Process Development for Benzyl Alcohol Production by Whole-Cell Biocatalysis in Stirred and Packed Bed Reactors

The ocean is an excellent source for new biocatalysts due to the tremendous genetic diversity of marine microorganisms, and it may contribute to the development of sustainable industrial processes. A marine bacterium was isolated and selected for the conversion of benzaldehyde to benzyl alcohol, whi...

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Main Authors: Carlos J. C. Rodrigues, Carla C. C. R. de Carvalho
Format: Article
Language:English
Published: MDPI AG 2022-05-01
Series:Microorganisms
Subjects:
Online Access:https://www.mdpi.com/2076-2607/10/5/966
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author Carlos J. C. Rodrigues
Carla C. C. R. de Carvalho
author_facet Carlos J. C. Rodrigues
Carla C. C. R. de Carvalho
author_sort Carlos J. C. Rodrigues
collection DOAJ
description The ocean is an excellent source for new biocatalysts due to the tremendous genetic diversity of marine microorganisms, and it may contribute to the development of sustainable industrial processes. A marine bacterium was isolated and selected for the conversion of benzaldehyde to benzyl alcohol, which is an important chemical employed as a precursor for producing esters for cosmetics and other industries. Enzymatic production routes are of interest for sustainable processes. To overcome benzaldehyde low water solubility, DMSO was used as a biocompatible cosolvent up to a concentration of 10% (<i>v</i>/<i>v</i>). A two-phase system with <i>n</i>-hexane, <i>n</i>-heptane, or <i>n</i>-hexadecane as organic phase allowed at least a 44% higher relative conversion of benzaldehyde than the aqueous system, and allowed higher initial substrate concentrations. Cell performance decreased with increasing product concentration but immobilization of cells in alginate improved four-fold the robustness of the biocatalyst: free and immobilized cells were inhibited at concentrations of benzyl alcohol of 5 and 20 mM, respectively. Scaling up to a 100 mL stirred reactor, using a fed-batch approach, enabled a 1.5-fold increase in benzyl alcohol productivity when compared with batch mode. However, product accumulation in the reactor hindered the conversion. The use of a continuous flow reactor packed with immobilized cells enabled a 9.5-fold increase in productivity when compared with the fed-batch stirred reactor system.
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spelling doaj.art-f4d4f31113374fbfb7f4a5a168923b472023-11-23T12:15:45ZengMDPI AGMicroorganisms2076-26072022-05-0110596610.3390/microorganisms10050966Process Development for Benzyl Alcohol Production by Whole-Cell Biocatalysis in Stirred and Packed Bed ReactorsCarlos J. C. Rodrigues0Carla C. C. R. de Carvalho1Department of Bioengineering, iBB—Institute for Bioengineering and Biosciences, Instituto Superior Técnico, Universidade de Lisboa, Av. Rovisco Pais, 1049-001 Lisbon, PortugalDepartment of Bioengineering, iBB—Institute for Bioengineering and Biosciences, Instituto Superior Técnico, Universidade de Lisboa, Av. Rovisco Pais, 1049-001 Lisbon, PortugalThe ocean is an excellent source for new biocatalysts due to the tremendous genetic diversity of marine microorganisms, and it may contribute to the development of sustainable industrial processes. A marine bacterium was isolated and selected for the conversion of benzaldehyde to benzyl alcohol, which is an important chemical employed as a precursor for producing esters for cosmetics and other industries. Enzymatic production routes are of interest for sustainable processes. To overcome benzaldehyde low water solubility, DMSO was used as a biocompatible cosolvent up to a concentration of 10% (<i>v</i>/<i>v</i>). A two-phase system with <i>n</i>-hexane, <i>n</i>-heptane, or <i>n</i>-hexadecane as organic phase allowed at least a 44% higher relative conversion of benzaldehyde than the aqueous system, and allowed higher initial substrate concentrations. Cell performance decreased with increasing product concentration but immobilization of cells in alginate improved four-fold the robustness of the biocatalyst: free and immobilized cells were inhibited at concentrations of benzyl alcohol of 5 and 20 mM, respectively. Scaling up to a 100 mL stirred reactor, using a fed-batch approach, enabled a 1.5-fold increase in benzyl alcohol productivity when compared with batch mode. However, product accumulation in the reactor hindered the conversion. The use of a continuous flow reactor packed with immobilized cells enabled a 9.5-fold increase in productivity when compared with the fed-batch stirred reactor system.https://www.mdpi.com/2076-2607/10/5/966biocatalysistwo-phase biocatalysisstirred tank reactorpacked bed reactorwhole cellsimmobilization
spellingShingle Carlos J. C. Rodrigues
Carla C. C. R. de Carvalho
Process Development for Benzyl Alcohol Production by Whole-Cell Biocatalysis in Stirred and Packed Bed Reactors
Microorganisms
biocatalysis
two-phase biocatalysis
stirred tank reactor
packed bed reactor
whole cells
immobilization
title Process Development for Benzyl Alcohol Production by Whole-Cell Biocatalysis in Stirred and Packed Bed Reactors
title_full Process Development for Benzyl Alcohol Production by Whole-Cell Biocatalysis in Stirred and Packed Bed Reactors
title_fullStr Process Development for Benzyl Alcohol Production by Whole-Cell Biocatalysis in Stirred and Packed Bed Reactors
title_full_unstemmed Process Development for Benzyl Alcohol Production by Whole-Cell Biocatalysis in Stirred and Packed Bed Reactors
title_short Process Development for Benzyl Alcohol Production by Whole-Cell Biocatalysis in Stirred and Packed Bed Reactors
title_sort process development for benzyl alcohol production by whole cell biocatalysis in stirred and packed bed reactors
topic biocatalysis
two-phase biocatalysis
stirred tank reactor
packed bed reactor
whole cells
immobilization
url https://www.mdpi.com/2076-2607/10/5/966
work_keys_str_mv AT carlosjcrodrigues processdevelopmentforbenzylalcoholproductionbywholecellbiocatalysisinstirredandpackedbedreactors
AT carlaccrdecarvalho processdevelopmentforbenzylalcoholproductionbywholecellbiocatalysisinstirredandpackedbedreactors