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Deciphering the effect of microbead size distribution on the kinetics of heterogeneous biocatalysts through single-particle analysis based on fluorescence microscopy

Authors :
Pedro Ramos-Cabrer
Fernando López-Gallego
Emilio Muñoz-Morales
Susana Velasco-Lozano
Ana I. Benítez-Mateos
María J. Marín
Consejo Nacional de Ciencia y Tecnología (México)
Ministerio de Economía y Competitividad (España)
Ministerio de Ciencia, Innovación y Universidades (España)
Agencia Estatal de Investigación (España)
ARAID Foundation
European Commission
Ikerbasque Basque Foundation for Science
Ramos-Cabrer, Pedro
López-Gallego, Fernando
Ramos-Cabrer, Pedro [0000-0003-0368-7031]
López-Gallego, Fernando [0000-0003-0031-1880]
Source :
Catalysts, Volume 9, Issue 11, Catalysts, Vol 9, Iss 11, p 896 (2019), Zaguán: Repositorio Digital de la Universidad de Zaragoza, Universidad de Zaragoza, Digital.CSIC. Repositorio Institucional del CSIC, instname, Zaguán. Repositorio Digital de la Universidad de Zaragoza
Publication Year :
2019
Publisher :
Multidisciplinary Digital Publishing Institute, 2019.

Abstract

This article belongs to the Special Issue Advances in the Design and Characterization of Heterogeneous Biocatalysts.<br />Understanding the functionality of immobilized enzymes with spatiotemporal resolution and under operando conditions is an unmet need in applied biocatalysis, as well as priceless information to guide the optimization of heterogeneous biocatalysts for industrial purposes. Unfortunately, enzyme immobilization still relies on trial-and-error approximations that prevail over rational designs. Hence, a modern fabrication process to achieve efficient and robust heterogeneous biocatalysts demands comprehensive characterization techniques to track and understand the immobilization process at the protein–material interface. Recently, our group has developed a new generation of self-sufficient heterogeneous biocatalysts based on alcohol dehydrogenases co-immobilized with nicotinamide cofactors on agarose porous microbeads. Harnessing the autofluorescence of NAD+(P)H and using time-lapse fluorescence microscopy, enzyme activity toward the redox cofactors can be monitored inside the beads. To analyze these data, herein we present an image analytical tool to quantify the apparent Michaelis–Menten parameters of alcohol dehydrogenases co-immobilized with NAD(P)+/H at the single-particle level. Using this tool, we found a strong negative correlation between the apparent catalytic performance of the immobilized enzymes and the bead radius when using exogenous bulky substrates in reduction reactions. Therefore, applying image analytics routines to microscopy studies, we can directly unravel the functional heterogeneity of different heterogeneous biocatalyst samples tested under different reaction conditions.<br />A.I.B.-M. and F.L.-G. are grateful to MINECO (BIO2015-69887-R, BIO2014-61838-EXP and PCI2018-092984) and HOMBIOCAT ERA-CoBioTech project for funding their research. We also thank ARAID and IKERBASQUE foundations for funding F.L.-G. and P.R.-C., and S.V.-L. thanks the Mexican Council of Science and Technology (CONACyT) for the postdoctoral fellowship she received.

Details

Language :
English
Database :
OpenAIRE
Journal :
Catalysts, Volume 9, Issue 11, Catalysts, Vol 9, Iss 11, p 896 (2019), Zaguán: Repositorio Digital de la Universidad de Zaragoza, Universidad de Zaragoza, Digital.CSIC. Repositorio Institucional del CSIC, instname, Zaguán. Repositorio Digital de la Universidad de Zaragoza
Accession number :
edsair.doi.dedup.....2f4ccf8fe2d10e874f6da2cfb3ae2278