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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Algal polysaccharides as matrices for the immobilization of urease in lipid ultrathin films studied with tensiometry and vibrational spectroscopy: Physical-chemical properties and implications in the enzyme activity

Full text
Author(s):
de Brito, Audrey Kalinouski [1] ; Nordi, Cristina S. F. [1] ; Caseli, Luciano [1]
Total Authors: 3
Affiliation:
[1] Univ Fed Sao Paulo, UNIFESP, Inst Ciencias Ambientais Quim & Farmaceut, Diadema, SP - Brazil
Total Affiliations: 1
Document type: Journal article
Source: COLLOIDS AND SURFACES B-BIOINTERFACES; v. 135, p. 639-645, NOV 1 2015.
Web of Science Citations: 10
Abstract

Currently, many biological substances extracted from algae have received special attention because of their intrinsic characteristics, which can be applied to different areas of biotechnology. Therefore, in the current study, exopolysaccharides (EPS) from the microalgae Cryptomonas tetrapirenoidosa were employed as an aqueous subphase of a monolayer formed by the lipid dioctadecyldimethylammonium bromide (DODAB). The primary objective of this approach was to evaluate whether EPS could serve as a matrix for the immobilization of the enzyme urease to produce biosensors for urea. After DODAB was spread on the EPS solutions, urease was injected into the aqueous subphase, and the surface was submitted to compression using lateral barriers. The monolayers were subsequently characterized by surface pressure-area isotherms and polarization modulation infrared reflection-absorption spectroscopy (PM-IRRAS). The results indicated that EPS enhanced the adsorption of the enzyme on the lipid monolayer. The mixed films were later transferred to solid supports using the Langmuir-Blodgett (LB) technique and were characterized by transfer ratio, PM-IRRAS, quartz crystal microbalance, and atomic force microscopy. The immobilization of the enzyme on solid supports was fundamental for providing an ideal geometrical accommodation of urease because the interaction of EPS with urease in solution causes a decrease of the relative activity of urease. Therefore, these LB films are promising for the fabrication of future urea biosensors, the architecture of which can be manipulated and enhanced at the molecular level. (C) 2015 Elsevier B.V. All rights reserved. (AU)

FAPESP's process: 11/14289-7 - Adsorption of pollutants metals and enzymes in hybrid Langmuir-Blodgett films immobilized with algal polysaccharides / phospholipids
Grantee:Audrey Kalinouski de Brito
Support Opportunities: Scholarships in Brazil - Master
FAPESP's process: 13/10213-1 - Interaction of bioactive materials in ultrathin films organized in models for biointerfaces models for investigation of molecular recognition processes and associated molecular mechanisms
Grantee:Luciano Caseli
Support Opportunities: Regular Research Grants