The DNA sequence on bacteriophage G4 recognized by the Escherichia coli B restriction enzyme

1979 ◽  
Vol 131 (4) ◽  
pp. 871-875 ◽  
Author(s):  
James A. Lautenberger ◽  
Marshall H. Edgell ◽  
Clyde A. Hutchison ◽  
G.Nigel Godson
1978 ◽  
Vol 75 (5) ◽  
pp. 2271-2275 ◽  
Author(s):  
J. A. Lautenberger ◽  
N. C. Kan ◽  
D. Lackey ◽  
S. Linn ◽  
M. H. Edgell ◽  
...  

PLoS ONE ◽  
2017 ◽  
Vol 12 (6) ◽  
pp. e0179853 ◽  
Author(s):  
Alexey Fomenkov ◽  
Zhiyi Sun ◽  
Deborah K. Dila ◽  
Brian P. Anton ◽  
Richard J. Roberts ◽  
...  

1978 ◽  
Vol 75 (10) ◽  
pp. 4724-4728 ◽  
Author(s):  
L. Greenfield ◽  
T. Boone ◽  
G. Wilcox

1980 ◽  
Vol 8 (22) ◽  
pp. 5267-5274 ◽  
Author(s):  
C.Garrett Miyada ◽  
Arnold H. Horwitz ◽  
Laura G. Cass ◽  
Josef Timko ◽  
Gary Wilcox

Author(s):  
Manfred E. Bayer

Bacterial viruses adsorb specifically to receptors on the host cell surface. Although the chemical composition of some of the cell wall receptors for bacteriophages of the T-series has been described and the number of receptor sites has been estimated to be 150 to 300 per E. coli cell, the localization of the sites on the bacterial wall has been unknown.When logarithmically growing cells of E. coli are transferred into a medium containing 20% sucrose, the cells plasmolize: the protoplast shrinks and becomes separated from the somewhat rigid cell wall. When these cells are fixed in 8% Formaldehyde, post-fixed in OsO4/uranyl acetate, embedded in Vestopal W, then cut in an ultramicrotome and observed with the electron microscope, the separation of protoplast and wall becomes clearly visible, (Fig. 1, 2). At a number of locations however, the protoplasmic membrane adheres to the wall even under the considerable pull of the shrinking protoplast. Thus numerous connecting bridges are maintained between protoplast and cell wall. Estimations of the total number of such wall/membrane associations yield a number of about 300 per cell.


1966 ◽  
Vol 241 (13) ◽  
pp. 3090-3096
Author(s):  
Sally E. Jorgensen ◽  
James F. Koerner

Genetics ◽  
1990 ◽  
Vol 126 (3) ◽  
pp. 519-533 ◽  
Author(s):  
F W Stahl ◽  
L C Thomason ◽  
I Siddiqi ◽  
M M Stahl

Abstract When one of two infecting lambda phage types in a replication-blocked cross is chi + and DNA packaging is divorced from the RecBCD-chi interaction, complementary chi-stimulated recombinants are recovered equally in mass lysates only if the chi + parent is in excess in the infecting parental mixture. Otherwise, the chi 0 recombinant is recovered in excess. This observation implies that, along with the chi 0 chromosome, two chi + parent chromosomes are involved in the formation of each chi + recombinant. The trimolecular nature of chi +-stimulated recombination is manifest in recombination between lambda and a plasmid. When lambda recombines with a plasmid via the RecBCD pathway, the resulting chromosome has an enhanced probability of undergoing lambda x lambda recombination in the interval into which the plasmid was incorporated. These two observations support a model in which DNA is degraded by Exo V from cos, the sequence that determines the end of packaged lambda DNA and acts as point of entry for RecBCD enzyme, to chi, the DNA sequence that stimulates the RecBCD enzyme to effect recombination. The model supposes that chi acts by ejecting the RecD subunit from the RecBCD enzyme with two consequences. (1) ExoV activity is blocked leaving a highly recombinagenic, frayed duplex end near chi, and (2) as the enzyme stripped of the RecD subunit travels beyond chi it is competent to catalyze reciprocal recombination.


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