Previous Article | Next Article ![]()
Appl. Environ. Microbiol., Nov 1995, 3826-3831, Vol 61, No. 11
J Ceron, A Ortiz, R Quintero, L Guereca and A Bravo
In this paper we describe a PCR strategy that can be used to rapidly
identify Bacillus thuringiensis strains that harbor any of the known cryI
or cryIII genes. Four general PCR primers which amplify DNA fragments from
the known cryI or cryIII genes were selected from conserved regions. Once a
strain was identified as an organism that contains a particular type of cry
gene, it could be easily characterized by performing additional PCR with
specific cryI and cryIII primers selected from variable regions. The method
described in this paper can be used to identify the 10 different cryI genes
and the five different cryIII genes. One feature of this screening method
is that each cry gene is expected to produce a PCR product having a precise
molecular weight. The genes which produce PCR products having different
sizes probably represent strains that harbor a potentially novel cry gene.
Finally, we present evidence that novel crystal genes can be identified by
the method described in this paper.
Copyright © 1995, American Society for Microbiology
Specific PCR primers directed to identify cryI and cryIII genes within a Bacillus thuringiensis strain collection
Instituto de Biotecnologia, Universidad Nacional de Colombia, Ciudad Universitaria, Bogota, Colombia.
This article has been cited by other articles:
| J. Bacteriol. | Microbiol. Mol. Biol. Rev. | Eukaryot. Cell | All ASM Journals |
|---|