Literature DB >> 1548708

Crystallization and preliminary X-ray study of a lipase from Pseudomonas glumae.

A Cleasby1, E Garman, M R Egmond, M Batenburg.   

Abstract

Lipase from Pseudomonas glumae has been purified and crystallized in two forms, using the hanging drop method of vapour diffusion at 4 degrees C and 15 degrees C. Both forms grew at pH 9.0 from 0.1 M-Tris buffer in the presence of 10% (v/v) acetone. Form 1 was crystallized from 27 to 29% polyethylene glycol in the presence of less than 0.5% (v/v) n-dodecyl-beta-D-glucopyranoside. Form 2 was grown from 17 to 19% ammonium sulphate in the presence of 1% n-octyl-beta-D-glucopyranoside. Form 1 is orthorhombic with space group P2(1)2(1)2(1), and cell dimensions of a = 158.1 A, b = 158.6 A, c = 63.4 A, Form 2 is tetragonal with space group P4(1)2(1)2 (or P4(3)2(1)2) and cell dimensions of a = 89.3 A, c = 180.4 A. Form 1 probably has four molecules per asymmetric unit and diffracts to at least 2.5 A. Form 2 has two molecules per asymmetric unit and diffracts to at least 3.0 A.

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Year:  1992        PMID: 1548708     DOI: 10.1016/0022-2836(92)90593-9

Source DB:  PubMed          Journal:  J Mol Biol        ISSN: 0022-2836            Impact factor:   5.469


  2 in total

1.  Crystallization and crystal manipulation of a steric chaperone in complex with its lipase substrate.

Authors:  Kris Pauwels; Remy Loris; Guy Vandenbussche; Jean Marie Ruysschaert; Lode Wyns; Patrick Van Gelder
Journal:  Acta Crystallogr Sect F Struct Biol Cryst Commun       Date:  2005-07-30

2.  Cloning of the Pseudomonas glumae lipase gene and determination of the active site residues.

Authors:  L G Frenken; M R Egmond; A M Batenburg; J W Bos; C Visser; C T Verrips
Journal:  Appl Environ Microbiol       Date:  1992-12       Impact factor: 4.792

  2 in total

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