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A multiplexed nanostructure-initiator mass spectrometry (NIMS) assay for simultaneously detecting glycosyl hydrolase and lignin modifying enzyme activities
Lignocellulosic biomass is composed of three major biopolymers: cellulose, hemicellulose and lignin. Analytical tools capable of quickly detecting both glycan and lignin deconstruction are needed to support the development and characterization of efficient enzymes/enzyme cocktails. Previously we hav...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8175421/ https://www.ncbi.nlm.nih.gov/pubmed/34083602 http://dx.doi.org/10.1038/s41598-021-91181-8 |
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author | Ing, Nicole Deng, Kai Chen, Yan Aulitto, Martina Gin, Jennifer W. Pham, Thanh Le Mai Petzold, Christopher J. Singer, Steve W. Bowen, Benjamin Sale, Kenneth L. Simmons, Blake A. Singh, Anup K. Adams, Paul D. Northen, Trent R. |
author_facet | Ing, Nicole Deng, Kai Chen, Yan Aulitto, Martina Gin, Jennifer W. Pham, Thanh Le Mai Petzold, Christopher J. Singer, Steve W. Bowen, Benjamin Sale, Kenneth L. Simmons, Blake A. Singh, Anup K. Adams, Paul D. Northen, Trent R. |
author_sort | Ing, Nicole |
collection | PubMed |
description | Lignocellulosic biomass is composed of three major biopolymers: cellulose, hemicellulose and lignin. Analytical tools capable of quickly detecting both glycan and lignin deconstruction are needed to support the development and characterization of efficient enzymes/enzyme cocktails. Previously we have described nanostructure-initiator mass spectrometry-based assays for the analysis of glycosyl hydrolase and most recently an assay for lignin modifying enzymes. Here we integrate these two assays into a single multiplexed assay against both classes of enzymes and use it to characterize crude commercial enzyme mixtures. Application of our multiplexed platform based on nanostructure-initiator mass spectrometry enabled us to characterize crude mixtures of laccase enzymes from fungi Agaricus bisporus (Ab) and Myceliopthora thermophila (Mt) revealing activity on both carbohydrate and aromatic substrates. Using time-series analysis we determined that crude laccase from Ab has the higher GH activity and that laccase from Mt has the higher activity against our lignin model compound. Inhibitor studies showed a significant reduction in Mt GH activity under low oxygen conditions and increased activities in the presence of vanillin (common GH inhibitor). Ultimately, this assay can help to discover mixtures of enzymes that could be incorporated into biomass pretreatments to deconstruct diverse components of lignocellulosic biomass. |
format | Online Article Text |
id | pubmed-8175421 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-81754212021-06-04 A multiplexed nanostructure-initiator mass spectrometry (NIMS) assay for simultaneously detecting glycosyl hydrolase and lignin modifying enzyme activities Ing, Nicole Deng, Kai Chen, Yan Aulitto, Martina Gin, Jennifer W. Pham, Thanh Le Mai Petzold, Christopher J. Singer, Steve W. Bowen, Benjamin Sale, Kenneth L. Simmons, Blake A. Singh, Anup K. Adams, Paul D. Northen, Trent R. Sci Rep Article Lignocellulosic biomass is composed of three major biopolymers: cellulose, hemicellulose and lignin. Analytical tools capable of quickly detecting both glycan and lignin deconstruction are needed to support the development and characterization of efficient enzymes/enzyme cocktails. Previously we have described nanostructure-initiator mass spectrometry-based assays for the analysis of glycosyl hydrolase and most recently an assay for lignin modifying enzymes. Here we integrate these two assays into a single multiplexed assay against both classes of enzymes and use it to characterize crude commercial enzyme mixtures. Application of our multiplexed platform based on nanostructure-initiator mass spectrometry enabled us to characterize crude mixtures of laccase enzymes from fungi Agaricus bisporus (Ab) and Myceliopthora thermophila (Mt) revealing activity on both carbohydrate and aromatic substrates. Using time-series analysis we determined that crude laccase from Ab has the higher GH activity and that laccase from Mt has the higher activity against our lignin model compound. Inhibitor studies showed a significant reduction in Mt GH activity under low oxygen conditions and increased activities in the presence of vanillin (common GH inhibitor). Ultimately, this assay can help to discover mixtures of enzymes that could be incorporated into biomass pretreatments to deconstruct diverse components of lignocellulosic biomass. Nature Publishing Group UK 2021-06-03 /pmc/articles/PMC8175421/ /pubmed/34083602 http://dx.doi.org/10.1038/s41598-021-91181-8 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Ing, Nicole Deng, Kai Chen, Yan Aulitto, Martina Gin, Jennifer W. Pham, Thanh Le Mai Petzold, Christopher J. Singer, Steve W. Bowen, Benjamin Sale, Kenneth L. Simmons, Blake A. Singh, Anup K. Adams, Paul D. Northen, Trent R. A multiplexed nanostructure-initiator mass spectrometry (NIMS) assay for simultaneously detecting glycosyl hydrolase and lignin modifying enzyme activities |
title | A multiplexed nanostructure-initiator mass spectrometry (NIMS) assay for simultaneously detecting glycosyl hydrolase and lignin modifying enzyme activities |
title_full | A multiplexed nanostructure-initiator mass spectrometry (NIMS) assay for simultaneously detecting glycosyl hydrolase and lignin modifying enzyme activities |
title_fullStr | A multiplexed nanostructure-initiator mass spectrometry (NIMS) assay for simultaneously detecting glycosyl hydrolase and lignin modifying enzyme activities |
title_full_unstemmed | A multiplexed nanostructure-initiator mass spectrometry (NIMS) assay for simultaneously detecting glycosyl hydrolase and lignin modifying enzyme activities |
title_short | A multiplexed nanostructure-initiator mass spectrometry (NIMS) assay for simultaneously detecting glycosyl hydrolase and lignin modifying enzyme activities |
title_sort | multiplexed nanostructure-initiator mass spectrometry (nims) assay for simultaneously detecting glycosyl hydrolase and lignin modifying enzyme activities |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8175421/ https://www.ncbi.nlm.nih.gov/pubmed/34083602 http://dx.doi.org/10.1038/s41598-021-91181-8 |
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