Literature DB >> 22369488

Purification of polyhydroxybutyrate synthase from its native organism, Ralstonia eutropha: implications for the initiation and elongation of polymer formation in vivo.

Mimi Cho1, Christopher J Brigham, Anthony J Sinskey, JoAnne Stubbe.   

Abstract

Class I polyhydroxybutyrate (PHB) synthase (PhaC) from Ralstonia eutropha catalyzes the formation of PHB from (R)-3-hydroxybutyryl-CoA, ultimately resulting in the formation of insoluble granules. Previous mechanistic studies of R. eutropha PhaC, purified from Escherichia coli (PhaC(Ec)), demonstrated that the polymer elongation rate is much faster than the initiation rate. In an effort to identify a factor(s) from the native organism that might prime the synthase and increase the rate of polymer initiation, an N-terminally Strep2-tagged phaC (Strep2-PhaC(Re)) was constructed and integrated into the R. eutropha genome in place of wild-type phaC. Strep2-PhaC(Re) was expressed and purified by affinity chromatography from R. eutropha grown in nutrient-rich TSB medium for 4 h (peak production PHB, 15% cell dry weight) and 24 h (PHB, 2% cell dry weight). Analysis of the purified PhaC by size exclusion chromatography, sodium dodecyl sulfate-polyacrylamide gel electrophoresis, and gel permeation chromatography revealed that it unexpectedly copurified with the phasin protein, PhaP1, and with soluble PHB (M(w) = 350 kDa) in a "high-molecular weight" (HMW) complex and in monomeric/dimeric (M/D) forms with no associated PhaP1 or PHB. Assays for monitoring the formation of PHB in the HMW complex showed no lag phase in CoA release, in contrast to M/D forms of PhaC(Re) (and PhaC(Ec)), suggesting that PhaC in the HMW fraction has been isolated in a PHB-primed form. The presence of primed and nonprimed PhaC suggests that the elongation rate for PHB formation is also faster than the initiation rate in vivo. A modified micelle model for granule genesis is proposed to accommodate the reported observations.

Entities:  

Mesh:

Substances:

Year:  2012        PMID: 22369488      PMCID: PMC3326396          DOI: 10.1021/bi2013596

Source DB:  PubMed          Journal:  Biochemistry        ISSN: 0006-2960            Impact factor:   3.162


  51 in total

1.  Class I and III polyhydroxyalkanoate synthases from Ralstonia eutropha and Allochromatium vinosum: characterization and substrate specificity studies.

Authors:  W Yuan; Y Jia; J Tian; K D Snell; U Müh; A J Sinskey; R H Lambalot; C T Walsh; J Stubbe
Journal:  Arch Biochem Biophys       Date:  2001-10-01       Impact factor: 4.013

2.  Roles of multiple acetoacetyl coenzyme A reductases in polyhydroxybutyrate biosynthesis in Ralstonia eutropha H16.

Authors:  Charles F Budde; Alison E Mahan; Jingnan Lu; Chokyun Rha; Anthony J Sinskey
Journal:  J Bacteriol       Date:  2010-08-20       Impact factor: 3.490

3.  Chaperones specific for the membrane-bound [NiFe]-hydrogenase interact with the Tat signal peptide of the small subunit precursor in Ralstonia eutropha H16.

Authors:  Torsten Schubert; Oliver Lenz; Eberhard Krause; Rudolf Volkmer; Bärbel Friedrich
Journal:  Mol Microbiol       Date:  2007-09-10       Impact factor: 3.501

4.  PHA synthase activity controls the molecular weight and polydispersity of polyhydroxybutyrate in vivo.

Authors:  S J Sim; K D Snell; S A Hogan; J Stubbe; C Rha; A J Sinskey
Journal:  Nat Biotechnol       Date:  1997-01       Impact factor: 54.908

5.  Metabolism of poly-beta-hydroxybutyrate. I. Purification, composition, and properties of native poly-beta-hydroxybutyrate granules from Bacillus megaterium.

Authors:  R Griebel; Z Smith; J M Merrick
Journal:  Biochemistry       Date:  1968-10       Impact factor: 3.162

6.  Oleosin is bifunctional enzyme that has both monoacylglycerol acyltransferase and phospholipase activities.

Authors:  Velayoudame Parthibane; Sona Rajakumari; Varadarajan Venkateshwari; Ramachandiran Iyappan; Ram Rajasekharan
Journal:  J Biol Chem       Date:  2011-11-29       Impact factor: 5.157

7.  Overexpression and purification of the soluble polyhydroxyalkanoate synthase from Alcaligenes eutrophus: evidence for a required posttranslational modification for catalytic activity.

Authors:  T U Gerngross; K D Snell; O P Peoples; A J Sinskey; E Csuhai; S Masamune; J Stubbe
Journal:  Biochemistry       Date:  1994-08-09       Impact factor: 3.162

8.  Poly(hydroxyalkanoic acid) Biosynthesis in Ectothiorhodospirashaposhnikovii: Characterization and Reactivity of a Type III PHA Synthase.

Authors:  Shiming Zhang; Steven Kolvek; Steve Goodwin; Robert W Lenz
Journal:  Biomacromolecules       Date:  2004 Jan-Feb       Impact factor: 6.988

9.  Ralstonia eutropha H16 encodes two and possibly three intracellular Poly[D-(-)-3-hydroxybutyrate] depolymerase genes.

Authors:  Gregory M York; Joachim Lupberger; Jiamin Tian; Adam G Lawrence; JoAnne Stubbe; Anthony J Sinskey
Journal:  J Bacteriol       Date:  2003-07       Impact factor: 3.490

10.  Purification and characterization of the poly(hydroxyalkanoic acid) synthase from Chromatium vinosum and localization of the enzyme at the surface of poly(hydroxyalkanoic acid) granules.

Authors:  M Liebergesell; K Sonomoto; M Madkour; F Mayer; A Steinbüchel
Journal:  Eur J Biochem       Date:  1994-11-15
View more
  15 in total

1.  Development of a transferable bimolecular fluorescence complementation system for the investigation of interactions between poly(3-hydroxybutyrate) granule-associated proteins in Gram-negative bacteria.

Authors:  Daniel Pfeiffer; Dieter Jendrossek
Journal:  Appl Environ Microbiol       Date:  2013-02-22       Impact factor: 4.792

2.  Comparative proteome analysis reveals four novel polyhydroxybutyrate (PHB) granule-associated proteins in Ralstonia eutropha H16.

Authors:  Anna Sznajder; Daniel Pfeiffer; Dieter Jendrossek
Journal:  Appl Environ Microbiol       Date:  2014-12-29       Impact factor: 4.792

3.  Trapping of intermediates with substrate analog HBOCoA in the polymerizations catalyzed by class III polyhydroxybutyrate (PHB) synthase from Allochromatium vinosum.

Authors:  Chao Chen; Ruikai Cao; Ruben Shrestha; Christina Ward; Benjamin B Katz; Christopher J Fischer; John M Tomich; Ping Li
Journal:  ACS Chem Biol       Date:  2015-02-25       Impact factor: 5.100

4.  New Insights into PhaM-PhaC-Mediated Localization of Polyhydroxybutyrate Granules in Ralstonia eutropha H16.

Authors:  Stephanie Bresan; Dieter Jendrossek
Journal:  Appl Environ Microbiol       Date:  2017-05-31       Impact factor: 4.792

5.  Phasin proteins activate Aeromonas caviae polyhydroxyalkanoate (PHA) synthase but not Ralstonia eutropha PHA synthase.

Authors:  Kazunori Ushimaru; Yoko Motoda; Keiji Numata; Takeharu Tsuge
Journal:  Appl Environ Microbiol       Date:  2014-02-28       Impact factor: 4.792

6.  PhaM is the physiological activator of poly(3-hydroxybutyrate) (PHB) synthase (PhaC1) in Ralstonia eutropha.

Authors:  Daniel Pfeiffer; Dieter Jendrossek
Journal:  Appl Environ Microbiol       Date:  2013-11-08       Impact factor: 4.792

7.  Study of Class I and Class III Polyhydroxyalkanoate (PHA) Synthases with Substrates Containing a Modified Side Chain.

Authors:  Kaimin Jia; Ruikai Cao; Duy H Hua; Ping Li
Journal:  Biomacromolecules       Date:  2016-03-22       Impact factor: 6.988

8.  Whole-genome microarray and gene deletion studies reveal regulation of the polyhydroxyalkanoate production cycle by the stringent response in Ralstonia eutropha H16.

Authors:  Christopher J Brigham; Daan R Speth; ChoKyun Rha; Anthony J Sinskey
Journal:  Appl Environ Microbiol       Date:  2012-09-07       Impact factor: 4.792

9.  Localization of poly(3-hydroxybutyrate) (PHB) granule-associated proteins during PHB granule formation and identification of two new phasins, PhaP6 and PhaP7, in Ralstonia eutropha H16.

Authors:  Daniel Pfeiffer; Dieter Jendrossek
Journal:  J Bacteriol       Date:  2012-08-24       Impact factor: 3.490

10.  PHB granules are attached to the nucleoid via PhaM in Ralstonia eutropha.

Authors:  Andreas Wahl; Nora Schuth; Daniel Pfeiffer; Stephan Nussberger; Dieter Jendrossek
Journal:  BMC Microbiol       Date:  2012-11-16       Impact factor: 3.605

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.