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Nucleotide sequence and analysis of the Vibrio alginolyticus sucrose uptake-encoding region

Identifieur interne : 003682 ( Istex/Corpus ); précédent : 003681; suivant : 003683

Nucleotide sequence and analysis of the Vibrio alginolyticus sucrose uptake-encoding region

Auteurs : Gregory L. Blatch ; Renate R. Scholle ; David R. Woods

Source :

RBID : ISTEX:43C3427E988CA1CBF881954A89E28C53F7D120D6

Abstract

The nucleotide sequence of the Vibrio alginolyticus sucrose uptake-encoding region was determined, and contained two genes, scrA and scrK. The scrA gene encodes an enzyme IISucrose (EIIScr) protein of the phosphoenolpyruvate dependent phosphotransferase system and the scrK gene encodes a fructokinase. The deduced amino acid (aa)_sequence for the V. alginolyticus EIIScr protein was homologous with the EIIScr protein from Streptococcus mutants, Salmonella typhimurium (pUR400 system) and Bacillus subtilis. The deduced aa sequence for the V. alginolyticus fructokinase was homologous with the Escherichia coli enzymes, 6-phosphofructokinase (isoenzyme 2) and ribokinase. Transposon phoA mutagenesis experiments indicated that the EIIScr protein was a membrane-bound protein with a region that extended into the periplasm.

Url:
DOI: 10.1016/0378-1119(90)90408-J

Links to Exploration step

ISTEX:43C3427E988CA1CBF881954A89E28C53F7D120D6

Le document en format XML

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<div type="abstract" xml:lang="en">The nucleotide sequence of the Vibrio alginolyticus sucrose uptake-encoding region was determined, and contained two genes, scrA and scrK. The scrA gene encodes an enzyme IISucrose (EIIScr) protein of the phosphoenolpyruvate dependent phosphotransferase system and the scrK gene encodes a fructokinase. The deduced amino acid (aa)_sequence for the V. alginolyticus EIIScr protein was homologous with the EIIScr protein from Streptococcus mutants, Salmonella typhimurium (pUR400 system) and Bacillus subtilis. The deduced aa sequence for the V. alginolyticus fructokinase was homologous with the Escherichia coli enzymes, 6-phosphofructokinase (isoenzyme 2) and ribokinase. Transposon phoA mutagenesis experiments indicated that the EIIScr protein was a membrane-bound protein with a region that extended into the periplasm.</div>
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<term>enzyme IISucrose</term>
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<item>
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<term>PTS</term>
<term>phosphotransferase system</term>
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<term>V. alginolyticus sucrose uptake-encoding gene</term>
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<term>V. alginolyticus fructokinase-encoding gene</term>
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<ce:section-title>Abstract</ce:section-title>
<ce:abstract-sec>
<ce:simple-para id="SP0005">The nucleotide sequence of the
<ce:italic>Vibrio alginolyticus</ce:italic>
sucrose uptake-encoding region was determined, and contained two genes,
<ce:italic>scrA</ce:italic>
and
<ce:italic>scrK</ce:italic>
. The
<ce:italic>scrA</ce:italic>
gene encodes an enzyme II
<ce:sup>Sucrose</ce:sup>
(EII
<ce:sup>Scr</ce:sup>
) protein of the phosphoenolpyruvate dependent phosphotransferase system and the
<ce:italic>scrK</ce:italic>
gene encodes a fructokinase. The deduced amino acid (aa)_sequence for the
<ce:italic>V. alginolyticus</ce:italic>
EII
<ce:sup>Scr</ce:sup>
protein was homologous with the EII
<ce:sup>Scr</ce:sup>
protein from
<ce:italic>Streptococcus mutants, Salmonella typhimurium</ce:italic>
(pUR400 system) and
<ce:italic>Bacillus subtilis</ce:italic>
. The deduced aa sequence for the
<ce:italic>V. alginolyticus</ce:italic>
fructokinase was homologous with the
<ce:italic>Escherichia coli</ce:italic>
enzymes, 6-phosphofructokinase (isoenzyme 2) and ribokinase. Transposon
<ce:italic>phoA</ce:italic>
mutagenesis experiments indicated that the EII
<ce:sup>Scr</ce:sup>
protein was a membrane-bound protein with a region that extended into the periplasm.</ce:simple-para>
</ce:abstract-sec>
</ce:abstract>
<ce:keywords>
<ce:section-title>Keywords</ce:section-title>
<ce:keyword>
<ce:text>
<ce:italic>Bacillus subtilis</ce:italic>
</ce:text>
</ce:keyword>
<ce:keyword>
<ce:text>
<ce:italic>Streptococcus mutants</ce:italic>
</ce:text>
</ce:keyword>
<ce:keyword>
<ce:text>sucrase</ce:text>
</ce:keyword>
<ce:keyword>
<ce:text>fructokinase</ce:text>
</ce:keyword>
<ce:keyword>
<ce:text>transposon</ce:text>
</ce:keyword>
<ce:keyword>
<ce:text>recombinant DNA</ce:text>
</ce:keyword>
</ce:keywords>
<ce:keywords class="abr">
<ce:section-title>Abbreviations</ce:section-title>
<ce:keyword>
<ce:text>
<ce:italic>A</ce:italic>
<ce:inf>600</ce:inf>
</ce:text>
<ce:keyword>
<ce:text>absorbance at 600 nm</ce:text>
</ce:keyword>
</ce:keyword>
<ce:keyword>
<ce:text>aa</ce:text>
<ce:keyword>
<ce:text>amino acid(s)</ce:text>
</ce:keyword>
</ce:keyword>
<ce:keyword>
<ce:text>Ap</ce:text>
<ce:keyword>
<ce:text>ampicillin</ce:text>
</ce:keyword>
</ce:keyword>
<ce:keyword>
<ce:text>
<ce:italic>B.</ce:italic>
</ce:text>
<ce:keyword>
<ce:text>
<ce:italic>Bacillus</ce:italic>
</ce:text>
</ce:keyword>
</ce:keyword>
<ce:keyword>
<ce:text>bp</ce:text>
<ce:keyword>
<ce:text>base pair(s)</ce:text>
</ce:keyword>
</ce:keyword>
<ce:keyword>
<ce:text>Δ</ce:text>
<ce:keyword>
<ce:text>deletion</ce:text>
</ce:keyword>
</ce:keyword>
<ce:keyword>
<ce:text>EI, EII and EIII</ce:text>
<ce:keyword>
<ce:text>enzymes I, II and III, respectively, of the PTS</ce:text>
</ce:keyword>
</ce:keyword>
<ce:keyword>
<ce:text>EII
<ce:sup>Scr</ce:sup>
</ce:text>
<ce:keyword>
<ce:text>enzyme II
<ce:sup>Sucrose</ce:sup>
</ce:text>
</ce:keyword>
</ce:keyword>
<ce:keyword>
<ce:text>HPr</ce:text>
<ce:keyword>
<ce:text>heat-stable protein</ce:text>
</ce:keyword>
</ce:keyword>
<ce:keyword>
<ce:text>kb</ce:text>
<ce:keyword>
<ce:text>kilobase(s) or 1000 bp</ce:text>
</ce:keyword>
</ce:keyword>
<ce:keyword>
<ce:text>LB</ce:text>
<ce:keyword>
<ce:text>Luria-Bertani (medium)</ce:text>
</ce:keyword>
</ce:keyword>
<ce:keyword>
<ce:text>nt</ce:text>
<ce:keyword>
<ce:text>nucleotide(s)</ce:text>
</ce:keyword>
</ce:keyword>
<ce:keyword>
<ce:text>ORF</ce:text>
<ce:keyword>
<ce:text>open reading frame</ce:text>
</ce:keyword>
</ce:keyword>
<ce:keyword>
<ce:text>p</ce:text>
<ce:keyword>
<ce:text>plasmid</ce:text>
</ce:keyword>
</ce:keyword>
<ce:keyword>
<ce:text>PEP</ce:text>
<ce:keyword>
<ce:text>phosphoenolpyruvate</ce:text>
</ce:keyword>
</ce:keyword>
<ce:keyword>
<ce:text>PTS</ce:text>
<ce:keyword>
<ce:text>phosphotransferase system</ce:text>
</ce:keyword>
</ce:keyword>
<ce:keyword>
<ce:text>
<ce:italic>S.</ce:italic>
</ce:text>
<ce:keyword>
<ce:text>
<ce:italic>Streptococcus</ce:italic>
</ce:text>
</ce:keyword>
</ce:keyword>
<ce:keyword>
<ce:text>
<ce:italic>scrA</ce:italic>
</ce:text>
<ce:keyword>
<ce:text>
<ce:italic>V. alginolyticus</ce:italic>
sucrose uptake-encoding gene</ce:text>
</ce:keyword>
</ce:keyword>
<ce:keyword>
<ce:text>
<ce:italic>scrB</ce:italic>
</ce:text>
<ce:keyword>
<ce:text>
<ce:italic>V. alginolyticus</ce:italic>
sucrase-encoding gene</ce:text>
</ce:keyword>
</ce:keyword>
<ce:keyword>
<ce:text>
<ce:italic>scrK</ce:italic>
</ce:text>
<ce:keyword>
<ce:text>
<ce:italic>V. alginolyticus</ce:italic>
fructokinase-encoding gene</ce:text>
</ce:keyword>
</ce:keyword>
<ce:keyword>
<ce:text>Tn</ce:text>
<ce:keyword>
<ce:text>transposon</ce:text>
</ce:keyword>
</ce:keyword>
<ce:keyword>
<ce:text>
<ce:italic>V.</ce:italic>
</ce:text>
<ce:keyword>
<ce:text>
<ce:italic>Vibrio</ce:italic>
</ce:text>
</ce:keyword>
</ce:keyword>
<ce:keyword>
<ce:text>[]</ce:text>
<ce:keyword>
<ce:text>denotes plasmid-carrier state</ce:text>
</ce:keyword>
</ce:keyword>
<ce:keyword>
<ce:text>::</ce:text>
<ce:keyword>
<ce:text>novel joint (fusion)</ce:text>
</ce:keyword>
</ce:keyword>
</ce:keywords>
</head>
</converted-article>
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<title>Nucleotide sequence and analysis of the Vibrio alginolyticus sucrose uptake-encoding region</title>
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<title>Nucleotide sequence and analysis of the</title>
</titleInfo>
<name type="personal">
<namePart type="given">Gregory L.</namePart>
<namePart type="family">Blatch</namePart>
<affiliation>Department of Microbiology, University of Cape Town, Rondebosch, 7700, South Africa</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">Renate R.</namePart>
<namePart type="family">Scholle</namePart>
<affiliation>Department of Microbiology, University of Cape Town, Rondebosch, 7700, South Africa</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">David R.</namePart>
<namePart type="family">Woods</namePart>
<affiliation>Department of Microbiology, University of Cape Town, Rondebosch, 7700, South Africa</affiliation>
<description>Correspondence to: Dr. D.R. Woods, Dept. of Microbiology, University of Cape Town, Rondebosch 7700, South Africa Tel. (021) 650-2173; Fax (021) 650-2138.</description>
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<publisher>ELSEVIER</publisher>
<dateIssued encoding="w3cdtf">1990</dateIssued>
<dateValid encoding="w3cdtf">1990-06-30</dateValid>
<dateModified encoding="w3cdtf">1990-03-14</dateModified>
<copyrightDate encoding="w3cdtf">1990</copyrightDate>
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<abstract lang="en">The nucleotide sequence of the Vibrio alginolyticus sucrose uptake-encoding region was determined, and contained two genes, scrA and scrK. The scrA gene encodes an enzyme IISucrose (EIIScr) protein of the phosphoenolpyruvate dependent phosphotransferase system and the scrK gene encodes a fructokinase. The deduced amino acid (aa)_sequence for the V. alginolyticus EIIScr protein was homologous with the EIIScr protein from Streptococcus mutants, Salmonella typhimurium (pUR400 system) and Bacillus subtilis. The deduced aa sequence for the V. alginolyticus fructokinase was homologous with the Escherichia coli enzymes, 6-phosphofructokinase (isoenzyme 2) and ribokinase. Transposon phoA mutagenesis experiments indicated that the EIIScr protein was a membrane-bound protein with a region that extended into the periplasm.</abstract>
<note>Received by J. Davison</note>
<subject>
<genre>Keywords</genre>
<topic>Bacillus subtilis</topic>
<topic>Streptococcus mutants</topic>
<topic>sucrase</topic>
<topic>fructokinase</topic>
<topic>transposon</topic>
<topic>recombinant DNA</topic>
</subject>
<subject>
<genre>Abbreviations</genre>
<topic>A600 : absorbance at 600 nm</topic>
<topic>aa : amino acid(s)</topic>
<topic>Ap : ampicillin</topic>
<topic>B. : Bacillus</topic>
<topic>bp : base pair(s)</topic>
<topic>Δ : deletion</topic>
<topic>EI, EII and EIII : enzymes I, II and III, respectively, of the PTS</topic>
<topic>EIIScr : enzyme IISucrose</topic>
<topic>HPr : heat-stable protein</topic>
<topic>kb : kilobase(s) or 1000 bp</topic>
<topic>LB : Luria-Bertani (medium)</topic>
<topic>nt : nucleotide(s)</topic>
<topic>ORF : open reading frame</topic>
<topic>p : plasmid</topic>
<topic>PEP : phosphoenolpyruvate</topic>
<topic>PTS : phosphotransferase system</topic>
<topic>S. : Streptococcus</topic>
<topic>scrA : V. alginolyticus sucrose uptake-encoding gene</topic>
<topic>scrB : V. alginolyticus sucrase-encoding gene</topic>
<topic>scrK : V. alginolyticus fructokinase-encoding gene</topic>
<topic>Tn : transposon</topic>
<topic>V. : Vibrio</topic>
<topic>[] : denotes plasmid-carrier state</topic>
<topic>:: : novel joint (fusion)</topic>
</subject>
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<titleInfo type="abbreviated">
<title>GENE</title>
</titleInfo>
<genre type="Journal">journal</genre>
<originInfo>
<dateIssued encoding="w3cdtf">19901030</dateIssued>
</originInfo>
<identifier type="ISSN">0378-1119</identifier>
<identifier type="PII">S0378-1119(00)X0513-6</identifier>
<part>
<date>19901030</date>
<detail type="volume">
<number>95</number>
<caption>vol.</caption>
</detail>
<detail type="issue">
<number>1</number>
<caption>no.</caption>
</detail>
<extent unit="issue pages">
<start>1</start>
<end>163</end>
</extent>
<extent unit="pages">
<start>17</start>
<end>23</end>
</extent>
</part>
</relatedItem>
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<identifier type="DOI">10.1016/0378-1119(90)90408-J</identifier>
<identifier type="PII">0378-1119(90)90408-J</identifier>
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