Metabolic Responses in Biofilms

References

• Allison D G., Evans D J., Brown M R., Gilbert P. Possible involvement of the division cycle in dispersal of Escherichia coli from biofilms. Journal of Bacteriology 1990; 172: 1667–1669
   PubMed Web of Science ®Google Scholar
• Anwar H, Strap J L., Costerton J W. Establishment of aging biofilms: possible mechanism of bacterial resistance to antimicrobial therapy. Antimicrobial Agents and Chemotherapy 1992; 36: 1347–1351
   PubMed Web of Science ®Google Scholar
• Berry C W., Henry C A. The effect of adsorption on the acid production of caries and noncaries-producing streptococci. Journal of Dental Research 1977; 56: 1193–1200
   Web of Science ®Google Scholar
• Bradshaw D J., Marsh P D., Watson G K., Schilling K. Effect of oxygen and inoculum composition on development of mixed culture biofilm. Journal of Dental Research 1994; 73: 849, (abstract 504)
   Google Scholar
• Colbourne J S. Materials usage and their effects on the microbiological quality of water supplies. Journal of Applied Bacteriology Symposium Supplement 1985; 47S–59S
   Google Scholar
• Costerton J W., Cheng K J., Geesey G G., Ladd T I., Nickel J C., Dasgupta M, Marrie T J. Bacterial biofilms in nature and disease. Annual Reviews in Microbiology 1987; 41: 435–464
   PubMed Web of Science ®Google Scholar
• Davies D G., Chakrabarty A M., Geesey G G. Exopolysaccharide production in biofilms: substratum activation of alginate gene expression by Pseudomonas aeruginosa. Applied and Environmental Microbiology 1993; 59: 1181–1186
   PubMed Web of Science ®Google Scholar
• Dibdin G H., Shellis R P. Physical and biochemical studies of Streptococcus mutans sediments suggest new factors linking the cariogenicity of plaque with its extracellular polysaccharide content. Journal of Dental Research 1988; 67: 890–895
   Web of Science ®Google Scholar
• Duguid I G., Evans E, Brown M R., Gilbert P. Effect of biofilm culture upon the susceptibility of Staphylococcus epidermidis to tobramycin. Journal of Antimicrobial Chemotherapy 1992; 30: 803–810
   PubMed Web of Science ®Google Scholar
• Ellwood D C., Keevil C W., Marsh P D., Brown C M., Wardell J N. Surface-associated growth. Philosophical Transactions of the Royal Society of London Series B 1982; 297: 517–532
   PubMed Web of Science ®Google Scholar
• Evans D J., Allison D G., Brown M R., Gilbert P. Effect of growth-rate on resistance of Gram-negative biofilms to cetrimide. Journal of Antimicrobial Chemotherapy 1990; 26: 473–478
   PubMed Web of Science ®Google Scholar
• Gilbert P, Allison D G., Evans D J., Handley P S., Brown M RW. Growth rate control of adherent bacterial populations. Applied and Environmental Microbiology 1989; 55: 1308–1311
   PubMed Web of Science ®Google Scholar
• Gilbert P, Collier P J., Brown M R. Influence of growth rate on susceptibility to antimicrobial agents: biofilms, cell cycle, dormancy, and stringent response. Antimicrobial Agents and Chemotherapy 1990; 34: 1865–1868
   PubMed Web of Science ®Google Scholar
• Giwercman B, Fomsgaard A, Mansa B, Hoiby N. Polyacrylamide gel electrophoresis analysis of lipopolysaccharide from Pseudomonas aeruginosa growing planktonically and as biofilm. FEMS Microbiology Immunology 1992; 4: 225–230
   Google Scholar
• Hattori R, Hattori T. Growth rate and molar growth yield of Escherichia coli adsorbed on an anion exchange resin. Journal of General and Applied Microbiology 1981; 27: 287–298
   Web of Science ®Google Scholar
• Heukelekian H, Heller A. Relation between food concentration and surface for bacterial growth. Journal of Bacteriology 1940; 40: 547–558
   PubMedGoogle Scholar
• Hudson M C., Curtiss R, III. Regulation of expression of Streptococcus mutans genes important to virulence. Infection and Immunity 1990; 58: 464–470
   Web of Science ®Google Scholar
• Kolenbrander P E. Intergeneric coaggregation among human oral bacteria and ecology of dental plaque. Annual Reviews in Microbiology 1988; 42: 627–656
   PubMed Web of Science ®Google Scholar
• Lorenz M G., Aardema B W., Krumbein W E. Interaction of marine sediments with DNA and DNA availability to nucleases. Marine Biology 1981; 64: 225–230
   Web of Science ®Google Scholar
• Lorenz M G., Aardema B W., Wackernagel W. Highly efficient genetic transformation of Bacillus subtilis attached to sand grains. Journal of General Microbiology 1988; 134: 107–112
   PubMedGoogle Scholar
• Lorenz M G., Reipschlager K, Wackernagel W. Plasmid transformation of naturally competent Acinetobacter calcoaceticus in non-sterile soil extract and groundwater. Archives of Microbiology 1992; 157: 355–360
   Web of Science ®Google Scholar
• Lorenz M G., Wackernagel W. Adsorption of DNA to sand and variable degradation rates of adsorbed DNA. Applied and Environmental Microbiology 1987; 53: 2948–2952
   PubMed Web of Science ®Google Scholar
• Mikx F HM, Van der Hoeven J S. Symbiosis of Streptococcus mutans and Veillonella alcalescens in mixed continuous culture. Archives of Oral Biology 1976; 20: 401–410
   Web of Science ®Google Scholar
• Millward T A., Wilson M. The effect of chlorhexidine on Streptococcus sanguis biofilms. Microbios 1989; 58: 155–164
   Google Scholar
• Morisaki H. The electric current from Escherichia coli and the effect of resin on it. Journal of General and Applied Microbiology 1982; 28: 73–86
   Web of Science ®Google Scholar
• Nichols W W. Biofilm permeability to antibacterial agents. Bacterial biofilms and their control in medicine and industry, WW Nichols, JWT Wimpenny, DJ Stickler, H Lappin-Scott. University of Wales College of Cardiff, Cardiff 1993; 53–57
   Google Scholar
• Noorda W D., Purdell-Lewis D J., De Koning W, Van Montfort A MAP, Weerkamp A H. A new apparatus for continuous cultivation of bacterial plaque on solid surfaces and human dental enamel. Journal of Applied Bacteriology 1985; 58: 563–569
   PubMedGoogle Scholar
• Romanowski G, Lorenz M G., Wackernagel W. Adsorption of plasmid DNA to mineral surfaces and protection against DNAase I. Applied and Environmental Microbiology 1991; 57: 1057–1061
   PubMed Web of Science ®Google Scholar
• Stotzky G, Rem L T. Influence of clay minerals on microorganisms. I. Montmorillonite and kaolinte on bacteria. Canadian Journal of Microbiology 1966; 12: 547–563
   PubMed Web of Science ®Google Scholar
• Stotzky G, Rem L T. Influence of clay minerals on microorganisms. II. Effect of various clay species, homionic clays and other particles on bacteria. Canadian Journal of Microbiology 1966; 12: 831–848
   PubMed Web of Science ®Google Scholar
• Stotzky G, Rem L T. Influence of clay minerals on microorganisms. III. Effect of particle size cation exchange capacity and surface area on bacteria. Canadian Journal of Microbiology 1966; 12: 1235–1246
   PubMed Web of Science ®Google Scholar
• Tempest D W. The place of continuous culture in microbiological research. Advances in Microbial Physiology, AH Rose, JF Wilkinson. Academic Press, London & New York 1970; 223–250
   Google Scholar
• Van Loosdrecht M CM, Lyklema J, Norde W, Zehnder A JB. Influence of interfaces on microbial activity. Microbiological Reviews 1990; 54: 75–87
   PubMedGoogle Scholar
• White D J., Nancollas G H. Physical and chemical considerations of the role of firmly and loosely bound fluoride in caries prevention. Journal of Dental Research 1990; 69: 587–594
   PubMedGoogle Scholar
• Zero D T., Van Houte J, Russo J. The intraoral effect on enamel demineralisation of extracellular matrix material synthesized from sucrose by Streptococcus mutans. Journal of Dental Research 1986; 65: 918–923
   Web of Science ®Google Scholar
• ZoBell C E. The effect of solid surfaces upon bacterial growth. Journal of Bacteriology 1943; 46: 39–56
   PubMedGoogle Scholar