Exploitation of Hetero- and Phototrophic Metabolic Modules for Redox-Intensive Whole-Cell Biocatalysis

The successful realization of a sustainable manufacturing bioprocess and the maximization of its production potential and capacity are the main concerns of a bioprocess engineer. A main step towards this endeavor is the development of an efficient biocatalyst. Isolated enzyme(s), microbial cells, or...

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Main Authors: Eleni Theodosiou, Adrian Tüllinghoff, Jörg Toepel, Bruno Bühler
Format: Article
Language:English
Published: Frontiers Media S.A. 2022-04-01
Series:Frontiers in Bioengineering and Biotechnology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fbioe.2022.855715/full
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author Eleni Theodosiou
Adrian Tüllinghoff
Jörg Toepel
Bruno Bühler
author_facet Eleni Theodosiou
Adrian Tüllinghoff
Jörg Toepel
Bruno Bühler
author_sort Eleni Theodosiou
collection DOAJ
description The successful realization of a sustainable manufacturing bioprocess and the maximization of its production potential and capacity are the main concerns of a bioprocess engineer. A main step towards this endeavor is the development of an efficient biocatalyst. Isolated enzyme(s), microbial cells, or (immobilized) formulations thereof can serve as biocatalysts. Living cells feature, beside active enzymes, metabolic modules that can be exploited to support energy-dependent and multi-step enzyme-catalyzed reactions. Metabolism can sustainably supply necessary cofactors or cosubstrates at the expense of readily available and cheap resources, rendering external addition of costly cosubstrates unnecessary. However, for the development of an efficient whole-cell biocatalyst, in depth comprehension of metabolic modules and their interconnection with cell growth, maintenance, and product formation is indispensable. In order to maximize the flux through biosynthetic reactions and pathways to an industrially relevant product and respective key performance indices (i.e., titer, yield, and productivity), existing metabolic modules can be redesigned and/or novel artificial ones established. This review focuses on whole-cell bioconversions that are coupled to heterotrophic or phototrophic metabolism and discusses metabolic engineering efforts aiming at 1) increasing regeneration and supply of redox equivalents, such as NAD(P/H), 2) blocking competing fluxes, and 3) increasing the availability of metabolites serving as (co)substrates of desired biosynthetic routes.
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spelling doaj.art-57e80b3da55b471fbbfab2f62031e3112022-12-22T02:06:53ZengFrontiers Media S.A.Frontiers in Bioengineering and Biotechnology2296-41852022-04-011010.3389/fbioe.2022.855715855715Exploitation of Hetero- and Phototrophic Metabolic Modules for Redox-Intensive Whole-Cell BiocatalysisEleni Theodosiou0Adrian Tüllinghoff1Jörg Toepel2Bruno Bühler3Institute of Applied Biosciences, Centre for Research and Technology Hellas, Thessaloniki, GreeceDepartment of Solar Materials, Helmholtz Centre for Environmental Research GmbH—UFZ, Leipzig, GermanyDepartment of Solar Materials, Helmholtz Centre for Environmental Research GmbH—UFZ, Leipzig, GermanyDepartment of Solar Materials, Helmholtz Centre for Environmental Research GmbH—UFZ, Leipzig, GermanyThe successful realization of a sustainable manufacturing bioprocess and the maximization of its production potential and capacity are the main concerns of a bioprocess engineer. A main step towards this endeavor is the development of an efficient biocatalyst. Isolated enzyme(s), microbial cells, or (immobilized) formulations thereof can serve as biocatalysts. Living cells feature, beside active enzymes, metabolic modules that can be exploited to support energy-dependent and multi-step enzyme-catalyzed reactions. Metabolism can sustainably supply necessary cofactors or cosubstrates at the expense of readily available and cheap resources, rendering external addition of costly cosubstrates unnecessary. However, for the development of an efficient whole-cell biocatalyst, in depth comprehension of metabolic modules and their interconnection with cell growth, maintenance, and product formation is indispensable. In order to maximize the flux through biosynthetic reactions and pathways to an industrially relevant product and respective key performance indices (i.e., titer, yield, and productivity), existing metabolic modules can be redesigned and/or novel artificial ones established. This review focuses on whole-cell bioconversions that are coupled to heterotrophic or phototrophic metabolism and discusses metabolic engineering efforts aiming at 1) increasing regeneration and supply of redox equivalents, such as NAD(P/H), 2) blocking competing fluxes, and 3) increasing the availability of metabolites serving as (co)substrates of desired biosynthetic routes.https://www.frontiersin.org/articles/10.3389/fbioe.2022.855715/fullwhole-cell redox biocatalysiscentral metabolismTCA cyclemetabolic engineeringcyanobacteriaredox balance
spellingShingle Eleni Theodosiou
Adrian Tüllinghoff
Jörg Toepel
Bruno Bühler
Exploitation of Hetero- and Phototrophic Metabolic Modules for Redox-Intensive Whole-Cell Biocatalysis
Frontiers in Bioengineering and Biotechnology
whole-cell redox biocatalysis
central metabolism
TCA cycle
metabolic engineering
cyanobacteria
redox balance
title Exploitation of Hetero- and Phototrophic Metabolic Modules for Redox-Intensive Whole-Cell Biocatalysis
title_full Exploitation of Hetero- and Phototrophic Metabolic Modules for Redox-Intensive Whole-Cell Biocatalysis
title_fullStr Exploitation of Hetero- and Phototrophic Metabolic Modules for Redox-Intensive Whole-Cell Biocatalysis
title_full_unstemmed Exploitation of Hetero- and Phototrophic Metabolic Modules for Redox-Intensive Whole-Cell Biocatalysis
title_short Exploitation of Hetero- and Phototrophic Metabolic Modules for Redox-Intensive Whole-Cell Biocatalysis
title_sort exploitation of hetero and phototrophic metabolic modules for redox intensive whole cell biocatalysis
topic whole-cell redox biocatalysis
central metabolism
TCA cycle
metabolic engineering
cyanobacteria
redox balance
url https://www.frontiersin.org/articles/10.3389/fbioe.2022.855715/full
work_keys_str_mv AT elenitheodosiou exploitationofheteroandphototrophicmetabolicmodulesforredoxintensivewholecellbiocatalysis
AT adriantullinghoff exploitationofheteroandphototrophicmetabolicmodulesforredoxintensivewholecellbiocatalysis
AT jorgtoepel exploitationofheteroandphototrophicmetabolicmodulesforredoxintensivewholecellbiocatalysis
AT brunobuhler exploitationofheteroandphototrophicmetabolicmodulesforredoxintensivewholecellbiocatalysis