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Crystallization of a genetically engineered water-soluble primary penicillin target enzyme. The high molecular mass PBP2x of Streptococcus pneumoniae.
Charlier, P; Buisson, G; Dideberg, O; Wierenga, J; Keck, W; Laible, G; Hakenbeck, R.
Afiliação
  • Charlier P; Institut de Physique, Crystallographie, Université de Liège, Belgium.
J Mol Biol ; 232(3): 1007-9, 1993 Aug 05.
Article em En | MEDLINE | ID: mdl-8355266
A genetically engineered water-soluble derivative of PBP2x of Streptococcus pneumoniae has been produced, purified and crystallized in a form suitable for X-ray diffraction analysis. The best crystals have been grown at 15 degrees C, from solutions containing 8% polyethylene glycol 10,000 at pH values ranging from 3.9 to 6.0. These crystals diffract to a resolution of 3.5 A and have a space group P6(1)22 (or enantiomorph) with unit cell dimensions of a = b = 162.2 A, c = 171.8 A, alpha = beta = 90 degrees, gamma = 120 degrees. The molecular mass and cell dimensions suggest that there is one molecule of enzyme per asymmetric unit. The breakdown of a chromogenic cephalosporin derivative diffused into a crystal reveals clearly that the enzyme is active in the crystalline state.
Assuntos
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Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 1993 Tipo de documento: Article
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Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 1993 Tipo de documento: Article