scholarly journals A recombinant foot-and-mouth disease virus antigen inhibits DNA replication and triggers the SOS response inEscherichia coli

1995 ◽  
Vol 129 (2-3) ◽  
pp. 157-162
Author(s):  
A. Benito ◽  
E. Viaplana ◽  
J.L. Corchero ◽  
X. Carbonell ◽  
A. Villaverde
2001 ◽  
Vol 96 (2) ◽  
pp. 189-202 ◽  
Author(s):  
Scott M Reid ◽  
Nigel P Ferris ◽  
Anke Brüning ◽  
Geoffrey H Hutchings ◽  
Zofia Kowalska ◽  
...  

Nature ◽  
1965 ◽  
Vol 205 (4976) ◽  
pp. 1135-1136 ◽  
Author(s):  
P. B. CAPSTICK ◽  
A. J. GARLAND ◽  
W. G. CHAPMAN ◽  
R. C. MASTERS

1990 ◽  
Vol 29 (1) ◽  
pp. 33-41 ◽  
Author(s):  
N.P. Ferris ◽  
R.P. Kitching ◽  
J.M. Oxtoby ◽  
R.M. Philpot ◽  
R. Rendle

Author(s):  
S. S. Breese ◽  
H. L. Bachrach

Models for the structure of foot-and-mouth disease virus (FMDV) have been proposed from chemical and physical measurements (Brown, et al., 1970; Talbot and Brown, 1972; Strohmaier and Adam, 1976) and from rotational image-enhancement electron microscopy (Breese, et al., 1965). In this report we examine the surface structure of FMDV particles by high resolution electron microscopy and compare it with that of particles in which the outermost capsid protein VP3 (ca. 30, 000 daltons) has been split into smaller segments, two of which VP3a and VP3b have molecular weights of about 15, 000 daltons (Bachrach, et al., 1975).Highly purified and concentrated type A12, strain 119 FMDV (5 mg/ml) was prepared as previously described (Bachrach, et al., 1964) and stored at 4°C in 0. 2 M KC1-0. 5 M potassium phosphate buffer at pH 7. 5. For electron microscopy, 1. 0 ml samples of purified virus and trypsin-treated virus were dialyzed at 4°C against 0. 2 M NH4OAC at pH 7. 3, deposited onto carbonized formvar-coated copper screens and stained with phosphotungstic acid, pH 7. 3.


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