ATP fosters the tuning of nanostructured CeO2 peroxidase-like activity for promising antibacterial performance. (24th June 2020)
- Record Type:
- Journal Article
- Title:
- ATP fosters the tuning of nanostructured CeO2 peroxidase-like activity for promising antibacterial performance. (24th June 2020)
- Main Title:
- ATP fosters the tuning of nanostructured CeO2 peroxidase-like activity for promising antibacterial performance
- Authors:
- Chishti, Benazir
Fouad, H.
Seo, H. K.
Alothman, Othman Y.
Ansari, Z. A.
Ansari, S. G. - Abstract:
- Abstract : Recyclable nano CeO2 POD mimic records a K m reduction (∼30% and ∼19.72% for TMB and H2 O2, respectively) in 900 seconds at pH 4.5. ATP boosts catalytic feasibility in nano CeO2 at physiological pH. Abstract : An enduring and formidable challenge in nanozyme catalysis is low sensitivity and operational instability, which impedes their biological usage. In this contribution fluorite-structured cerium oxide nanocrystals (CeO2 NCs) with ∼23.04% Ce 3+ fraction were found to possess recyclable (10 cycles) peroxidase (POD)-like activity capable of catalyzing the oxidation of 3, 3′, 5, 5′-tetramethylbenzidine (TMB) when hydrogen peroxide (H2 O2 ) serves as oxidant, and exhibit high substrate affinity under acidic conditions. We tuned this catalytic activity at neutral pH (7.4) using adenosine triphosphate (ATP). It was found that ATP stabilizes the oxidation product and improves catalytic performance at neutral pH. Mechanistic investigation reveals that oxidation of TMB originates from catalyst (CeO2 NCs)-directed decomposition of H2 O2, which pools hydroxyl (˙OH) radicals under acidic and neutral environments; kinetic studies indicate a Michaelis–Menten enzyme kinetic model. Notably, above pH 4.5, ATP facilitates a drop in catalyst K m values of about 2.5 and 4.79 times for TMB and H2 O2, respectively, suggesting high affinity favouring reaction feasibility at neutral pH. Screening of other relevant modulators shows the following order in promoting catalysis at neutralAbstract : Recyclable nano CeO2 POD mimic records a K m reduction (∼30% and ∼19.72% for TMB and H2 O2, respectively) in 900 seconds at pH 4.5. ATP boosts catalytic feasibility in nano CeO2 at physiological pH. Abstract : An enduring and formidable challenge in nanozyme catalysis is low sensitivity and operational instability, which impedes their biological usage. In this contribution fluorite-structured cerium oxide nanocrystals (CeO2 NCs) with ∼23.04% Ce 3+ fraction were found to possess recyclable (10 cycles) peroxidase (POD)-like activity capable of catalyzing the oxidation of 3, 3′, 5, 5′-tetramethylbenzidine (TMB) when hydrogen peroxide (H2 O2 ) serves as oxidant, and exhibit high substrate affinity under acidic conditions. We tuned this catalytic activity at neutral pH (7.4) using adenosine triphosphate (ATP). It was found that ATP stabilizes the oxidation product and improves catalytic performance at neutral pH. Mechanistic investigation reveals that oxidation of TMB originates from catalyst (CeO2 NCs)-directed decomposition of H2 O2, which pools hydroxyl (˙OH) radicals under acidic and neutral environments; kinetic studies indicate a Michaelis–Menten enzyme kinetic model. Notably, above pH 4.5, ATP facilitates a drop in catalyst K m values of about 2.5 and 4.79 times for TMB and H2 O2, respectively, suggesting high affinity favouring reaction feasibility at neutral pH. Screening of other relevant modulators shows the following order in promoting catalysis at neutral pH: ATP > histidine ≥ ADP >AMP. This pH-tunable POD-mimic CeO2 nanozyme realizes a nanocatalytic strategy for sourcing ˙OH radicals, which contributes to anti-bacterial performance. This study provides new insight for designing nanozymes and expanding the use of nanozymes in biomedicine. … (more)
- Is Part Of:
- New journal of chemistry. Volume 44:Number 26(2020)
- Journal:
- New journal of chemistry
- Issue:
- Volume 44:Number 26(2020)
- Issue Display:
- Volume 44, Issue 26 (2020)
- Year:
- 2020
- Volume:
- 44
- Issue:
- 26
- Issue Sort Value:
- 2020-0044-0026-0000
- Page Start:
- 11291
- Page End:
- 11303
- Publication Date:
- 2020-06-24
- Subjects:
- Chemistry -- Periodicals
Chimie -- Périodiques
540 - Journal URLs:
- http://www.rsc.org/ ↗
http://www.rsc.org/is/journals/current/newjchem/njc.htm ↗ - DOI:
- 10.1039/c9nj05955e ↗
- Languages:
- English
- ISSNs:
- 1144-0546
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6084.319900
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 13834.xml