Crystallization and preliminary X-ray analysis of xylanase B from Clostridium stercorarium

Recombinant mature xylanase B from Clostridium stercorarium has been prepared and crystallized by the sitting‐drop vapour‐diffusion method using 4 mg ml−1 purified enzyme, 10.3%(w/v) polyethylene glycol 1500, 8.6%(v/v) glycerol and 0.34 M non‐detergent sulfobetaine 195. A suitable crystal grew after...

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Published inActa crystallographica. Section D, Biological crystallography. Vol. 60; no. 2; pp. 342 - 343
Main Authors Nishimoto, Mamoru, Fushinobu, Shinya, Miyanaga, Akimasa, Wakagi, Takayoshi, Shoun, Hirofumi, Sakka, Kazuo, Ohmiya, Kunio, Nirasawa, Satoru, Kitaoka, Motomitsu, Hayashi, Kiyoshi
Format Journal Article
LanguageEnglish
Published 5 Abbey Square, Chester, Cheshire CH1 2HU, England International Union of Crystallography 01.02.2004
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Summary:Recombinant mature xylanase B from Clostridium stercorarium has been prepared and crystallized by the sitting‐drop vapour‐diffusion method using 4 mg ml−1 purified enzyme, 10.3%(w/v) polyethylene glycol 1500, 8.6%(v/v) glycerol and 0.34 M non‐detergent sulfobetaine 195. A suitable crystal grew after incubation for ten weeks at 293 K. The crystal belonged to space group P212121, with unit‐cell parameters a = 64.76, b = 96.60, c = 138.44 Å. X‐ray diffraction data were collected to 1.80 Å resolution.
Bibliography:ark:/67375/WNG-4L6CB0D2-Q
ArticleID:AYDBE5008
istex:B0A42710B8E997C7CAF7E63DC42B58BB20799B65
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:1399-0047
0907-4449
1399-0047
DOI:10.1107/S090744490302715X