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Rapid determination of kappa-carrageenan using a biosensor from immobilized Pseudomonas carrageenovora cells

A potentiometric whole cell biosensor based on immobilized marine bacterium, Pseudomonas carrageenovora producing κ-carrageenase and glycosulfatase enzymes for specific and direct determination of κ-carrageenan, is described. The bacterial cells were immobilized on the self-plasticized hydrogen ion...

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Autores principales: Hassan, Riyadh Abdulmalek, Heng, Lee Yook, Ahmad, Asmat, Tan, Ling Ling
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6467376/
https://www.ncbi.nlm.nih.gov/pubmed/30990847
http://dx.doi.org/10.1371/journal.pone.0214580
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author Hassan, Riyadh Abdulmalek
Heng, Lee Yook
Ahmad, Asmat
Tan, Ling Ling
author_facet Hassan, Riyadh Abdulmalek
Heng, Lee Yook
Ahmad, Asmat
Tan, Ling Ling
author_sort Hassan, Riyadh Abdulmalek
collection PubMed
description A potentiometric whole cell biosensor based on immobilized marine bacterium, Pseudomonas carrageenovora producing κ-carrageenase and glycosulfatase enzymes for specific and direct determination of κ-carrageenan, is described. The bacterial cells were immobilized on the self-plasticized hydrogen ion (H(+))-selective acrylic membrane electrode surface to form a catalytic layer. Hydrogen ionophore I was incorporated in the poly(n-butyl acrylate) [poly(nBA)] as a pH ionophore. Catalytic decomposition of κ-carrageenan by the bienzymatic cascade reaction produced neoagarobiose, an inorganic sulfate ion and a proton. The latter was detectable by H(+) ion transducer for indirect potentiometric quantification of κ-carrageenan concentration. The use of a disposable screen-printed Ag/AgCl electrode (SPE) provided no cleaning requirement and enabled κ-carrageenan detection to be carried out conveniently without cross contamination in a complex food sample. The SPE-based microbial biosensor response was found to be reproducible with high reproducibility and relative standard deviation (RSD) at 2.6% (n = 3). The whole cell biosensor demonstrated a broad dynamic linear response range to κ-carrageenan from 0.2–100 ppm in 20 mM phosphate buffer saline (PBS) at pH 7.5 with a detection limit at 0.05 ppm and a Nernstian sensitivity of 58.78±0.87 mV/decade (R(2) = 0.995). The biosensor showed excellent selectivity towards κ-carrageenan compared to other types of carrageenans tested e.g. ι-carrageenan and λ-carrageenan. No pretreatment to the food sample was necessary when the developed whole cell biosensor was employed for direct assay of κ-carrageenan in dairy product.
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spelling pubmed-64673762019-05-03 Rapid determination of kappa-carrageenan using a biosensor from immobilized Pseudomonas carrageenovora cells Hassan, Riyadh Abdulmalek Heng, Lee Yook Ahmad, Asmat Tan, Ling Ling PLoS One Research Article A potentiometric whole cell biosensor based on immobilized marine bacterium, Pseudomonas carrageenovora producing κ-carrageenase and glycosulfatase enzymes for specific and direct determination of κ-carrageenan, is described. The bacterial cells were immobilized on the self-plasticized hydrogen ion (H(+))-selective acrylic membrane electrode surface to form a catalytic layer. Hydrogen ionophore I was incorporated in the poly(n-butyl acrylate) [poly(nBA)] as a pH ionophore. Catalytic decomposition of κ-carrageenan by the bienzymatic cascade reaction produced neoagarobiose, an inorganic sulfate ion and a proton. The latter was detectable by H(+) ion transducer for indirect potentiometric quantification of κ-carrageenan concentration. The use of a disposable screen-printed Ag/AgCl electrode (SPE) provided no cleaning requirement and enabled κ-carrageenan detection to be carried out conveniently without cross contamination in a complex food sample. The SPE-based microbial biosensor response was found to be reproducible with high reproducibility and relative standard deviation (RSD) at 2.6% (n = 3). The whole cell biosensor demonstrated a broad dynamic linear response range to κ-carrageenan from 0.2–100 ppm in 20 mM phosphate buffer saline (PBS) at pH 7.5 with a detection limit at 0.05 ppm and a Nernstian sensitivity of 58.78±0.87 mV/decade (R(2) = 0.995). The biosensor showed excellent selectivity towards κ-carrageenan compared to other types of carrageenans tested e.g. ι-carrageenan and λ-carrageenan. No pretreatment to the food sample was necessary when the developed whole cell biosensor was employed for direct assay of κ-carrageenan in dairy product. Public Library of Science 2019-04-16 /pmc/articles/PMC6467376/ /pubmed/30990847 http://dx.doi.org/10.1371/journal.pone.0214580 Text en © 2019 Hassan et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Hassan, Riyadh Abdulmalek
Heng, Lee Yook
Ahmad, Asmat
Tan, Ling Ling
Rapid determination of kappa-carrageenan using a biosensor from immobilized Pseudomonas carrageenovora cells
title Rapid determination of kappa-carrageenan using a biosensor from immobilized Pseudomonas carrageenovora cells
title_full Rapid determination of kappa-carrageenan using a biosensor from immobilized Pseudomonas carrageenovora cells
title_fullStr Rapid determination of kappa-carrageenan using a biosensor from immobilized Pseudomonas carrageenovora cells
title_full_unstemmed Rapid determination of kappa-carrageenan using a biosensor from immobilized Pseudomonas carrageenovora cells
title_short Rapid determination of kappa-carrageenan using a biosensor from immobilized Pseudomonas carrageenovora cells
title_sort rapid determination of kappa-carrageenan using a biosensor from immobilized pseudomonas carrageenovora cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6467376/
https://www.ncbi.nlm.nih.gov/pubmed/30990847
http://dx.doi.org/10.1371/journal.pone.0214580
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