Literature DB >> 10660553

The multiple activities of polyphosphate kinase of Escherichia coli and their subunit structure determined by radiation target analysis.

C M Tzeng1, A Kornberg.   

Abstract

Polyphosphate kinase (PPK), the principal enzyme required for the synthesis of inorganic polyphosphate (polyP) from ATP, also exhibits other enzymatic activities, which differ significantly in their biochemical optima and responses to chemical agents. These several activities include: polyP synthesis (forward reaction), nATP --> polyP(n) + nADP (Equation 1); ATP synthesis from polyP (reverse reaction), ADP + polyP(n) --> ATP + polyP(n - 1) (Equation 2); general nucleoside-diphosphate kinase, GDP + polyP(n) --> GTP + polyP(n - 1) (Equation 3); linear guanosine 5'-tetraphosphate (ppppG) synthesis, GDP + polyP(n) --> ppppG + polyP(n - 2) (Equation 4); and autophosphorylation, PPK + ATP --> PPK-P + ADP (Equation 5). The Mg(2+) optima are 5, 2, 1, and 0.2 mM, respectively, for the activities in Equations 1, 2, 3, and 4. Inorganic pyrophosphate inhibits the activities in Equations 1 and 3 but stimulates that in Equation 4. The kinetics of the activities in Equations 1, 2, and 3 are highly processive, whereas the transfer of a pyrophosphoryl group from polyP to GDP (Equation 4) is distributive and demonstrates a rapid equilibrium, random Bi-Bi catalytic mechanism. Radiation target analysis revealed that the principal functional unit of the homotetrameric PPK is a dimer. Exceptions are a trimer for the synthesis of ppppG (Equation 4) and a tetrameric state for the autophosphorylation of PPK (Equation 5) at low ATP concentrations. Thus, the diverse functions of this enzyme involve different subunit organizations and conformations. The highly conserved homology of PPK among 18 microorganisms was used to determine important residues and conserved regions by alanine substitution, by site-directed mutagenesis, and by deletion mutagenesis. Of 46 single-site mutants, seven exhibit none of the five enzymatic activities; in one mutant, ATP synthesis from polyP is reduced relative to GTP synthesis. Among deletion mutants, some lost all five PPK activities, but others retained partial activity for some reactions but not for others.

Entities:  

Mesh:

Substances:

Year:  2000        PMID: 10660553     DOI: 10.1074/jbc.275.6.3977

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  14 in total

1.  Mutations in Escherichia coli Polyphosphate Kinase That Lead to Dramatically Increased In Vivo Polyphosphate Levels.

Authors:  Amanda K Rudat; Arya Pokhrel; Todd J Green; Michael J Gray
Journal:  J Bacteriol       Date:  2018-02-23       Impact factor: 3.490

Review 2.  Model systems for studying polyphosphate biology: a focus on microorganisms.

Authors:  Alix Denoncourt; Michael Downey
Journal:  Curr Genet       Date:  2021-01-09       Impact factor: 3.886

3.  PAS-A domain of phosphorelay sensor kinase A: a catalytic ATP-binding domain involved in the initiation of development in Bacillus subtilis.

Authors:  K Stephenson; J A Hoch
Journal:  Proc Natl Acad Sci U S A       Date:  2001-12-04       Impact factor: 11.205

4.  The glycogen-bound polyphosphate kinase from Sulfolobus acidocaldarius is actually a glycogen synthase.

Authors:  S Cardona; F Remonsellez; N Guiliani; C A Jerez
Journal:  Appl Environ Microbiol       Date:  2001-10       Impact factor: 4.792

5.  Regulation of ppk expression and in vivo function of Ppk in Streptomyces lividans TK24.

Authors:  Sofiane Ghorbel; Aleksey Smirnov; Hichem Chouayekh; Brice Sperandio; Catherine Esnault; Jan Kormanec; Marie-Joelle Virolle
Journal:  J Bacteriol       Date:  2006-09       Impact factor: 3.490

6.  Inorganic polyphosphate in Vibrio cholerae: genetic, biochemical, and physiologic features.

Authors:  N Ogawa; C M Tzeng; C D Fraley; A Kornberg
Journal:  J Bacteriol       Date:  2000-12       Impact factor: 3.490

7.  Polyphosphatase activity of CthTTM, a bacterial triphosphate tunnel metalloenzyme.

Authors:  Ruchi Jain; Stewart Shuman
Journal:  J Biol Chem       Date:  2008-09-08       Impact factor: 5.157

Review 8.  Inorganic polyphosphate in the microbial world. Emerging roles for a multifaceted biopolymer.

Authors:  Tomás Albi; Aurelio Serrano
Journal:  World J Microbiol Biotechnol       Date:  2016-01-09       Impact factor: 3.312

9.  Role of polyphosphate kinase in biofilm formation by Porphyromonas gingivalis.

Authors:  Wen Chen; Robert J Palmer; Howard K Kuramitsu
Journal:  Infect Immun       Date:  2002-08       Impact factor: 3.441

10.  A polyphosphate kinase 1 (ppk1) mutant of Pseudomonas aeruginosa exhibits multiple ultrastructural and functional defects.

Authors:  Cresson D Fraley; M Harunur Rashid; Sam S K Lee; Rebecca Gottschalk; Janine Harrison; Pauline J Wood; Michael R W Brown; Arthur Kornberg
Journal:  Proc Natl Acad Sci U S A       Date:  2007-02-22       Impact factor: 11.205

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.