THE TRANSCRIPTIONAL REGULATOR LEVR OF BACILLUS-SUBTILIS HAS DOMAINS HOMOLOGOUS TO BOTH SIGMA-54-DEPENDENT AND PHOSPHOTRANSFERASE SYSTEM-DEPENDENT REGULATORS
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DEBARBOUILLE, M
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机构:U.́ de Biochimie Microbienne, URA 1300 Ctr. Natl. Res. Sci., Departement des biotechnologies, 75724 Paris, Cedex 15
DEBARBOUILLE, M
MARTINVERSTRAETE, I
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机构:U.́ de Biochimie Microbienne, URA 1300 Ctr. Natl. Res. Sci., Departement des biotechnologies, 75724 Paris, Cedex 15
MARTINVERSTRAETE, I
KLIER, A
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机构:U.́ de Biochimie Microbienne, URA 1300 Ctr. Natl. Res. Sci., Departement des biotechnologies, 75724 Paris, Cedex 15
KLIER, A
RAPOPORT, G
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机构:U.́ de Biochimie Microbienne, URA 1300 Ctr. Natl. Res. Sci., Departement des biotechnologies, 75724 Paris, Cedex 15
RAPOPORT, G
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[1] U.́ de Biochimie Microbienne, URA 1300 Ctr. Natl. Res. Sci., Departement des biotechnologies, 75724 Paris, Cedex 15
The regulatory gene levR of the levanase operon of Bacillus subtilis was cloned and sequenced. It encodes a polypeptide of M(r) 106,064 with two domains homologous to members of two families of bacterial activators. One domain in LevR is homologous with one region of bacterial regulators including SacT and SacY of B. subtilis and BglG from Escherichia coli. Another domain of LevR is homologous to one part of the central domain of NifA and NtrC, which control nitrogen assimilation in Gram-negative bacteria. The levanase promoter contains two regions almost identical to the -12, -24 consensus regions present in sigma-54-dependent promoters. The expression of the levanase operon in E. coli was strongly dependent on sigma-54. Taken together, these results suggest that the operon is expressed from a -12, -24 promoter regulated by a sigma-54-like-dependent system in B. subtilis.