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Genetic control of violacein biosynthesis to enable a pigment-based whole-cell lead biosensor
Environmental risks continue to grow due to heavy metal contamination caused by anthropogenic activities. Accumulation of harmful quantities of lead poses a threat to aquatic organisms, plants, and human beings. Whole-cell biosensors, which can proliferate independently, can detect the bioavailable...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9055639/ https://www.ncbi.nlm.nih.gov/pubmed/35519119 http://dx.doi.org/10.1039/d0ra04815a |
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author | Hui, Chang-ye Guo, Yan Liu, Lisa Zhang, Nai-xing Gao, Chao-xian Yang, Xue-qin Yi, Juan |
author_facet | Hui, Chang-ye Guo, Yan Liu, Lisa Zhang, Nai-xing Gao, Chao-xian Yang, Xue-qin Yi, Juan |
author_sort | Hui, Chang-ye |
collection | PubMed |
description | Environmental risks continue to grow due to heavy metal contamination caused by anthropogenic activities. Accumulation of harmful quantities of lead poses a threat to aquatic organisms, plants, and human beings. Whole-cell biosensors, which can proliferate independently, can detect the bioavailable fraction to assess the effect of target heavy metal on the environmental ecosystem. In this study, the biosynthesis pathway of violacein was heterogeneously constructed under the control of the T7 lac promoter in E. coli. A dose–response relationship existed between the inducer and the production of violacein. The biosynthesis pathway of violacein was finally engineered under the regulation of Pb(ii)-dependent metalloregulator PbrR to assemble Pb(ii)-inducible whole-cell biosensor. It permitted specific biosensing of Pb(ii) with extraordinary selectivity, and could resist the interferences from various metal ions. Color change by the intracellular accumulation of violacein could be recognized with the naked eye directly with high concentration of lead exposure, and quantified by determining the absorbance at 490 nm after butanol extraction. A good linear range for Pb(ii) concentrations of 0.1875–1.5 μM was obtained. The novel pigment-based whole-cell biosensor could detect concentrations as low as 0.1875 μM Pb(ii) based on in vitro quantification of violacein extracted by butanol, which is significantly lower than reported fluorescent protein-based PbrR-regulated biosensors based on direct measurement of whole cell fluorescence. These results indicate that genetically controlled violacein biosynthesis can enable a sensitive, visual, and qualitative biosensor for monitoring the presence of bioavailable Pb(ii) in lead-contaminated water. |
format | Online Article Text |
id | pubmed-9055639 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90556392022-05-04 Genetic control of violacein biosynthesis to enable a pigment-based whole-cell lead biosensor Hui, Chang-ye Guo, Yan Liu, Lisa Zhang, Nai-xing Gao, Chao-xian Yang, Xue-qin Yi, Juan RSC Adv Chemistry Environmental risks continue to grow due to heavy metal contamination caused by anthropogenic activities. Accumulation of harmful quantities of lead poses a threat to aquatic organisms, plants, and human beings. Whole-cell biosensors, which can proliferate independently, can detect the bioavailable fraction to assess the effect of target heavy metal on the environmental ecosystem. In this study, the biosynthesis pathway of violacein was heterogeneously constructed under the control of the T7 lac promoter in E. coli. A dose–response relationship existed between the inducer and the production of violacein. The biosynthesis pathway of violacein was finally engineered under the regulation of Pb(ii)-dependent metalloregulator PbrR to assemble Pb(ii)-inducible whole-cell biosensor. It permitted specific biosensing of Pb(ii) with extraordinary selectivity, and could resist the interferences from various metal ions. Color change by the intracellular accumulation of violacein could be recognized with the naked eye directly with high concentration of lead exposure, and quantified by determining the absorbance at 490 nm after butanol extraction. A good linear range for Pb(ii) concentrations of 0.1875–1.5 μM was obtained. The novel pigment-based whole-cell biosensor could detect concentrations as low as 0.1875 μM Pb(ii) based on in vitro quantification of violacein extracted by butanol, which is significantly lower than reported fluorescent protein-based PbrR-regulated biosensors based on direct measurement of whole cell fluorescence. These results indicate that genetically controlled violacein biosynthesis can enable a sensitive, visual, and qualitative biosensor for monitoring the presence of bioavailable Pb(ii) in lead-contaminated water. The Royal Society of Chemistry 2020-07-28 /pmc/articles/PMC9055639/ /pubmed/35519119 http://dx.doi.org/10.1039/d0ra04815a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Hui, Chang-ye Guo, Yan Liu, Lisa Zhang, Nai-xing Gao, Chao-xian Yang, Xue-qin Yi, Juan Genetic control of violacein biosynthesis to enable a pigment-based whole-cell lead biosensor |
title | Genetic control of violacein biosynthesis to enable a pigment-based whole-cell lead biosensor |
title_full | Genetic control of violacein biosynthesis to enable a pigment-based whole-cell lead biosensor |
title_fullStr | Genetic control of violacein biosynthesis to enable a pigment-based whole-cell lead biosensor |
title_full_unstemmed | Genetic control of violacein biosynthesis to enable a pigment-based whole-cell lead biosensor |
title_short | Genetic control of violacein biosynthesis to enable a pigment-based whole-cell lead biosensor |
title_sort | genetic control of violacein biosynthesis to enable a pigment-based whole-cell lead biosensor |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9055639/ https://www.ncbi.nlm.nih.gov/pubmed/35519119 http://dx.doi.org/10.1039/d0ra04815a |
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