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Expression and Refolding of the Plant Chitinase From Drosera capensis for Applications as a Sustainable and Integrated Pest Management

Recently, the study of chitinases has become an important target of numerous research projects due to their potential for applications, such as biocontrol pest agents. Plant chitinases from carnivorous plants of the genus Drosera are most aggressive against a wide range of phytopathogens. However, l...

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Autores principales: Sinelnikov, Igor G., Siedhoff, Niklas E., Chulkin, Andrey M., Zorov, Ivan N., Schwaneberg, Ulrich, Davari, Mehdi D., Sinitsyna, Olga A., Shcherbakova, Larisa A., Sinitsyn, Arkady P., Rozhkova, Aleksandra M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8490864/
https://www.ncbi.nlm.nih.gov/pubmed/34621729
http://dx.doi.org/10.3389/fbioe.2021.728501
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author Sinelnikov, Igor G.
Siedhoff, Niklas E.
Chulkin, Andrey M.
Zorov, Ivan N.
Schwaneberg, Ulrich
Davari, Mehdi D.
Sinitsyna, Olga A.
Shcherbakova, Larisa A.
Sinitsyn, Arkady P.
Rozhkova, Aleksandra M.
author_facet Sinelnikov, Igor G.
Siedhoff, Niklas E.
Chulkin, Andrey M.
Zorov, Ivan N.
Schwaneberg, Ulrich
Davari, Mehdi D.
Sinitsyna, Olga A.
Shcherbakova, Larisa A.
Sinitsyn, Arkady P.
Rozhkova, Aleksandra M.
author_sort Sinelnikov, Igor G.
collection PubMed
description Recently, the study of chitinases has become an important target of numerous research projects due to their potential for applications, such as biocontrol pest agents. Plant chitinases from carnivorous plants of the genus Drosera are most aggressive against a wide range of phytopathogens. However, low solubility or insolubility of the target protein hampered application of chitinases as biofungicides. To obtain plant chitinase from carnivorous plants of the genus Drosera in soluble form in E.coli expression strains, three different approaches including dialysis, rapid dilution, and refolding on Ni-NTA agarose to renaturation were tested. The developed « Rapid dilution » protocol with renaturation buffer supplemented by 10% glycerol and 2M arginine in combination with the redox pair of reduced/oxidized glutathione, increased the yield of active soluble protein to 9.5 mg per 1 g of wet biomass. A structure-based removal of free cysteines in the core domain based on homology modeling of the structure was carried out in order to improve the soluble of chitinase. One improved chitinase variant (C191A/C231S/C286T) was identified which shows improved expression and solubility in E. coli expression systems compared to wild type. Computational analyzes of the wild-type and the improved variant revealed overall higher fluctuations of the structure while maintaining a global protein stability. It was shown that free cysteines on the surface of the protein globule which are not involved in the formation of inner disulfide bonds contribute to the insolubility of chitinase from Drosera capensis. The functional characteristics showed that chitinase exhibits high activity against colloidal chitin (360 units/g) and high fungicidal properties of recombinant chitinases against Parastagonospora nodorum. Latter highlights the application of chitinase from D. capensis as a promising enzyme for the control of fungal pathogens in agriculture.
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spelling pubmed-84908642021-10-06 Expression and Refolding of the Plant Chitinase From Drosera capensis for Applications as a Sustainable and Integrated Pest Management Sinelnikov, Igor G. Siedhoff, Niklas E. Chulkin, Andrey M. Zorov, Ivan N. Schwaneberg, Ulrich Davari, Mehdi D. Sinitsyna, Olga A. Shcherbakova, Larisa A. Sinitsyn, Arkady P. Rozhkova, Aleksandra M. Front Bioeng Biotechnol Bioengineering and Biotechnology Recently, the study of chitinases has become an important target of numerous research projects due to their potential for applications, such as biocontrol pest agents. Plant chitinases from carnivorous plants of the genus Drosera are most aggressive against a wide range of phytopathogens. However, low solubility or insolubility of the target protein hampered application of chitinases as biofungicides. To obtain plant chitinase from carnivorous plants of the genus Drosera in soluble form in E.coli expression strains, three different approaches including dialysis, rapid dilution, and refolding on Ni-NTA agarose to renaturation were tested. The developed « Rapid dilution » protocol with renaturation buffer supplemented by 10% glycerol and 2M arginine in combination with the redox pair of reduced/oxidized glutathione, increased the yield of active soluble protein to 9.5 mg per 1 g of wet biomass. A structure-based removal of free cysteines in the core domain based on homology modeling of the structure was carried out in order to improve the soluble of chitinase. One improved chitinase variant (C191A/C231S/C286T) was identified which shows improved expression and solubility in E. coli expression systems compared to wild type. Computational analyzes of the wild-type and the improved variant revealed overall higher fluctuations of the structure while maintaining a global protein stability. It was shown that free cysteines on the surface of the protein globule which are not involved in the formation of inner disulfide bonds contribute to the insolubility of chitinase from Drosera capensis. The functional characteristics showed that chitinase exhibits high activity against colloidal chitin (360 units/g) and high fungicidal properties of recombinant chitinases against Parastagonospora nodorum. Latter highlights the application of chitinase from D. capensis as a promising enzyme for the control of fungal pathogens in agriculture. Frontiers Media S.A. 2021-09-21 /pmc/articles/PMC8490864/ /pubmed/34621729 http://dx.doi.org/10.3389/fbioe.2021.728501 Text en Copyright © 2021 Sinelnikov, Siedhoff, Chulkin, Zorov, Schwaneberg, Davari, Sinitsyna, Shcherbakova, Sinitsyn and Rozhkova. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Bioengineering and Biotechnology
Sinelnikov, Igor G.
Siedhoff, Niklas E.
Chulkin, Andrey M.
Zorov, Ivan N.
Schwaneberg, Ulrich
Davari, Mehdi D.
Sinitsyna, Olga A.
Shcherbakova, Larisa A.
Sinitsyn, Arkady P.
Rozhkova, Aleksandra M.
Expression and Refolding of the Plant Chitinase From Drosera capensis for Applications as a Sustainable and Integrated Pest Management
title Expression and Refolding of the Plant Chitinase From Drosera capensis for Applications as a Sustainable and Integrated Pest Management
title_full Expression and Refolding of the Plant Chitinase From Drosera capensis for Applications as a Sustainable and Integrated Pest Management
title_fullStr Expression and Refolding of the Plant Chitinase From Drosera capensis for Applications as a Sustainable and Integrated Pest Management
title_full_unstemmed Expression and Refolding of the Plant Chitinase From Drosera capensis for Applications as a Sustainable and Integrated Pest Management
title_short Expression and Refolding of the Plant Chitinase From Drosera capensis for Applications as a Sustainable and Integrated Pest Management
title_sort expression and refolding of the plant chitinase from drosera capensis for applications as a sustainable and integrated pest management
topic Bioengineering and Biotechnology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8490864/
https://www.ncbi.nlm.nih.gov/pubmed/34621729
http://dx.doi.org/10.3389/fbioe.2021.728501
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