Literature DB >> 893408

Micrococcus luteus correndonucleases. I. resolution and purification of two endonucleases specific for DNA containing pyrimidine dimers.

S Riazuddin, L Grossman.   

Abstract

Five peaks of endonuclease activity showing a preference for ultraviolet-damaged DNA have been chromatographically identified from extracts of Micrococcus luteus. They are numerically designated as I to V in order of their elution from phosphocellulose (Whatman P-11) columns. The first two of these peaks have been highly purified by a combination of gel filtration and affinity chromatography and are catalytically homogeneous judging from their effect on transforming DNAs. Peak I, which has an isoelectric point of 4.7, is heat-stable, requires high ionic strength for optimal activity, acts with equal facility on ultraviolet-irradiated native and denatured DNA, and has been designated as Py pyrimidine dimer Py correndonuclease I. Peak II which has a pI value of 8.7, is heat-labile, is inhibited by high ionic strength, acts on ultraviolet-irradiated native but not denatured DNA, and has been designated as Py pyrimidine dimer Py correndonuclease II. Both enzymes are inhibited by Ca2+ and Zn2+, do not show any cofactor or sulfhydryl requirement, act optimally between pH 7.0 and 7.4, and have molecular weights between 11,000 and 15,000. Py pyrimidine dimer Py correndonuclease I requires a dose about 1.6 times that for Py pyrimidine dimers Py correndonuclease II for incision saturation of irradiated phiX174 RFI DNA.

Entities:  

Mesh:

Substances:

Year:  1977        PMID: 893408

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  20 in total

1.  Unusual conformation of (dA)n.(dT)n-tracts as revealed by cyclobutane thymine-thymine dimer formation.

Authors:  V Lyamichev
Journal:  Nucleic Acids Res       Date:  1991-08-25       Impact factor: 16.971

2.  UV endonuclease of Micrococcus luteus, a cyclobutane pyrimidine dimer-DNA glycosylase/abasic lyase: cloning and characterization of the gene.

Authors:  S Shiota; H Nakayama
Journal:  Proc Natl Acad Sci U S A       Date:  1997-01-21       Impact factor: 11.205

3.  T4 DNA polymerase (3'-5') exonuclease, an enzyme for the detection and quantitation of stable DNA lesions: the ultraviolet light example.

Authors:  P W Doetsch; G L Chan; W A Haseltine
Journal:  Nucleic Acids Res       Date:  1985-05-10       Impact factor: 16.971

4.  Reconstitution of an Escherichia coli repair endonuclease activity from the separated uvrA+ and uvrB+/uvrC+ gene products.

Authors:  E Seeberg
Journal:  Proc Natl Acad Sci U S A       Date:  1978-06       Impact factor: 11.205

5.  Protein complexes formed during the incision reaction catalyzed by the Escherichia coli UvrABC endonuclease.

Authors:  A T Yeung; W B Mattes; L Grossman
Journal:  Nucleic Acids Res       Date:  1986-03-25       Impact factor: 16.971

6.  Physical association of pyrimidine dimer DNA glycosylase and apurinic/apyrimidinic DNA endonuclease essential for repair of ultraviolet-damaged DNA.

Authors:  Y Nakabeppu; M Sekiguchi
Journal:  Proc Natl Acad Sci U S A       Date:  1981-05       Impact factor: 11.205

Review 7.  DNA glycosylases.

Authors:  S J Caradonna; Y C Cheng
Journal:  Mol Cell Biochem       Date:  1982-07-07       Impact factor: 3.396

8.  Selection of Arabidopsis cDNAs that partially correct phenotypes of Escherichia coli DNA-damage-sensitive mutants and analysis of two plant cDNAs that appear to express UV-specific dark repair activities.

Authors:  Q Pang; J B Hays; I Rajagopal; T S Schaefer
Journal:  Plant Mol Biol       Date:  1993-06       Impact factor: 4.076

9.  Endonucleolytic activity directed towards 8-(2-hydroxy-2-propyl) purines in double-stranded DNA.

Authors:  Z Livneh; D Elad; J Sperling
Journal:  Proc Natl Acad Sci U S A       Date:  1979-11       Impact factor: 11.205

10.  Apurinic/apyrimidinic endonucleases in repair of pyrimidine dimers and other lesions in DNA.

Authors:  H R Warner; B F Demple; W A Deutsch; C M Kane; S Linn
Journal:  Proc Natl Acad Sci U S A       Date:  1980-08       Impact factor: 11.205

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.