unit-cell parameters a = b = 122.58, c = 150.49 Å, = 120°. With one molecule per asymmetric unit, the crystal volume per unit protein weight (V M) is 2.78 Å3 Da-1. The structure was solved by the single anomalous dispersion method and structure refinement is in progress.

Original languageEnglish
Pages (from-to)689-691
Number of pages3
JournalActa Crystallographica Section F: Structural Biology and Crystallization Communications
Volume67
Issue number6
DOIs
StatePublished - Jun 2011

Keywords

  • glucuronic acid dehydrogenase
  • seaweed
  • short-chain dehydrogenase/ oxidoreductase family

Fingerprint

Dive into the research topics of 'Cloning, expression, purification, crystallization and X-ray crystallographic analysis of glucuronic acid dehydrogenase from Chromohalobacter salexigens'. Together they form a unique fingerprint.

Cite this