NDLI: The transcriptional regulator LevR of Bacillus subtilis has domains homologous to both sigma 54- and phosphotransferase system-dependent regulators.

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The transcriptional regulator LevR of Bacillus subtilis has domains homologous to both sigma 54- and phosphotransferase system-dependent regulators.

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The transcriptional regulator LevR of Bacillus subtilis has domains homologous to both sigma 54- and phosphotransferase system-dependent regulators.

Content Provider	World Health Organization (WHO)-Global Index Medicus
Author	Klier, A. Rapoport, G. Débarbouillé, M. Martin-verstraete, I.
Description	Author Affiliation: Débarbouillé M ( Unité de Biochimie Microbienne, URA 1300 du Centre National de la Recherche Scientifique, Paris, France.);
Abstract	The regulatory gene levR of the levanase operon of Bacillus subtilis was cloned and sequenced. It encodes a polypeptide of Mr 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.
ISSN	00278424
e-ISSN	10916490
Journal	Proceedings of the National Academy of Sciences of the United States of America
Issue Number	6
Volume Number	88
Language	English
Publisher	National Academy of Sciences
Publisher Date	1991-04-01
Publisher Place	United States
Access Restriction	Open
Subject Keyword	Bacillus Subtilis Genetics Bacterial Proteins Genes, Regulator Glycoside Hydrolases Operon Transcription Factors Amino Acid Sequence Enzymology Cloning, Molecular DNA, Bacterial Escherichia Coli Molecular Sequence Data Oligonucleotide Probes Polymerase Chain Reaction Promoter Regions, Genetic Recombinant Fusion Proteins Metabolism Restriction Mapping Sequence Homology, Nucleic Acid Beta-Galactosidase Comparative Study Research Support, Non-U.S. Gov't Multidisciplinary
Content Type	Text
Resource Type	Article
Subject	Multidisciplinary

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