Abstract
Strains of Streptococcus mutans are very susceptible to growth inhibition by benzylpenicillin, but are tolerant to lysis when exposed to even high concentrations of this drug. These properties enabled this study of S. mutans GS-5 surface growth and peptidoglycan, ribonucleic acid, protein, and deoxyribonucleic acid syntheses in the absence of osmotic stabilization. Inhibition of syntheses of peptidoglycan, ribonucleic acid, and protein was dose dependent. Synthesis of peptidoglycan was most susceptible. Substantial but less severe inhibitions of ribonucleic acid and protein syntheses rapidly followed decreased peptidoglycan synthesis, whereas inhibition of deoxyribonucleic acid synthesis was delayed and minimal. Computer-assisted reconstructions of surface growth zones and poles observed in electron micrographs of replicas were performed and indicated that at low concentrations of benzylpenicillin (0.03 micrograms/ml), growth sites reached abnormally large sizes and surface/volume ratios. The observed shifts in surface/volume ratio were attributed to an inhibition of the normal constrictive division mechanism. The poles of these cells also increased in size over those of the controls, but the relatively smaller change in surface/volume ratio confirmed the visual impression that the shape of the poles was much less altered than the shape of the growth sites. As the concentration of benzylpenicillin used was raised from 0.03 to 2 micrograms/ml, the ability of growth sites and poles to enlarge was restricted in a manner that most closely agreed with the extent of inhibition of peptidoglycan (rather than deoxyribonucleic acid, ribonucleic acid, or protein) synthesis. This correlation suggested that increases in cell size may be regulated by the supply of peptidoglycan precursors.
Full text
PDF





Images in this article
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Edelstein E. M., Rosenzweig M. S., Daneo-Moore L., Higgins M. L. Unit cell hypothesis for Streptococcus faecalis. J Bacteriol. 1980 Jul;143(1):499–505. doi: 10.1128/jb.143.1.499-505.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Higgins M. L. Three-dimensional reconstruction of whole cells of Streptococcus faecalis from thin sections of cells. J Bacteriol. 1976 Sep;127(3):1337–1345. doi: 10.1128/jb.127.3.1337-1345.1976. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kolenbrander P. E., Hohman R. J. Electron microscopic study of cell surface rings during cell division and morphogenesis of Arthrobacter crystallopoietes. J Bacteriol. 1977 Jun;130(3):1345–1356. doi: 10.1128/jb.130.3.1345-1356.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Mattingly S. J., Daneo-Moore L., Shockman G. D. Factors regulating cell wall thickening and intracellular iodophilic polysaccharide storage in Streptococcus mutans. Infect Immun. 1977 Jun;16(3):967–973. doi: 10.1128/iai.16.3.967-973.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Mychajlonka M., McDowell T. D., Shockman G. D. Conservation of cell wall peptidoglycan by strains of Streptococcus mutans and Streptococcus sanguis. Infect Immun. 1980 Apr;28(1):65–73. doi: 10.1128/iai.28.1.65-73.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Mychajlonka M., McDowell T. D., Shockman G. D. Inhibition of peptidoglycan, ribonucleic acid, and protein synthesis in tolerant strains of Streptococcus mutans. Antimicrob Agents Chemother. 1980 Apr;17(4):572–582. doi: 10.1128/aac.17.4.572. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Schwarz U., Asmus A., Frank H. Autolytic enzymes and cell division of Escherichia coli. J Mol Biol. 1969 May 14;41(3):419–429. doi: 10.1016/0022-2836(69)90285-x. [DOI] [PubMed] [Google Scholar]
- Shockman G. D., Daneo-Moore L., Cornett J. B., Mychajlonka M. Does penicillin kill bacteria?. Rev Infect Dis. 1979 Sep-Oct;1(5):787–796. doi: 10.1093/clinids/1.5.787. [DOI] [PubMed] [Google Scholar]
- Shockman G. D. Symposium on the fine structure and replication of bacteria and their parts. IV. Unbalanced cell-wall synthesis: autolysis and cell-wall thickening. Bacteriol Rev. 1965 Sep;29(3):345–358. doi: 10.1128/br.29.3.345-358.1965. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Spratt B. G. Distinct penicillin binding proteins involved in the division, elongation, and shape of Escherichia coli K12. Proc Natl Acad Sci U S A. 1975 Aug;72(8):2999–3003. doi: 10.1073/pnas.72.8.2999. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Terleckyj B., Willett N. P., Shockman G. D. Growth of several cariogenic strains of oral streptococci in a chemically defined medium. Infect Immun. 1975 Apr;11(4):649–655. doi: 10.1128/iai.11.4.649-655.1975. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Tomasz A. The role of autolysins in cell death. Ann N Y Acad Sci. 1974 May 10;235(0):439–447. doi: 10.1111/j.1749-6632.1974.tb43282.x. [DOI] [PubMed] [Google Scholar]
- WEIDEL W., PELZER H. BAGSHAPED MACROMOLECULES--A NEW OUTLOOK ON BACTERIAL CELL WALLS. Adv Enzymol Relat Areas Mol Biol. 1964;26:193–232. doi: 10.1002/9780470122716.ch5. [DOI] [PubMed] [Google Scholar]

