author_facet Trach, K
Chapman, J W
Piggot, P
LeCoq, D
Hoch, J A
Trach, K
Chapman, J W
Piggot, P
LeCoq, D
Hoch, J A
author Trach, K
Chapman, J W
Piggot, P
LeCoq, D
Hoch, J A
spellingShingle Trach, K
Chapman, J W
Piggot, P
LeCoq, D
Hoch, J A
Journal of Bacteriology
Complete sequence and transcriptional analysis of the spo0F region of the Bacillus subtilis chromosome
Molecular Biology
Microbiology
author_sort trach, k
spelling Trach, K Chapman, J W Piggot, P LeCoq, D Hoch, J A 0021-9193 1098-5530 American Society for Microbiology Molecular Biology Microbiology http://dx.doi.org/10.1128/jb.170.9.4194-4208.1988 <jats:p>The total sequence of a 6,314-base-pair BglII fragment of the Bacillus subtilis chromosome containing the spo0F locus has been accomplished. Several genes of interest have been identified on this DNA fragment. The ctrA locus was recognized as coding for CTP synthetase by comparison of its deduced sequence with that of Escherichia coli CTP synthetase. A total of 53% of the residues are identical between the enzymes from these organisms. The spo0F locus was followed immediately by a locus, tsr, required for RNA synthesis in this organism. Temperature-sensitive mutations within the tsr locus have been identified, but strains with deletions of the locus are nonviable. It was concluded that tsr codes for an unknown essential component of the RNA synthesis machinery. The tsr gene was followed by another open reading frame which could code for a protein of 19,975 Mr. This gene was translated in vivo, but deletion-insertion mutations within the gene had no phenotype. The gene was cotranscribed with the tsr gene, although about 50% of the transcripts terminated between the two genes. The rev-4 mutation which reverts the sporulation-defective phenotype of erythromycin-resistant mutants was located to a partial open reading frame at the end of the fragment. Disruption of this open reading frame by deletion-insertion mutation did not result in a discernible phenotype. S1 protection experiments located the start sites of transcription for several of the genes on this fragment. The spo0F gene was found to be monocistronic. Regulation of the identified genes was investigated by using beta-galactosidase gene fusions.</jats:p> Complete sequence and transcriptional analysis of the spo0F region of the Bacillus subtilis chromosome Journal of Bacteriology
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series Journal of Bacteriology
source_id 49
title Complete sequence and transcriptional analysis of the spo0F region of the Bacillus subtilis chromosome
title_unstemmed Complete sequence and transcriptional analysis of the spo0F region of the Bacillus subtilis chromosome
title_full Complete sequence and transcriptional analysis of the spo0F region of the Bacillus subtilis chromosome
title_fullStr Complete sequence and transcriptional analysis of the spo0F region of the Bacillus subtilis chromosome
title_full_unstemmed Complete sequence and transcriptional analysis of the spo0F region of the Bacillus subtilis chromosome
title_short Complete sequence and transcriptional analysis of the spo0F region of the Bacillus subtilis chromosome
title_sort complete sequence and transcriptional analysis of the spo0f region of the bacillus subtilis chromosome
topic Molecular Biology
Microbiology
url http://dx.doi.org/10.1128/jb.170.9.4194-4208.1988
publishDate 1988
physical 4194-4208
description <jats:p>The total sequence of a 6,314-base-pair BglII fragment of the Bacillus subtilis chromosome containing the spo0F locus has been accomplished. Several genes of interest have been identified on this DNA fragment. The ctrA locus was recognized as coding for CTP synthetase by comparison of its deduced sequence with that of Escherichia coli CTP synthetase. A total of 53% of the residues are identical between the enzymes from these organisms. The spo0F locus was followed immediately by a locus, tsr, required for RNA synthesis in this organism. Temperature-sensitive mutations within the tsr locus have been identified, but strains with deletions of the locus are nonviable. It was concluded that tsr codes for an unknown essential component of the RNA synthesis machinery. The tsr gene was followed by another open reading frame which could code for a protein of 19,975 Mr. This gene was translated in vivo, but deletion-insertion mutations within the gene had no phenotype. The gene was cotranscribed with the tsr gene, although about 50% of the transcripts terminated between the two genes. The rev-4 mutation which reverts the sporulation-defective phenotype of erythromycin-resistant mutants was located to a partial open reading frame at the end of the fragment. Disruption of this open reading frame by deletion-insertion mutation did not result in a discernible phenotype. S1 protection experiments located the start sites of transcription for several of the genes on this fragment. The spo0F gene was found to be monocistronic. Regulation of the identified genes was investigated by using beta-galactosidase gene fusions.</jats:p>
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author Trach, K, Chapman, J W, Piggot, P, LeCoq, D, Hoch, J A
author_facet Trach, K, Chapman, J W, Piggot, P, LeCoq, D, Hoch, J A, Trach, K, Chapman, J W, Piggot, P, LeCoq, D, Hoch, J A
author_sort trach, k
container_issue 9
container_start_page 4194
container_title Journal of Bacteriology
container_volume 170
description <jats:p>The total sequence of a 6,314-base-pair BglII fragment of the Bacillus subtilis chromosome containing the spo0F locus has been accomplished. Several genes of interest have been identified on this DNA fragment. The ctrA locus was recognized as coding for CTP synthetase by comparison of its deduced sequence with that of Escherichia coli CTP synthetase. A total of 53% of the residues are identical between the enzymes from these organisms. The spo0F locus was followed immediately by a locus, tsr, required for RNA synthesis in this organism. Temperature-sensitive mutations within the tsr locus have been identified, but strains with deletions of the locus are nonviable. It was concluded that tsr codes for an unknown essential component of the RNA synthesis machinery. The tsr gene was followed by another open reading frame which could code for a protein of 19,975 Mr. This gene was translated in vivo, but deletion-insertion mutations within the gene had no phenotype. The gene was cotranscribed with the tsr gene, although about 50% of the transcripts terminated between the two genes. The rev-4 mutation which reverts the sporulation-defective phenotype of erythromycin-resistant mutants was located to a partial open reading frame at the end of the fragment. Disruption of this open reading frame by deletion-insertion mutation did not result in a discernible phenotype. S1 protection experiments located the start sites of transcription for several of the genes on this fragment. The spo0F gene was found to be monocistronic. Regulation of the identified genes was investigated by using beta-galactosidase gene fusions.</jats:p>
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spelling Trach, K Chapman, J W Piggot, P LeCoq, D Hoch, J A 0021-9193 1098-5530 American Society for Microbiology Molecular Biology Microbiology http://dx.doi.org/10.1128/jb.170.9.4194-4208.1988 <jats:p>The total sequence of a 6,314-base-pair BglII fragment of the Bacillus subtilis chromosome containing the spo0F locus has been accomplished. Several genes of interest have been identified on this DNA fragment. The ctrA locus was recognized as coding for CTP synthetase by comparison of its deduced sequence with that of Escherichia coli CTP synthetase. A total of 53% of the residues are identical between the enzymes from these organisms. The spo0F locus was followed immediately by a locus, tsr, required for RNA synthesis in this organism. Temperature-sensitive mutations within the tsr locus have been identified, but strains with deletions of the locus are nonviable. It was concluded that tsr codes for an unknown essential component of the RNA synthesis machinery. The tsr gene was followed by another open reading frame which could code for a protein of 19,975 Mr. This gene was translated in vivo, but deletion-insertion mutations within the gene had no phenotype. The gene was cotranscribed with the tsr gene, although about 50% of the transcripts terminated between the two genes. The rev-4 mutation which reverts the sporulation-defective phenotype of erythromycin-resistant mutants was located to a partial open reading frame at the end of the fragment. Disruption of this open reading frame by deletion-insertion mutation did not result in a discernible phenotype. S1 protection experiments located the start sites of transcription for several of the genes on this fragment. The spo0F gene was found to be monocistronic. Regulation of the identified genes was investigated by using beta-galactosidase gene fusions.</jats:p> Complete sequence and transcriptional analysis of the spo0F region of the Bacillus subtilis chromosome Journal of Bacteriology
spellingShingle Trach, K, Chapman, J W, Piggot, P, LeCoq, D, Hoch, J A, Journal of Bacteriology, Complete sequence and transcriptional analysis of the spo0F region of the Bacillus subtilis chromosome, Molecular Biology, Microbiology
title Complete sequence and transcriptional analysis of the spo0F region of the Bacillus subtilis chromosome
title_full Complete sequence and transcriptional analysis of the spo0F region of the Bacillus subtilis chromosome
title_fullStr Complete sequence and transcriptional analysis of the spo0F region of the Bacillus subtilis chromosome
title_full_unstemmed Complete sequence and transcriptional analysis of the spo0F region of the Bacillus subtilis chromosome
title_short Complete sequence and transcriptional analysis of the spo0F region of the Bacillus subtilis chromosome
title_sort complete sequence and transcriptional analysis of the spo0f region of the bacillus subtilis chromosome
title_unstemmed Complete sequence and transcriptional analysis of the spo0F region of the Bacillus subtilis chromosome
topic Molecular Biology, Microbiology
url http://dx.doi.org/10.1128/jb.170.9.4194-4208.1988