Literature DB >> 8454327

Expression of gtfS is essential for normal insoluble glucan synthesis by Streptococcus downei.

K S Gilmore1, R R Russell, J J Ferretti.   

Abstract

The gtfI and gtfS genes of Streptococcus downei were investigated to determine the contribution of the respective enzymes to glucan production in the presence and absence of other glucosyltransferases. Extracts of Escherichia coli expressing cloned gtfS produced a short linear dextran from sucrose which could act as a primer for insoluble glucan synthesis when mixed with extracts of a strain expressing recombinant gtfI. To elucidate the contribution of gtfS to glucan production by S. downei, a mutant was constructed by insertionally inactivating gtfS. S. downei (gtfS mutant) colonies exhibited a marked phenotypic change on sucrose-containing media and a decreased ability to adhere to glass and produced no detectable water-insoluble glucan. These experiments confirm that expression of gtfS is essential for normal insoluble glucan synthesis by S. downei.

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Year:  1993        PMID: 8454327      PMCID: PMC281354          DOI: 10.1128/iai.61.4.1246-1250.1993

Source DB:  PubMed          Journal:  Infect Immun        ISSN: 0019-9567            Impact factor:   3.441


  20 in total

1.  Isolation and characterization of the Streptococcus mutans gtfC gene, coding for synthesis of both soluble and insoluble glucans.

Authors:  N Hanada; H K Kuramitsu
Journal:  Infect Immun       Date:  1988-08       Impact factor: 3.441

2.  Cloning and expression of two Streptococcus mutans glucosyltransferases in Escherichia coli K-12.

Authors:  M L Gilpin; R R Russell; P Morrissey
Journal:  Infect Immun       Date:  1985-08       Impact factor: 3.441

3.  Synthesis of adherent insoluble glucan by the concerted action of the two glucosyltransferase components of Streptococcus mutans.

Authors:  M Inoue; T Koga; S Sato; S Hamada
Journal:  FEBS Lett       Date:  1982-06-21       Impact factor: 4.124

Review 4.  Biology, immunology, and cariogenicity of Streptococcus mutans.

Authors:  S Hamada; H D Slade
Journal:  Microbiol Rev       Date:  1980-06

5.  Cloning of a Streptococcus mutans glucosyltransferase gene coding for insoluble glucan synthesis.

Authors:  H Aoki; T Shiroza; M Hayakawa; S Sato; H K Kuramitsu
Journal:  Infect Immun       Date:  1986-09       Impact factor: 3.441

6.  Peptide sequences for sucrose splitting and glucan binding within Streptococcus sobrinus glucosyltransferase (water-insoluble glucan synthetase).

Authors:  H Abo; T Matsumura; T Kodama; H Ohta; K Fukui; K Kato; H Kagawa
Journal:  J Bacteriol       Date:  1991-02       Impact factor: 3.490

7.  Isolation and characterization of the Streptococcus mutans gtfD gene, coding for primer-dependent soluble glucan synthesis.

Authors:  N Hanada; H K Kuramitsu
Journal:  Infect Immun       Date:  1989-07       Impact factor: 3.441

8.  Analysis of the Streptococcus downei gtfS gene, which specifies a glucosyltransferase that synthesizes soluble glucans.

Authors:  K S Gilmore; R R Russell; J J Ferretti
Journal:  Infect Immun       Date:  1990-08       Impact factor: 3.441

9.  Mechanism of adherence of Streptococcus mutans to smooth surfaces. I. Roles of insoluble dextran-levan synthetase enzymes and cell wall polysaccharide antigen in plaque formation.

Authors:  H Mukasa; H D Slade
Journal:  Infect Immun       Date:  1973-10       Impact factor: 3.441

10.  Cloning of a Streptococcus sobrinus gtf gene that encodes a glucosyltransferase which produces a high-molecular-weight water-soluble glucan.

Authors:  N Hanada; Y Yamashita; Y Shibata; S Sato; T Katayama; T Takehara; M Inoue
Journal:  Infect Immun       Date:  1991-10       Impact factor: 3.441

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  1 in total

1.  Purification, characterization, and specificity of dextranase inhibitor (Dei) expressed from Streptococcus sobrinus UAB108 gene cloned in Escherichia coli.

Authors:  J W Sun; S Y Wanda; R Curtiss
Journal:  J Bacteriol       Date:  1995-04       Impact factor: 3.490

  1 in total

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