Promoter vectors with restriction-site banks

Citations of this article
Mendeley users who have this article in their library.
Get full text


New vectors harboring the promoter for the chloramphenicol acetyl transferase gene (cat promoter) have been constructed. These vectors are all derived from pJRD184 [Heusterspreute et al., Gene 39 (1985) 299-304], which contains a restriction-site bank. The cat promoter has been inserted at various positions and in reverse orientations so that almost all the restriction sites originally present on pJRD184 can be used in cloning experiments. The expression of the aceK gene of Escherichia coli cloned under the control of the cat promoter has been tested. A large increase in the synthesis of the isocitrate dehydrogenase kinase, the aceK gene product, has demonstrated the efficiency of the newly constructed vectors. © 1988.




Bleicher, F., Deville, F., Cortay, J. C., Négre, D., Cozzone, A. J., & Cenatiempo, Y. (1988). Promoter vectors with restriction-site banks. Gene, 63(1), 135–139.

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free