TY - JOUR
T1 - Electrified Nanoconfined Biocatalysis with Rapid Cofactor Recycling
AU - Megarity, Clare F.
AU - Siritanaratkul, Bhavin
AU - Cheng, Beichen
AU - Morello, Giorgio
AU - Wan, Lei
AU - Sills, Adam J.
AU - Heath, Rachel S.
AU - Turner, Nicholas J.
AU - Armstrong, Fraser A.
N1 - Funding Information:
Fraser Armstrong, Bhavin Siritanaratkul and Clare Megarity gratefully acknowledge support from the Biotechnology and Biological Sciences Research Council (BB/P023797/1) and the EPA Cephalosporin Fund (CF 327). We thank colleagues, particularly Josceline Dunne and Sacha Tchen for help with experiments. Giorgio Morello thanks Wadham College, Oxford – Richards Graduate Scholarship.
Publisher Copyright:
© 2019 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim
PY - 2019/12/5
Y1 - 2019/12/5
N2 - In living cells, the overall rates of catalytic reaction chains (cascades) are massively enhanced by nanoconfinement of enzymes in tiny enclosed volumes: presented in such a way, interdependent catalysts are highly concentrated, and distances (active site-to-active site) across which intermediates and cofactors must diffuse, may be tiny. In a parallel technology exploiting this principle, enzyme cascades are powered, amplified, and monitored in real time as they work in concert, being nanoconfined within the pores of an electrically conductive metal oxide electrode. The technology, nicknamed the electrochemical leaf, mimics chloroplast biosynthesis by exploiting nicotinamide adenine dinucleotide (NADP(H)) recycling catalysed by the flavoenzyme, ferredoxin NADP+ reductase (FNR). Adsorbed on the inner walls of the nanopores, FNR rapidly transfers electrons between the electrode and NADP(H). This activity is coupled to an oxidoreductase enzyme, also nanoconfined within the pores, which recycles the cofactor and selectively synthesises a desired product or senses an analyte. Use of catalyst and cofactor is very efficient. The technology is simple, inexpensive and adaptable, and scalable to both microscopic levels (diagnostics) and macroscopic levels (organic synthesis). Whereas native FNR is specific for NADP(H), the technology can be extended by genetic engineering to include NAD(H) as recycling cofactor.
AB - In living cells, the overall rates of catalytic reaction chains (cascades) are massively enhanced by nanoconfinement of enzymes in tiny enclosed volumes: presented in such a way, interdependent catalysts are highly concentrated, and distances (active site-to-active site) across which intermediates and cofactors must diffuse, may be tiny. In a parallel technology exploiting this principle, enzyme cascades are powered, amplified, and monitored in real time as they work in concert, being nanoconfined within the pores of an electrically conductive metal oxide electrode. The technology, nicknamed the electrochemical leaf, mimics chloroplast biosynthesis by exploiting nicotinamide adenine dinucleotide (NADP(H)) recycling catalysed by the flavoenzyme, ferredoxin NADP+ reductase (FNR). Adsorbed on the inner walls of the nanopores, FNR rapidly transfers electrons between the electrode and NADP(H). This activity is coupled to an oxidoreductase enzyme, also nanoconfined within the pores, which recycles the cofactor and selectively synthesises a desired product or senses an analyte. Use of catalyst and cofactor is very efficient. The technology is simple, inexpensive and adaptable, and scalable to both microscopic levels (diagnostics) and macroscopic levels (organic synthesis). Whereas native FNR is specific for NADP(H), the technology can be extended by genetic engineering to include NAD(H) as recycling cofactor.
KW - biocatalysis
KW - cascade
KW - cofactor regeneration
KW - electrosynthesis
KW - ferredoxin-NADP reductase
UR - https://www.scopus.com/pages/publications/85074798168
U2 - 10.1002/cctc.201901245
DO - 10.1002/cctc.201901245
M3 - Article
AN - SCOPUS:85074798168
SN - 1867-3880
VL - 11
SP - 5662
EP - 5670
JO - ChemCatChem
JF - ChemCatChem
IS - 23
ER -