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J. Bacteriol., Jul 1996, 4012-4019, Vol 178, No. 14
K Kruger and F Pfeifer
Halobacterium salinarium PHH4 synthesizes gas vesicles in the stationary
growth phase by the expression of 14 gyp genes arranged in two clusters.
The chromosomal gvpACNO (c-gvpACNO) gene cluster (encoding the major
structural gas vesicle protein GvpA and the minor structural protein GvpC
was transcribed as three mRNA species starting at one promoter during the
stationary phase of growth. The second gene cluster, c-gvpDEFGHIKLM), was
transcribed during all stages of growth as a relatively unstable, single
mRNA with a maximal length of 6 kb. In addition, a 1.7-kb c-gvpD transcript
was synthesized during stationary growth starting at the same promotor as
that of the cgvpDEFGHIJKLM mRNA. The expression of the first two genes
located in this unit (c- gvpD and c-gvpE) was also monitored by Western
blot (immunoblot) analyses using antisera raised against these proteins
synthesized in Escherichia coli. While the cGvpD protein was present only
during early exponential growth and disappeared during gas vesicle
formation, the cGvpE protein was present during cGvpA and gas vesicle
synthesis in the early stationary phase of growth. Previous data indicated
that cGvpD is involved in repression of gas vesicle formation, whereas
cGvpE is a transcriptional activator for the c-gvpA promoter. The
appearance of both proteins during the growth cycle is in line with the
functions of these proteins in gas vesicle synthesis. The mechanism of the
differential translation of cGvpD and cGvpE from the c-gvpDEFGHIJKLM rnRNA
still has to be elucidated, but antisense RNAs complementary to the 5'
terminus as well as the 3' portion of the c-gvpD mRNA might be involved in
this regulation. Such RNAs occurred during early stationary growth when the
cGvpD protein level decreased and may possibly inhibit the translation of
the c-gvpD mRNA.
Copyright © 1996, American Society for Microbiology
Transcript analysis of the c-vac region and differential synthesis of the two regulatory gas vesicle proteins GvpD and GvpE in Halobacterium salinarium PHH4
Institut fur Mikrobiologie und Genetik, Technische Hochschule Darmstadt, Germany.
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