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

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 synthesi...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:The Journal of biological chemistry 2000-02, Vol.275 (6), p.3977-3983
Hauptverfasser: Tzeng, C M, Kornberg, A
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 3983
container_issue 6
container_start_page 3977
container_title The Journal of biological chemistry
container_volume 275
creator Tzeng, C M
Kornberg, A
description 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.
doi_str_mv 10.1074/jbc.275.6.3977
format Article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_proquest_miscellaneous_17464819</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>17464819</sourcerecordid><originalsourceid>FETCH-LOGICAL-p238t-cac395c2207391ca4c180618c308b36399b5939a66911868e843947c0f51a2e93</originalsourceid><addsrcrecordid>eNo1kD1PwzAYhD2AaCmsjMgTW4IdJ449oqp8SJVYyhy9cd4Sl3zhD6T8Av42VJRbTjo9d8MRcsNZylmZ3x9qk2ZlkcpU6LI8I0vGMp7orFALcun9gf0q1_yCLDiTkhWFWJLvXYu0j12wU4cUTLBfNlj0dNzTaezmqR391EJA-mEH8HjMN9606KxpLVAzdpbC0NDQonXUxzoONlAfXDQhOqQNBnS9HbCh9UwdNBaCHQcawL1j-K1CN3vrr8j5HjqP1ydfkbfHzW79nGxfn17WD9tkyoQKiQEjdGGyjJVCcwO54YpJroxgqhZSaF0XWmiQUnOupEKVC52Xhu0LDhlqsSJ3f7uTGz8j-lD11hvsOhhwjL7iZS5zxY_g7QmMdY9NNTnbg5ur_-vED-cPcMs</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>17464819</pqid></control><display><type>article</type><title>The multiple activities of polyphosphate kinase of Escherichia coli and their subunit structure determined by radiation target analysis</title><source>MEDLINE</source><source>EZB-FREE-00999 freely available EZB journals</source><source>Alma/SFX Local Collection</source><creator>Tzeng, C M ; Kornberg, A</creator><creatorcontrib>Tzeng, C M ; Kornberg, A</creatorcontrib><description>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 --&gt; polyP(n) + nADP (Equation 1); ATP synthesis from polyP (reverse reaction), ADP + polyP(n) --&gt; ATP + polyP(n - 1) (Equation 2); general nucleoside-diphosphate kinase, GDP + polyP(n) --&gt; GTP + polyP(n - 1) (Equation 3); linear guanosine 5'-tetraphosphate (ppppG) synthesis, GDP + polyP(n) --&gt; ppppG + polyP(n - 2) (Equation 4); and autophosphorylation, PPK + ATP --&gt; 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.</description><identifier>ISSN: 0021-9258</identifier><identifier>DOI: 10.1074/jbc.275.6.3977</identifier><identifier>PMID: 10660553</identifier><language>eng</language><publisher>United States</publisher><subject>Amino Acid Sequence ; Bacterial Proteins - chemistry ; Diphosphates - pharmacology ; Enzyme Inhibitors - pharmacology ; Escherichia coli ; Escherichia coli - enzymology ; Gamma Rays ; Guanidine - pharmacology ; Guanosine Tetraphosphate - biosynthesis ; Kinetics ; Magnesium - pharmacology ; Molecular Sequence Data ; Mutation ; Nucleotides - metabolism ; Phosphorylation - radiation effects ; Phosphotransferases (Phosphate Group Acceptor) - chemistry ; Phosphotransferases (Phosphate Group Acceptor) - metabolism ; Phosphotransferases (Phosphate Group Acceptor) - radiation effects ; Polyphosphates - metabolism ; Protein Conformation ; Sequence Alignment</subject><ispartof>The Journal of biological chemistry, 2000-02, Vol.275 (6), p.3977-3983</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10660553$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tzeng, C M</creatorcontrib><creatorcontrib>Kornberg, A</creatorcontrib><title>The multiple activities of polyphosphate kinase of Escherichia coli and their subunit structure determined by radiation target analysis</title><title>The Journal of biological chemistry</title><addtitle>J Biol Chem</addtitle><description>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 --&gt; polyP(n) + nADP (Equation 1); ATP synthesis from polyP (reverse reaction), ADP + polyP(n) --&gt; ATP + polyP(n - 1) (Equation 2); general nucleoside-diphosphate kinase, GDP + polyP(n) --&gt; GTP + polyP(n - 1) (Equation 3); linear guanosine 5'-tetraphosphate (ppppG) synthesis, GDP + polyP(n) --&gt; ppppG + polyP(n - 2) (Equation 4); and autophosphorylation, PPK + ATP --&gt; 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.</description><subject>Amino Acid Sequence</subject><subject>Bacterial Proteins - chemistry</subject><subject>Diphosphates - pharmacology</subject><subject>Enzyme Inhibitors - pharmacology</subject><subject>Escherichia coli</subject><subject>Escherichia coli - enzymology</subject><subject>Gamma Rays</subject><subject>Guanidine - pharmacology</subject><subject>Guanosine Tetraphosphate - biosynthesis</subject><subject>Kinetics</subject><subject>Magnesium - pharmacology</subject><subject>Molecular Sequence Data</subject><subject>Mutation</subject><subject>Nucleotides - metabolism</subject><subject>Phosphorylation - radiation effects</subject><subject>Phosphotransferases (Phosphate Group Acceptor) - chemistry</subject><subject>Phosphotransferases (Phosphate Group Acceptor) - metabolism</subject><subject>Phosphotransferases (Phosphate Group Acceptor) - radiation effects</subject><subject>Polyphosphates - metabolism</subject><subject>Protein Conformation</subject><subject>Sequence Alignment</subject><issn>0021-9258</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo1kD1PwzAYhD2AaCmsjMgTW4IdJ449oqp8SJVYyhy9cd4Sl3zhD6T8Av42VJRbTjo9d8MRcsNZylmZ3x9qk2ZlkcpU6LI8I0vGMp7orFALcun9gf0q1_yCLDiTkhWFWJLvXYu0j12wU4cUTLBfNlj0dNzTaezmqR391EJA-mEH8HjMN9606KxpLVAzdpbC0NDQonXUxzoONlAfXDQhOqQNBnS9HbCh9UwdNBaCHQcawL1j-K1CN3vrr8j5HjqP1ydfkbfHzW79nGxfn17WD9tkyoQKiQEjdGGyjJVCcwO54YpJroxgqhZSaF0XWmiQUnOupEKVC52Xhu0LDhlqsSJ3f7uTGz8j-lD11hvsOhhwjL7iZS5zxY_g7QmMdY9NNTnbg5ur_-vED-cPcMs</recordid><startdate>20000211</startdate><enddate>20000211</enddate><creator>Tzeng, C M</creator><creator>Kornberg, A</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7QL</scope><scope>C1K</scope></search><sort><creationdate>20000211</creationdate><title>The multiple activities of polyphosphate kinase of Escherichia coli and their subunit structure determined by radiation target analysis</title><author>Tzeng, C M ; Kornberg, A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p238t-cac395c2207391ca4c180618c308b36399b5939a66911868e843947c0f51a2e93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>Amino Acid Sequence</topic><topic>Bacterial Proteins - chemistry</topic><topic>Diphosphates - pharmacology</topic><topic>Enzyme Inhibitors - pharmacology</topic><topic>Escherichia coli</topic><topic>Escherichia coli - enzymology</topic><topic>Gamma Rays</topic><topic>Guanidine - pharmacology</topic><topic>Guanosine Tetraphosphate - biosynthesis</topic><topic>Kinetics</topic><topic>Magnesium - pharmacology</topic><topic>Molecular Sequence Data</topic><topic>Mutation</topic><topic>Nucleotides - metabolism</topic><topic>Phosphorylation - radiation effects</topic><topic>Phosphotransferases (Phosphate Group Acceptor) - chemistry</topic><topic>Phosphotransferases (Phosphate Group Acceptor) - metabolism</topic><topic>Phosphotransferases (Phosphate Group Acceptor) - radiation effects</topic><topic>Polyphosphates - metabolism</topic><topic>Protein Conformation</topic><topic>Sequence Alignment</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tzeng, C M</creatorcontrib><creatorcontrib>Kornberg, A</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Environmental Sciences and Pollution Management</collection><jtitle>The Journal of biological chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tzeng, C M</au><au>Kornberg, A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The multiple activities of polyphosphate kinase of Escherichia coli and their subunit structure determined by radiation target analysis</atitle><jtitle>The Journal of biological chemistry</jtitle><addtitle>J Biol Chem</addtitle><date>2000-02-11</date><risdate>2000</risdate><volume>275</volume><issue>6</issue><spage>3977</spage><epage>3983</epage><pages>3977-3983</pages><issn>0021-9258</issn><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 --&gt; polyP(n) + nADP (Equation 1); ATP synthesis from polyP (reverse reaction), ADP + polyP(n) --&gt; ATP + polyP(n - 1) (Equation 2); general nucleoside-diphosphate kinase, GDP + polyP(n) --&gt; GTP + polyP(n - 1) (Equation 3); linear guanosine 5'-tetraphosphate (ppppG) synthesis, GDP + polyP(n) --&gt; ppppG + polyP(n - 2) (Equation 4); and autophosphorylation, PPK + ATP --&gt; 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.</abstract><cop>United States</cop><pmid>10660553</pmid><doi>10.1074/jbc.275.6.3977</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0021-9258
ispartof The Journal of biological chemistry, 2000-02, Vol.275 (6), p.3977-3983
issn 0021-9258
language eng
recordid cdi_proquest_miscellaneous_17464819
source MEDLINE; EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection
subjects Amino Acid Sequence
Bacterial Proteins - chemistry
Diphosphates - pharmacology
Enzyme Inhibitors - pharmacology
Escherichia coli
Escherichia coli - enzymology
Gamma Rays
Guanidine - pharmacology
Guanosine Tetraphosphate - biosynthesis
Kinetics
Magnesium - pharmacology
Molecular Sequence Data
Mutation
Nucleotides - metabolism
Phosphorylation - radiation effects
Phosphotransferases (Phosphate Group Acceptor) - chemistry
Phosphotransferases (Phosphate Group Acceptor) - metabolism
Phosphotransferases (Phosphate Group Acceptor) - radiation effects
Polyphosphates - metabolism
Protein Conformation
Sequence Alignment
title The multiple activities of polyphosphate kinase of Escherichia coli and their subunit structure determined by radiation target analysis
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-21T11%3A41%3A13IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=The%20multiple%20activities%20of%20polyphosphate%20kinase%20of%20Escherichia%20coli%20and%20their%20subunit%20structure%20determined%20by%20radiation%20target%20analysis&rft.jtitle=The%20Journal%20of%20biological%20chemistry&rft.au=Tzeng,%20C%20M&rft.date=2000-02-11&rft.volume=275&rft.issue=6&rft.spage=3977&rft.epage=3983&rft.pages=3977-3983&rft.issn=0021-9258&rft_id=info:doi/10.1074/jbc.275.6.3977&rft_dat=%3Cproquest_pubme%3E17464819%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=17464819&rft_id=info:pmid/10660553&rfr_iscdi=true