Affiliation:
1. Department of Molecular Biology and Biotechnology, University of Sheffield, Sheffield S10 2TN,1 and
2. Unilever Research, Sharnbrook, Bedfordshire MK44 1LQ,2 United Kingdom
Abstract
ABSTRACT
The GerAA, -AB, and -AC proteins of the
Bacillus subtilis
spore are required for the germination response to
l
-alanine as the sole germinant. They are likely to encode the components of the germination apparatus that respond directly to this germinant, mediating the spore's response; multiple homologues of the
gerA
genes are found in every spore former so far examined. The
gerA
operon is expressed in the forespore, and the level of expression of the operon appears to be low. The GerA proteins are predicted to be membrane associated. In an attempt to localize GerA proteins, spores of
B. subtilis
were broken and fractionated to give integument, membrane, and soluble fractions. Using antibodies that detect Ger proteins specifically, as confirmed by the analysis of strains lacking GerA and the related GerB proteins, the GerAA protein and the GerAC+GerBC protein homologues were localized to the membrane fraction of fragmented spores. The spore-specific penicillin-binding protein PBP5∗, a marker for the outer forespore membrane, was absent from this fraction. Extraction of spores to remove coat layers did not release the GerAC or AA protein from the spores. Both experimental approaches suggest that GerAA and GerAC proteins are located in the inner spore membrane, which forms a boundary around the cellular compartment of the spore. The results provide support for a model of germination in which, in order to initiate germination, germinant has to permeate the coat and cortex of the spore and bind to a germination receptor located in the inner membrane.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Cited by
111 articles.
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