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Título
A comprehensive study on levan nanoparticles formation: Kinetics and self-assembly modeling
Autor(es)
Palabras clave
Levan
Kinetic modeling
Self-assembly
Fecha de publicación
2020
Editor
Elsevier
Citación
Álvaro González-Garcinuño, Antonio Tabernero, Gema Marcelo, Eva Martín del Valle, A comprehensive study on levan nanoparticles formation: Kinetics and self-assembly modeling, International Journal of Biological Macromolecules, Volume 147, 2020, Pages 1089-1098, ISSN 0141-8130, https://doi.org/10.1016/j.ijbiomac.2019.10.076. (https://www.sciencedirect.com/science/article/pii/S0141813019359914)
Resumen
[EN]Levan nanoparticles formation is a complicated phenomenon involving simultaneously polymeric reaction kinetics
and nanoparticles self-assembly theory. These phenomena are studied in this work with experimental and
computationalmethodologies. Specifically, the effect of different parameters on levan kinetics and nanoparticles
production in a cell-free system environment have been studied. Results point out that 37 °C is the best temperature
for synthesizing levan as well as the existence of a substrate inhibition effect for polymeric reaction. This
work also highlights that raffinose can be used for producing and that an increase on the ratio enzymesubstrate
increases the velocity of conversion. However, the previous experimental conditions did not produce
an important effect on self-assembly formed levan nanoparticles (always 110 nm) as long as the required
levan concentration (CAC) for nanoparticles reorganization is achieved. To have a better understanding of
these results, a model was developed to explain numerically levan kinetics and nanoparticle self-assembly.
This model was built by taking into account enzyme poisoning effect (also demonstrated experimentally) and
a diffusion limited cluster model for the aggregation phenomenon. Simulation results fit properly experimental
data and catalytic parameters as well as predicting accurately the value of CAC for producing its reorganization
into nanoparticles by self-assembly.
URI
ISSN
0141-8130
DOI
10.1016/j.ijbiomac.2019.10.076
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