نتایج جستجو برای: urease covalent binding

تعداد نتایج: 435933  

Journal: :Journal of leukocyte biology 2006
Justin T Schwartz Lee-Ann H Allen

Previous studies have demonstrated that Helicobacter pylori (Hp) delays its entry into macrophages and persists inside megasomes, which are poorly acidified and accumulate early endosome autoantigen 1. Herein, we explored the role of Hp urease in bacterial survival in murine peritoneal macrophages and J774 cells. Plasmid-free mutagenesis was used to replace ureA and ureB with chloramphenicol ac...

Abdol-Khalegh Bordbar

In the present study, the binding isotherms for interaction of a homologous series of n-alkyltrimethyl ammonium bromides with bovine serum albumin (BSA) have been analyzed on basis of intrinsic thermodynamic quantities. In this regards, the intrinsic Gibbs free energy of binding, AGb(i,)„ has been estimated at various surfactant concentrations and its trend of variation for both binding sets ha...

2014
Ramesh Kumar

Studies of our experiment are related to the binding of enzymes to antibodies. This involves the formation of a stable, covalent linkage between an enzyme & antibody. We used different Enzymes for this studies which are altered in binding action. Enzymes we used-e.g. Horseradish peroxidase (HRPO), urease, or alkaline phosphatase. Studies of Enzyme and an antigen-specific monoclonal or polyclona...

Journal: :Molecules 2017
Sherif T S Hassan Emil Švajdlenka

Studies on enzyme inhibition remain a crucial area in drug discovery since these studies have led to the discoveries of new lead compounds useful in the treatment of several diseases. In this study, protocatechuic acid (PCA), an active compound from Hibiscus sabdariffa L. has been evaluated for its inhibitory properties against jack bean urease (JBU) as well as its possible toxic effect on huma...

Journal: :British journal of pharmacology 1979
A R Boobis M J Brodie C J Bulpitt D S Davies

using lung and liver microsomes in the presence of paraquat, to generate superoxide and covalently bind a metabolite of DOPA. Male Wistar rats (150-250 g) were killed by decapitation and their lungs were perfused with ice cold normal saline. The lungs and livers were removed, homogenised and the microsomal fraction was isolated by differential centrifugation. The covalent binding of DOPA to was...

2012
Iwona Konieczna Paulina Żarnowiec Marek Kwinkowski Beata Kolesińska Justyna Frączyk Zbigniew Kamiński Wiesław Kaca

Urease is a virulence factor found in various pathogenic bacteria. It is essential in colonization of a host organism and in maintenance of bacterial cells in tissues. Due to its enzymatic activity, urease has a toxic effect on human cells. The presence of ureolytic activity is an important marker of a number of bacterial infections. Urease is also an immunogenic protein and is recognized by an...

Journal: :Infection and immunity 1996
M Clyne B Drumm

Helicobacter pylori urease is essential for colonization of the gastric mucosa irrespective of whether the stomach is acidic or hypochlorhydric. It has therefore been speculated that the enzyme functions as an adhesin. The aim of this study was to compare the adherence of H. pylori N6 with the adherence of an isogenic urease-negative mutant, strain N6(ureB::TnKm), to gastric cells. Strain N6 or...

Journal: :journal of physical & theoretical chemistry 2005
m. vahdi k. zare a. boos z. asfari

the adsorption of pyrazolone(hpmsp), calix[4]-arene,cu and cs, on carbon nanotube(cnt) atroom temperature has been investigated using spectroscopy.uv spectroscopy indicated that pyrazolone molecules adsorbed on carbon nanotube at roomtemperature in compared calix[4]- arene molecules adsorbed approximately same.the amount ofpyrazolone(hpmsp) adsorb 3.8. le mol/g and amount calix[4]-arene adsorbe...

Journal: :The Biochemical journal 1993
S Edmonds A Gibb E Sim

Thiol compounds have been investigated as inhibitors of the covalent binding reaction of human complement protein C4 using Sepharose-C1s as a combined activating and binding surface. o- and p-substituted aminothiophenols are equally effective inhibitors, whereas the m-substituted compound is a less potent inhibitor. The anti-hypertensive drug captopril is also shown to inhibit the covalent bind...

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