Literature DB >> 25286954

Crystallization and preliminary crystallographic analysis of poly(3-hydroxybutyrate) depolymerase from Bacillus thuringiensis.

Yung Lin Wang1, Yi Ting Lin2, Chia Lin Chen1, Gwo Chyuan Shaw1, Shwu Huey Liaw1.   

Abstract

Poly[(R)-3-hydroxybutyrate] (PHB) is a microbial biopolymer that has been commercialized as biodegradable plastics. The key enzyme for the degradation is PHB depolymerase (PhaZ). A new intracellular PhaZ from Bacillus thuringiensis (BtPhaZ) has been screened for potential applications in polymer biodegradation. Recombinant BtPhaZ was crystallized using 25% polyethylene glycol 3350, 0.2 M ammonium acetate, 0.1 M bis-tris pH 6.5 at 288 K. The crystals belonged to space group P1, with unit-cell parameters a = 42.97, b = 83.23, c = 85.50 Å, α = 73.45, β = 82.83, γ = 83.49°. An X-ray diffraction data set was collected to 1.42 Å resolution with an Rmerge of 6.4%. Unexpectedly, a molecular-replacement solution was obtained using the crystal structure of Streptomyces lividans chloroperoxidase as a template, which shares 24% sequence identity to BtPhaZ. This is the first crystal structure of an intracellular poly(3-hydroxybutyrate) depolymerase.

Entities:  

Keywords:  Bacillus thuringiensis; PhaZ; depolymerase; poly(3-hydroxybutyrate)

Mesh:

Substances:

Year:  2014        PMID: 25286954      PMCID: PMC4188094          DOI: 10.1107/S2053230X14019347

Source DB:  PubMed          Journal:  Acta Crystallogr F Struct Biol Commun        ISSN: 2053-230X            Impact factor:   1.056


  18 in total

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Authors:  Robert Schwarzenbacher; Adam Godzik; Slawomir K Grzechnik; Lukasz Jaroszewski
Journal:  Acta Crystallogr D Biol Crystallogr       Date:  2004-06-22

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Review 3.  Polyhydroxyalkanoate granules are complex subcellular organelles (carbonosomes).

Authors:  Dieter Jendrossek
Journal:  J Bacteriol       Date:  2009-03-06       Impact factor: 3.490

4.  Biochemical analysis and structure determination of Paucimonas lemoignei poly(3-hydroxybutyrate) (PHB) depolymerase PhaZ7 muteins reveal the PHB binding site and details of substrate-enzyme interactions.

Authors:  Dieter Jendrossek; Siska Hermawan; Bishwa Subedi; Anastassios C Papageorgiou
Journal:  Mol Microbiol       Date:  2013-09-30       Impact factor: 3.501

5.  Identification and characterization of the Bacillus thuringiensis phaZ gene, encoding new intracellular poly-3-hydroxybutyrate depolymerase.

Authors:  Chi-Ling Tseng; Hui-Ju Chen; Gwo-Chyuan Shaw
Journal:  J Bacteriol       Date:  2006-08-25       Impact factor: 3.490

6.  Solvent content of protein crystals.

Authors:  B W Matthews
Journal:  J Mol Biol       Date:  1968-04-28       Impact factor: 5.469

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Journal:  Microbiol Rev       Date:  1990-12

8.  The structure of PhaZ7 at atomic (1.2 A) resolution reveals details of the active site and suggests a substrate-binding mode.

Authors:  Sachin Wakadkar; Siska Hermawan; Dieter Jendrossek; Anastassios C Papageorgiou
Journal:  Acta Crystallogr Sect F Struct Biol Cryst Commun       Date:  2010-05-25

9.  Structural basis of poly(3-hydroxybutyrate) hydrolysis by PhaZ7 depolymerase from Paucimonas lemoignei.

Authors:  Anastassios C Papageorgiou; Siska Hermawan; Chouhan Bhanupratap Singh; Dieter Jendrossek
Journal:  J Mol Biol       Date:  2008-08-05       Impact factor: 5.469

10.  The PHA Depolymerase Engineering Database: A systematic analysis tool for the diverse family of polyhydroxyalkanoate (PHA) depolymerases.

Authors:  Michael Knoll; Thomas M Hamm; Florian Wagner; Virginia Martinez; Jürgen Pleiss
Journal:  BMC Bioinformatics       Date:  2009-03-18       Impact factor: 3.169

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  1 in total

1.  Poly-β-hydroxybutyrate Metabolism Is Unrelated to the Sporulation and Parasporal Crystal Protein Formation in Bacillus thuringiensis.

Authors:  Xun Wang; Zhou Li; Xin Li; Hongliang Qian; Xia Cai; Xinfeng Li; Jin He
Journal:  Front Microbiol       Date:  2016-06-15       Impact factor: 5.640

  1 in total

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