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Open AccessJournal ArticleDOI

Rate of translocation of bacteriophage T7 DNA across the membranes of Escherichia coli.

L. R. Garcia, +1 more
- 01 Jul 1995 - 
- Vol. 177, Iss: 14, pp 4066-4076
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TLDR
A GATC site located between the early E. coli promoters and the coding sequences of the first T7 protein made after infection is not methylated before the protein is synthesized, a result supporting the idea that only certain proteins are permitted access to the entering T7 DNA.
Abstract
Translocation of bacteriophage T7 DNA from the capsid into the cell has been assayed by measuring the time after infection that each GATC site on the phage genome is methylated by cells containing high levels of DNA adenine methylase. Methylation at GATC sites on T7 DNA renders both the infecting genome and any newly synthesized molecules sensitive to the restriction enzyme DpnI. In a normal infection at 30 degrees C, translocation of the T7 genome into the cell takes between 9 and 12 min. In contrast, translocation of the entire phage lambda genome or of a T7 genome ejected from a lambda capsid can be detected within the first minute of infection. Entry of the leading end of the T7 genome occurs by a transcription-independent mechanism that brings both Escherichia coli and T7 promoters into the cell. Further translocation of the genome normally involves transcription by the RNA polymerases of both E. coli and T7; the rates of DNA translocation into the cell when catalyzed by each enzyme are comparable to the estimated rates of transcription of the respective enzymes. A GATC site located between the early E. coli promoters and the coding sequences of the first T7 protein made after infection is not methylated before the protein is synthesized, a result supporting the idea (B. A. Moffatt and F. W. Studier, J. Bacteriol. 170:2095-2105, 1988) that only certain proteins are permitted access to the entering T7 DNA. In the absence of transcription, the genomes of most T7 strains do not completely enter the cell. However, the entire genome of a mutant that lacks bp 3936 to 808 of T7 DNA enters the cell in a transcription-independent process at an average overall rate of 50 bp per s.

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Refactoring bacteriophage T7

TL;DR: The viability of the initial design suggests that the genomes encoding natural biological systems can be systematically redesigned and built anew in service of scientific understanding or human intention.
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TL;DR: Current data suggest a highly speculative model, in which two of the proteins ejected from the phages head establish a molecular motor that ratchets the phage genome into the cell.
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Exclusion of T4 phage by the hok/sok killer locus from plasmid R1.

TL;DR: Results suggest that single cells exhibit altruistic behavior and investigate whether the hok/sok locus evolved as a phage-exclusion mechanism.
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The Bacteriophage T7 Virion Undergoes Extensive Structural Remodeling During Infection

TL;DR: Cryo–electron tomography captures T7 bacteriophage virions at successive stages of bacterial infection and reveals the de novo formation of an extended tail by the ejection of internal head proteins, in order to form the channel for DNA transport into the cytoplasm.
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Biological Consequences of Tightly Bent DNA: The Other Life of a Macromolecular Celebrity

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References
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Book

Molecular Cloning: A Laboratory Manual

TL;DR: Molecular Cloning has served as the foundation of technical expertise in labs worldwide for 30 years as mentioned in this paper and has been so popular, or so influential, that no other manual has been more widely used and influential.
Journal ArticleDOI

Complete nucleotide sequence of bacteriophage T7 DNA and the locations of T7 genetic elements

TL;DR: The complete nucleotide sequence of bacteriophage T7 DNA, 39,936 base-pairs, has been determined and the amino acid sequences and compositions predicted for all of the T7 proteins (except the proteins produced by frameshifting) are given.
PatentDOI

Cloning and expression of the gene for bacteriophage T7 RNA polymerase

TL;DR: In this paper, the authors describe a method to clone a functional gene for bacteriophage T7 RNA polymerase, which is useful for synthesizing large amounts of RNA in vivo or in vitro, and can produce a single RNA selectively from a complex mixture of DNAs.
Book

Encyclopedia of virology

TL;DR: The Encyclopedia of Virology focuses on the effects of viruses on the immune system, the role of viruses in disease, oncology, gene therapy, and evolution, plus a wide range of related topics.
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