dc.contributor.author |
Samal, RR |
|
dc.contributor.author |
Subudhi, U |
|
dc.date.accessioned |
2025-07-22T08:55:18Z |
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dc.date.available |
2025-07-22T08:55:18Z |
|
dc.date.issued |
2024 |
|
dc.identifier.citation |
International Journal Of Biological Macromolecules, 283, 2024; 137820 |
|
dc.identifier.issn |
0141-8130 |
|
dc.identifier.uri |
http://ore.immt.res.in/handle/2018/3624 |
|
dc.description |
Department of Science and Technology, Government of India |
|
dc.description.abstract |
The present study highlights the hazardous effect of heavy and light rare earth elements (REEs) on bovine liver catalase (BLC) using a combination of spectroscopic and computational methods. The presence of Praseodymium chloride (PrCl3) and Gadolinium chloride (GdCl3) resulted in a substantial reduction in catalytic efficiency of BLC by approximately 1.8 and 2.6 fold, respectively. The compromised activity was further accompanied by conformational rearrangements at the secondary and tertiary levels as evidenced by circular dichroism (CD) and fluorescence spectroscopy. These analyses revealed a significant decrease in alpha-helical content and a simultaneous increase in random coils, disrupting intramolecular hydrogen bonding. Furthermore, the zeta potential (zeta) of BLC demonstrated a reversal from negative to positive zeta values upon the addition of PrCl3 and GdCl3, indicating BLClanthanide complex formation. Isothermal titration calorimetry (ITC) supports spontaneous interaction with negative free energy favouring endothermic reaction. This was further supported by docking studies which revealed the binding of PrCl3 and GdCl3 within the active site of BLC thus interfering with the catalytic ability to degrade hydrogen peroxide (H2O2). Nevertheless, a significant decline in the melting temperature (Tm) of BLC was observed in the presence of lanthanides suggesting the thermal instability of the enzyme. Thus, a similar approach could be applied to evaluate the hazardous effects of lanthanides on structural and functional changes in other proteins or similar biomolecules. |
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dc.language |
en |
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dc.publisher |
Elsevier |
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dc.relation.isreferencedby |
SCI |
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dc.rights |
Copyright [2024]. All efforts have been made to respect the copyright to the best of our knowledge. Inadvertent omissions, if brought to our notice, stand for correction and withdrawal of document from this repository. |
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dc.subject |
Biochemistry & Molecular Biology |
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dc.subject |
Chemical Sciences |
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dc.subject |
Polymer Science |
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dc.title |
Modulation of antioxidant enzyme by light and heavy rare earth metals: A case study with catalase |
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dc.type |
Journal Article |
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dc.affiliation.author |
CSIR-Institute of Minerals and Materials Technology, Bhubaneswar 751013, Odisha, India |
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