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Genetic analysis of scrA and scrB from Streptococcus sobrinus 6715

  • Y. Y.M. Chen
  • , D. J. LeBlanc*
  • *Corresponding author for this work
  • University of Texas Health Science Center at San Antonio

Research output: Contribution to journalJournal Article peer-review

25 Scopus citations

Abstract

A DNA fragment containing scrA and scrB, which encode enzyme II of the phosphoenolpyruvate-dependent sucrose phosphotransferase system and sucrose- 6-phosphate hydrolase, respectively, was isolated from a λgt10 genomic DNA library of Streptococcus sobrinus 6715. Both genes were located on a 4.2-kb DNA fragment which was maintained stably in Escherichia coli on low-copy- number vector pGB2. The recombinant E. coli clone expressed sucrose- hydrolytic activity on MacConkey agar base supplemented with raffinose or sucrose. Results from deletion analysis showed that the sucrose-metabolic activity was contained within a 3.5-kb region. The lactic acid bacterium Lactococcus lactis subsp. lactis LM0230, which is devoid of sucrose-metabolic activity, was used to study the enzyme activities encoded by scrA and scrB from S. sobrinus 6715. L. lactis transformants carrying the 4.2-kb S. sobrinus-derived DNA fragment on E. coli-Streptococcus shuttle vector pDL278 were able to grow at the expense of sucrose and exhibited enzyme II and sucrose-6-phosphate hydrolase activities. Results from hybridization studies and a comparison of the restriction endonuclease maps of the scrA- and scrB- containing chromosomal regions from S. mutans GS5 and S. sobrinus 6715 suggested considerable divergence.

Original languageEnglish
Pages (from-to)3739-3746
Number of pages8
JournalInfection and Immunity
Volume60
Issue number9
StatePublished - 1992
Externally publishedYes

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