Bacteriophage T4 Host Range is Expanded by Duplications of a Small Domain of the Tail Fiber Adhesin

1996 ◽  
Vol 258 (5) ◽  
pp. 726-731 ◽  
Author(s):  
F. Tétart ◽  
F. Repoila ◽  
C. Monod ◽  
H.M. Krisch
Genetics ◽  
1989 ◽  
Vol 122 (3) ◽  
pp. 471-479
Author(s):  
M Snyder ◽  
W B Wood

Abstract Gene 37 of T4 encodes the major subunit of the distal half of the tail fiber. The distal tip of the fiber, comprised of the carboxy-terminal ends of two molecules of gene 37 product (gp37), carries the principal determinant of the phage host range. The gp37 carboxyl termini recognize the bacterial surface during infection, and, in addition, include a site required for interaction with the product of gp38 during distal half-fiber assembly. In the absence of interaction with gp38, gp37 polypeptides do not dimerize. Eleven temperature-sensitive mutants with defects located near the promoter-distal end of gene 37 were tested at nonpermissive temperatures for production of an antigen that is diagnostic of distal half-fiber assembly. Six of the mutations prevent distal half-fiber assembly. The other five allow assembly of distal half fibers, which combine with proximal half fibers and attach to phage particles, but the resulting phage do not adsorb to bacteria. These two classes of mutations define two adjacent but separate genetic regions, corresponding to two different functional domains in gp37. These two regions and the neighboring gene 38 comprise a functional unit that can be considered as a host-range "cassette," with features that are strikingly similar to corresponding functional units in other unrelated as well as related phages.


2017 ◽  
Vol 10 (2) ◽  
pp. 463-471 ◽  
Author(s):  
Paul Hyman ◽  
Mark van Raaij

PHAGE ◽  
2020 ◽  
Vol 1 (2) ◽  
pp. 87-90 ◽  
Author(s):  
Maarten Boon ◽  
Dominique Holtappels ◽  
Cédric Lood ◽  
Vera van Noort ◽  
Rob Lavigne

1967 ◽  
Vol 9 (2) ◽  
pp. 149-158 ◽  
Author(s):  
B. de Groot

Analysis of the inheritance of the three bar-properties of bacteriophage T4: exclusion of T2 from the progeny of crosses, glucosylation of the hydroxymethylcytosine (HMC)moiety of the DNA according to T4, and plating with large plaques on E. coli K strains, was carried out by means of marker rescue from T4 by T2 on E. coli K (λh) as a selective indicator. Five of the strains isolated plated with large plaques on K (λh), but did not exclude T2 and showed T2 glucosylation; plating on E. coli K (λh) was found to segregate from the other two bar-properties. The sixth isolate showed, in addition to plating with large plaques on K, partial non-excludability by the parental T4 and T4 glucosylation of HMC. If partial non-excludability is the result of T4 glucosylation, the role of the additional glucose substitutions might be a protective effect on the DNA against the exclusion factor of T4. This proposal is supported by the analysis of the progeny from a single burst from a cross of T4 and T2. The following T2 genes were partially excluded: host-range, no exclusion of parental T2, sensitivity to ultraviolet, and limited plating efficiency on E. coli K (λh). The exclusion factor of T4 is not transmitted to all progeny and does not behave like a bar-property. Only resistance to exclusion and T4 glucosylation were transmitted to all twenty-seven progeny of the single burst. The elimination of sensitivity to exclusion and T2 glucosylation is explained by assuming that the recombinant class with the exclusion factor of T4 and T2 α-glucosylation will exclude itself and be suicidal upon infection of a new host. Exclusion and differential glucosylation are discussed with regard to restriction and modification, respectively.


Virology ◽  
1993 ◽  
Vol 194 (1) ◽  
pp. 117-127 ◽  
Author(s):  
A.M. Makhov ◽  
B.L. Trus ◽  
J.F. Conway ◽  
M.N. Simon ◽  
T.G. Zurabishvili ◽  
...  

1977 ◽  
Vol 74 (8) ◽  
pp. 3355-3359 ◽  
Author(s):  
T. J. Snopek ◽  
W. B. Wood ◽  
M. P. Conley ◽  
P. Chen ◽  
N. R. Cozzarelli

Viruses ◽  
2017 ◽  
Vol 9 (7) ◽  
pp. 168 ◽  
Author(s):  
Meritxell Granell ◽  
Mikiyoshi Namura ◽  
Sara Alvira ◽  
Shuji Kanamaru ◽  
Mark van Raaij

Genetics ◽  
1980 ◽  
Vol 94 (3) ◽  
pp. 531-547
Author(s):  
Jack N Levy ◽  
Edward B Goldberg

ABSTRACT In this paper, we present results of crosses designed to elucidate the structure of recombinants in the tail-fiber region of bacteriophage T4, in which a glucosylation-dependent recombination mechanism is operative, and the cause of this "special" recombination in glucosylated crosses is discussed. We present evidence that, when phage are nonglucosylated, recombination in the tail-fiber region proceeds via long heteroduplex overlaps. Mismatched bases within such regions (in nonglucosylated phage) are repaired efficiently (as contrasted to those of glucosylated phage), bnt asymmetrically; that is, there may not be an equal probability of resolving the mismatch to mutant or wild type.


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