Regulation of Recombination between gtfB/gtfC Genes in Streptococcus mutans by Recombinase A

Streptococcus mutans produces 3 types of glucosyltransferases (GTFs), whose cooperative action is essential for cellular adhesion. The recombinase A (RecA) protein is required for homologous recombination. In our previous study, we isolated several strains with a smooth colony morphology and low GTF...

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Main Authors: Satoko Inagaki, Kazuyo Fujita, Yukiko Takashima, Kayoko Nagayama, Arifah C. Ardin, Yuki Matsumi, Michiyo Matsumoto-Nakano
Format: Article
Language:English
Published: Wiley 2013-01-01
Series:The Scientific World Journal
Online Access:http://dx.doi.org/10.1155/2013/405075
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author Satoko Inagaki
Kazuyo Fujita
Yukiko Takashima
Kayoko Nagayama
Arifah C. Ardin
Yuki Matsumi
Michiyo Matsumoto-Nakano
author_facet Satoko Inagaki
Kazuyo Fujita
Yukiko Takashima
Kayoko Nagayama
Arifah C. Ardin
Yuki Matsumi
Michiyo Matsumoto-Nakano
author_sort Satoko Inagaki
collection DOAJ
description Streptococcus mutans produces 3 types of glucosyltransferases (GTFs), whose cooperative action is essential for cellular adhesion. The recombinase A (RecA) protein is required for homologous recombination. In our previous study, we isolated several strains with a smooth colony morphology and low GTF activity, characteristics speculated to be derived from the GTF fusions. The purpose of the present study was to investigate the mechanism of those fusions. S. mutans strain MT8148 was grown in the presence of recombinant RecA (rRecA) protein, after which smooth colonies were isolated. The biological functions and sequences of the gtfB and gtfC genes of this as well as other clinical strains were determined. The sucrose-dependent adherence rates of those strains were reduced as compared to that of MT8148. Determination of the sequences of the gtfB and gtfC genes showed that an approximately 3500 bp region was deleted from the area between them. Furthermore, expression of the recA gene was elevated in those strains as compared to MT8148. These results suggest that RecA has an important role in fusions of gtfB and gtfC genes, leading to alteration of colony morphology and reduction in sucrose-dependent adhesion.
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institution Kabale University
issn 1537-744X
language English
publishDate 2013-01-01
publisher Wiley
record_format Article
series The Scientific World Journal
spelling doaj-art-11bea8fd058646b9bd49a1cf76c0a4992025-02-03T01:31:31ZengWileyThe Scientific World Journal1537-744X2013-01-01201310.1155/2013/405075405075Regulation of Recombination between gtfB/gtfC Genes in Streptococcus mutans by Recombinase ASatoko Inagaki0Kazuyo Fujita1Yukiko Takashima2Kayoko Nagayama3Arifah C. Ardin4Yuki Matsumi5Michiyo Matsumoto-Nakano6Department of Pediatric Dentistry, Osaka University Graduate School of Dentistry, 1-8 Yamada-oka, Suita, Osaka 565-0871, JapanDepartment of Pediatric Dentistry, Osaka University Graduate School of Dentistry, 1-8 Yamada-oka, Suita, Osaka 565-0871, JapanDepartment of Pediatric Dentistry, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, 2-5-1 Shikata-cho, Kita-ku, Okayama 700-8558, JapanDepartment of Pediatric Dentistry, Osaka University Graduate School of Dentistry, 1-8 Yamada-oka, Suita, Osaka 565-0871, JapanDepartment of Pediatric Dentistry, Osaka University Graduate School of Dentistry, 1-8 Yamada-oka, Suita, Osaka 565-0871, JapanDepartment of Pediatric Dentistry, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, 2-5-1 Shikata-cho, Kita-ku, Okayama 700-8558, JapanDepartment of Pediatric Dentistry, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, 2-5-1 Shikata-cho, Kita-ku, Okayama 700-8558, JapanStreptococcus mutans produces 3 types of glucosyltransferases (GTFs), whose cooperative action is essential for cellular adhesion. The recombinase A (RecA) protein is required for homologous recombination. In our previous study, we isolated several strains with a smooth colony morphology and low GTF activity, characteristics speculated to be derived from the GTF fusions. The purpose of the present study was to investigate the mechanism of those fusions. S. mutans strain MT8148 was grown in the presence of recombinant RecA (rRecA) protein, after which smooth colonies were isolated. The biological functions and sequences of the gtfB and gtfC genes of this as well as other clinical strains were determined. The sucrose-dependent adherence rates of those strains were reduced as compared to that of MT8148. Determination of the sequences of the gtfB and gtfC genes showed that an approximately 3500 bp region was deleted from the area between them. Furthermore, expression of the recA gene was elevated in those strains as compared to MT8148. These results suggest that RecA has an important role in fusions of gtfB and gtfC genes, leading to alteration of colony morphology and reduction in sucrose-dependent adhesion.http://dx.doi.org/10.1155/2013/405075
spellingShingle Satoko Inagaki
Kazuyo Fujita
Yukiko Takashima
Kayoko Nagayama
Arifah C. Ardin
Yuki Matsumi
Michiyo Matsumoto-Nakano
Regulation of Recombination between gtfB/gtfC Genes in Streptococcus mutans by Recombinase A
The Scientific World Journal
title Regulation of Recombination between gtfB/gtfC Genes in Streptococcus mutans by Recombinase A
title_full Regulation of Recombination between gtfB/gtfC Genes in Streptococcus mutans by Recombinase A
title_fullStr Regulation of Recombination between gtfB/gtfC Genes in Streptococcus mutans by Recombinase A
title_full_unstemmed Regulation of Recombination between gtfB/gtfC Genes in Streptococcus mutans by Recombinase A
title_short Regulation of Recombination between gtfB/gtfC Genes in Streptococcus mutans by Recombinase A
title_sort regulation of recombination between gtfb gtfc genes in streptococcus mutans by recombinase a
url http://dx.doi.org/10.1155/2013/405075
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