cir, a gene conferring resistance to colicin I maps between mgl and fpk on the Escherichia coli chromosome (original) (raw)
We’re sorry, something doesn't seem to be working properly.
Please try refreshing the page. If that doesn't work, please contact support so we can address the problem.
Summary
With the help of the tetracycline resistance transposon Tn_10_ in and around the mgl genes the gene cir was mapped. cir is 80% cotransducible with mgl by P1 transduction. The sequence of the surrounding markers in clockwise order was established as: cdd fpk cir mgl gyrA. The direction of transcription in cir was determined as clockwise on the Escherichia coli chromosome. The gene product of cir, an outer membrane receptor for colicin I, is not part of the mgl operon. It is not regulated by D-fucose, the inducer of the mgl system and mutants defective in cir are unimpaired in the uptake of substrates of the _mgl_-dependent transport system.
Access this article
Subscribe and save
- Get 10 units per month
- Download Article/Chapter or eBook
- 1 Unit = 1 Article or 1 Chapter
- Cancel anytime Subscribe now
Buy Now
Price excludes VAT (USA)
Tax calculation will be finalised during checkout.
Instant access to the full article PDF.
Similar content being viewed by others
References
- Argast M, Boos W (1980) Co-regulation in Escherichia coli of a novel transport system for _sn_-glycerol-3-phosphate and outer membrane protein Ic (e, E) with alkaline phosphatase and phosphate-binding protein. J Bacteriol 143:142–150
Google Scholar - Bachmann BJ, Low KB (1980) Linkage map of Escherichia coli K12. Microbiol Rev 44:1–56
Google Scholar - Boos W (1982) Synthesis of (2R)-glycerol-o-β-D-galacto-pyranoside by β-galactosidase. Methods Enzymol 89:59–64
Google Scholar - Boos W, Sarvas M (1970) Close linkage between a galactose binding protein and the β-methylgalactoside permease in Escherichia coli. Eur J Biochem 13:526–533
Google Scholar - Boos W, Steinacher I, Engelhardt-Altendorf D (1981) Mapping of mglB, the structural gene of the galactose-binding protein of Escherichia coli. Mol Gen Genet 184:508–518
Google Scholar - Bowles LK, Minguel AG, Konisky J (1983) Purification of the colicin I receptor. J Biol Chem 258:1215–1220
Google Scholar - Cardelli J, Konisky J (1974) Isolation and characterization of an Escherichia coli mutant tolerant to colicin Ia and Ib. J Bacteriol 119:379–385
Google Scholar - Casadaban M (1976) Transposition and fusion of the lac genes to selected promotors in Escherichia coli using bacteriophage lambda and Mu. J Mol Biol 104:541–555
Google Scholar - Eckhardt T (1977) Use of argA-lac fusions to generate lambda-argA-lac bacteriophages and to determine the direction of transcription of argA transcription in Escherichia coli. J Bacteriol 132:60–66
Google Scholar - Ferenci T, Kornberg HL (1974) The role of phosphotransferasemediated syntheses of fructose-1-phosphate and fructose-6-phosphate in the growth of Escherichia coli on fructose. Proc R Soc London Ser B 187:105–119
Google Scholar - Ferenci T, Boos W (1980) The role of the Escherichia coli λ receptor in the transport of maltose and maltodextrins. J Supramolec Struct 13:101–116
Google Scholar - Hantke K (1976) Phage T6 — colicin K receptor and nucleoside transport in Escherichia coli. FEBS Lett 70:109–112
Google Scholar - Hantke K (1981) Regulation of ferric iron transport in Escherichia coli K12 isolation of a constitutive mutant. Mol Gen Genet 182:288–292
Google Scholar - Harayama Y, Bollinger J, Iino T, Hazelbauer GL (1983) Characterization of the mgl operon of Escherichia coli by transposon mutagenesis and molecular cloning. J Bacteriol 153:408–415
Google Scholar - Hazelbauer GL, Adler J (1971) Role of the galactose-binding protein in the chemotaxis of Escherichia coli toward galactose. Nature (London) New Biol 12:101–104
Google Scholar - Kleckner N, Roth J, Botstein D (1977) Genetic engineering in vivo using translocatable drug-resistance elements; new methods in bacterial genetics. J Mol Biol 116:125–159
Google Scholar - Kleckner N, Barker D, Ross DG, Botstein D, Swan JA, Zaben M (1978) Properties of the tetracycline-resistance element Tn_10_ in Escherichia coli and bacteriophage lambda. Genetics 90:427–461
Google Scholar - Komeda Y, Iino T (1979) Regulation of expression of the flagellin gene (hag) in Escherichia coli K-12: Analysis of hag-lac gene fusions. J Bacteriol 139:721–729
Google Scholar - Konisky J (1971) Characterization of colicin Ia and colicin Ib; chemical studies of protein structure. J Biol Chem 247:3750–3755
Google Scholar - Konisky J, Soucek S, Frick K, Davies JK, Hammond C (1976) Relationship between the transport of iron and the amount of specific colicin Ia membrane receptors in Escherichia coli. J Bacteriol 127:249–257
Google Scholar - Laemmli UK (1970) Cleavage of structural protein during the assembly of the head of bacteriophage T4. Nature (London) 227:680–685
Google Scholar - Ludtke D, Larson TJ, Beck C, Boos W (1982) Only one gene is required for the _glpT_-dependent transport of _sn_-glycerol-3-phosphate in Escherichia coli. Mol Gen Genet 186:540–547
Google Scholar - Miller JH (1972) Experiments in Molecular Genetics. Cold Spring Harbor Laboratories, Cold Spring Harbor, New York
Google Scholar - Parnes JR, Boos W (1973) Unidirectional transport activity mediated by the galactose-binding protein of Escherichia coli. J Biol Chem 248:4436–4445
Google Scholar - Rotman B, Guzman R (1982) Identification of the mglA gene product in the β-methylgalactoside transport system of Escherichia coli using plasmid DNA deletions generated in vitro. J Biol Chem 257:9030–9034
Google Scholar - Silhavy TJ, Boos W (1974) Selection procedure for mutants defective in the β-methylgalactoside transport system of Escherichia coli utilizing the compound 2R-glyceryl-β-D-galactopyranoside. J Bacteriol 120:424–432
Google Scholar - Tabor H, Hafner WE, Tabor CW (1980) Construction of an Escherichia coli strain unable to synthesize putrescine, spermidine or cadaverine: characterization of two genes controlling lysine decarboxylase. J Bacteriol 144:952–956
Google Scholar - Worsham LP, Konisky J (1981) Use of cir-lac operon fusions to study transcriptional regulation of the colicin Ia receptor in Escherichia coli K-12. J Bacteriol 145:647–650
Google Scholar
Author information
Authors and Affiliations
- Department of Biology, University of Konstanz, P.O. Box 5560, D-7750, Konstanz, Germany
Winfried Boos, Christine Bantlow, Dorothee Benner & Elke Roller
Authors
- Winfried Boos
You can also search for this author inPubMed Google Scholar - Christine Bantlow
You can also search for this author inPubMed Google Scholar - Dorothee Benner
You can also search for this author inPubMed Google Scholar - Elke Roller
You can also search for this author inPubMed Google Scholar
Additional information
Communicated by E. Bautz
Rights and permissions
About this article
Cite this article
Boos, W., Bantlow, C., Benner, D. et al. cir, a gene conferring resistance to colicin I maps between mgl and fpk on the Escherichia coli chromosome.Molec. Gen. Genet. 191, 401–406 (1983). https://doi.org/10.1007/BF00425754
- Received: 07 May 1983
- Issue Date: January 1983
- DOI: https://doi.org/10.1007/BF00425754