A 35.7 kb DNA fragment from the Bacillus subtilis chromosome containing a putative 12.3 kb operon involved in hexuronate catabolism and a perfectly symmetrical hypothetical catabolite-responsive element.

The Bacillus subtilis strain 168 chromosomal region extending from 109 degrees to 112 degrees has been sequenced. Among the 35 ORFs identified, cotT and rapA were the only genes that had been previously mapped and sequenced. Out of ten ORFs belonging to a single putative transcription unit, seven are probably involved in hexuronate catabolism. Their sequences are homologous to Escherichia coli genes exuT, uidB, uxaA, uxaB, uxaC, uxuA and uxuB, which are all required for the uptake of free D-glucuronate, D-galacturonate and beta-glucuronide, and their transformation into glyceraldehyde 3-phosphate and pyruvate via 2-keto-3-deoxygluconate. The remaining three ORFs encode two dehydrogenases and a transcriptional regulator. The operon is preceded by a putative catabolite-responsive element (CRE), located between a hypothetical promoter and the RBS of the first gene. This element, the longest and the only so far described that is fully symmetrical, consists of a 26 bp palindrome matching the theoretical B. subtilis CRE sequence. The remaining predicted amino acid sequences that share homologies with other proteins comprise: a cytochrome P-450, a glycosyltransferase, an ATP-binding cassette transporter, a protein similar to the formate dehydrogenase alpha-subunit (FdhA), protein similar to NADH dehydrogenases, and three homologues of polypeptides that have undefined functions.

[1]  L. Merson-Davies,et al.  Analysis of five tylosin biosynthetic genes from the tyllBA region of the Streptomyces fradiae genome. , 1994, Molecular microbiology.

[2]  N. Welker,et al.  Cloning and characterization of a glutamine transport operon of Bacillus stearothermophilus NUB36: effect of temperature on regulation of transcription , 1991, Journal of bacteriology.

[3]  A Danchin,et al.  Bacillus subtilis genome project: cloning and sequencing of the 97 kb region from 325° to 333deg; , 1993, Molecular microbiology.

[4]  S. Wong,et al.  Sorbitol dehydrogenase from Bacillus subtilis. Purification, characterization, and gene cloning. , 1992, The Journal of biological chemistry.

[5]  D. Barstow,et al.  The pMTL nic- cloning vectors. I. Improved pUC polylinker regions to facilitate the use of sonicated DNA for nucleotide sequencing. , 1988, Gene.

[6]  H. Sahm,et al.  Biochemical characterization and sequence analysis of the gluconate:NADP 5-oxidoreductase gene from Gluconobacter oxydans , 1995, Journal of bacteriology.

[7]  Y. Fujita,et al.  Specific recognition of the Bacillus subtilis gnt cis‐acting catabolite‐responsive element by a protein complex formed between CcpA and seryl‐phosphorylated HPr , 1995, Molecular microbiology.

[8]  W. Nicholson,et al.  Catabolite repression of α amylase gene expression in Bacillus subtilis involves a trans‐acting gene product homologous to the Escherichia coli lacl and galR repressors , 1991, Molecular microbiology.

[9]  J. Devereux,et al.  A comprehensive set of sequence analysis programs for the VAX , 1984, Nucleic Acids Res..

[10]  A. Aronson,et al.  Gene structure and precursor processing of a novel Bacillus subtilis spore coat protein , 1989, Molecular microbiology.

[11]  M. Sargent Synchronous Cultures of Bacillus subtilis Obtained by Filtration with Glass Fiber Filters , 1973, Journal of bacteriology.

[12]  F. Pichinoty,et al.  Nutrition carbonée et étude taxonomique de Bacillus subtilis et B. licheniformis , 1979 .

[13]  E. Cundliffe,et al.  Cloning and characterization of two genes from Streptomyces lividans that confer inducible resistance to lincomycin and macrolide antibiotics. , 1991, Gene.

[14]  H. Mori,et al.  A 718-kb DNA sequence of the Escherichia coli K-12 genome corresponding to the 12.7-28.0 min region on the linkage map. , 1996, DNA research : an international journal for rapid publication of reports on genes and genomes.

[15]  N. Hugouvieux-Cotte-Pattat,et al.  Hexuronate catabolism in Erwinia chrysanthemi , 1987, Journal of bacteriology.

[16]  F. Blattner,et al.  Analysis of the Escherichia coli genome VI: DNA sequence of the region from 92.8 through 100 minutes. , 1995, Nucleic acids research.

[17]  W. Hillen,et al.  Catabolite repression in Bacillus subtilis: a global regulatory mechanism for the Gram‐positive bacteria? , 1995, Molecular microbiology.

[18]  F. Blattner,et al.  DNA sequence and analysis of 136 kilobases of the Escherichia coli genome: organizational symmetry around the origin of replication. , 1993, Genomics.

[19]  L. Merson-Davies,et al.  Analysis of five tyiosin biosynthetic genes from the tyllBA region of the Streptomyces fradiae genome , 1994, Molecular microbiology.

[20]  A. Wahba,et al.  Uronic acid metabolism in bacteria. I. Purification and properties of uronic acid isomerase in Escherichia coli. , 1960, The Journal of biological chemistry.

[21]  T. Niermann,et al.  Properties and primary structure of the L-malate dehydrogenase from the extremely thermophilic archaebacterium Methanothermus fervidus. , 1990, European journal of biochemistry.

[22]  R. Fleischmann,et al.  Complete Genome Sequence of the Methanogenic Archaeon, Methanococcus jannaschii , 1996, Science.

[23]  Mark Borodovsky,et al.  GENMARK: Parallel Gene Recognition for Both DNA Strands , 1993, Comput. Chem..

[24]  D. McConnell,et al.  Bacillus licheniformis alpha-amylase gene, amyL, is subject to promoter-independent catabolite repression in Bacillus subtilis , 1989, Journal of bacteriology.

[25]  I. Paulsen,et al.  Catabolite repression and inducer control in Gram-positive bacteria. , 1996, Microbiology.

[26]  J. Pouysségur,et al.  Le métabolisme des hexuronides et des hexuronates chez Escherichia coli K 12: Aspects physiologiques et génétiques de sa régulation , 1974 .

[27]  A. Sonenshein,et al.  Transcriptional regulation of Bacillus subtilis glucose starvation-inducible genes: control of gsiA by the ComP-ComA signal transduction system , 1992, Journal of bacteriology.

[28]  E. Myers,et al.  Basic local alignment search tool. , 1990, Journal of molecular biology.

[29]  C. Yanisch-Perron,et al.  Improved M13 phage cloning vectors and host strains: nucleotide sequences of the M13mp18 and pUC19 vectors. , 1985, Gene.

[30]  D. Turner,et al.  Improved free-energy parameters for predictions of RNA duplex stability. , 1986, Proceedings of the National Academy of Sciences of the United States of America.

[31]  J. Hoch,et al.  1 – The Genetic Map of Bacillus subtilis , 1982 .

[32]  S. Ehrlich,et al.  Sequence analysis of the Bacillus subtilis chromosome region between the serA and kdg loci cloned in a yeast artificial chromosome. , 1996, Microbiology.

[33]  K. Ahn,et al.  Variations and coding features of the sequence spanning the replication terminus of Bacillus subtilis 168 and W23 chromosomes. , 1991, Gene.

[34]  M. Weickert,et al.  Site-directed mutagenesis of a catabolite repression operator sequence in Bacillus subtilis. , 1990, Proceedings of the National Academy of Sciences of the United States of America.