28 Activated toxins bind to the target protein/s (specific receptor molecules), insert into the cell membranes and create pores, resulting in osmotic imbalance and ultimately lyses of midgut epithelial cells 29 and the eventual death of the host. 30 The brush border membranes of susceptible insects possess specific receptor molecules which play important roles in the insecticidal specificities of Cry1 type toxins. 31 Bt toxin Cry1Ac was found to bind the recombinant peptides Selleck BKM120 corresponding to extracellular regions of a cadherin

protein (BtR) in a major cotton pest, Pectinophora gossypiella. 32 At least four different binding sites have been described for Cry1A toxins in different lepidopteran insects: a cadherin-like protein (CADR), a glycosylphosphatidyl-inositol (GPI)-anchored aminopeptidase-N

(APN), a GPI-anchored alkaline phosphatase (ALP) and a 270 kDa glycoconjugate. 33 Alkaline phosphatase has also been proposed as Cry1Ac receptor. 34 List of receptors for Cry1 halotype protoxins in some organisms are given in Table 3. cry1Aa gene is a typical example of a sporulation-dependent cry gene, expressed only in the mother cell compartment of B. thuringiensis. Two overlapping transcription start sites have find more been mapped; defining two overlapping promoters (BtI and BtII) which are used sequentially. 41 BtI is active between about T2 and T6 of sporulation and BtII is active from about T5 onwards (where Tn is n hours after the end of the exponential phase). Two sigma factors, σ35 and σ28,

that specifically direct transcription of cry1Aa from BtI and BtII, respectively were isolated. In vitro transcription experiments have also indicated that other cry genes (e.g. cry1Ba) contain either BtI alone or BtI with BtII. 42 and 43 The genes encoding σ35 and σ28 have been cloned and sequenced. 44 Their deduced amino acid sequences had showed 88 and 85% identity with σE and σK of Bacillus subtilis respectively. The σE and σK factors of B. subtilis are activated during the sporulation stage. 45B. thuringiensis σE and σK (encoding sigma 35 and sigma 28, respectively) mutants were constructed and cry1Aa gene expression was analyzed in these mutants. 46 The results indicated that these two sigma factors regulated expression of a cry1Aa9-9lacZ transcriptional fusion in vivo. The σK mutant Ribonucleotide reductase produced about 50% less β-galactosidase than the wild-type strain whereas no β-galactosidase synthesis was obtained in the σE mutant. The latter result was anticipated as σE controls σK synthesis. Consensus sequences of promoters recognized by B. thuringiensis RNA polymerase containing σE or σK have been deduced from the alignment of the promoter regions of these genes. 47 The results indicate that the transcription of cry1Ba is likely to be σE or σK dependent. The mRNAs encoding the crystal proteins have average half-lives of 10 min.