Literature DB >> 17318541

Peculiarities of PHA granules preparation and PHA depolymerase activity determination.

Dieter Jendrossek1.   

Abstract

An extensive amount of knowledge on biochemistry of poly(3-hydroxyalkanoic acid) (PHA) synthesis and on its biodegradation has accumulated during the last two decades. Numerous genes encoding enzymes involved in the formation of PHA and in PHA degradation (PHA depolymerases) were cloned and characterized from many microorganisms. A large variety of methods exists for determination of PHA depolymerase activity and for preparation of the polymeric substrate (PHA). Unfortunately, results obtained with these different methods cannot be compared directly because they highly depend on the assay method applied and on the history of PHA granules preparation. In this contribution, the peculiarities, advantages, disadvantages and limitations of existing PHA depolymerase assay methods are described.

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Year:  2007        PMID: 17318541     DOI: 10.1007/s00253-007-0860-9

Source DB:  PubMed          Journal:  Appl Microbiol Biotechnol        ISSN: 0175-7598            Impact factor:   4.813


  16 in total

1.  Poly(3-hydroxybutyrate) (PHB) depolymerase PhaZa1 is involved in mobilization of accumulated PHB in Ralstonia eutropha H16.

Authors:  Keiichi Uchino; Terumi Saito; Dieter Jendrossek
Journal:  Appl Environ Microbiol       Date:  2007-12-21       Impact factor: 4.792

Review 2.  Polyhydroxyalkanoate granules are complex subcellular organelles (carbonosomes).

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

3.  Identification and characterization of a novel intracellular poly(3-hydroxybutyrate) depolymerase from Bacillus megaterium.

Authors:  Hui-Ju Chen; Shih-Chuan Pan; Gwo-Chyuan Shaw
Journal:  Appl Environ Microbiol       Date:  2009-06-26       Impact factor: 4.792

4.  Identification and characterization of a novel class of extracellular poly(3-hydroxybutyrate) depolymerase from Bacillus sp. strain NRRL B-14911.

Authors:  Wan-Ting Ma; Ju-Hui Lin; Hui-Ju Chen; Syuan-Yi Chen; Gwo-Chyuan Shaw
Journal:  Appl Environ Microbiol       Date:  2011-09-23       Impact factor: 4.792

5.  To be or not to be a poly(3-hydroxybutyrate) (PHB) depolymerase: PhaZd1 (PhaZ6) and PhaZd2 (PhaZ7) of Ralstonia eutropha, highly active PHB depolymerases with no detectable role in mobilization of accumulated PHB.

Authors:  Anna Sznajder; Dieter Jendrossek
Journal:  Appl Environ Microbiol       Date:  2014-06-06       Impact factor: 4.792

6.  Characterization of a novel immobilized biocatalyst obtained by matrix-assisted refolding of recombinant polyhydroxyoctanoate depolymerase from Pseudomonas putida KT2442 isolated from inclusion bodies.

Authors:  M Arroyo; J García-Hidalgo; M Villalón; L de Eugenio; D Hormigo; C Acebal; J L García; M A Prieto; Isabel de la Mata
Journal:  J Ind Microbiol Biotechnol       Date:  2010-11-20       Impact factor: 3.346

7.  Absence of ppGpp Leads to Increased Mobilization of Intermediately Accumulated Poly(3-Hydroxybutyrate) in Ralstonia eutropha H16.

Authors:  Janina R Juengert; Marina Borisova; Christoph Mayer; Christiane Wolz; Christopher J Brigham; Anthony J Sinskey; Dieter Jendrossek
Journal:  Appl Environ Microbiol       Date:  2017-06-16       Impact factor: 4.792

8.  Isolated poly(3-hydroxybutyrate) (PHB) granules are complex bacterial organelles catalyzing formation of PHB from acetyl coenzyme A (CoA) and degradation of PHB to acetyl-CoA.

Authors:  Keiichi Uchino; Terumi Saito; Birgit Gebauer; Dieter Jendrossek
Journal:  J Bacteriol       Date:  2007-08-24       Impact factor: 3.490

9.  Impact of Ralstonia eutropha's poly(3-Hydroxybutyrate) (PHB) Depolymerases and Phasins on PHB storage in recombinant Escherichia coli.

Authors:  Jessica Eggers; Alexander Steinbüchel
Journal:  Appl Environ Microbiol       Date:  2014-10-03       Impact factor: 4.792

10.  Poly(3-hydroxybutyrate) degradation in Ralstonia eutropha H16 is mediated stereoselectively to (S)-3-hydroxybutyryl coenzyme A (CoA) via crotonyl-CoA.

Authors:  Jessica Eggers; Alexander Steinbüchel
Journal:  J Bacteriol       Date:  2013-05-10       Impact factor: 3.490

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