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Journal of Bacteriology, April 2000, p. 1916-1922, Vol. 182, No. 7
0021-9193/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Purification and Characterization of the DeoR
Repressor of Bacillus subtilis
Xianmin
Zeng,1
Hans H.
Saxild,1,* and
Robert L.
Switzer2
Department of Microbiology, Technical
University of Denmark, DK-2800 Lyngby,
Denmark,1 and Department of
Biochemistry, University of Illinois, Urbana,
Illinois2
Received 24 September 1999/Accepted 13 December 1999
Transcription of the Bacillus subtilis dra-nupC-pdp
operon is repressed by the DeoR repressor protein. The DeoR repressor with an N-terminal His tag was overproduced with a plasmid under control of a phage T5 promoter in Escherichia
coli and was purified to near homogeneity by one affinity
chromatography step. Gel filtration experimental results showed
that native DeoR has a mass of 280 kDa and appears to exist as an
octamer. Binding of DeoR to the operator DNA of the
dra-nupC-pdp operon was characterized by using an
electrophoretic gel mobility shift assay. An apparent
dissociation constant of 22 nM was determined for binding of DeoR to
operator DNA, and the binding curve indicated that the binding of DeoR to the operator DNA was cooperative. In the presence of
low-molecular-weight effector deoxyribose-5-phosphate, the dissociation
constant was higher than 1,280 nM. The dissociation constant remained
unchanged in the presence of deoxyribose-1-phosphate. DNase I
footprinting exhibited a protected region that extends over more than
43 bp, covering a palindrome together with a direct repeat to one half of the palindrome and the nucleotides between them.
*
Corresponding author. Mailing address: Department of
Microbiology, Technical University of Denmark, Building 301, DK-2800 Lyngby, Denmark. Phone: 45 25 24 95. Fax: 45 88 26 60. E-mail: imhhs{at}pop.dtu.dk.
Journal of Bacteriology, April 2000, p. 1916-1922, Vol. 182, No. 7
0021-9193/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
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