scholarly journals COMPLEMENTARITY BETWEEN LAMBDA ( ) PHAGE AND ESCHERICHIA COLI

1963 ◽  
Vol 50 (6) ◽  
pp. 1177-1184 ◽  
Author(s):  
M. H. Green
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.


Gene ◽  
1993 ◽  
Vol 124 (1) ◽  
pp. 29-35 ◽  
Author(s):  
J.P. Doherty ◽  
R. Lindeman ◽  
R.J. Trent ◽  
M.W. Graham ◽  
D.M. Woodcock

1993 ◽  
Vol 90 (22) ◽  
pp. 10861-10865 ◽  
Author(s):  
C. Herman ◽  
T. Ogura ◽  
T. Tomoyasu ◽  
S. Hiraga ◽  
Y. Akiyama ◽  
...  

1966 ◽  
Vol 41 (3) ◽  
pp. 247-249 ◽  
Author(s):  
YOSHINOBU SUGINO ◽  
AKIKO SORAI ◽  
TOKIO KOGOMA ◽  
YUKINORI HIROTA ◽  
REIJI OKAZAKI

1991 ◽  
Vol 173 (2) ◽  
pp. 896-899 ◽  
Author(s):  
S H Phadnis ◽  
S Kulakauskas ◽  
B R Krishnan ◽  
J Hiemstra ◽  
D E Berg

2012 ◽  
Vol 75 (5) ◽  
pp. 959-965 ◽  
Author(s):  
TOMÁS SUBILS ◽  
VIRGINIA AQUILI ◽  
GUILLERMO EBNER ◽  
CLAUDIA BALAGUÉ

Toxin synthesis by Shiga toxin–producing Escherichia coli (STEC) appears to be coregulated through the induction of the integrated bacteriophages that encode the toxin genes. These phages might be the principal means for the dissemination and release of Shiga toxins. We evaluated the effect of three common food preservatives, potassium sorbate, sodium benzoate, and sodium propionate, on the propagation of the phages and Shiga toxins. We tested each preservative at four concentrations, 1, 1.25, 2.5, and 5 mg/ml, both on free phages and on lysogenic phages in bacteria. We also evaluated the expression of a lambdoid phage, which was exposed to increasing concentrations of preservatives, by measuring β-galactosidase activity from SPC105, a transductant strain. Furthermore, we tested the effect of the preservatives on cytotoxigenic activity of Shiga toxin on Vero cells. We detected an increase of the inhibitory effect of the phage lytic activity, both in lysogenic and free phages, as the preservative concentration increased. However, the inhibition was higher on the lysogenic phages release than on free phages. Sodium benzoate and potassium sorbate were about equal at inhibiting phages; they were more effective than sodium propionate. A significant decrease of lacZ expression, encoded in a lambda phage, was observed. We also found a reduction in Shiga toxin titer caused by exposure of E. coli O157:H7 to 5 mg/ml sodium benzoate or potassium sorbate. These results imply that these three preservatives, used to inhibit microbial spoilage of foods, also act to inhibit lytic activity and dispersion of a phage carrying the gene encoding powerful Shiga cytotoxins. Also notable was the inactivation of Shiga toxin activity, although this effect was detected using concentrations of preservatives greater than those allowed by the Argentine Food Code.


2000 ◽  
Vol 182 (3) ◽  
pp. 842-847 ◽  
Author(s):  
Dana Boyd ◽  
David S. Weiss ◽  
Joseph C. Chen ◽  
Jon Beckwith

ABSTRACT We describe a simple system for reversible, stable integration of plasmid-borne genes into the Escherichia coli chromosome. Most ordinary E. coli strains and a variety of pBR322-derived ampicillin-resistant plasmids can be used. A single genetic element, a lambda phage, is the only specialized vector required. The resultant strains have a single copy of the plasmid fragment inserted stably at the lambda attachment site on the chromosome, with nearly the entire lambda genome deleted.


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