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Temperature-sensitive mutants of the EcoRI endonuclease.

Publication ,  Journal Article
Muir, RS; Flores, H; Zinder, ND; Model, P; Soberon, X; Heitman, J
Published in: J Mol Biol
December 19, 1997

The EcoRI endonuclease is an important recombinant DNA tool and a paradigm of sequence-specific DNA-protein interactions. We have isolated temperature-sensitive (TS) EcoRI endonuclease mutants (R56Q, G78D, P90S, V97I, R105K, M157I, C218Y, A235E, M255I, T261I and L263F) and characterized activity in vivo and in vitro. Although the majority were TS for function in vivo, all of the mutant enzymes were stably expressed and largely soluble at both 30 degrees C and 42 degrees C in vivo and none of the mutants was found to be TS in vitro. These findings suggest that these mutations may affect folding of the enzyme at elevated temperature in vivo. Both non-conservative and conservative substitutions occurred but were not correlated with severity of the mutation. Of the 12 residues identified, 11 are conserved between EcoRI and the isoschizomer RsrI (which shares 50% identity), a further indication that these residues are critical for EcoRI structure and function. Inspection of the 2.8 A resolution X-ray crystal structure of the wild-type EcoRI endonuclease-DNA complex revealed that: (1) the TS mutations cluster in one half of the globular enzyme; (2) several of the substituted residues interact with each other; (3) most mutations would be predicted to disrupt local structures; (4) two mutations may affect the dimer interface (G78D and A235E); (5) one mutation (P90S) occurred in a residue that is part of, or immediately adjacent to, the EcoRI active site and which is conserved in the distantly related EcoRV endonuclease. Finally, one class of mutants restricted phage in vivo and was active in vitro, whereas a second class did not restrict and was inactive in vitro. The two classes of mutants may differ in kinetic properties or cleavage mechanism. In summary, these mutations provide insights into EcoRI structure and function, and complement previous genetic, biochemical, and structural analyses.

Duke Scholars

Published In

J Mol Biol

DOI

ISSN

0022-2836

Publication Date

December 19, 1997

Volume

274

Issue

5

Start / End Page

722 / 737

Location

Netherlands

Related Subject Headings

  • Temperature
  • Mutation
  • Models, Molecular
  • Escherichia coli
  • Deoxyribonuclease EcoRI
  • DNA, Bacterial
  • DNA Repair
  • DNA Mutational Analysis
  • DNA Damage
  • Crystallography, X-Ray
 

Citation

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Muir, R. S., Flores, H., Zinder, N. D., Model, P., Soberon, X., & Heitman, J. (1997). Temperature-sensitive mutants of the EcoRI endonuclease. J Mol Biol, 274(5), 722–737. https://doi.org/10.1006/jmbi.1997.1419
Muir, R. S., H. Flores, N. D. Zinder, P. Model, X. Soberon, and J. Heitman. “Temperature-sensitive mutants of the EcoRI endonuclease.J Mol Biol 274, no. 5 (December 19, 1997): 722–37. https://doi.org/10.1006/jmbi.1997.1419.
Muir RS, Flores H, Zinder ND, Model P, Soberon X, Heitman J. Temperature-sensitive mutants of the EcoRI endonuclease. J Mol Biol. 1997 Dec 19;274(5):722–37.
Muir, R. S., et al. “Temperature-sensitive mutants of the EcoRI endonuclease.J Mol Biol, vol. 274, no. 5, Dec. 1997, pp. 722–37. Pubmed, doi:10.1006/jmbi.1997.1419.
Muir RS, Flores H, Zinder ND, Model P, Soberon X, Heitman J. Temperature-sensitive mutants of the EcoRI endonuclease. J Mol Biol. 1997 Dec 19;274(5):722–737.
Journal cover image

Published In

J Mol Biol

DOI

ISSN

0022-2836

Publication Date

December 19, 1997

Volume

274

Issue

5

Start / End Page

722 / 737

Location

Netherlands

Related Subject Headings

  • Temperature
  • Mutation
  • Models, Molecular
  • Escherichia coli
  • Deoxyribonuclease EcoRI
  • DNA, Bacterial
  • DNA Repair
  • DNA Mutational Analysis
  • DNA Damage
  • Crystallography, X-Ray