Journal article
Chelating agents inhibit activity and prevent expression of streptococcal glucan-binding lectins
Infection and immunity, Vol.60(9), pp.3807-3813
09/1992
DOI: 10.1128/iai.60.9.3807-3813.1992
PMCID: PMC257393
PMID: 1500189
Abstract
Several of the cariogenic mutans streptococci produce cell wall-associated glucan-binding lectins (GBLs). The lectins bind alpha-1,6-linked glucans and have no affinity for other polysaccharides or anomeric linkages. When citrate or lactate was included in the growth medium, expression of the activities of the GBLs of Streptococcus cricetus and S. sobrinus was prevented. Furthermore, chelating agents, including citrate, lactate, EDTA, and acetylacetone, were able to reversibly inhibit glucan-induced aggregation of GBL+ streptococci. In addition, the chelating agents prevented sucrose-dependent streptococcal adhesion to glass surfaces and dispersed preformed adherent masses of the streptococci. Neither citrate nor other chelating agents modified the activities of glucosyltransferases. Expression of the lectin could only be achieved by the addition of manganous ion to the growth medium. Chloramphenicol and other metabolic inhibitors prevented synthesis of GBL in cells obtained from manganese-deficient medium and shifted to manganous ion-sufficient medium. The GBL may be a manganoprotein, the manganese of which may be perturbed, but not removed, by chelating agents. During synthesis of the GBL, manganous ion may be required in order for the protein to achieve an active conformation. Citrate or other chelating agents may have promise as anticaries agents.
Details
- Title: Subtitle
- Chelating agents inhibit activity and prevent expression of streptococcal glucan-binding lectins
- Creators
- Lü-Lü - University of LouisvilleJ S Singh - University of LouisvilleM Y Galperin - University of LouisvilleD Drake - University of LouisvilleK G Taylor - University of LouisvilleR J Doyle - University of Louisville
- Resource Type
- Journal article
- Publication Details
- Infection and immunity, Vol.60(9), pp.3807-3813
- DOI
- 10.1128/iai.60.9.3807-3813.1992
- PMID
- 1500189
- PMCID
- PMC257393
- NLM abbreviation
- Infect Immun
- ISSN
- 0019-9567
- eISSN
- 1098-5522
- Language
- English
- Date published
- 09/1992
- Academic Unit
- Endodontics; Dental Research
- Record Identifier
- 9984367728602771
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