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PMID: 1716611 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Sucrose-promoted accumulation of growing glucosyltransferase variants of Streptococcus gordonii on hydroxyapatite surfaces.

Infection and immunity ·Vol. 59 ·No. 10 ·1991-10-00 ·Pages 3523-30

Vickerman MM, Clewell DB, Jones GW

Abstract

Streptococcus gordonii exhibits a phase variation involving expression of high (Spp+) or low (Spp-) glucosyltransferase activity. The related bacterial accumulation on hydroxyapatite (HA) and saliva-coated HA surfaces was examined and found to be significant. Spp+ cells growing anaerobically in a defined medium utilize about 30% of the glucose available from sucrose to make insoluble glucans. These glucans formed cohesive masses on HA beads, which contained 80 to 90% of the total bacteria. The bacterial polymer mass had a volume of about 40 microns3 and contained more than 5 x 10(10) viable cells per cm3. In the absence of sucrose, the beads were saturated by 1 x 10(8) to 2 x 10(8) Spp+ cells. Spp- bacteria, which make 30-fold less glucan than do Spp+ bacteria, did not accumulate on surfaces in numbers significantly above the saturation level of 1 x 10(8) to 2 x 10(8) cells in the presence or absence of sucrose. Insoluble glucan synthesized by Spp+ cells from sucrose also enabled these bacteria to accumulate on saliva-coated HA seven times more effectively than the Spp- cells and 10 times more effectively than the Spp+ cells grown in medium without sucrose.

MeSH Terms
Culture Media Dextrans/pharmacology Durapatite Glucosyltransferases/analysis Humans Hydroxyapatites/pharmacology Male Saliva/physiology Streptococcus/enzymology,growth & development Sucrose/pharmacology
Chemicals
Culture Media Dextrans Hydroxyapatites Sucrose Durapatite Glucosyltransferases
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Vickerman M M
Department of Microbiology, School of Medicine, University of Michigan, Ann Arbor 48109.
Clewell D B
Jones G W
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Article Info
Journal
Infection and immunity
Abbr.
Infect Immun
ISSN
0019-9567
Published
1991-10-00
Pages
3523-30
Language
English
Region
United States
NLM ID
0246127
PMCID
PMC258916
Subset
IM
Grants
NIDCR NIH HHS · DE00154 · United States
NIDCR NIH HHS · DE02731 · United States
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