The novel cry52Ca1 gene from an Indian Bacillus thuringiensis (Bt) isolate was cloned in an expression vector (pET301/CT-DEST, 6xHis). The gene expressed as a ∼77.2 kDa protein in E. coli BL21-CodonPlus (DE3)-RIPL cells upon induction with isopropyl-thio-galactoside (IPTG) for 18 h at 28 °C. Cry52Ca1 protein was toxic to Helicoverpa armigera (cotton bollworm) neonate larvae (LC 36.66 µg per ml and MIC 3.051 µg per ml) in diet-based laboratory assays. This gene has potential for deployment in insect-resistant transgenic crops.
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http://dx.doi.org/10.1016/j.jip.2018.11.002 | DOI Listing |
J Invertebr Pathol
November 2018
ICAR-National Research Centre on Plant Biotechnology, Pusa Campus, New Delhi 110012, India. Electronic address:
The novel cry52Ca1 gene from an Indian Bacillus thuringiensis (Bt) isolate was cloned in an expression vector (pET301/CT-DEST, 6xHis). The gene expressed as a ∼77.2 kDa protein in E.
View Article and Find Full Text PDFAppl Microbiol Biotechnol
February 2018
ICAR-National Research Centre on Plant Biotechnology, Pusa Campus, New Delhi, 110012, India.
Novel genes from Bacillus thuringiensis (Bt) are required for effective deployment in agriculture, human health, and forestry. In an improvement over conventional PCR-based screening, next generation sequencing (NGS) has been used for identification of new genes of potential interest from Bt strains, but cost becomes a constraint when several isolates are to be sequenced. We demonstrate the potential of a DNA pooling strategy known as pool deconvolution to identify commercially important toxin genes from 36 native Bt isolates.
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