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Localization of sugar-binding sites in Staphylococcus aureus using gold-labeled neoglycoprotein.
Author(s) -
Hiroyuki Morioka,
A Suganuma,
M. Tachibana
Publication year - 1994
Publication title -
journal of histochemistry and cytochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.971
H-Index - 124
eISSN - 1551-5044
pISSN - 0022-1554
DOI - 10.1177/42.12.7983361
Subject(s) - wheat germ agglutinin , bovine serum albumin , cell wall , staphylococcus aureus , staining , lectin , chemistry , cytoplasm , bacterial cell structure , biochemistry , negative stain , acetylglucosamine , microbiology and biotechnology , bacteria , enzyme , biology , electron microscope , physics , optics , genetics
We studied post- and pre-embedding staining of sugar-binding sites on thin sections of Staphylococcus aureus with an electron microscopic neoglycoprotein-gold technique. Although gold particles of cellobiosyl bovine serum albumin (BSA)-glycosylated BSA-, lactosyl BSA-, and melibiosyl BSA-gold did not label, heavy labeling of N-acetylglucosaminide-BSA-gold was observed in both the cell wall and the cytoplasm on Spurr-embedded thin sections of S. aureus. Inhibition of labeling with wheat germ agglutinin-biotin and N-acetylglucosaminidase indicated that the labeling was due to N-acetylglucosamine. These data suggested that molecules that bind specifically with N-acetylglucosamine occur in the cell wall and cytoplasm of S. aureus. Pre-embedding staining revealed that these molecules are abundant at the surface of the cell wall and that the abundance differs depending on the bacterial strain. An N-acetylglucosamine-specific lectin-like substance, glucosaminidase, and toxins are proposed as candidates for molecules responsible for the labeling, and the possible functional significance of the findings is discussed briefly.

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