Nucleotide sequence of the Q gene and the Q to S intergenic region of bacteriophage lambda

Virology ◽  
1982 ◽  
Vol 117 (1) ◽  
pp. 81-92 ◽  
Author(s):  
Donna L. Daniels ◽  
Freferick R. Blattner
2005 ◽  
Vol 7 (1) ◽  
pp. 33-39 ◽  
Author(s):  
Toshiki Watanabe ◽  
Mutsumi Nishida ◽  
Katsutoshi Watanabe ◽  
Defny S. Wewengkang ◽  
Michio Hidaka

Virology ◽  
1986 ◽  
Vol 154 (1) ◽  
pp. 155-167 ◽  
Author(s):  
David D. Auperin ◽  
Donna R. Sasso ◽  
Joseph B. McCormick

1998 ◽  
Vol 45 (1) ◽  
pp. 261-270 ◽  
Author(s):  
D Kuchanny ◽  
G Klein ◽  
J Krzewska ◽  
A Czyz ◽  
B Lipińska

groES and groEL genes encode two co-operating proteins GroES and GroEL, belonging to a class of chaperone proteins highly conserved during evolution. The GroE chaperones are indispensable for the growth of bacteriophage lambda in Escherichia coli cells. In order to clone the groEL and groES genes of the marine bacterium Vibrio harveyi, we constructed the V. harveyi genomic library in the lambdaEMBL1 vector, and selected clones which were able to complement mutations in both groE genes of E. coli for bacteriophage lambda growth. Using Southern hybridization, in one of these clones we identified a DNA fragment homologous to the E. coli groE region. Analysis of the nucleotide sequence of this fragment showed that the cloned region contained a sequence in 71.7% homologous to the 3' end of the groEL gene of E. coli. This confirmed that the lambda clone indeed carries the groE region of V. harveyi. The positive result of our strategy of cloning with the use of the genomic library in lambda vector suggests that the same method might be useful in the isolation of the groE homologues from other bacteria. The V. harveyi cloned groE genes did not suppress thermosensitivity of the E. coli groE mutants.


1981 ◽  
Vol 37 (1) ◽  
pp. 336-342 ◽  
Author(s):  
G R Smith ◽  
M Comb ◽  
D W Schultz ◽  
D L Daniels ◽  
F R Blattner

Gene ◽  
1985 ◽  
Vol 35 (3) ◽  
pp. 313-320 ◽  
Author(s):  
Frank H. Stephenson
Keyword(s):  

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