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Modernized Machine Learning Approach to Illuminate Enzyme Immobilization for Biocatalysis
[Image: see text] Biocatalysis is an established technology with significant application in the pharmaceutical industry. Immobilization of enzymes offers significant benefits for commercial and practical purposes to enhance the stability and recyclability of biocatalysts. Determination of the spatia...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10604017/ https://www.ncbi.nlm.nih.gov/pubmed/37901174 http://dx.doi.org/10.1021/acscentsci.3c00757 |
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author | Wei, Hong Smith, Joseph P. |
author_facet | Wei, Hong Smith, Joseph P. |
author_sort | Wei, Hong |
collection | PubMed |
description | [Image: see text] Biocatalysis is an established technology with significant application in the pharmaceutical industry. Immobilization of enzymes offers significant benefits for commercial and practical purposes to enhance the stability and recyclability of biocatalysts. Determination of the spatial and chemical distributions of immobilized enzymes on solid support materials is essential for an optimal catalytic performance. However, current analytical methodologies often fall short of rapidly identifying and characterizing immobilized enzyme systems. Herein, we present a new analytical methodology that combines non-negative matrix factorization (NMF)—an unsupervised machine learning tool—with Raman hyperspectral imaging to simultaneously resolve the spatial and spectral characteristics of all individual species involved in enzyme immobilization. Our novel approach facilitates the determination of the optimal NMF model using new data-driven, quantitative selection criteria that fully resolve all chemical species present, offering a robust methodology for analyzing immobilized enzymes. Specifically, we demonstrate the ability of NMF with Raman hyperspectral imaging to resolve the spatial and spectral profiles of an engineered pantothenate kinase immobilized on two different commercial microporous resins. Our results demonstrate that this approach can accurately identify and spatially resolve all species within this enzyme immobilization process. To the best of our knowledge, this is the first report of NMF within hyperspectral imaging for enzyme immobilization analysis, and as such, our methodology can now provide a new powerful tool to streamline biocatalytic process development within the pharmaceutical industry. |
format | Online Article Text |
id | pubmed-10604017 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-106040172023-10-28 Modernized Machine Learning Approach to Illuminate Enzyme Immobilization for Biocatalysis Wei, Hong Smith, Joseph P. ACS Cent Sci [Image: see text] Biocatalysis is an established technology with significant application in the pharmaceutical industry. Immobilization of enzymes offers significant benefits for commercial and practical purposes to enhance the stability and recyclability of biocatalysts. Determination of the spatial and chemical distributions of immobilized enzymes on solid support materials is essential for an optimal catalytic performance. However, current analytical methodologies often fall short of rapidly identifying and characterizing immobilized enzyme systems. Herein, we present a new analytical methodology that combines non-negative matrix factorization (NMF)—an unsupervised machine learning tool—with Raman hyperspectral imaging to simultaneously resolve the spatial and spectral characteristics of all individual species involved in enzyme immobilization. Our novel approach facilitates the determination of the optimal NMF model using new data-driven, quantitative selection criteria that fully resolve all chemical species present, offering a robust methodology for analyzing immobilized enzymes. Specifically, we demonstrate the ability of NMF with Raman hyperspectral imaging to resolve the spatial and spectral profiles of an engineered pantothenate kinase immobilized on two different commercial microporous resins. Our results demonstrate that this approach can accurately identify and spatially resolve all species within this enzyme immobilization process. To the best of our knowledge, this is the first report of NMF within hyperspectral imaging for enzyme immobilization analysis, and as such, our methodology can now provide a new powerful tool to streamline biocatalytic process development within the pharmaceutical industry. American Chemical Society 2023-09-27 /pmc/articles/PMC10604017/ /pubmed/37901174 http://dx.doi.org/10.1021/acscentsci.3c00757 Text en © 2023 Merck & Co., Inc., Rahway, NJ, USA and its affiliates. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Wei, Hong Smith, Joseph P. Modernized Machine Learning Approach to Illuminate Enzyme Immobilization for Biocatalysis |
title | Modernized Machine
Learning Approach to Illuminate
Enzyme Immobilization for Biocatalysis |
title_full | Modernized Machine
Learning Approach to Illuminate
Enzyme Immobilization for Biocatalysis |
title_fullStr | Modernized Machine
Learning Approach to Illuminate
Enzyme Immobilization for Biocatalysis |
title_full_unstemmed | Modernized Machine
Learning Approach to Illuminate
Enzyme Immobilization for Biocatalysis |
title_short | Modernized Machine
Learning Approach to Illuminate
Enzyme Immobilization for Biocatalysis |
title_sort | modernized machine
learning approach to illuminate
enzyme immobilization for biocatalysis |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10604017/ https://www.ncbi.nlm.nih.gov/pubmed/37901174 http://dx.doi.org/10.1021/acscentsci.3c00757 |
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