Engineering of a vaccinia virus bacterial artificial chromosome in Escherichia coli by bacteriophage λ–based recombination

2005 ◽  
Vol 2 (2) ◽  
pp. 95-97 ◽  
Author(s):  
Arban Domi ◽  
Bernard Moss
2002 ◽  
Vol 76 (9) ◽  
pp. 4655-4661 ◽  
Author(s):  
José M. González ◽  
Zoltan Pénzes ◽  
Fernando Almazán ◽  
Enrique Calvo ◽  
Luis Enjuanes

ABSTRACT The stable propagation of a full-length transmissible gastroenteritis coronavirus (TGEV) cDNA in Escherichia coli cells as a bacterial artificial chromosome has been considerably improved by the insertion of an intron to disrupt a toxic region identified in the viral genome. The viral RNA was expressed in the cell nucleus under the control of the cytomegalovirus promoter and the intron was efficiently removed during translocation of this RNA to the cytoplasm. The insertion in two different positions allowed stable plasmid amplification for at least 200 generations. Infectious TGEV was efficiently recovered from cells transfected with the modified cDNAs.


2019 ◽  
Vol 305 ◽  
pp. 43-50
Author(s):  
Gustav Sjöberg ◽  
Mónica Guevara-Martínez ◽  
Antonius J.A. van Maris ◽  
Martin Gustavsson

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