Journal of Bacteriology, August 1999, p. 4584-4591, Vol. 181, No. 15
0021-9193/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Faculty of Pharmaceutical Sciences,
Received 11 March 1999/Accepted 21 May 1999
The expression of 21 novel genes located in the region from
dnaA to abrB of the Bacillus
subtilis chromosome was analyzed. One of the genes,
yaaH, had a predicted promoter sequence conserved among
SigE-dependent genes. Northern blot analysis revealed that yaaH mRNA was first detected from 2 h after the cessation
of logarithmic growth (T2) of sporulation
in wild-type cells and in spoIIIG (SigG
) and
spoIVCB (SigK
) mutants but not in
spoIIAC (SigF
) and spoIIGAB
(SigE
) mutants. The transcription start point was
determined by primer extension analysis; the
10 and
35 regions are
very similar to the consensus sequences recognized by SigE-containing
RNA polymerase. A YaaH-His tag fusion encoded by a plasmid with a
predicted promoter for the yaaH gene was produced from
T2 of sporulation in a B. subtilis transformant and extracted from mature spores,
indicating that the yaaH gene product is a spore protein.
Inactivation of the yaaH gene by insertion of an
erythromycin resistance gene did not affect vegetative growth or spore
resistance to heat, chloroform, and lysozyme. The germination of
yaaH mutant spores in a mixture of
L-asparagine, D-glucose,
D-fructose, and potassium chloride was almost the same as
that of wild-type spores, but the mutant spores were defective in
L-alanine-stimulated germination. These results suggest
that yaaH is a novel gene encoding a spore protein produced
in the mother cell compartment from T2 of
sporulation and that it is required for the
L-alanine-stimulated germination pathway.
*
Corresponding author. Mailing address: Faculty of
Pharmaceutical Sciences, Setsunan University, Hirakata, Osaka 573-0101, Japan. Phone: (81) 720-66-3112 or -3114. Fax: (81) 720-66-3112 or
-3114. E-mail: watabe{at}pharm.setsunan.ac.jp.
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