ArticleSaudi journal of biological sciences2019
Isolation, characterization, cloning and bioinformatics analysis of a novel receptor from black cut worm (
Article in Saudi journal of biological sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.
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Who cites it
10 citing papers in PubMed.
- Helicoverpa zea selected on Bt corn have wing shapes better suited to long distance flight.Environmental entomology · 2026Article
- Cross-pollination in seed-blended refuge and selection for Vip3A resistance in a lepidopteran pest as detected by genomic monitoring.Proceedings of the National Academy of Sciences of the United States of America · 2024Article
- Article
- PHB2 affects the virulence of Vip3Aa to Sf9 cells through internalization and mitochondrial stability.Virulence · 2022Article
- Article
- In vivo competition assays between Vip3 proteins confirm the occurrence of shared binding sites in Spodoptera littoralis.Scientific reports · 2022Article
- Critical Domains in the Specific Binding of Radiolabeled Vip3Af Insecticidal Protein to Brush Border Membrane Vesicles fromApplied and environmental microbiology · 2021Article
- Vegetative Insecticidal Protein (Vip): A Potential Contender FromFrontiers in microbiology · 2021Review
- Current Insights on Vegetative Insecticidal Proteins (Vip) as Next Generation Pest Killers.Toxins · 2020Review
- Characterization, cloning, expression and bioassay ofSaudi journal of biological sciences · 2020Article
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Authors and funding
10 authors.
Funding
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Abstract
Black cutworm (BCW) is an economically important lepidopteran insect. The control of this insect by a Bt toxin and the understanding of the interaction between the Bt toxin and its receptor molecule were the objectives of this research work. A gene coding for a Vip3A receptor molecule was identified, characterized, and cloned, from the brush border membrane vesicles (BBMV) of the BCW. The nucleotide sequence analysis of the cloned putative Vip3A-receptor gene revealed that the gene was 1.3-kb long and exhibited no homology with any gene in the gene bank. We succeeded in identifying and characterizing most of the Vip3A-receptor gene sequence; and the nucleotide sequence analysis of the cloned putative Vip3A-receptor gene (accession no. KX858809) revealed about 92% of the expected sequence was recovered, which exhibited no homology with any gene in the GenBank.
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