Supported Pt Enabled Proton-Driven NAD(P)+ Regeneration for Biocatalytic Oxidation.

The utilization of biocatalytic oxidations has evolved from the niche applications of the early 21st century to a widely recognized tool for general chemical synthesis. One of the major drawbacks that hinders commercialization is the dependence on expensive nicotinamide adenine dinucleotide (NAD(P)+) cofactors, and so, their regeneration is essential. Here, we report the design of carbon-supported Pt catalysts that can regenerate NAD(P)+ by proton-driven NAD(P)H oxidation with concurrent hydrogen formation. The carbon support was modified to tune the electronic nature of the Pt nanoparticles, and it was found that the best catalyst for NAD(P)+ regeneration (TOF = 581 h-1) was electron-rich Pt on carbon. Finally, the heterogeneous Pt catalyst was applied in the biocatalytic oxidation of a variety of alcohols catalyzed by different alcohol dehydrogenases. The Pt catalyst exhibited good compatibility with the biocatalytic system. Its NAD(P)+ regeneration function successfully supported biocatalytic conversion from alcohols to corresponding ketone or lactone products. This work provides a promising strategy for chemical synthesis via NAD(P)+-dependent pathways utilizing a cooperative inorganic-enzymatic catalytic system.

[1]  Joseph W. H. Burnett,et al.  NADH Regeneration: A Case Study of Pt-Catalyzed NAD+ Reduction with H2 , 2020, ACS Catalysis.

[2]  Haiyan Song,et al.  Platinum nanoparticle-deposited multi-walled carbon nanotubes as a NADH oxidase mimic: characterization and applications. , 2020, Nanoscale.

[3]  Wilm Jones,et al.  Improving Photocatalytic Energy Conversion via NAD(P)H , 2020, Joule.

[4]  Masatake Haruta,et al.  Oxidation of β-Nicotinamide Adenine Dinucleotide (NADH) by Au Cluster and Nanoparticle Catalysts Aiming for Coenzyme Regeneration in Enzymatic Glucose Oxidation , 2020 .

[5]  J. Andexer,et al.  Round, round we go - strategies for enzymatic cofactor regeneration. , 2020, Natural product reports.

[6]  S. Minteer,et al.  The progress and outlook of bioelectrocatalysis for the production of chemicals, fuels and materials , 2020, Nature Catalysis.

[7]  Joseph W. H. Burnett,et al.  A facile analytical method for reliable selectivity examination in cofactor NADH regeneration. , 2020, Chemical communications.

[8]  F. G. Mutti,et al.  Generation of amine dehydrogenases with increased catalytic performance and substrate scope from ε-deaminating L-Lysine dehydrogenase , 2019, Nature Communications.

[9]  R. Zare,et al.  Highly active enzyme–metal nanohybrids synthesized in protein–polymer conjugates , 2019, Nature Catalysis.

[10]  M. Richmond,et al.  Hydrogenase biomimics containing redox-active ligands: Fe2(CO)4(μ-edt)(κ2-bpcd) with electron-acceptor 4,5-bis(diphenylphosphino)-4-cyclopenten-1,3-dione (bpcd) as a potential [Fe4-S4]H surrogate. , 2019, Dalton transactions.

[11]  Christopher K Prier,et al.  Recent preparative applications of redox enzymes. , 2019, Current opinion in chemical biology.

[12]  P. Ekins,et al.  The role of hydrogen and fuel cells in the global energy system , 2019, Energy & Environmental Science.

[13]  J. Hartwig,et al.  Cooperative asymmetric reactions combining photocatalysis and enzymatic catalysis , 2018, Nature.

[14]  Ye-Wang Zhang,et al.  Immobilization of glycerol dehydrogenase and NADH oxidase for enzymatic synthesis of 1,3‐dihydroxyacetone with in situ cofactor regeneration , 2018 .

[15]  Shuke Wu,et al.  Recent advances in enzymatic oxidation of alcohols. , 2018, Current opinion in chemical biology.

[16]  Yejing Liu,et al.  Manipulating the d-Band Electronic Structure of Platinum-Functionalized Nanoporous Gold Bowls: Synergistic Intermetallic Interactions Enhance Catalysis , 2016 .

[17]  Qiuyong Zhao,et al.  Conversion of glycerol to 1,3-dihydroxyacetone by glycerol dehydrogenase co-expressed with an NADH oxidase for cofactor regeneration , 2016, Biotechnology Letters.

[18]  Nicholas J Turner,et al.  Artificial concurrent catalytic processes involving enzymes. , 2015, Chemical communications.

[19]  Youngmee Kim,et al.  Visible-Light-Driven Photoproduction of Hydrogen Using Rhodium Catalysts and Platinum Nanoparticles with Formate , 2014 .

[20]  Huimin Zhao,et al.  Cooperative tandem catalysis by an organometallic complex and a metalloenzyme. , 2014, Angewandte Chemie.

[21]  S. Ntais,et al.  Particle size effect on catalytic activity of carbon-supported Pt nanoparticles for complete ethylene oxidation , 2013 .

[22]  Zhongyi Jiang,et al.  Methods for the regeneration of nicotinamide coenzymes , 2013 .

[23]  Z Jane Wang,et al.  A supramolecular approach to combining enzymatic and transition metal catalysis , 2013, Nature Chemistry.

[24]  Frank Hollmann,et al.  Synthetic cascades are enabled by combining biocatalysts with artificial metalloenzymes , 2012, Nature Chemistry.

[25]  S. Barton,et al.  Quantitative analysis of bioactive NAD+ regenerated by NADH electro-oxidation , 2012 .

[26]  G. Huisman,et al.  Engineering the third wave of biocatalysis , 2012, Nature.

[27]  P. Sadler,et al.  Organometallic ruthenium and iridium transfer-hydrogenation catalysts using coenzyme NADH as a cofactor. , 2012, Angewandte Chemie.

[28]  S. Fukuzumi,et al.  Efficient catalytic interconversion between NADH and NAD+ accompanied by generation and consumption of hydrogen with a water-soluble iridium complex at ambient pressure and temperature. , 2012, Journal of the American Chemical Society.

[29]  O. Lenz,et al.  A modular system for regeneration of NAD cofactors using graphite particles modified with hydrogenase and diaphorase moieties. , 2012, Chemical communications.

[30]  I. Arends,et al.  On the nature of mutual inactivation between [Cp*Rh(bpy)(H2O)]2+ and enzymes – analysis and potential remedies , 2010 .

[31]  B. Feringa Dynamic Kinetic Resolution of Racemic β‐Haloalcohols: Direct Access to Enantioenriched Epoxides. , 2009 .

[32]  Ping Wang,et al.  Cofactor regeneration for sustainable enzymatic biosynthesis. , 2007, Biotechnology advances.

[33]  W. Yuan,et al.  Characterization of surface oxygen complexes on carbon nanofibers by TPD, XPS and FT-IR , 2007 .

[34]  G. Gökaǧaç,et al.  Different Sized Platinum Nanoparticles Supported on Carbon: An XPS Study on These Methanol Oxidation Catalysts , 2007 .

[35]  T. Moore,et al.  Enzyme‐assisted Reforming of Glucose to Hydrogen in a Photoelectrochemical Cell ¶ , 2005, Photochemistry and photobiology.

[36]  W. Hummel,et al.  NADH oxidase from Lactobacillus brevis: a new catalyst for the regeneration of NAD , 2003 .

[37]  S. Parker,et al.  Characterization of Activated Carbon Using X-ray Photoelectron Spectroscopy and Inelastic Neutron Scattering Spectroscopy , 2002 .

[38]  Chi-Huey Wong,et al.  Enzymes for chemical synthesis , 2001, Nature.

[39]  L. Kubota,et al.  Study of NADH stability using ultraviolet-visible spectrophotometric analysis and factorial design. , 1998, Analytical biochemistry.

[40]  Kurt Faber,et al.  Biotransformations in Organic Chemistry — A Textbook , 1996 .

[41]  G. Abraham,et al.  Spontaneous reactions of 1,3-substituted 1,4-dihydropyridines with acids in water at neutrality. I. Kinetic analysis and mechanism of the reactions of dihydronicotinamide--adenine dinucleotide with orthophosphates. , 1965, Biochemistry.

[42]  G. Berkelhammer,et al.  A Study of the Primary Acid Reaction on Model Compounds of Reduced Diphosphopyridine Nucleotide1,2 , 1958 .

[43]  Florian Rudroff,et al.  Opportunities and challenges for combining chemo- and biocatalysis , 2018, Nature Catalysis.

[44]  J. Reek,et al.  UvA-DARE (Digital Academic Repository) An iron-iron hydrogenase mimic with appended electron reservoir for efficient proton reduction in aqueous media , 2016 .

[45]  M. Bayer Catalysis Concepts And Green Applications , 2016 .

[46]  G. Shirane,et al.  Temperature (k) , 2008 .