Literature DB >> 15103129

Structure determination of the extracellular xylanase from Geobacillus stearothermophilus by selenomethionyl MAD phasing.

A Teplitsky1, A Mechaly, V Stojanoff, G Sainz, G Golan, H Feinberg, R Gilboa, V Reiland, G Zolotnitsky, D Shallom, A Thompson, Y Shoham, G Shoham.   

Abstract

Xylanases are hemicellulases that hydrolyze the internal beta-1,4-glycoside bonds of xylan. The extracellular thermostable endo-1,4-beta-xylanase (EC 3.2.1.8; XT6) produced by the thermophilic bacterium Geobacillus stearothermophilus T-6 was shown to bleach pulp optimally at pH 9 and 338 K and was successfully used in a large-scale biobleaching mill trial. The xylanase gene was cloned and sequenced. The mature enzyme consists of 379 amino acids, with a calculated molecular weight of 43 808 Da and a pI of 9.0. Crystallographic studies of XT6 were performed in order to study the mechanism of catalysis and to provide a structural basis for the rational introduction of enhanced thermostability by site-specific mutagenesis. XT6 was crystallized in the primitive trigonal space group P3(2)21, with unit-cell parameters a = b = 112.9, c = 122.7 A. A full diffraction data set for wild-type XT6 has been measured to 2.4 A resolution on flash-frozen crystals using synchrotron radiation. A fully exchanged selenomethionyl XT6 derivative (containing eight Se atoms per XT6 molecule) was also prepared and crystallized in an isomorphous crystal form, providing full selenium MAD data at three wavelengths and enabling phase solution and structure determination. The structure of wild-type XT6 was refined at 2.4 A resolution to a final R factor of 15.6% and an R(free) of 18.6%. The structure demonstrates that XT6 is made up of an eightfold TIM-barrel containing a deep active-site groove, consistent with its 'endo' mode of action. The two essential catalytic carboxylic residues (Glu159 and Glu265) are located at the active site within 5.5 A of each other, as expected for 'retaining' glycoside hydrolases. A unique subdomain was identified in the carboxy-terminal part of the enzyme and was suggested to have a role in xylan binding. The three-dimensional structure of XT6 is of great interest since it provides a favourable starting point for the rational improvement of its already high thermal and pH stabilities, which are required for a number of biotechnological and industrial applications.

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Year:  2004        PMID: 15103129     DOI: 10.1107/S0907444904004123

Source DB:  PubMed          Journal:  Acta Crystallogr D Biol Crystallogr        ISSN: 0907-4449


  18 in total

1.  Mapping glycoside hydrolase substrate subsites by isothermal titration calorimetry.

Authors:  Gennady Zolotnitsky; Uri Cogan; Noam Adir; Vered Solomon; Gil Shoham; Yuval Shoham
Journal:  Proc Natl Acad Sci U S A       Date:  2004-07-26       Impact factor: 11.205

2.  A two-component system regulates the expression of an ABC transporter for xylo-oligosaccharides in Geobacillus stearothermophilus.

Authors:  Smadar Shulami; Galia Zaide; Gennady Zolotnitsky; Yael Langut; Geoff Feld; Abraham L Sonenshein; Yuval Shoham
Journal:  Appl Environ Microbiol       Date:  2006-12-01       Impact factor: 4.792

3.  Cloning, sequence analysis, and expression of a gene encoding an endoxylanase from Bacillus halodurans S7.

Authors:  Gashaw Mamo; Osvaldo Delgado; Alejandra Martinez; Bo Mattiasson; Rajni Hatti-Kaul
Journal:  Mol Biotechnol       Date:  2006-06       Impact factor: 2.695

4.  Crystallization and preliminary crystallographic analysis of a family 43 beta-D-xylosidase from Geobacillus stearothermophilus T-6.

Authors:  Christian Brüx; Karsten Niefind; Alon Ben-David; Maya Leon; Gil Shoham; Yuval Shoham; Dietmar Schomburg
Journal:  Acta Crystallogr Sect F Struct Biol Cryst Commun       Date:  2005-11-12

5.  Crystallization and preliminary X-ray crystallographic studies of XynX, a family 10 xylanase from Aeromonas punctata ME-1.

Authors:  Zui Fujimoto; Kengo Usui; Yukari Kondo; Kazumasa Yasui; Keiichi Kawai; Tohru Suzuki
Journal:  Acta Crystallogr Sect F Struct Biol Cryst Commun       Date:  2005-02-01

Review 6.  Thermostable enzymes as biocatalysts in the biofuel industry.

Authors:  Carl J Yeoman; Yejun Han; Dylan Dodd; Charles M Schroeder; Roderick I Mackie; Isaac K O Cann
Journal:  Adv Appl Microbiol       Date:  2010-03-06       Impact factor: 5.086

7.  Preliminary crystallographic analysis of Xyn52B2, a GH52 β-D-xylosidase from Geobacillus stearothermophilus T6.

Authors:  Roie Dann; Shifra Lansky; Noa Lavid; Arie Zehavi; Valery Belakhov; Timor Baasov; Hay Dvir; Babu Manjasetty; Hassan Belrhali; Yuval Shoham; Gil Shoham
Journal:  Acta Crystallogr F Struct Biol Commun       Date:  2014-11-28       Impact factor: 1.056

Review 8.  Genomics review of holocellulose deconstruction by aspergilli.

Authors:  Fernando Segato; André R L Damásio; Rosymar C de Lucas; Fabio M Squina; Rolf A Prade
Journal:  Microbiol Mol Biol Rev       Date:  2014-12       Impact factor: 11.056

9.  Cross-utilization of β-galactosides and cellobiose in Geobacillus stearothermophilus.

Authors:  Smadar Shulami; Arie Zehavi; Valery Belakhov; Rachel Salama; Shifra Lansky; Timor Baasov; Gil Shoham; Yuval Shoham
Journal:  J Biol Chem       Date:  2020-06-03       Impact factor: 5.157

10.  Purification, crystallization and preliminary crystallographic analysis of Gan1D, a GH1 6-phospho-β-galactosidase from Geobacillus stearothermophilus T1.

Authors:  Shifra Lansky; Arie Zehavi; Roie Dann; Hay Dvir; Hassan Belrhali; Yuval Shoham; Gil Shoham
Journal:  Acta Crystallogr F Struct Biol Commun       Date:  2014-01-21       Impact factor: 1.056

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