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Appl. Environ. Microbiol., Apr 1996, 1369-1377, Vol 62, No. 4
WS Kuo and KF Chak
Two pairs of universal oligonucleotide primers were designed to probe the
most conserved regions of all known cryI-type gene sequences so that the
amplified PCR fragments of the DNA template from Bacillus thuringiensis
strains may contain all possible cryI-type gene sequences. The restriction
fragment length polymorphism (RFLP) patterns of the PCR-amplified fragments
revealed that 14 distinct cry-type genes have been identified from 20 B.
thuringiensis strains. Those cry-type genes included cryIA(a), cryIA(a),
cryIA(b), cryIA(b), cryIA(c), cryIB, cryIC, cryIC, cryIC(b), cryID, cryIE,
cryIF, cryIF, and cryIII (a dagger at the end of a gene designation
indicates a novel cry-type gene determined by restriction mapping or DNA
sequences). Among them, the sequences of cryIA(a), cryIA(b), cryIB, cryIC,
cryIF, and cryIII were found to be different from the corresponding
published cry gene sequences. Interestingly, five cry-type genes
[cryIA(a)-, cryIB-, cryIC- , cryIC(b)-, and cryIF-type genes] and seven
cry-type genes [cryIA(a)-, cryIA(b)-, cryIB-, cryIC-, cryIC(b)-, cryIF-,
and cryIII-type genes] have been detected from B. thuringiensis subsp.
morrisoni HD-12 and B. thuringiensis subsp. wuhanensis, respectively.
Therefore, the PCR-RFLP typing system is a facile method to detect both
known and novel cry genes existing in B. thuringiensis strains.
Copyright © 1996, American Society for Microbiology
Identification of novel cry-type genes from Bacillus thuringiensis strains on the basis of restriction fragment length polymorphism of the PCR-amplified DNA
Institute of Biochemistry, National Yang Ming University, Taipei, Taiwan, Republic of China.
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