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Lactobacilli isolated from kefir grains: evidence of the presence of S-layer proteins

Published online by Cambridge University Press:  04 May 2004

Graciela Liliana Garrote
Affiliation:
Centro de Investigación y Desarrollo en Criotecnología de Alimentos (CIDCA), 47 y 116 (1900), Facultad de Ciencias Exactas, Universidad Nacional de La Plata, La Plata, Argentina
Lucrecia Delfederico
Affiliation:
Laboratorio de Microbiología Molecular, Departamento de Ciencia y Tecnología, Universidad Nacional de Quilmes, Bernal, Argentina
Rodrigo Bibiloni
Affiliation:
Centro de Investigación y Desarrollo en Criotecnología de Alimentos (CIDCA), 47 y 116 (1900), Facultad de Ciencias Exactas, Universidad Nacional de La Plata, La Plata, Argentina
Analia Graciela Abraham
Affiliation:
Centro de Investigación y Desarrollo en Criotecnología de Alimentos (CIDCA), 47 y 116 (1900), Facultad de Ciencias Exactas, Universidad Nacional de La Plata, La Plata, Argentina
Pablo Fernando Pérez
Affiliation:
Centro de Investigación y Desarrollo en Criotecnología de Alimentos (CIDCA), 47 y 116 (1900), Facultad de Ciencias Exactas, Universidad Nacional de La Plata, La Plata, Argentina
Liliana Semorile
Affiliation:
Laboratorio de Microbiología Molecular, Departamento de Ciencia y Tecnología, Universidad Nacional de Quilmes, Bernal, Argentina
Graciela Liliana De Antoni
Affiliation:
Centro de Investigación y Desarrollo en Criotecnología de Alimentos (CIDCA), 47 y 116 (1900), Facultad de Ciencias Exactas, Universidad Nacional de La Plata, La Plata, Argentina

Abstract

In the present study we report for the first time the presence of S-layer proteins in Lactobacillus kefir and Lactobacillus parakefir isolated from kefir grains. Soluble whole-cell protein profile obtained either by mechanical disruption (X-press) or by a combined treatment with lysozyme and SDS on whole cells, showed a significant band of apparent molecular mass of 66–71 kDa as measured by SDS–PAGE. The intensity of this band was considerably reduced when cells were treated with 5 M-LiCl. The above mentioned proteins were recovered in the LiCl extracts. After dialysis and concentration, the proteins extracted were able to reassemble in a regular array. Negative staining of these protein preparations were analysed by transmission electron microscopy and a paracrystalline arrangement was seen. Thin sections of bacteria analysed by transmission electron micrographs showed an outermost layer over the bacterial cell wall, that was lost after the LiCl treatment. The production of this surface structure under different culture conditions was also evaluated. Finally, the relationship between the presence of S-layer proteins and surface properties (e.g. adhesion to Caco-2 cells, autoaggregation, and hemagglutination) was investigated.

Type
Research Article
Copyright
Proprietors of Journal of Dairy Research 2004

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