the enzyme is used as anticancer agent, which is verified by using three concentration of enzyme (0.010, 0.015, 0.020 mM/ml) which show a significant kill for Mcf-7 cells at (0.015 mg/ml), with cytotoxicity activity reaching (45%)
application of molecular absorption properties of horseradish peroxidase for self-indicating enzymatic interactions and analytical methods. This method can be applied for glucose determination where there is a low concentration (or an absence) of proteins
use of nanoporous TiO2 electrodes as a substrate for enzyme immobilization in order to enhance the electron transport across the semiconductor electrode-electrolyte interface. The immobilized HRP enzyme is stable and the overall electron transfer process is predominantly controlled by a diffusion process. The application for H2O2 biosensors is demonstrated by monitoring its reduction process using cyclic voltammetry
biodegradation of toxic and carcinogenic phenolic contaminants and related compounds in industrial effluents. Calotropis procera is a drought-resistant local plant that grows wild in the natural habitat of Nigerian throughout the year. Calotropis procera root could be an environmentally sustainable source of peroxidase for a low technological solution for phenol remediation
study of kinetic characterization, thermal stability and synergistic effect of temperature and pH for peroxidase (POD) and pectin methylesterase (PME) in tomato puree. Inactivation of both enzymes is very important, since these enzymes can have very negative effects on the color, odor, flavor and texture of juices and vegetable beverages during storage. The browning and loss of stability in juices and vegetable beverages, such as tomato puree, can be controlled by applying temperature and pH combinations capable of inactivating these enzymes in a total or partial way, but while respecting the limits organoleptic and legal for juices and vegetable beverages
the immobilized enzyme (entrapped onto a carboxymethyl cellulose/Fe3O4 magnetic hybrid material) maintains its activity upon storage at 4 and 25°C for 8 weeks, and upon recycling for up to 15 uses. It appears to be candidate for industrial applications
the enzyme shows high antibacterial activity in 100 mM thiocyanate, 100 mM H2O2 medium for some pathogenic bacteria, such as Aeromonas hydrophila ATCC 79666, Micrococcus luteus LA 2971, Mycobacterium smegmatis RUT, Bacillus subtilis IMG22, Pseudomonas pyocyanea, Bacillus subtilis var. niger ATCC 10, Pseudomonas aeruginosa ATCC 27853, Enterococcus faecalis ATCC 15753, Bacillus brevis FMC3, Klebsiella pneumoniae FMC5, Corynebacterium xerosis UC9165, Bacillus cereus EÜ, Bacillus megaterium NRS, Yersinia enterocolitica, Listeria monocytogenes scoot A, Bacillus megaterium EÜ, Bacillus megaterium DSM32, Klebsiella oxytoca, Staphylococcus aerogenes, Streptococcus faecalis, Mycobacterium smegmatis CCM 2067. The lactoperoxidase(100 mM)/thiocyanate(100 mM)/H2O2 system is purposed as an effective agent against many of the diseases causing organisms in human and animals
QPO is a potential drug target to inhibit the expression of leukotoxin LtxA from Aggregatibacter actinomycetemcomitans for the treatment and prevention of localized aggressive periodontitis
QPO is a potential drug target to inhibit the expression of leukotoxin LtxA from Aggregatibacter actinomycetemcomitans for the treatment and prevention of localized aggressive periodontitis
heterologous production in Pichia pastoris is greatlyenhanced by the addition of hemin with a titer of 0.41 U/ml peroxidase activity at the second day ofincubation
preparation of starch-g-poly(butyl acrylate) copolymers using horseradish peroxidase, in the presence of hydrogen peroxide and acetylacetone. Poly(butyl acrylate) is successfully grafted onto starch by HRP-mediated graft copolymerization, improving the thermal stability of starch
protein engineering to obtain an active and stable HRP variant with reduced surface glycosylation during production in Pichia pastoris. Mutant N13D/N57S/N255D/N268D produced in the Pichia pastoris benchmark strain shows considerable catalytic activity and thermal stability and is less glycosylated
self-crosslinking of fibroin molecules and p-hydroxyphenylacetamide, as a model compound of tyrosine residues in fibroins, using the hydrogen peroxide-horseradish peroxidase system. Incubation leads to p-hydroxyphenylacetamide polymerization, and the molecular weight of fibroin proteins is also noticeably increased by treatment. The mechanical properties and thermal behavior for the modified fibroin membrane are improved. The obtained membrane exhibits good biocompatibility
1.11.1.7 peroxidase
results (
results (
top
