Research output: Contribution to journal › Article › peer-review
Expression of a stress- and starvation-induced dps/pexB-homologous gene is controlled by the alternative sigma factor σ(B) in Bacillus subtilis. / Antelmann, Haike; Engelmann, Susanne; Schmid, Roland; Sorokin, Alexei; Lapidus, Alla; Hecker, Michael.
In: Journal of Bacteriology, Vol. 179, No. 23, 12.1997, p. 7251-7256.Research output: Contribution to journal › Article › peer-review
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TY - JOUR
T1 - Expression of a stress- and starvation-induced dps/pexB-homologous gene is controlled by the alternative sigma factor σ(B) in Bacillus subtilis
AU - Antelmann, Haike
AU - Engelmann, Susanne
AU - Schmid, Roland
AU - Sorokin, Alexei
AU - Lapidus, Alla
AU - Hecker, Michael
PY - 1997/12
Y1 - 1997/12
N2 - σ(B)-dependent general stress proteins (Gsps) of Bacillus subtilis are essential for the development of glucose-starvation-induced cross-resistance to oxidative challenge. However, the proteins directly involved in this nonspecific resistance to oxidative stress have to be identified. We found that one prominent Gsp displayed strong sequence similarity to the previously characterized oxidative-stress-inducible MrgA protein of B. subtilis and to the starvation-induced Dps/PexB protein of Escherichia coli. We therefore designated this prominent Gsp Dps. While MrgA belongs to the peroxide- stress-inducible proteins needed for the H2O2-inducible adaptive response to oxidative stress, Dps belongs to the proteins induced by heat, salt, or ethanol stress and after starvation for glucose but not by a sublethal oxidative challenge. Primer extension experiments identified two overlapping promoters upstream of the coding region of dps, one being σ(B) dependent (P(B)) and the other being σ(B) independent (P1). Both promoters contribute to the basal level of dps during growth. After stress or during entry into the stationary phase, transcription from P1 strongly increased whereas transcription from P1 decreased. Mutant strains lacking Dps completely failed to develop glucose-starvation-induced resistance to oxidative stress. These results confirm our suggestion that σ(B)-dependent general stress proteins of B. subtilis are absolutely required for the development of nonspecific resistance to oxidative stress.
AB - σ(B)-dependent general stress proteins (Gsps) of Bacillus subtilis are essential for the development of glucose-starvation-induced cross-resistance to oxidative challenge. However, the proteins directly involved in this nonspecific resistance to oxidative stress have to be identified. We found that one prominent Gsp displayed strong sequence similarity to the previously characterized oxidative-stress-inducible MrgA protein of B. subtilis and to the starvation-induced Dps/PexB protein of Escherichia coli. We therefore designated this prominent Gsp Dps. While MrgA belongs to the peroxide- stress-inducible proteins needed for the H2O2-inducible adaptive response to oxidative stress, Dps belongs to the proteins induced by heat, salt, or ethanol stress and after starvation for glucose but not by a sublethal oxidative challenge. Primer extension experiments identified two overlapping promoters upstream of the coding region of dps, one being σ(B) dependent (P(B)) and the other being σ(B) independent (P1). Both promoters contribute to the basal level of dps during growth. After stress or during entry into the stationary phase, transcription from P1 strongly increased whereas transcription from P1 decreased. Mutant strains lacking Dps completely failed to develop glucose-starvation-induced resistance to oxidative stress. These results confirm our suggestion that σ(B)-dependent general stress proteins of B. subtilis are absolutely required for the development of nonspecific resistance to oxidative stress.
UR - http://www.scopus.com/inward/record.url?scp=0030665283&partnerID=8YFLogxK
U2 - 10.1128/jb.179.23.7251-7256.1997
DO - 10.1128/jb.179.23.7251-7256.1997
M3 - Article
C2 - 9393687
AN - SCOPUS:0030665283
VL - 179
SP - 7251
EP - 7256
JO - Journal of Bacteriology
JF - Journal of Bacteriology
SN - 0021-9193
IS - 23
ER -
ID: 90042981