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Journal of Bacteriology, August 2001, p. 4648-4651, Vol. 183, No. 15
Department of Marine Science, School of
Marine Science and Technology, University of Tokai, Shimizu,
Shizuoka 424-8610, Japan
Received 16 April 2001/Accepted 19 April 2001
Expression of Bacillus subtilis aprE, encoding an
extracellular alkaline protease, is positively regulated by
phosphorylated DegU, the regulator of a two-component regulatory
system, DegS-DegU. We found that the expression of an
aprE'-'lacZ fusion was greatly reduced in a disruption
mutant with a mutation of relA, which encodes the stringent
factor RelA. The level of DegU in the relA mutant was
similar to that in the wild-type cell. A relA degU double
mutation did not result in a further decrease of the
aprE'-'lacZ level found in a degU single
mutant. The expression of the aprE'-'lacZ fusion in the
relA mutant was stimulated by multicopy degR or the degU32(Hy) and degS200(Hy) mutations that
cause the stabilization of phosphorylated DegU. Furthermore, the
expression of sacB'-'lacZ, which is also dependent on
phosphorylated DegU, was stimulated by the relA mutation,
and this stimulation was not seen in the relA degU double
mutant. These results show that RelA (or its product
guanosine-3',5'-bisdiphosphate [pp Gpp]) does not affect the
phosphorylation of DegU and suggest that it participates in the
expression of aprE and sacB through the
regulation of DegU-dependent transcription.
0021-9193/01/$04.00+0 DOI: 10.1128/JB.183.15.4648-4651.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Involvement of Stringent Factor RelA in Expression
of the Alkaline Protease Gene aprE in Bacillus
subtilis
*
Corresponding author. Mailing address: Department of
Marine Science, School of Marine Science and Technology, Tokai
University, Shimizu, Shizuoka 424-8610, Japan. Phone: (543) 34-0411. Fax: (543) 34-9834. E-mail:
teruot{at}scc.u-tokai.ac.jp.
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