Lambdoid phages that simplify the recovery of in vitro recombinants

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Beggs, J.D., Guerineau, M., Atkins, J.F.: A map of the restriction targets in yeast 2 micron plasmid DNA cloned on bacteriophage lambda. Molec. gen. Genet. (in press) 1976

Bellett, A.J.D., Busse, H.G., Baldwin, R.L.: Tandem genetic duplications in a derivative of phage lambda. The bacteriophage lambda, ed. by A.D. Hershey, pp. 501–514 (1971)

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Borck, K., Beggs, J.D., Brammar, W.J., Hopkins, A.S., Murray, N.E.: The construction in vitro of transducing derivatives of phage lambda. Molec. gen. Genet.146, 199–207 (1976)

Campbell, A.: Sensitive mutants of bacteriophage λ. Virology14, 22–32 (1961)

Clark, A.J.: The beginning of a genetic analysis of recombination proficiency. J. cell. Phys., Suppl. to Vol.70, No. 2 (Part II), 165–180 (1967)

Clark, L., Carbon, J.: Biochemical construction and selection of hybrid plasmids containing specific segments of theEscherichia coli genome. Proc. nat. Acad. Sci. (Wash.)72, 4361–4365 (1975)

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davies, J., Jacob, F.: Genetic mapping of the regulator and operator genes of thelac operon. J. molec. Biol.36, 413–416 (1968)

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Enquist, L., Tiemeier, D., Leder, P., Weisberg, R., Sternberg, N.: Safer derivatives of bacteriophage λgt. λC for use in cloning of recombinant DNA molecules. Nature (Lond.)259 596–598 (1976)

Franklin, N.C.: TheN operon of lambda: extent and regulation as observed in fusions to the tryptophan operon ofEscherichia coli. In: The bacteriophage lambda (ed. A.D. Hershey), pp. 621–638. New York: Cold Spring Harbor Laboratories 1971

Franklin, N.C.: Altered reading of genetic signals fused to theN operon of bacteriophage λ: genetic evidence for modification of polymerase by the protein product of theN gene. J. molec. Biol.89, 33–48 (1974)

Goldberg, A.R., Howe, M.: New mutations in theS cistron of bacteriophage λ affecting host cell lysis. Virology38, 200–202 (1969)

Gottesman, M.M., Gottesman, M.E., Gottesman, S., Gellert, M.: Characterisation of bacteriophage λ reverse as anEscherichia coli phage carrying a unique set of host-derived recombination function. J. molec. Biol.88, 471–487 (1974)

Grunstein, M., Hogness, D.S.: Colony hybridisation: a method for the isolation of cloned DNAs that contain a specific gene. Proc. nat. Acad. Sci. (Wash.)72, 3961–3963 (1975)

Haggerty, D.M., Schlief, R.F.: Location in bacteriophage lambda DNA of cleavage sites of the site-specific endonuclease fromBacillus amyloliquefaciens H. J. Virol.18, 659–663 (1976)

Hedgpeth, J., Goodman, H.M., Boyer, H.W.: DNA nucleotide sequence restricted by the RI endonuclease. Proc. nat. Acad. Sci. (Wash.)69, 3448–3502 (1972)

Helinski, D.R., Falkow, S., Curtiss, R., Szybalski, W.: Guidelines for research involving recombinant DNA molecules, Appendix C. National Institutes for Health, Bethesda, Maryland, U.S.A. (1976)

Horwitz, J.P., Chua, J., Curby, R.J., Tomson, A.J., Da Rooge, M.A., Fisher, B.E., Mauricio, J., Klundt, I.: Substrate for cytochemical demonstration of enzyme activity. I. Some substituted 3-indolyl-β-D-glycopyranosides. J. med. Chem.7, 574–583 (1964)

Ippen, K., Shapiro, J.A., Beckwith, J.R.: Transposition of thelac region to thegal region of theEscherichia coli chromosome: Isolation of λlac transducing bacteriophages. J. Bact.108, 5–9 (1971)

Jones, K.W., Murray, K.: A procedure for detection of heterologous DNA sequences in lambdoid phages by in situ hybridisation. J. molec. Biol.96, 455–460 (1975)

Kaiser, A.D., Hogness, D.S.: The transformation ofEscherichia coli with Deoxyribonucleic acid isolated from bacteriophage λdg. J. molec. Biol.2, 392–415 (1960)

Kaiser, A.D., Jacob, F.: Recombination between related temperate bacteriophage and the genetic control of immunity and prophage localisation. Virology4, 509–521 (1957)

Lederberg, E.M., Cohen, S.N.: Transformation ofSalmonella typhimurium by plasmid deoxyribonucleic acid. J. Bact.119, 1072–1074 (1974)

Liedke-Kulke, M., Kaiser, A.D.: The c-region of coliphage 21. Virology32, 475–481 (1967)

Lennox, E.S.: Transduction of linked characters of the host of bacteriophage P1. Virology1, 190–206 (1955)

Mandel, M., Higa, A.: Calcium-dependent bacteriophage DNA infection. J. molec. Biol.53, 159–162 (1970)

Marmur, J.: A procedure for the isolation of Deoxyribonucleic acid from microorganisms. J. molec. Biol.3, 208–218 (1961)

Mertz, J.E., Davis, R.W.: Cleavage of DNA by RI restriction endonuclease generates cohesive ends. Proc. nat. Acad. Sci. (Wash.)69, 3370–3374 (1972)

Moir, A., Brammar, W.J.: The use of specialised transducing phages in the amplification of enzyme production. Molec. gen. Genet. (in press) (1976)

Murray, N.E., Manduca de Ritis, P., Foster, L.A.: DNA targets for theEscherichia coli K restriction system analysed genetically in recombinants between phages phi 80 and lambda Molec. gen. Genet.120, 261–281 (1973)

Murray, N.E., Manduca de Ritis, P., Foster, L.A.: DNA targets in phage λ to form receptor chromosomes for DNA fragments. Nature (Lond.)251, 476–481 (1974)

Murray, K., Murray, N.E.: Phage lambda receptor chromosomes for DNA fragments made with restriction endonuclease III ofHaemophilus influenzae and restriction endonuclease I ofEscherichia coli. J. molec. Biol.98, 551–564 (1975)

Old, R., Murray, K., Roizes, G.: Recognition sequence of restriction endonuclease III fromHaemophilus influenzae. J. Molec. Biol.92, 331–339 (1975)

Parkinson, J.S.: Genetics of the left arm of the chromosome of bacteriophage lambda. Genetics59, 311–325 (1968)

Parkinson, J.S.: Deletion mutants of bacteriophage lambda. II. Genetic properties ofatt-defective mutants. J. molec. Biol.56, 385–401 (1971)

Parkinson, J.S., Huskey, R.J.: Deletion mutants of bacteriophage lambda. I. Isolation and initial characterisation. J. molec. Biol.56, 369–384 (1971)

Perricaudet, M., Tiollais, P.: Defective bacteriophage lambda chromosome, potential vector for DNA fragments obtained after cleavage byBacillus amyloliquifaciens endonuclease (Bam1). FEBS Letters56, 7–11 (1975)

Philippsen, P., Streeck, R.E., Zauchau, H.G.: Defined fragments of calf, human and rat DNA produced by restriction nucleases. Europ. J. Biochem.45, 475–488 (1974)

Rambach, A., Tiollais, P.: Bacteriophage λ havingEcoRI endonuclease sites only in the non-essential region of the genome. Proc. nat. Acad. Sci. (Wash.)71, 3927–3930 (1974)

Sharp, P.A., Sugden, B., Sambrook, J.: Detection of two restriction endonuclease activities inHaemophilus parainfluenzae using analytical agarose ethidium bromide electrophoresis. Biochemistry12, 3055–3063 (1973)

Shimada, K., Weisberg, R.A., Gottesman, M.E.: Prophage lambda at unusual chromosomal locations. I. Location of the secondary attachment sites and the properties of the lysogens. J. molec. Biol.63, 483–503 (1972)

Shulman, M., Gottesman, M.: Lambdaatt 2: a transducing phage capable of intra molecularint-xis Promoted Recombination. In: The bacteriophage lambda (ed. A.D. Hershey), pp. 477–488. New York: Cold Spring Harbor Laboratories 1971

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Smith, J.D., Barnett, L., Brenner, S., Russell, R.L.: More mutant tyrosine transfer RNAs. J. molec. Biol.54, 1–14 (1970)

Spizizen, J.: Transformation of biochemically deficient strains ofBacillus subtilis by deoxyribonucleate. Proc. nat. Acad. Sci. (Wash.)44, 1072–1078 (1958)

Stacey, K.A., Simson, E.: Improved method for the isolation of thymine-requiring mutants ofEscherichia coli. J. Bact.90, 554–555 (1965)

Szybalski, W., Kubinski, H., Hradecna, Z., Summers, W.C.: Analytical and preparative separation of the complementary DNA strands. Mechanics in enzymology, Vol. XXI, pp. 383–413. New York: Academic Press, Inc.

Thomas, M., Cameron, J.R., Davis, R.W.: Viable molecular hybrids of bacteriophage λ and eukaryotic DNA. Proc. nat. Acad. Sci. (Wash.)71, 4579–4583 (1974)

Ullmann, A., Jacob, F., Monod, J.: Characterisation by in vitro complementation of a peptide corresponding to an operatorproximal segment of the β-galactosidase structural gene ofE. coli. J. molec. Biol.24, 339–343 (1967)

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Wensink, P.C., Finnegan, D.J., Donelson, J.E., Hogness, D.S.: A system for mapping DNA sequences in the chromosomes ofDrosophila melanogaster. Cell3, 315–325 (1974)

Wilson, G.A., Young, F.E.: Isolation of a sequence-specific endonuclease (BamI) fromBacillus amyloliquefaciens. J. molec. Biol.97, 123–125 (1975)

Wood, W.B.: Host specificity of DNA produced byE. coli: Bacterial mutations affecting the restriction and modification of DNA. J. molec. Biol.16, 118–133 (1966)

Yanofsky, C., Lennox, E.S.: Transduction and recombination study of linkage relationships among the genes controlling tryptophan synthesis inEscherichia coli. Virology8, 425–447 (1959)

Yoshimori, R.N.: A genetic and biochemical analysis of the restriction and modification of DNA by resistance transfer factors. Ph. D. Thesis, University of California. (1971)

Zissler, J., Signer, E.R., Schaefer, F.: The role of recombination in growth of bacteriophage lambda. I. The gamma gene. The bacteriophage lambda, ed. A.D. Hershey, pp. 455–475 New York: Cold Spring Harbor Laboratories 1971