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Improving Cry8Ka toxin activity towards the cotton boll weevil (Anthonomus grandis)

BACKGROUND: The cotton boll weevil (Anthonomus grandis) is a serious insect-pest in the Americas, particularly in Brazil. The use of chemical or biological insect control is not effective against the cotton boll weevil because of its endophytic life style. Therefore, the use of biotechnological tool...

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Autores principales: Oliveira, Gustavo R, Silva, Maria CM, Lucena, Wagner A, Nakasu, Erich YT, Firmino, Alexandre AP, Beneventi, Magda A, Souza, Djair SL, Gomes, José E, de Souza, José DA, Rigden, Daniel J, Ramos, Hudson B, Soccol, Carlos R, Grossi-de-Sa, Maria F
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3179717/
https://www.ncbi.nlm.nih.gov/pubmed/21906288
http://dx.doi.org/10.1186/1472-6750-11-85
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author Oliveira, Gustavo R
Silva, Maria CM
Lucena, Wagner A
Nakasu, Erich YT
Firmino, Alexandre AP
Beneventi, Magda A
Souza, Djair SL
Gomes, José E
de Souza, José DA
Rigden, Daniel J
Ramos, Hudson B
Soccol, Carlos R
Grossi-de-Sa, Maria F
author_facet Oliveira, Gustavo R
Silva, Maria CM
Lucena, Wagner A
Nakasu, Erich YT
Firmino, Alexandre AP
Beneventi, Magda A
Souza, Djair SL
Gomes, José E
de Souza, José DA
Rigden, Daniel J
Ramos, Hudson B
Soccol, Carlos R
Grossi-de-Sa, Maria F
author_sort Oliveira, Gustavo R
collection PubMed
description BACKGROUND: The cotton boll weevil (Anthonomus grandis) is a serious insect-pest in the Americas, particularly in Brazil. The use of chemical or biological insect control is not effective against the cotton boll weevil because of its endophytic life style. Therefore, the use of biotechnological tools to produce insect-resistant transgenic plants represents an important strategy to reduce the damage to cotton plants caused by the boll weevil. The present study focuses on the identification of novel molecules that show improved toxicity against the cotton boll weevil. In vitro directed molecular evolution through DNA shuffling and phage display screening was applied to enhance the insecticidal activity of variants of the Cry8Ka1 protein of Bacillus thuringiensis. RESULTS: Bioassays carried out with A. grandis larvae revealed that the LC(50 )of the screened mutant Cry8Ka5 toxin was 3.15-fold higher than the wild-type Cry8Ka1 toxin. Homology modelling of Cry8Ka1 and the Cry8Ka5 mutant suggested that both proteins retained the typical three-domain Cry family structure. The mutated residues were located mostly in loops and appeared unlikely to interfere with molecular stability. CONCLUSIONS: The improved toxicity of the Cry8Ka5 mutant obtained in this study will allow the generation of a transgenic cotton event with improved potential to control A. grandis.
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spelling pubmed-31797172011-09-25 Improving Cry8Ka toxin activity towards the cotton boll weevil (Anthonomus grandis) Oliveira, Gustavo R Silva, Maria CM Lucena, Wagner A Nakasu, Erich YT Firmino, Alexandre AP Beneventi, Magda A Souza, Djair SL Gomes, José E de Souza, José DA Rigden, Daniel J Ramos, Hudson B Soccol, Carlos R Grossi-de-Sa, Maria F BMC Biotechnol Research Article BACKGROUND: The cotton boll weevil (Anthonomus grandis) is a serious insect-pest in the Americas, particularly in Brazil. The use of chemical or biological insect control is not effective against the cotton boll weevil because of its endophytic life style. Therefore, the use of biotechnological tools to produce insect-resistant transgenic plants represents an important strategy to reduce the damage to cotton plants caused by the boll weevil. The present study focuses on the identification of novel molecules that show improved toxicity against the cotton boll weevil. In vitro directed molecular evolution through DNA shuffling and phage display screening was applied to enhance the insecticidal activity of variants of the Cry8Ka1 protein of Bacillus thuringiensis. RESULTS: Bioassays carried out with A. grandis larvae revealed that the LC(50 )of the screened mutant Cry8Ka5 toxin was 3.15-fold higher than the wild-type Cry8Ka1 toxin. Homology modelling of Cry8Ka1 and the Cry8Ka5 mutant suggested that both proteins retained the typical three-domain Cry family structure. The mutated residues were located mostly in loops and appeared unlikely to interfere with molecular stability. CONCLUSIONS: The improved toxicity of the Cry8Ka5 mutant obtained in this study will allow the generation of a transgenic cotton event with improved potential to control A. grandis. BioMed Central 2011-09-09 /pmc/articles/PMC3179717/ /pubmed/21906288 http://dx.doi.org/10.1186/1472-6750-11-85 Text en Copyright ©2011 Oliveira et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Oliveira, Gustavo R
Silva, Maria CM
Lucena, Wagner A
Nakasu, Erich YT
Firmino, Alexandre AP
Beneventi, Magda A
Souza, Djair SL
Gomes, José E
de Souza, José DA
Rigden, Daniel J
Ramos, Hudson B
Soccol, Carlos R
Grossi-de-Sa, Maria F
Improving Cry8Ka toxin activity towards the cotton boll weevil (Anthonomus grandis)
title Improving Cry8Ka toxin activity towards the cotton boll weevil (Anthonomus grandis)
title_full Improving Cry8Ka toxin activity towards the cotton boll weevil (Anthonomus grandis)
title_fullStr Improving Cry8Ka toxin activity towards the cotton boll weevil (Anthonomus grandis)
title_full_unstemmed Improving Cry8Ka toxin activity towards the cotton boll weevil (Anthonomus grandis)
title_short Improving Cry8Ka toxin activity towards the cotton boll weevil (Anthonomus grandis)
title_sort improving cry8ka toxin activity towards the cotton boll weevil (anthonomus grandis)
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3179717/
https://www.ncbi.nlm.nih.gov/pubmed/21906288
http://dx.doi.org/10.1186/1472-6750-11-85
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