Literature DB >> 5326110

Methylated bases in the host-modified deoxyribonucleic acid of Escherichia coli and bacteriophage lambda.

M Gough, S Lederberg.   

Abstract

Gough, Michael (Brown University, Providence, R.I.), and Seymour Lederberg. Methylated bases in the host-modified deoxyribonucleic acid of Escherichia coli and bacteriophage lambda. J. Bacteriol. 91:1460-1468. 1966.-The deoxyribonucleic acid (DNA) from strains of Escherichia coli and phage lambda was examined to determine whether the types or amounts of methionine-derived methylated bases present correlated with the host-specific modification of that DNA. The DNA of strain C600 (which has K-12 modification specificity) and of a modificationless mutant of C600 are similar in their content of 5-methylcytosine and 6-methylaminopurine. Strains Bc251 and its P1-lysogen differ in P1-controlled specificity, but they have the same content of 6-methylaminopurine, and both lack 5-methylcytosine in their DNA. Phage lambda contains the same methylated bases as its host of origin, but in reduced amounts and in different proportions. Although minor amounts of these methylated bases may have importance as a result of their location, the presence of the majority of these methylated bases is irrelevant to the specificity of host modification of DNA.

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Year:  1966        PMID: 5326110      PMCID: PMC316064          DOI: 10.1128/jb.91.4.1460-1468.1966

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  36 in total

1.  HOST SPECIFICITY OF DNA PRODUCED BY ESCHERICHIA COLI. IV. HOST SPECIFICITY OF INFECTIOUS DNA FROM BACTERIOPHAGE LAMBDA.

Authors:  D DUSSOIX; W ARBER
Journal:  J Mol Biol       Date:  1965-02       Impact factor: 5.469

2.  [On a thermosensitive repression system in the Escherichia coli lambda bacteriophage].

Authors:  R SUSSMAN; F JACOB
Journal:  C R Hebd Seances Acad Sci       Date:  1962-02-19

3.  Host specificity of DNA produced by Escherichia coli. I. Host controlled modification of bacteriophage lambda.

Authors:  W ARBER; D DUSSOIX
Journal:  J Mol Biol       Date:  1962-07       Impact factor: 5.469

4.  N-Methylation of uridylic acid and preparation of oligonucleotides of 3-methyluridylic acid.

Authors:  W SZER; D SHUGAR
Journal:  Acta Biochim Pol       Date:  1960       Impact factor: 2.149

5.  The transformation of Escherichia coli with deoxyribonucleic acid isolated from bacteriophage lambda-dg.

Authors:  A D KAISER; D S HOGNESS
Journal:  J Mol Biol       Date:  1960-12       Impact factor: 5.469

6.  A fine-structure genetic and chemical study of the enzyme alkaline phosphatase of E. coli. I. Purification and characterization of alkaline phosphatase.

Authors:  A GAREN; C LEVINTHAL
Journal:  Biochim Biophys Acta       Date:  1960-03-11

7.  A variant of phage P2 originating in Escherichia coli, strain B.

Authors:  D COHEN
Journal:  Virology       Date:  1959-01       Impact factor: 3.616

8.  Suppression of the multiplication of heterologous bacteriophages in lysogenic bacteria.

Authors:  S LEDERBERG
Journal:  Virology       Date:  1957-06       Impact factor: 3.616

9.  Microdetermination of purines and pyrimidines in biological materials.

Authors:  A MARSHAK; H J VOGEL
Journal:  J Biol Chem       Date:  1951-04       Impact factor: 5.157

10.  Utilization of ribosylhomocysteine by various microorganisms.

Authors:  J A Duerre; P M Bowden
Journal:  Biochem Biophys Res Commun       Date:  1964-06-01       Impact factor: 3.575

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  14 in total

1.  Methylation pattern of lambda deoxyribonucleic acid.

Authors:  C Hidalgo; H A Nash
Journal:  J Virol       Date:  1972-11       Impact factor: 5.103

2.  In vivo suppression of coding associated with bacteriophage-induced S-adenosylmethionine hydrolase.

Authors:  P W Siersma; S Lederberg
Journal:  J Bacteriol       Date:  1970-02       Impact factor: 3.490

3.  Host specificity of DNA produced by Escherichia coli, X. In vitro restriction of phage fd replicative form.

Authors:  S Linn; W Arber
Journal:  Proc Natl Acad Sci U S A       Date:  1968-04       Impact factor: 11.205

4.  Deoxyribonucleic acid-cytosine methylation by host- and plasmid-controlled enzymes.

Authors:  M S May; S Hattaman
Journal:  J Bacteriol       Date:  1975-04       Impact factor: 3.490

5.  Restriction and modification in B. subtilis. The biochemical basis of modification against endo R. Bsu R restriction.

Authors:  U Günthert; J Stutz; G Klotz
Journal:  Mol Gen Genet       Date:  1975-12-30

6.  Methylation of cytosine residues in DNA controlled by a drug resistance factor (host-induced modification-R factors-N 6 -methyladenine-5-methylcytosine).

Authors:  S Hattman; E Gold; A Plotnik
Journal:  Proc Natl Acad Sci U S A       Date:  1972-01       Impact factor: 11.205

7.  Variation of 6-methylaminopurine content in bacteriophage P22 deoxyribonucleic acid as a function of host specificity.

Authors:  S Hattman
Journal:  J Virol       Date:  1971-05       Impact factor: 5.103

8.  DNA methylase from HeLa cell nuclei.

Authors:  P H Roy; A Weissbach
Journal:  Nucleic Acids Res       Date:  1975-10       Impact factor: 16.971

9.  Isolation of a mutant of Escherichia coli defective in cytosine-specific deoxyribonucleic acid methylase activity and in partial protection of bacteriophage lambda against restriction by cells containing the N-3 drug-resistance factor.

Authors:  S Hattman; S Schlagman; L Cousens
Journal:  J Bacteriol       Date:  1973-09       Impact factor: 3.490

10.  Mutants of the N-3 R-factor conditionally defective in hspII modification and deoxyribonucleic acid-cytosine methylase activity.

Authors:  S Schlagman; S Hattman
Journal:  J Bacteriol       Date:  1974-10       Impact factor: 3.490

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