Cloning, nucleotide sequence, and expression of the Bacillus subtilis lon gene.

Standard

Cloning, nucleotide sequence, and expression of the Bacillus subtilis lon gene. / Riethdorf, Sabine; Völker, U; Gerth, U; Winkler, A; Engelmann, S; Hecker, M.

In: J BACTERIOL, Vol. 176, No. 21, 21, 1994, p. 6518-6527.

Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

Harvard

Riethdorf, S, Völker, U, Gerth, U, Winkler, A, Engelmann, S & Hecker, M 1994, 'Cloning, nucleotide sequence, and expression of the Bacillus subtilis lon gene.', J BACTERIOL, vol. 176, no. 21, 21, pp. 6518-6527. <http://www.ncbi.nlm.nih.gov/pubmed/7961402?dopt=Citation>

APA

Vancouver

Riethdorf S, Völker U, Gerth U, Winkler A, Engelmann S, Hecker M. Cloning, nucleotide sequence, and expression of the Bacillus subtilis lon gene. J BACTERIOL. 1994;176(21):6518-6527. 21.

Bibtex

@article{ca075bc37c854c0cad37cb4c4fdbf467,
title = "Cloning, nucleotide sequence, and expression of the Bacillus subtilis lon gene.",
abstract = "The lon gene of Escherichia coli encodes the ATP-dependent serine protease La and belongs to the family of sigma 32-dependent heat shock genes. In this paper, we report the cloning and characterization of the lon gene from the gram-positive bacterium Bacillus subtilis. The nucleotide sequence of the lon locus, which is localized upstream of the hemAXCDBL operon, was determined. The lon gene codes for an 87-kDa protein consisting of 774 amino acid residues. A comparison of the deduced amino acid sequence with previously described lon gene products from E. coli, Bacillus brevis, and Myxococcus xanthus revealed strong homologies among all known bacterial Lon proteins. Like the E. coli lon gene, the B. subtilis lon gene is induced by heat shock. Furthermore, the amount of lon-specific mRNA is increased after salt, ethanol, and oxidative stress as well as after treatment with puromycin. The potential promoter region does not show similarities to promoters recognized by sigma 32 of E. coli but contains sequences which resemble promoters recognized by the vegetative RNA polymerase E sigma A of B. subtilis. A second gene designated orfX is suggested to be transcribed together with lon and encodes a protein with 195 amino acid residues and a calculated molecular weight of 22,000.",
keywords = "Amino Acid Sequence, Molecular Sequence Data, Base Sequence, Sequence Analysis, DNA, Hot Temperature, Cloning, Molecular, Gene Rearrangement, *Gene Expression Regulation, Bacterial, ATP-Dependent Proteases, Bacillus subtilis/*genetics, Bacterial Proteins/classification/genetics, Escherichia coli/genetics, *Escherichia coli Proteins, Genes, Bacterial/*genetics, Heat-Shock Proteins/classification/*genetics, Mutagenesis, Insertional, Open Reading Frames/genetics, *Protease La, Recombinant Proteins/biosynthesis, Serine Endopeptidases/*genetics, Amino Acid Sequence, Molecular Sequence Data, Base Sequence, Sequence Analysis, DNA, Hot Temperature, Cloning, Molecular, Gene Rearrangement, *Gene Expression Regulation, Bacterial, ATP-Dependent Proteases, Bacillus subtilis/*genetics, Bacterial Proteins/classification/genetics, Escherichia coli/genetics, *Escherichia coli Proteins, Genes, Bacterial/*genetics, Heat-Shock Proteins/classification/*genetics, Mutagenesis, Insertional, Open Reading Frames/genetics, *Protease La, Recombinant Proteins/biosynthesis, Serine Endopeptidases/*genetics",
author = "Sabine Riethdorf and U V{\"o}lker and U Gerth and A Winkler and S Engelmann and M Hecker",
year = "1994",
language = "English",
volume = "176",
pages = "6518--6527",
journal = "J BACTERIOL",
issn = "0021-9193",
publisher = "American Society for Microbiology",
number = "21",

}

RIS

TY - JOUR

T1 - Cloning, nucleotide sequence, and expression of the Bacillus subtilis lon gene.

AU - Riethdorf, Sabine

AU - Völker, U

AU - Gerth, U

AU - Winkler, A

AU - Engelmann, S

AU - Hecker, M

PY - 1994

Y1 - 1994

N2 - The lon gene of Escherichia coli encodes the ATP-dependent serine protease La and belongs to the family of sigma 32-dependent heat shock genes. In this paper, we report the cloning and characterization of the lon gene from the gram-positive bacterium Bacillus subtilis. The nucleotide sequence of the lon locus, which is localized upstream of the hemAXCDBL operon, was determined. The lon gene codes for an 87-kDa protein consisting of 774 amino acid residues. A comparison of the deduced amino acid sequence with previously described lon gene products from E. coli, Bacillus brevis, and Myxococcus xanthus revealed strong homologies among all known bacterial Lon proteins. Like the E. coli lon gene, the B. subtilis lon gene is induced by heat shock. Furthermore, the amount of lon-specific mRNA is increased after salt, ethanol, and oxidative stress as well as after treatment with puromycin. The potential promoter region does not show similarities to promoters recognized by sigma 32 of E. coli but contains sequences which resemble promoters recognized by the vegetative RNA polymerase E sigma A of B. subtilis. A second gene designated orfX is suggested to be transcribed together with lon and encodes a protein with 195 amino acid residues and a calculated molecular weight of 22,000.

AB - The lon gene of Escherichia coli encodes the ATP-dependent serine protease La and belongs to the family of sigma 32-dependent heat shock genes. In this paper, we report the cloning and characterization of the lon gene from the gram-positive bacterium Bacillus subtilis. The nucleotide sequence of the lon locus, which is localized upstream of the hemAXCDBL operon, was determined. The lon gene codes for an 87-kDa protein consisting of 774 amino acid residues. A comparison of the deduced amino acid sequence with previously described lon gene products from E. coli, Bacillus brevis, and Myxococcus xanthus revealed strong homologies among all known bacterial Lon proteins. Like the E. coli lon gene, the B. subtilis lon gene is induced by heat shock. Furthermore, the amount of lon-specific mRNA is increased after salt, ethanol, and oxidative stress as well as after treatment with puromycin. The potential promoter region does not show similarities to promoters recognized by sigma 32 of E. coli but contains sequences which resemble promoters recognized by the vegetative RNA polymerase E sigma A of B. subtilis. A second gene designated orfX is suggested to be transcribed together with lon and encodes a protein with 195 amino acid residues and a calculated molecular weight of 22,000.

KW - Amino Acid Sequence

KW - Molecular Sequence Data

KW - Base Sequence

KW - Sequence Analysis, DNA

KW - Hot Temperature

KW - Cloning, Molecular

KW - Gene Rearrangement

KW - Gene Expression Regulation, Bacterial

KW - ATP-Dependent Proteases

KW - Bacillus subtilis/genetics

KW - Bacterial Proteins/classification/genetics

KW - Escherichia coli/genetics

KW - Escherichia coli Proteins

KW - Genes, Bacterial/genetics

KW - Heat-Shock Proteins/classification/genetics

KW - Mutagenesis, Insertional

KW - Open Reading Frames/genetics

KW - Protease La

KW - Recombinant Proteins/biosynthesis

KW - Serine Endopeptidases/genetics

KW - Amino Acid Sequence

KW - Molecular Sequence Data

KW - Base Sequence

KW - Sequence Analysis, DNA

KW - Hot Temperature

KW - Cloning, Molecular

KW - Gene Rearrangement

KW - Gene Expression Regulation, Bacterial

KW - ATP-Dependent Proteases

KW - Bacillus subtilis/genetics

KW - Bacterial Proteins/classification/genetics

KW - Escherichia coli/genetics

KW - Escherichia coli Proteins

KW - Genes, Bacterial/genetics

KW - Heat-Shock Proteins/classification/genetics

KW - Mutagenesis, Insertional

KW - Open Reading Frames/genetics

KW - Protease La

KW - Recombinant Proteins/biosynthesis

KW - Serine Endopeptidases/genetics

M3 - SCORING: Journal article

VL - 176

SP - 6518

EP - 6527

JO - J BACTERIOL

JF - J BACTERIOL

SN - 0021-9193

IS - 21

M1 - 21

ER -