Relevant bibliographies by topics / Mutation (Biology) Bacteriophage Lambda

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  1. Journal articles
  2. Dissertations / Theses
  3. Book chapters

Academic literature on the topic 'Mutation (Biology) Bacteriophage Lambda'

Author: Grafiati
Published: 4 June 2021
Last updated: 12 February 2022

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Journal articles on the topic "Mutation (Biology) Bacteriophage Lambda"

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Poteete, Anthony R., Hsinju R. Wang та Patricia L. Foster. "Phage λ Red-Mediated Adaptive Mutation". Journal of Bacteriology 184, № 13 (2002): 3753–55. http://dx.doi.org/10.1128/jb.184.13.3753-3755.2002.

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ABSTRACT Replacement of the recBCD genes of Escherichia coli with the red recombination genes of bacteriophage lambda results in a strain in which adaptive mutation occurs at an elevated frequency. Like RecBCD-dependent adaptive mutation, Red-mediated adaptive mutation is dependent upon recA and ruvABC functions.
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Raab, R., G. Neal, J. Garrett, R. Grimaila, R. Fusselman, and R. Young. "Mutational analysis of bacteriophage lambda lysis gene S." Journal of Bacteriology 167, no. 3 (1986): 1035–42. http://dx.doi.org/10.1128/jb.167.3.1035-1042.1986.

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Leffers, Gerald G., and Susan Gottesman. "Lambda Xis Degradation In Vivo by Lon and FtsH." Journal of Bacteriology 180, no. 6 (1998): 1573–77. http://dx.doi.org/10.1128/jb.180.6.1573-1577.1998.

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ABSTRACT Lambda Xis, which is required for site-specific excision of phage lambda from the bacterial chromosome, has a much shorter functional half-life than Int, which is required for both integration and excision (R. A. Weisberg and M. E. Gottesman, p. 489–500,in A. D. Hershey, ed., The Bacteriophage Lambda, 1971). We found that Xis is degraded in vivo by two ATP-dependent proteases, Lon and FtsH (HflB). Xis was stabilized two- to threefold more than in the wild type in a lon mutant and as much as sixfold more in a lon ftsH double mutant at the nonpermissive temperature for the ftsH mutation
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Gimble, F. S., and R. T. Sauer. "Mutations in bacteriophage lambda repressor that prevent RecA-mediated cleavage." Journal of Bacteriology 162, no. 1 (1985): 147–54. http://dx.doi.org/10.1128/jb.162.1.147-154.1985.

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Rydman, Pia S., and Dennis H. Bamford. "Identification and Mutational Analysis of Bacteriophage PRD1 Holin Protein P35." Journal of Bacteriology 185, no. 13 (2003): 3795–803. http://dx.doi.org/10.1128/jb.185.13.3795-3803.2003.

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ABSTRACT Holin proteins are phage-induced integral membrane proteins which regulate the access of lytic enzymes to host cell peptidoglycan at the time of release of progeny viruses by host cell lysis. We describe the identification of the membrane-containing phage PRD1 holin gene (gene XXXV). The PRD1 holin protein (P35, 12.8 kDa) acts similarly to its functional counterpart from phage lambda (gene S), and the defect in PRD1 gene XXXV can be corrected by the presence of gene S of lambda. Several nonsense, missense, and insertion mutations in PRD1 gene XXXV were analyzed. These studies support
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Sippy, J., and M. Feiss. "Analysis of a mutation affecting the specificity domain for prohead binding of the bacteriophage lambda terminase." Journal of Bacteriology 174, no. 3 (1992): 850–56. http://dx.doi.org/10.1128/jb.174.3.850-856.1992.

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Davidson, A., P. Yau, H. Murialdo, and M. Gold. "Isolation and characterization of mutations in the bacteriophage lambda terminase genes." Journal of Bacteriology 173, no. 16 (1991): 5086–96. http://dx.doi.org/10.1128/jb.173.16.5086-5096.1991.

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Bauer, Carl E., Steven D. Hesse, Richard I. Gumport, and Jeffrey F. Gardner. "Mutational analysis of integrase arm-type binding sites of bacteriophage lambda." Journal of Molecular Biology 192, no. 3 (1986): 513–27. http://dx.doi.org/10.1016/0022-2836(86)90273-1.

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Hayes, Sidney, and Roderick A. Slavcev. "Polarity withinpMandpEpromoted phage lambdacI-rexA-rexBtranscription and its suppression." Canadian Journal of Microbiology 51, no. 1 (2005): 37–49. http://dx.doi.org/10.1139/w04-115.

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The cI-rexA-rexB operon of bacteriophage λ confers 2 phenotypes, Imm and Rex, to lysogenic cells. Immunity to homoimmune infecting λ phage depends upon the CI repressor. Rex exclusion of T4rII mutants requires RexA and RexB proteins. Both Imm and Rex share temperature-sensitive conditional phenotypes when expressed from cI[Ts]857 but not from cI+λ prophage. Plasmids were made in which cI-rexA-rexB was transcribed from a non-lambda promoter, pTet. The cI857-rexA-rexB plasmid exhibited Ts conditional Rex and CI phenotypes; the cI+-rexA-rexB plasmid did not. Polarity was observed within cI-rexA-r
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Kuchanny, D., G. Klein, J. Krzewska, A. Czyz, and B. Lipińska. "Cloning of the groE operon of the marine bacterium Vibrio harveyi using a lambda vector." Acta Biochimica Polonica 45, no. 1 (1998): 261–70. http://dx.doi.org/10.18388/abp.1998_4341.

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groES and groEL genes encode two co-operating proteins GroES and GroEL, belonging to a class of chaperone proteins highly conserved during evolution. The GroE chaperones are indispensable for the growth of bacteriophage lambda in Escherichia coli cells. In order to clone the groEL and groES genes of the marine bacterium Vibrio harveyi, we constructed the V. harveyi genomic library in the lambdaEMBL1 vector, and selected clones which were able to complement mutations in both groE genes of E. coli for bacteriophage lambda growth. Using Southern hybridization, in one of these clones we identified
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Dissertations / Theses on the topic "Mutation (Biology) Bacteriophage Lambda"

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Pakula, Andrew Arnold. "A genetic and biochemical analysis of the bacteriophage [lambda] cro protein." Thesis, Massachusetts Institute of Technology, 1988. http://hdl.handle.net/1721.1/14612.

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Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Biology, 1988.<br>On t.p. [lambda] appears as the original Greek letter.<br>Includes bibliographical references.<br>by Andrew Arnold Pakula.<br>Ph.D.
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Burcica, Cristina Irina. "Modeling a Class of Naturally Occurring Mechanisms for Use in Synthetic Biology." University of Cincinnati / OhioLINK, 2008. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1218772646.

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Lohman, Kenton L. "Isolation and Characterization of Temperature-sensitive Protein Synthesis Mutants of Escherichia Coli by Directed Mutagenesis of the Defective Bacteriophage Lambda Fus2." Digital Commons @ East Tennessee State University, 1985. https://dc.etsu.edu/etd/2722.

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Mutagenesis of the defective transducing bacteriophage lambda fus2 was used to isolate a collection of temperature-sensitive mutants of E. coli in the major ribosomal protein gene cluster. Four mutants were examined in detail. Two of the mutants were resistant to the ribosomal antibiotics neamine and spectinomycin. Another mutant was defective in 50S ribosomal subunit assembly at 42(DEGREES)C. The 30S subunit proteins S17 and S19 were changed in two different mutants. Each protein migrated as a more basic species in two-dimensional gels of ribosomal proteins. Ribosomes from each of the four mu
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Henry, Matthew S. "Characterization of a lambdoid phage gene encoding a host cell attachment spike." Bowling Green, Ohio : Bowling Green State University, 2008. http://rave.ohiolink.edu/etdc/view?acc%5Fnum=bgsu1214189208.

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Ivanov, Yury V. "The Roles of Moron Genes in the Escherichia Coli Enterobacteria Phage Phi-80." Bowling Green State University / OhioLINK, 2012. http://rave.ohiolink.edu/etdc/view?acc_num=bgsu1350778152.

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Sheldon, Katlyn. "Two Dimensional Genetic Approach to the Development of a Controllable Lytic Phage Display System." Thesis, 2013. http://hdl.handle.net/10012/7371.

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Bacteriophage Lambda (λ) has played a historical role as an essential model contributing to our current understanding of molecular genetics. Lambda’s major capsid protein “gpD” occurs on each capsid at 405 to 420 copies per phage in homotrimeric form and functions to stabilize the head and likely to compact the genomic DNA. The interesting conformation of this protein allows for its exploitation through the genetic fusion of peptides or proteins to either the amino or carboxy terminal end of gpD, while retaining phage assembly functionality and viability. The lytic nature of λ and the conforma
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Book chapters on the topic "Mutation (Biology) Bacteriophage Lambda"

1

Dale, Jeremy W. "Cloning in Bacteriophage Lambda." In Techniques in Molecular Biology. Springer US, 1987. http://dx.doi.org/10.1007/978-1-4615-9799-5_9.

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Thomason, Lynn C., Amos B. Oppenheim, and Donald L. Court. "Modifying Bacteriophage $\lambda$ with Recombineering." In Methods in Molecular Biology. Humana Press, 2009. http://dx.doi.org/10.1007/978-1-60327-164-6_21.

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Oppenheim, Amos B., Daniel Kornitzer, Shoshy Altuvia, and Donald L. Court. "Posttranscriptional Control of the Lysogenic Pathway in Bacteriophage Lambda." In Progress in Nucleic Acid Research and Molecular Biology. Elsevier, 1993. http://dx.doi.org/10.1016/s0079-6603(08)61017-x.

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FLAVELL, R. A., D. L. SABO, E. F. BANDLE, and C. WEISSMANN. "Site-directed Mutagenesis : Generation of an Extracistronic Mutation in Bacteriophage Qβ RNA." In Molecular Biology. Elsevier, 1989. http://dx.doi.org/10.1016/b978-0-12-131200-8.50038-1.

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Journal articles
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