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PMID: 2179048 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Mechanisms of activation of the cryptic cel operon of Escherichia coli K12.

Genetics ·Vol. 124 ·No. 3 ·1990-03-00 ·Pages 473-82

Parker LL, Hall BG

Abstract

The cel (cellobiose utilization) operon of Escherichia coli K12 is not expressed in the wild-type organism. However, mutants that can express the operon and thereby utilize the beta-glucoside sugars cellobiose, arbutin and salicin are easily isolated. Two kinds of mutations are capable of activating the operon. The first involves mutations that allow the repressor to recognize the substrates cellobiose, arbutin and salicin as inducers. We have identified the sequence changes in five different active alleles and found those differences to be single base pair changes at one of two lysine codons in the repressor gene. The second kind of mutation involves the integration of the insertion sequences IS1, IS2 or IS5 into a 108-bp region 72-180 bp upstream of the start of transcription. Integration occurs at several different sites and in different orientations. Transcription of the cel operon begins at the same base pair in all mutants examined. Of 44 independent cel+ mutants, 27 were activated by point mutations and 17 were activated by insertion sequences. The preferred mechanism of activation appears to be strain dependent, since one of the parents yielded 94% insertionally activated alleles, while another yielded 100% point mutation activated alleles.

MeSH Terms
Base Sequence Cellobiose/metabolism Disaccharides/metabolism Escherichia coli/genetics,metabolism Gene Expression Genotype Molecular Sequence Data Mutation Operon Restriction Mapping
Chemicals
Disaccharides Cellobiose
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Parker L L
Department of Molecular and Cell Biology, University of Connecticut, Storrs 06268.
Hall B G
References (31)
31 references, click to expand
  1. Mutations caused by the insertion of genetic material into the galactose operon of Escherichia coli.
    J Mol Biol. 1969 Feb 28;40(1):93-105 PMID: 4903362
  2. Beta-glucoside (bgl) operon of Escherichia coli K-12: nucleotide sequence, genetic organization, and possible evolutionary relationship to regulatory components of two Bacillus subtilis genes.
    J Bacteriol. 1987 Jun;169(6):2579-90 PMID: 3034860
  3. Formation, induction, and curing of bacteriophage P1 lysogens.
    Virology. 1972 Jun;48(3):679-89 PMID: 4555608
  4. Regulation of the beta-glucoside system in Escherchia coli K-12.
    J Bacteriol. 1974 Nov;120(2):638-50 PMID: 4616943
  5. Mutagenesis by insertion of a drug-resistance element carrying an inverted repetition.
    J Mol Biol. 1975 Oct 5;97(4):561-75 PMID: 1102715
  6. Sizing and mapping of early adenovirus mRNAs by gel electrophoresis of S1 endonuclease-digested hybrids.
    Cell. 1977 Nov;12(3):721-32 PMID: 922889
  7. Nucleotide sequence of an insertion element, IS1.
    Proc Natl Acad Sci U S A. 1978 Feb;75(2):615-9 PMID: 273224
  8. Properties of the translocatable tetracycline-resistance element Tn10 in Escherichia coli and bacteriophage lambda.
    Genetics. 1978 Nov;90(3):427-61 PMID: 365678
  9. Nucleotide sequence of the transposable DNA-element IS2.
    Nucleic Acids Res. 1979 Mar;6(3):1111-22 PMID: 375194
  10. The sequence of IS4.
    Mol Gen Genet. 1981;181(2):169-75 PMID: 6268937
  11. Insertion of DNA activates the cryptic bgl operon in E. coli K12.
    Nature. 1981 Oct 22;293(5834):625-9 PMID: 6270569
  12. Functional genes for cellobiose utilization in natural isolates of Escherichia coli.
    J Bacteriol. 1987 Jun;169(6):2713-7 PMID: 3034866
  13. Role of cryptic genes in microbial evolution.
    Mol Biol Evol. 1983 Dec;1(1):109-24 PMID: 6400646
  14. Directed evolution of cellobiose utilization in Escherichia coli K12.
    Mol Biol Evol. 1984 Feb;1(2):171-82 PMID: 6400650
  15. Maintenance of the cellobiose utilization genes of Escherichia coli in a cryptic state.
    Mol Biol Evol. 1986 Sep;3(5):389-402 PMID: 2832693
  16. A fourth Escherichia coli gene system with the potential to evolve beta-glucoside utilization.
    Genetics. 1988 Jul;119(3):485-90 PMID: 3042507
  17. Regulation of the bgl operon of Escherichia coli by transcriptional antitermination.
    EMBO J. 1988 Oct;7(10):3271-7 PMID: 2846278
  18. Characterization and nucleotide sequence of the cryptic cel operon of Escherichia coli K12.
    Genetics. 1990 Mar;124(3):455-71 PMID: 2179047
  19. Specific-purpose plasmid cloning vectors. I. Low copy number, temperature-sensitive, mobilization-defective pSC101-derived containment vectors.
    Gene. 1981 Dec;16(1-3):227-35 PMID: 6282694
  20. The molecular basis of DNA-protein recognition inferred from the structure of cro repressor.
    Nature. 1982 Aug 19;298(5876):718-23 PMID: 6213863
  21. Escherichia coli DNA topoisomerase I mutants have compensatory mutations in DNA gyrase genes.
    Cell. 1982 Nov;31(1):43-51 PMID: 6297752
  22. Insertion of IS2 creates a novel ampC promoter in Escherichia coli.
    Cell. 1983 Mar;32(3):809-16 PMID: 6187472
  23. Cro repressor protein and its interaction with DNA.
    Cold Spring Harb Symp Quant Biol. 1983;47 Pt 1:427-33 PMID: 6305561
  24. Mapping and properties of the gam and sot genes of phage mu: their possible roles in recombination.
    Cold Spring Harb Symp Quant Biol. 1984;49:261-6 PMID: 6241548
  25. Improved M13 phage cloning vectors and host strains: nucleotide sequences of the M13mp18 and pUC19 vectors.
    Gene. 1985;33(1):103-19 PMID: 2985470
  26. Mini-mu bacteriophage with plasmid replicons for in vivo cloning and lac gene fusing.
    J Bacteriol. 1986 Oct;168(1):357-64 PMID: 3020001
  27. Enhancement of bacterial gene expression by insertion elements or by mutation in a CAP-cAMP binding site.
    J Mol Biol. 1986 Sep 5;191(1):85-95 PMID: 3025456
  28. Functional promoters created by the insertion of transposable element IS1.
    J Mol Biol. 1986 Oct 5;191(3):383-93 PMID: 3029382
  29. Biochemical genetics of the cryptic gene system for cellobiose utilization in Escherichia coli K12.
    Genetics. 1987 Mar;115(3):419-29 PMID: 3552873
  30. Positive and negative regulation of the bgl operon in Escherichia coli.
    J Bacteriol. 1987 Jun;169(6):2570-8 PMID: 3294798
  31. O0 and strong-polar mutations in the gal operon are insertions.
    Mol Gen Genet. 1968;102(4):353-63 PMID: 5743437
Article Info
Journal
Genetics
Abbr.
Genetics
ISSN
0016-6731
Published
1990-03-00
Pages
473-82
Language
English
Region
United States
NLM ID
0374636
PMCID
PMC1203941
Subset
IM
Grants
NIGMS NIH HHS · GM 37110 · United States
Databases
GENBANK
M64438, X52890
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