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Appl. Environ. Microbiol., 01 1995, 200-204, Vol 61, No. 1
GB Leisman, J Waukau and SA Forst
We have examined the production of the outer membrane proteins of the
primary and secondary forms of Xenorhabdus nematophilus during exponential-
and stationary-phase growth at different temperatures. The most highly
expressed outer membrane protein of X. nematophilus was OpnP. The amino
acid composition of OpnP was very similar to those of the porin proteins
OmpF and OmpC of Escherichia coli. N-terminal amino acid sequence analysis
revealed that residues 1 to 27 of the mature OpnP shared 70 and 60%
sequence identities with OmpC and OmpF, respectively. These results suggest
that OpnP is a major porin protein in X. nematophilus. Three additional
proteins, OpnA, OpnB, and OpnS, were induced during stationary-phase
growth. OpnB was present at a high level in stationary-phase cells grown at
19 to 30 degrees C and was repressed in cells grown at 34 degrees C. OpnA
was optimally produced at 30 degrees C and was not present in cells grown
at lower and higher temperatures. The production of OpnS was not dependent
on growth temperature. In contrast, another outer membrane protein, OpnT,
was strongly induced as the growth temperature was elevated from 19 to 34
degrees C. In addition, we show that the stationary-phase proteins OpnA and
OpnB were not produced in secondary-form cells.
Copyright © 1995, American Society for Microbiology
Characterization and environmental regulation of outer membrane proteins in Xenorhabdus nematophilus
Department of Biological Sciences, University of Wisconsin, Milwaukee 53201.
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