scholarly journals Effect of polyethylene glycol on calcium-treatment transfection of Escherichia coli with bacteriophage .LAMBDA. DNA.

1979 ◽  
Vol 43 (2) ◽  
pp. 401-402
Author(s):  
Toshihiro SHIBATA ◽  
Michio HIMENO ◽  
Junji MORITA ◽  
Tohru KOMANO
1995 ◽  
Vol 42 (2) ◽  
pp. 233-239 ◽  
Author(s):  
A Szalewska-Pałasz ◽  
G Wegrzyn

Replication of lambda plasmid DNA is halted in amino acid-starved wild type (stringent) strains whereas it proceeds in relA (relaxed) mutants. The only transcription which could be important in lambda plasmid DNA replication in amino acid-starved Escherichia coli cells is that starting from the pR promoter. Using a fusion which consists of the lacZ gene under the control of bacteriophage lambda pR promoter we found that transcription starting from this promoter was inhibited during the stringent, but not the relaxed, response in E. coli. We confirmed our conclusion by estimating the relative level of the pR transcript by RNA-DNA hybridization. We propose that decreased transcription from the pR promoter which serves as transcriptional activation of ori lambda is responsible for inhibition of lambda plasmid replication during the stringent response. The results presented in this paper, combined with our recent findings (published elsewhere), indicate that the transcriptional activation of ori lambda may be a main regulatory process controlling lambda DNA replication not only during the relaxed response but also in normal growth conditions.


1990 ◽  
Vol 172 (2) ◽  
pp. 1030-1034 ◽  
Author(s):  
P Guzman ◽  
B E Rivera Chavira ◽  
D L Court ◽  
M E Gottesman ◽  
G Guarneros

2014 ◽  
Vol 111 (20) ◽  
pp. 7308-7312 ◽  
Author(s):  
A. Tal ◽  
R. Arbel-Goren ◽  
N. Costantino ◽  
D. L. Court ◽  
J. Stavans

1978 ◽  
Vol 164 (1) ◽  
pp. 9-14 ◽  
Author(s):  
J. Yochem ◽  
H. Uchida ◽  
M. Sunshine ◽  
H. Saito ◽  
C. P. Georgopoulos ◽  
...  

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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