Papers

Peer-reviewed
May, 2006

Crystallization and preliminary X-ray analysis of an exotype alginate lyase Atu3025 from Agrobacterium tumefaciens strain C58, a member of polysaccharide lyase family 15

Acta Crystallographica Section F: Structural Biology and Crystallization Communications
  • Akihito Ochiai
  • ,
  • Masayuki Yamasaki
  • ,
  • Bunzo Mikami
  • ,
  • Wataru Hashimoto
  • ,
  • Kousaku Murata

Volume
62
Number
5
First page
486
Last page
488
Language
English
Publishing type
Research paper (scientific journal)
DOI
10.1107/S1744309106014333

Almost all alginate lyases depolymerize alginate in an endolytical fashion via a β-elimination reaction. The alginate lyase Atu3025 from Agrobacterium tumefaciens strain C58, consisting of 776 amino-acid residues, is a novel exotype alginate lyase classified into polysaccharide lyase family 15. The enzyme was crystallized at 293 K by sitting-drop vapour diffusion with polyethylene glycol 4000 as a precipitant. Preliminary X-ray analysis showed that the Atu3025 crystal belonged to space group P21 and diffracted to 2.8 Å resolution, with unit-cell parameters a = 107.7, b = 108.3, c = 149.5 Å, β= 91.5°. © 2006 International Union of Crystallography. All rights reserved.

Link information
DOI
https://doi.org/10.1107/S1744309106014333
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/16682783
ID information
  • DOI : 10.1107/S1744309106014333
  • ISSN : 1744-3091
  • Pubmed ID : 16682783
  • SCOPUS ID : 33646851039

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