Aspartic acid based metal–organic frameworks with dual function of NADH peroxidase and glycerol dehydrogenase-mimicking activities. (6th October 2022)
- Record Type:
- Journal Article
- Title:
- Aspartic acid based metal–organic frameworks with dual function of NADH peroxidase and glycerol dehydrogenase-mimicking activities. (6th October 2022)
- Main Title:
- Aspartic acid based metal–organic frameworks with dual function of NADH peroxidase and glycerol dehydrogenase-mimicking activities
- Authors:
- Liu, Shuli
Wu, Xiaoling
Xiong, Jun
Yuan, Xin
Zong, Min-Hua
Lou, Wen-Yong - Abstract:
- Abstract : CuAsp with a fiber-like structure exhibited both NADH peroxidase- and glycerol dehydrogenase (GlyDH)-mimetic activities. Abstract : Enzymatic cofactor regeneration is of significant importance and highly desired for tremendous biocatalytic processes, which is hindered by fragility intrinsic to natural enzymes. Herein, we report a copper aspartic acid (CuAsp) metal–organic framework (MOF) with a fiber structure exhibiting both NADH peroxidase- and glycerol dehydrogenase (GlyDH)-mimicking activities. The growth mechanism of CuAsp was investigated by changing the functional groups of ligands, which demonstrated that the amino group and two carboxylate groups in aspartic acid were all involved in the formation of MOFs. The CuAsp MOF displayed high NADH peroxidase mimicking activity within a wide range of pH and temperature. A cofactor total turnover number (TTN) of up to 17 500 was obtained in a typical model reaction of glucose dehydrogenase-catalyzed oxidation of glucose. More interestingly, CuAsp exhibited glycerol dehydrogenase (GlyDH)-mimicking activity and showed higher catalytic efficiency (with k cat / K m of 14.42 mL g −1 min −1 ) than its native counterpart (with k cat / K m of 2.40 mL g −1 min −1 ). As a proof of concept, CuAsp with the dual function of NADH peroxidase and GlyDH-mimicking activities was used to catalyze the transformation of glycerol to 1, 3-dihydroxyacetone (DHA). Besides, free GlyDH was encapsulated into CuAsp via a facile self-assemblyAbstract : CuAsp with a fiber-like structure exhibited both NADH peroxidase- and glycerol dehydrogenase (GlyDH)-mimetic activities. Abstract : Enzymatic cofactor regeneration is of significant importance and highly desired for tremendous biocatalytic processes, which is hindered by fragility intrinsic to natural enzymes. Herein, we report a copper aspartic acid (CuAsp) metal–organic framework (MOF) with a fiber structure exhibiting both NADH peroxidase- and glycerol dehydrogenase (GlyDH)-mimicking activities. The growth mechanism of CuAsp was investigated by changing the functional groups of ligands, which demonstrated that the amino group and two carboxylate groups in aspartic acid were all involved in the formation of MOFs. The CuAsp MOF displayed high NADH peroxidase mimicking activity within a wide range of pH and temperature. A cofactor total turnover number (TTN) of up to 17 500 was obtained in a typical model reaction of glucose dehydrogenase-catalyzed oxidation of glucose. More interestingly, CuAsp exhibited glycerol dehydrogenase (GlyDH)-mimicking activity and showed higher catalytic efficiency (with k cat / K m of 14.42 mL g −1 min −1 ) than its native counterpart (with k cat / K m of 2.40 mL g −1 min −1 ). As a proof of concept, CuAsp with the dual function of NADH peroxidase and GlyDH-mimicking activities was used to catalyze the transformation of glycerol to 1, 3-dihydroxyacetone (DHA). Besides, free GlyDH was encapsulated into CuAsp via a facile self-assembly process, which enabled the synergistic biosynthesis of DHA. This study may provide new insights into amino acid-based MOFs and suggest the potential of multifunctional nanozymes in the application of biocatalysis and biosensing. … (more)
- Is Part Of:
- Materials chemistry frontiers. Volume 6:Number 22(2022)
- Journal:
- Materials chemistry frontiers
- Issue:
- Volume 6:Number 22(2022)
- Issue Display:
- Volume 6, Issue 22 (2022)
- Year:
- 2022
- Volume:
- 6
- Issue:
- 22
- Issue Sort Value:
- 2022-0006-0022-0000
- Page Start:
- 3391
- Page End:
- 3401
- Publication Date:
- 2022-10-06
- Subjects:
- Materials science -- Periodicals
Chemistry -- Periodicals
540 - Journal URLs:
- http://www.rsc.org/journals-books-databases/about-journals/materials-chemistry-frontiers/ ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/d2qm00770c ↗
- Languages:
- English
- ISSNs:
- 2052-1529
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5394.107200
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 24783.xml