Literature DB >> 20182929

Regeneration of nicotinamide coenzymes: principles and applications for the synthesis of chiral compounds.

Andrea Weckbecker1, Harald Gröger, Werner Hummel.   

Abstract

Dehydrogenases which depend on nicotinamide coenzymes are of increasing interest for the preparation of chiral compounds, either by reduction of a prochiral precursor or by oxidative resolution of their racemate. The regeneration of oxidized and reduced nicotinamide cofactors is a very crucial step because the use of these cofactors in stoichiometric amounts is too expensive for application. There are several possibilities to regenerate nicotinamide cofactors: established methods such as formate/formate dehydrogenase (FDH) for the regeneration of NADH, recently developed electrochemical methods based on new mediator structures, or the application of gene cloning methods for the construction of "designed" cells by heterologous expression of appropriate genes.A very promising approach is enzymatic cofactor regeneration. Only a few enzymes are suitable for the regeneration of oxidized nicotinamide cofactors. Glutamate dehydrogenase can be used for the oxidation of NADH as well as NADPH while L: -lactate dehydrogenase is able to oxidize NADH only. The reduction of NAD(+) is carried out by formate and FDH. Glucose-6-phosphate dehydrogenase and glucose dehydrogenase are able to reduce both NAD(+) and NADP(+). Alcohol dehydrogenases (ADHs) are either NAD(+)- or NADP(+)-specific. ADH from horse liver, for example, reduces NAD(+) while ADHs from Lactobacillus strains catalyze the reduction of NADP(+). These enzymes can be applied by their inclusion in whole cell biotransformations with an NAD(P)(+)-dependent primary reaction to achieve in situ the regeneration of the consumed cofactor.Another efficient method for the regeneration of nicotinamide cofactors is the electrochemical approach. Cofactors can be regenerated directly, for example at a carbon anode, or indirectly involving mediators such as redox catalysts based on transition-metal complexes.An increasing number of examples in technical scale applications are known where nicotinamide dependent enzymes were used together with cofactor regenerating enzymes.

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Year:  2010        PMID: 20182929     DOI: 10.1007/10_2009_55

Source DB:  PubMed          Journal:  Adv Biochem Eng Biotechnol        ISSN: 0724-6145            Impact factor:   2.635


  28 in total

1.  Characterization of alcohol dehydrogenase (ADH12) from Haloarcula marismortui, an extreme halophile from the Dead Sea.

Authors:  Leanne M Timpson; Diya Alsafadi; Cillín Mac Donnchadha; Susan Liddell; Michael A Sharkey; Francesca Paradisi
Journal:  Extremophiles       Date:  2011-10-21       Impact factor: 2.395

2.  NADP+-Preferring D-Lactate Dehydrogenase from Sporolactobacillus inulinus.

Authors:  Lingfeng Zhu; Xiaoling Xu; Limin Wang; Hui Dong; Bo Yu; Yanhe Ma
Journal:  Appl Environ Microbiol       Date:  2015-07-06       Impact factor: 4.792

3.  Activation of Dioxygen by a TAML Activator in Reverse Micelles: Characterization of an Fe(III)Fe(IV) Dimer and Associated Catalytic Chemistry.

Authors:  Liang L Tang; William A Gunderson; Andrew C Weitz; Michael P Hendrich; Alexander D Ryabov; Terrence J Collins
Journal:  J Am Chem Soc       Date:  2015-07-23       Impact factor: 15.419

4.  Major Role of NAD-Dependent Lactate Dehydrogenases in the Production of l-Lactic Acid with High Optical Purity by the Thermophile Bacillus coagulans.

Authors:  Limin Wang; Yumeng Cai; Lingfeng Zhu; Honglian Guo; Bo Yu
Journal:  Appl Environ Microbiol       Date:  2014-09-12       Impact factor: 4.792

Review 5.  1,4-Dihydropyridine Derivatives: Dihydronicotinamide Analogues-Model Compounds Targeting Oxidative Stress.

Authors:  Astrida Velena; Neven Zarkovic; Koraljka Gall Troselj; Egils Bisenieks; Aivars Krauze; Janis Poikans; Gunars Duburs
Journal:  Oxid Med Cell Longev       Date:  2016-01-06       Impact factor: 6.543

6.  Development of a whole-cell biocatalyst with NADPH regeneration system for biosulfoxidation.

Authors:  Xiao-Hong Zhai; Yuan-Hui Ma; Dun-Yue Lai; Shuo Zhou; Zhen-Ming Chen
Journal:  J Ind Microbiol Biotechnol       Date:  2013-06-02       Impact factor: 3.346

7.  Oxidation of fatty aldehydes to fatty acids by Escherichia coli cells expressing the Vibrio harveyi fatty aldehyde dehydrogenase (FALDH).

Authors:  Markus Buchhaupt; Jan Guder; Fenja Sporleder; Melanie Paetzold; Jens Schrader
Journal:  World J Microbiol Biotechnol       Date:  2012-11-21       Impact factor: 3.312

Review 8.  New approaches to NAD(P)H regeneration in the biosynthesis systems.

Authors:  Lei Han; Bo Liang
Journal:  World J Microbiol Biotechnol       Date:  2018-09-10       Impact factor: 3.312

9.  Recombinant Enzymatic Redox Systems for Preparation of Aroma Compounds by Biotransformation.

Authors:  Viktor Varga; Vladimír Štefuca; Lenka Mihálová; Zdenko Levarski; Eva Struhárňanská; Jaroslav Blaško; Robert Kubinec; Pavel Farkaš; Vladimír Sitkey; Ján Turňa; Michal Rosenberg; Stanislav Stuchlík
Journal:  Front Microbiol       Date:  2021-06-24       Impact factor: 5.640

10.  A water-forming NADH oxidase from Lactobacillus pentosus suitable for the regeneration of synthetic biomimetic cofactors.

Authors:  Claudia Nowak; Barbara Beer; André Pick; Teresa Roth; Petra Lommes; Volker Sieber
Journal:  Front Microbiol       Date:  2015-09-16       Impact factor: 5.640

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