Initial characterization of the Streptococcus gordonii htpX gene
Examination of the Streptococcus gordonii chromosomal region, which lies immediately upstream of the glucosyltransferase positive regulatory determinant rgg, revealed two open reading frames. Based on nucleotide sequences, these genes were similar to the Listeria monocytogenes lemA gene, which is involved in antigen presentation, and the Escherichia coli htpX heat shock gene, which has an unknown function. Northern hybridization analysis indicated that S. gordonii lemA and htpX genes were associated with a ca. 1.7-kb polycistronic transcript. Although levels of the lemA/htpX transcript did not increase in response to heat to levels seen with dnaK controls, insertional inactivation of htpX resulted in changes in adhesiveness, cellular morphology and detergent-extractable surface antigens in cells grown at 41 degrees C, implying that htpX may be involved in surface protein expression. Insertional inactivation of lemA and htpX indicated that, despite their proximity to rgg and the structural gene, gtfG, these upstream genes do not affect S. gordonii glucosyltransferase activity.
Medienart: |
Artikel |
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Erscheinungsjahr: |
2002 |
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Erschienen: |
2002 |
Enthalten in: |
Zur Gesamtaufnahme - volume:17 |
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Enthalten in: |
Oral microbiology and immunology - 17(2002), 1 vom: 15. Feb., Seite 22-31 |
Sprache: |
Englisch |
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Beteiligte Personen: |
Vickerman, M M [VerfasserIn] |
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Anmerkungen: |
Date Completed 04.06.2002 Date Revised 25.10.2019 published: Print GENBANK: AF017421 Citation Status MEDLINE |
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Förderinstitution / Projekttitel: |
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PPN (Katalog-ID): |
NLM117460206 |
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100 | 1 | |a Vickerman, M M |e verfasserin |4 aut | |
245 | 1 | 0 | |a Initial characterization of the Streptococcus gordonii htpX gene |
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500 | |a Date Completed 04.06.2002 | ||
500 | |a Date Revised 25.10.2019 | ||
500 | |a published: Print | ||
500 | |a GENBANK: AF017421 | ||
500 | |a Citation Status MEDLINE | ||
520 | |a Examination of the Streptococcus gordonii chromosomal region, which lies immediately upstream of the glucosyltransferase positive regulatory determinant rgg, revealed two open reading frames. Based on nucleotide sequences, these genes were similar to the Listeria monocytogenes lemA gene, which is involved in antigen presentation, and the Escherichia coli htpX heat shock gene, which has an unknown function. Northern hybridization analysis indicated that S. gordonii lemA and htpX genes were associated with a ca. 1.7-kb polycistronic transcript. Although levels of the lemA/htpX transcript did not increase in response to heat to levels seen with dnaK controls, insertional inactivation of htpX resulted in changes in adhesiveness, cellular morphology and detergent-extractable surface antigens in cells grown at 41 degrees C, implying that htpX may be involved in surface protein expression. Insertional inactivation of lemA and htpX indicated that, despite their proximity to rgg and the structural gene, gtfG, these upstream genes do not affect S. gordonii glucosyltransferase activity | ||
650 | 4 | |a Journal Article | |
650 | 4 | |a Research Support, U.S. Gov't, P.H.S. | |
650 | 7 | |a Antigens, Bacterial |2 NLM | |
650 | 7 | |a Bacterial Proteins |2 NLM | |
650 | 7 | |a DNA, Bacterial |2 NLM | |
650 | 7 | |a Escherichia coli Proteins |2 NLM | |
650 | 7 | |a Heat-Shock Proteins |2 NLM | |
650 | 7 | |a Transcription Factors |2 NLM | |
650 | 7 | |a HtpX protein, E coli |2 NLM | |
650 | 7 | |a 137804-77-4 |2 NLM | |
650 | 7 | |a lemA protein, bacterial |2 NLM | |
650 | 7 | |a EC 2.7.3.- |2 NLM | |
650 | 7 | |a Metalloproteases |2 NLM | |
650 | 7 | |a EC 3.4.- |2 NLM | |
700 | 1 | |a Mather, N M |e verfasserin |4 aut | |
700 | 1 | |a Minick, P E |e verfasserin |4 aut | |
700 | 1 | |a Edwards, C A |e verfasserin |4 aut | |
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