Affiliation:
1. National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland
Abstract
Beachey, Edwin
H. (National Institute of Allergy and Infectious Diseases, Bethesda, Md.),
and Roger M. Cole
. Cell wall replication in
Escherichia coli
, studied by immunofluorescence and immunoelectron microscopy. J. Bacteriol. 92:1245–1251. 1966.—Cell wall components of four different strains of
Escherichia coli
(B; B/r, try
−
; O5; and O86:B7) were labeled with homologous fluorescent antibodies (FLG); the way the label was dispersed on further growth in media free of antibody was followed by fluorescence microscopy. Fluorescence diminished diffusely along longitudinal wall but remained bright at cell poles (or cross walls); newly formed cross walls did not fluoresce. In agreement, reverse labeling (preincubation in unlabeled antibody, followed by staining on the slide with homologous FLG) showed that stainability of longitudinal wall increased gradually and diffusely with increased time of incubation, whereas polar wall remained nonfluorescent or stained only faintly; newly formed poles (or cross walls), on the other hand, stained brightly. These observations were confirmed by electron microscopy, after immunoferritin labeling. Although the mode of cross-wall formation remained unclear, our findings refuted reported ideas of segmental or polar growth of cell wall in
E. coli
and supported the idea of wall replication by diffuse intercalation, as described for
Salmonella
.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Cited by
34 articles.
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