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Biotoxicity assessment of cloned cry 11 protein gene from Bacillus thuringiensis 9NF

The current investigation describes the isolation and characterization of toxic Bt. local isolates harboring 99% homology with Bti. prototoxin Bacillus thuringiensis (AXJ97553.1 and novel OUB27301.1) which contains full length cry11 gene (1.9 kb). Initially, it was cloned in pTZ57R/T and then sub-cl...

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Autores principales: Fatima, Naureen, Rehman, Abdul, Bukhari, DilAra Abbas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9574506/
https://www.ncbi.nlm.nih.gov/pubmed/36263005
http://dx.doi.org/10.1016/j.sjbs.2022.103463
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author Fatima, Naureen
Rehman, Abdul
Bukhari, DilAra Abbas
author_facet Fatima, Naureen
Rehman, Abdul
Bukhari, DilAra Abbas
author_sort Fatima, Naureen
collection PubMed
description The current investigation describes the isolation and characterization of toxic Bt. local isolates harboring 99% homology with Bti. prototoxin Bacillus thuringiensis (AXJ97553.1 and novel OUB27301.1) which contains full length cry11 gene (1.9 kb). Initially, it was cloned in pTZ57R/T and then sub-cloned in pET30a(+) for expression. The optimized conditions for good expression were found 1 mM IPTG, 3.5–4 h incubation time, and 37 °C. Toxicological assays were determined against 3rd instar larvae of Aedes aegypti with expressed partially purified and crude recombinant protein using recombinant E. coli BL21, DE3 transformed with cry11 gene. It was found that partially purified Bt. protein is highly toxic against A. aegypti larvae with LC(50) value of 42.883 ± 6 µg/ml. B. thuringiensis strains producing Cry 11 toxic protein can be used as biopesticide to control resistance in insects.
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spelling pubmed-95745062022-10-18 Biotoxicity assessment of cloned cry 11 protein gene from Bacillus thuringiensis 9NF Fatima, Naureen Rehman, Abdul Bukhari, DilAra Abbas Saudi J Biol Sci Original Article The current investigation describes the isolation and characterization of toxic Bt. local isolates harboring 99% homology with Bti. prototoxin Bacillus thuringiensis (AXJ97553.1 and novel OUB27301.1) which contains full length cry11 gene (1.9 kb). Initially, it was cloned in pTZ57R/T and then sub-cloned in pET30a(+) for expression. The optimized conditions for good expression were found 1 mM IPTG, 3.5–4 h incubation time, and 37 °C. Toxicological assays were determined against 3rd instar larvae of Aedes aegypti with expressed partially purified and crude recombinant protein using recombinant E. coli BL21, DE3 transformed with cry11 gene. It was found that partially purified Bt. protein is highly toxic against A. aegypti larvae with LC(50) value of 42.883 ± 6 µg/ml. B. thuringiensis strains producing Cry 11 toxic protein can be used as biopesticide to control resistance in insects. Elsevier 2022-11 2022-09-27 /pmc/articles/PMC9574506/ /pubmed/36263005 http://dx.doi.org/10.1016/j.sjbs.2022.103463 Text en © 2022 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Fatima, Naureen
Rehman, Abdul
Bukhari, DilAra Abbas
Biotoxicity assessment of cloned cry 11 protein gene from Bacillus thuringiensis 9NF
title Biotoxicity assessment of cloned cry 11 protein gene from Bacillus thuringiensis 9NF
title_full Biotoxicity assessment of cloned cry 11 protein gene from Bacillus thuringiensis 9NF
title_fullStr Biotoxicity assessment of cloned cry 11 protein gene from Bacillus thuringiensis 9NF
title_full_unstemmed Biotoxicity assessment of cloned cry 11 protein gene from Bacillus thuringiensis 9NF
title_short Biotoxicity assessment of cloned cry 11 protein gene from Bacillus thuringiensis 9NF
title_sort biotoxicity assessment of cloned cry 11 protein gene from bacillus thuringiensis 9nf
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9574506/
https://www.ncbi.nlm.nih.gov/pubmed/36263005
http://dx.doi.org/10.1016/j.sjbs.2022.103463
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