Souza_2024_Molecules_29_

Reference

Title : Experimental and Computational Analysis of Synthesis Conditions of Hybrid Nanoflowers for Lipase Immobilization - Souza_2024_Molecules_29_
Author(s) : Souza DES , Santos LMF , Freitas JPA , Almeida LC , Santos JCB , Souza RL , Pereira MM , Lima A S , Soares CMF
Ref : Molecules , 29 : , 2024
Abstract :

This work presents a framework for evaluating hybrid nanoflowers using Burkholderia cepacia lipase. It was expanded on previous findings by testing lipase hybrid nanoflowers (hNF-lipase) formation over a wide range of pH values (5-9) and buffer concentrations (10-100 mM). The free enzyme activity was compared with that of hNF-lipase. The analysis, performed by molecular docking, described the effect of lipase interaction with copper ions. The morphological characterization of hNF-lipase was performed using scanning electron microscopy. Fourier Transform Infrared Spectroscopy performed the physical-chemical characterization. The results show that all hNF-lipase activity presented values higher than that of the free enzyme. Activity is higher at pH 7.4 and has the highest buffer concentration of 100 mM. Molecular docking analysis has been used to understand the effect of enzyme protonation on hNF-lipase formation and identify the main the main binding sites of the enzyme with copper ions. The hNF-lipase nanostructures show the shape of flowers in their micrographs from pH 6 to 8. The spectra of the nanoflowers present peaks typical of the amide regions I and II, current in lipase, and areas with P-O vibrations, confirming the presence of the phosphate group. Therefore, hNF-lipase is an efficient biocatalyst with increased catalytic activity, good nanostructure formation, and improved stability.

PubMedSearch : Souza_2024_Molecules_29_
PubMedID: 38338371

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Citations formats

Souza DES, Santos LMF, Freitas JPA, Almeida LC, Santos JCB, Souza RL, Pereira MM, Lima A S, Soares CMF (2024)
Experimental and Computational Analysis of Synthesis Conditions of Hybrid Nanoflowers for Lipase Immobilization
Molecules 29 :

Souza DES, Santos LMF, Freitas JPA, Almeida LC, Santos JCB, Souza RL, Pereira MM, Lima A S, Soares CMF (2024)
Molecules 29 :