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Production and characterization of the (13)C/(15)N single‐labeled insecticidal protein Cry1Ab/Ac using recombinant Escherichia coli
Synthetic Cry1Ab/Ac proteins expressed by genetically modified (GM) crops have a high potential to control insect pests without utilizing large amounts of chemical insecticides. Before these crops are used in agriculture, the environmental fate and interactions in the soil must be understood. Stable...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7658450/ https://www.ncbi.nlm.nih.gov/pubmed/33058518 http://dx.doi.org/10.1002/mbo3.1125 |
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author | Wang, Zibo Hu, Cong Sun, Yu Jiang, Wei Wu, Guogan Pan, Aihu Li, Peng Tang, Xueming |
author_facet | Wang, Zibo Hu, Cong Sun, Yu Jiang, Wei Wu, Guogan Pan, Aihu Li, Peng Tang, Xueming |
author_sort | Wang, Zibo |
collection | PubMed |
description | Synthetic Cry1Ab/Ac proteins expressed by genetically modified (GM) crops have a high potential to control insect pests without utilizing large amounts of chemical insecticides. Before these crops are used in agriculture, the environmental fate and interactions in the soil must be understood. Stable isotope‐labeled Cry1Ab/Ac protein is a highly useful tool for collecting such data. We developed a protocol to produce (13)C/(15)N single‐labeled Cry proteins. The artificially synthesized gene Cry1Ab/Ac of Bt rice Huahui No. 1, which has been certified by the Chinese government to be safe for human consumption, was subcloned into pUC57, and the expression vector pET‐28a‐CryAb/Ac was constructed and transformed into Escherichia coli BL21 (DE3) competent cells. Next, 0.2 mM isopropyl thiogalactoside (IPTG) was added to these cells and cultured at 37°C for 4 h to induce the synthesis and formation of inclusion bodies in M9 growth media containing either [U‐(13)C] glucose (5% (13)C‐enriched) or [(15)N] ammonium chloride (5% (15)N‐enriched). Then, Cry inclusion bodies were dissolved in urea and purified by affinity chromatography under denaturing conditions, renatured by dialysis, and further detected by sodium dodecyl sulfate–polyacrylamide gel electrophoresis (SDS‐PAGE) and Western blotting. The purities of (13)C/(15)N‐labeled Cry proteins reached 99% with amounts of 12.6 mg/L and 8.8 mg/L, respectively. The δ (13)C and ä (15)N values of (13)C‐labeled Cry protein and (15)N‐labeled Cry protein were 3,269‰ and 2,854‰, respectively. A bioassay test revealed that the labeled Cry1Ab/Ac proteins had strong insecticidal activity. The stable isotope‐labeled insecticidal Cry proteins produced for the first time in this study will provide an experimental basis for future metabolic studies on Cry proteins in soil and the characteristics of nitrogen (N) and carbon (C) transformations. Our findings may also be employed as a reference for elucidating the environmental behavior and ecological effects of BT plants and expressed products. |
format | Online Article Text |
id | pubmed-7658450 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-76584502020-11-17 Production and characterization of the (13)C/(15)N single‐labeled insecticidal protein Cry1Ab/Ac using recombinant Escherichia coli Wang, Zibo Hu, Cong Sun, Yu Jiang, Wei Wu, Guogan Pan, Aihu Li, Peng Tang, Xueming Microbiologyopen Original Articles Synthetic Cry1Ab/Ac proteins expressed by genetically modified (GM) crops have a high potential to control insect pests without utilizing large amounts of chemical insecticides. Before these crops are used in agriculture, the environmental fate and interactions in the soil must be understood. Stable isotope‐labeled Cry1Ab/Ac protein is a highly useful tool for collecting such data. We developed a protocol to produce (13)C/(15)N single‐labeled Cry proteins. The artificially synthesized gene Cry1Ab/Ac of Bt rice Huahui No. 1, which has been certified by the Chinese government to be safe for human consumption, was subcloned into pUC57, and the expression vector pET‐28a‐CryAb/Ac was constructed and transformed into Escherichia coli BL21 (DE3) competent cells. Next, 0.2 mM isopropyl thiogalactoside (IPTG) was added to these cells and cultured at 37°C for 4 h to induce the synthesis and formation of inclusion bodies in M9 growth media containing either [U‐(13)C] glucose (5% (13)C‐enriched) or [(15)N] ammonium chloride (5% (15)N‐enriched). Then, Cry inclusion bodies were dissolved in urea and purified by affinity chromatography under denaturing conditions, renatured by dialysis, and further detected by sodium dodecyl sulfate–polyacrylamide gel electrophoresis (SDS‐PAGE) and Western blotting. The purities of (13)C/(15)N‐labeled Cry proteins reached 99% with amounts of 12.6 mg/L and 8.8 mg/L, respectively. The δ (13)C and ä (15)N values of (13)C‐labeled Cry protein and (15)N‐labeled Cry protein were 3,269‰ and 2,854‰, respectively. A bioassay test revealed that the labeled Cry1Ab/Ac proteins had strong insecticidal activity. The stable isotope‐labeled insecticidal Cry proteins produced for the first time in this study will provide an experimental basis for future metabolic studies on Cry proteins in soil and the characteristics of nitrogen (N) and carbon (C) transformations. Our findings may also be employed as a reference for elucidating the environmental behavior and ecological effects of BT plants and expressed products. John Wiley and Sons Inc. 2020-10-15 /pmc/articles/PMC7658450/ /pubmed/33058518 http://dx.doi.org/10.1002/mbo3.1125 Text en © 2020 The Authors. MicrobiologyOpen published by John Wiley & Sons Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Original Articles Wang, Zibo Hu, Cong Sun, Yu Jiang, Wei Wu, Guogan Pan, Aihu Li, Peng Tang, Xueming Production and characterization of the (13)C/(15)N single‐labeled insecticidal protein Cry1Ab/Ac using recombinant Escherichia coli |
title | Production and characterization of the (13)C/(15)N single‐labeled insecticidal protein Cry1Ab/Ac using recombinant Escherichia coli
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title_full | Production and characterization of the (13)C/(15)N single‐labeled insecticidal protein Cry1Ab/Ac using recombinant Escherichia coli
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title_fullStr | Production and characterization of the (13)C/(15)N single‐labeled insecticidal protein Cry1Ab/Ac using recombinant Escherichia coli
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title_full_unstemmed | Production and characterization of the (13)C/(15)N single‐labeled insecticidal protein Cry1Ab/Ac using recombinant Escherichia coli
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title_short | Production and characterization of the (13)C/(15)N single‐labeled insecticidal protein Cry1Ab/Ac using recombinant Escherichia coli
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title_sort | production and characterization of the (13)c/(15)n single‐labeled insecticidal protein cry1ab/ac using recombinant escherichia coli |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7658450/ https://www.ncbi.nlm.nih.gov/pubmed/33058518 http://dx.doi.org/10.1002/mbo3.1125 |
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