Cloning and study of the expression of a novel cry1Ia-type gene from Bacillus thuringiensis subsp. kurstaki

J Appl Microbiol. 2003;95(1):23-8. doi: 10.1046/j.1365-2672.2003.t01-1-01947.x.

Abstract

Aims: Cloning and expression of a new cry1Ia-type gene of Bacillus thuringiensis.

Methods and results: PCR amplification, using gene cry1I-specific primers revealed the presence of such a gene in the strain BNS3 of Bacillus thuringiensis subsp. kurstaki. The cloning and sequencing from BNS3 of the cry1Ia-type gene, called crybns3-3, showed an open reading frame of 2160-bp, encoding a protein of 719 amino acid residues. Both nucleotide and amino acid sequences similarity analysis revealed that the crybns3-3 is a new cry1Ia-type gene, presenting several differences from the cry1Ia-type genes. The study of the expression of crybns3-3 by Northern blot and RT-PCR showed that it was transcribed. The expression of crybns3-3 under the control of BtI and BtII promoters revealed that Crybns3-3 would co-crystallize with the endogenous delta-endotoxins.

Conclusions: crybns3-3 is a novel cry1Ia gene isolated from B. thuringiensis subsp. kurstaki strain BNS3.

Significance and impact of the study: The characteristics of crybns3-3 indicate that it is a new cry1Ia-type gene. Amino acid residue substitutions presented in Crybns3-3 could be exploited for both toxicity and specificity studies. Crybns3-3 would interact and co-crystallize at least partially with the endogenous delta-endotoxins of BNS3, and then participate in the formation of the parasporal crystal inclusions.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bacillus thuringiensis / genetics*
  • Base Sequence / genetics
  • Blotting, Northern / methods
  • Cloning, Molecular / methods
  • Cryptochromes
  • DNA, Bacterial / genetics
  • Drosophila Proteins*
  • Eye Proteins*
  • Flavoproteins / genetics*
  • Gene Expression / genetics*
  • Genes, Bacterial / genetics*
  • Molecular Sequence Data
  • Nucleic Acid Hybridization / genetics
  • Photoreceptor Cells, Invertebrate*
  • Promoter Regions, Genetic / genetics
  • RNA, Bacterial / genetics
  • Receptors, G-Protein-Coupled
  • Restriction Mapping / methods
  • Reverse Transcriptase Polymerase Chain Reaction / methods

Substances

  • Cryptochromes
  • DNA, Bacterial
  • Drosophila Proteins
  • Eye Proteins
  • Flavoproteins
  • RNA, Bacterial
  • Receptors, G-Protein-Coupled
  • cry protein, Drosophila