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A procedure for removal of cyanuric acid in swimming pools using a cell-free thermostable cyanuric acid hydrolase
Cyanuric acid (CYA) is used commercially for maintaining active chlorine to inactivate microbial and viral pathogens in swimming pools and hot tubs. Repeated CYA addition can cause a lack of available chlorine and adequate disinfection. Acceptable CYA levels can potentially be restored via cyanuric...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9118981/ https://www.ncbi.nlm.nih.gov/pubmed/34788856 http://dx.doi.org/10.1093/jimb/kuab084 |
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author | Guo, Feng McAuliffe, Joseph C Bongiorni, Cristina Latone, Jacob A Pepsin, Mike J Chow, Marina S Dhaliwal, Raj S Hoffmann, Katherine M Brazil, Bill T Heng, Meng H Robinson, Serina L Wackett, Lawrence P Whited, Gregory M |
author_facet | Guo, Feng McAuliffe, Joseph C Bongiorni, Cristina Latone, Jacob A Pepsin, Mike J Chow, Marina S Dhaliwal, Raj S Hoffmann, Katherine M Brazil, Bill T Heng, Meng H Robinson, Serina L Wackett, Lawrence P Whited, Gregory M |
author_sort | Guo, Feng |
collection | PubMed |
description | Cyanuric acid (CYA) is used commercially for maintaining active chlorine to inactivate microbial and viral pathogens in swimming pools and hot tubs. Repeated CYA addition can cause a lack of available chlorine and adequate disinfection. Acceptable CYA levels can potentially be restored via cyanuric acid hydrolases (CAH), enzymes that hydrolyze CYA to biuret under mild conditions. Here we describe a previously unknown CAH enzyme from Pseudolabrys sp. Root1462 (CAH-PR), mined from public databases by bioinformatic analysis of potential CAH genes, which we show to be suitable in a cell-free form for industrial applications based upon favorable enzymatic and physical properties, combined with high-yield expression in aerobic cell culture. The kinetic parameters and modeled structure were similar to known CAH enzymes, but the new enzyme displayed a surprising thermal and storage stability. The new CAH enzyme was applied, following addition of inexpensive sodium sulfite, to hydrolyze CYA to biuret. At the desired endpoint, hypochlorite addition inactivated remaining enzyme and oxidized biuret to primarily dinitrogen and carbon dioxide gases. The mechanism of biuret oxidation with hypochlorite under conditions relevant to recreational pools is described. |
format | Online Article Text |
id | pubmed-9118981 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-91189812022-06-08 A procedure for removal of cyanuric acid in swimming pools using a cell-free thermostable cyanuric acid hydrolase Guo, Feng McAuliffe, Joseph C Bongiorni, Cristina Latone, Jacob A Pepsin, Mike J Chow, Marina S Dhaliwal, Raj S Hoffmann, Katherine M Brazil, Bill T Heng, Meng H Robinson, Serina L Wackett, Lawrence P Whited, Gregory M J Ind Microbiol Biotechnol Biocatalysis Cyanuric acid (CYA) is used commercially for maintaining active chlorine to inactivate microbial and viral pathogens in swimming pools and hot tubs. Repeated CYA addition can cause a lack of available chlorine and adequate disinfection. Acceptable CYA levels can potentially be restored via cyanuric acid hydrolases (CAH), enzymes that hydrolyze CYA to biuret under mild conditions. Here we describe a previously unknown CAH enzyme from Pseudolabrys sp. Root1462 (CAH-PR), mined from public databases by bioinformatic analysis of potential CAH genes, which we show to be suitable in a cell-free form for industrial applications based upon favorable enzymatic and physical properties, combined with high-yield expression in aerobic cell culture. The kinetic parameters and modeled structure were similar to known CAH enzymes, but the new enzyme displayed a surprising thermal and storage stability. The new CAH enzyme was applied, following addition of inexpensive sodium sulfite, to hydrolyze CYA to biuret. At the desired endpoint, hypochlorite addition inactivated remaining enzyme and oxidized biuret to primarily dinitrogen and carbon dioxide gases. The mechanism of biuret oxidation with hypochlorite under conditions relevant to recreational pools is described. Oxford University Press 2021-11-12 /pmc/articles/PMC9118981/ /pubmed/34788856 http://dx.doi.org/10.1093/jimb/kuab084 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of Society of Industrial Microbiology and Biotechnology. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Biocatalysis Guo, Feng McAuliffe, Joseph C Bongiorni, Cristina Latone, Jacob A Pepsin, Mike J Chow, Marina S Dhaliwal, Raj S Hoffmann, Katherine M Brazil, Bill T Heng, Meng H Robinson, Serina L Wackett, Lawrence P Whited, Gregory M A procedure for removal of cyanuric acid in swimming pools using a cell-free thermostable cyanuric acid hydrolase |
title | A procedure for removal of cyanuric acid in swimming pools using a cell-free thermostable cyanuric acid hydrolase |
title_full | A procedure for removal of cyanuric acid in swimming pools using a cell-free thermostable cyanuric acid hydrolase |
title_fullStr | A procedure for removal of cyanuric acid in swimming pools using a cell-free thermostable cyanuric acid hydrolase |
title_full_unstemmed | A procedure for removal of cyanuric acid in swimming pools using a cell-free thermostable cyanuric acid hydrolase |
title_short | A procedure for removal of cyanuric acid in swimming pools using a cell-free thermostable cyanuric acid hydrolase |
title_sort | procedure for removal of cyanuric acid in swimming pools using a cell-free thermostable cyanuric acid hydrolase |
topic | Biocatalysis |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9118981/ https://www.ncbi.nlm.nih.gov/pubmed/34788856 http://dx.doi.org/10.1093/jimb/kuab084 |
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