GOx@ZIF-8(NiPd) Nanoflower: An Artificial Enzyme System for Tandem Catalysis

2017 ◽  
Vol 129 (50) ◽  
pp. 16298-16301 ◽  
Author(s):  
Qingqing Wang ◽  
Xueping Zhang ◽  
Liang Huang ◽  
Zhiquan Zhang ◽  
Shaojun Dong
Keyword(s):  
Enzyme System ◽  
Tandem Catalysis ◽  
Artificial Enzyme

GOx@ZIF-8(NiPd) Nanoflower: An Artificial Enzyme System for Tandem Catalysis

2017 ◽  
Vol 56 (50) ◽  
pp. 16082-16085 ◽  
Author(s):  
Qingqing Wang ◽  
Xueping Zhang ◽  
Liang Huang ◽  
Zhiquan Zhang ◽  
Shaojun Dong
Keyword(s):  
Enzyme System ◽  
Tandem Catalysis ◽  
Artificial Enzyme

scholarly journals Single Nanoparticle to 3D Supercage: Framing for an Artificial Enzyme System

2015 ◽  
Vol 137 (43) ◽  
pp. 13957-13963 ◽  
Author(s):  
Ren Cai ◽  
Dan Yang ◽  
Shengjie Peng ◽  
Xigao Chen ◽  
Yun Huang ◽  
...  
Keyword(s):  
Enzyme System ◽  
Artificial Enzyme ◽  
Single Nanoparticle

Petal-shaped MOF assembled with gold nanocage and urate oxidase used as artificial enzyme nanohybrid for tandem catalysis and dual-channel biosensing

Nanoscale ◽  
2021 ◽  
Author(s):  
Zejun Sun ◽  
Yujiao Sun ◽  
Meng Yang ◽  
Hui Jin ◽  
Rijun Gui
Keyword(s):  
Metal Organic Frameworks ◽  
Urate Oxidase ◽  
Tandem Catalysis ◽  
Artificial Enzyme ◽  
One Pot ◽  
Mild Conditions ◽  
Dual Channel ◽  
Metal Organic

A facile one-pot precipitation was employed to prepare a petal-shaped hybrid in mild conditions. The hybrid is composed of urate oxidase (UOx) encapsulated into zeolite-like metal-organic frameworks (MOF) with doping...

Synergistic effect of ternary electrospun TiO2/Fe2O3/PPy composite nanofibers on peroxidase-like mimics with enhanced catalytic performance

RSC Advances ◽  
2016 ◽  
Vol 6 (37) ◽  
pp. 31107-31113 ◽  
Author(s):  
Yanzhou Jiang ◽  
Guangdi Nie ◽  
Maoqiang Chi ◽  
Zezhou Yang ◽  
Zhen Zhang ◽  
...  
Keyword(s):  
Synergistic Effect ◽  
Shell Structure ◽  
Composite Nanofibers ◽  
Enzyme System ◽  
Catalytic Performance ◽  
Core Shell ◽  
Artificial Enzyme ◽  
Core Shell Structure

In this work, we demonstrate the fabrication of polypyrrole (PPy) decorated TiO2/Fe2O3 (TiO2/Fe2O3/PPy) composite nanofibers with a core–shell structure as an artificial enzyme system with a high peroxidase-like activity.

Electron Microscopic and Isozyme Study of a Case of Ochronosis

1972 ◽  
Vol 30 ◽  
pp. 88-89
Author(s):  
Jay W. Cha ◽  
Perry J. Melnick
Keyword(s):  
Benzene Ring ◽  
Enzyme System ◽  
Homogentisic Acid ◽  
Degenerative Changes ◽  
Acid Oxidase ◽  
Electron Microscopic ◽  
Tyrosine Metabolism ◽  
Collagenous Tissues

Hereditary ochronosis in very few cases has been examined electron microscopically or histochemically. In this disease homogentisic acid, a normal intermediary of tyrosine metabolism, forms in excessive amounts. This is believed to be due to absence or defective activity of homogentisic acid oxidase, an enzyme system necessary to break the benzene ring and to further break it down to fumaric and acetoacetic acids. Ochronotic pigment, a polymerized form of homogentisic acid, deposits mainly in mesenchymal tissues. There has been a question whether the pigment originates from the collagenous tissues, or deposits passively, where in contrast to melanin it induces degenerative changes.

The Kidney and Fibrinolysis

1970 ◽  
Vol 24 (01/02) ◽  
pp. 026-032 ◽  
Author(s):  
N. A Marsh
Keyword(s):  
Molecular Weight ◽  
Plasminogen Activator ◽  
Enzyme System ◽  
Normal Animal ◽  
Fibrinolytic Enzyme ◽  
The Other ◽  
Exclusion Chromatography ◽  
Normal Urine ◽  
Renal Origin ◽  
Molecular Exclusion Chromatography

SummaryMolecular exclusion chromatography was performed on samples of urine from normal and aminonucleoside nephrotic rats. Normal urine contained 2 peaks of urokinase activity, one having a molecular weight of 22,000 and the other around 200,000. Nephrotic urine contained three peaks of activity with MW’s 126,000, 60,000 and 30,000. Plasma activator determined from euglobulin precipitate had a MW. in excess of 200,000. The results indicate that in the normal animal, plasma plasminogen activator does not escape into the urine in substantial quantities but under the conditions of extreme proteinuria there may be some loss through the kidney. The alteration in urokinase output in nephrotic animals indicates a greatly disordered renal fibrinolytic enzyme system.The findings of this study largely support the hypothesis that plasma plasminogen activator of renal origin and urinary plasminogen activator (urokinase) are different molecular species.

Arterio-Venous Differences in the Components of the Fibrinolytic Enzyme System

1966 ◽  
Vol 16 (01/02) ◽  
pp. 032-037 ◽  
Author(s):  
D Ogston ◽  
C. M Ogston ◽  
N. B Bennett
Keyword(s):  
Plasminogen Activator ◽  
Enzyme System ◽  
Venous Blood ◽  
Fibrinolytic Enzyme ◽  
Blood Levels ◽  
Activator Concentration ◽  
Blood Samples ◽  
Arterial Blood ◽  
Male Subjects

Summary1. The concentration of the major components of the fibrinolytic enzyme system was compared in venous and arterial blood samples from male subjects.2. The plasminogen activator concentration was higher in venous blood and the arterio-venous difference increased as its concentration rose, but the ratio of the arterial to venous level remained constant.3. No arterio-venous difference was found for anti-urokinase activity, antiplasmin, plasminogen and fibrinogen.4. It is concluded that venous blood determinations of the components of the fibrinolytic enzyme system reflect satisfactorily arterial blood levels.

Kinetic Aspects of the Interaction of Blood Clotting Enzymes

1965 ◽  
Vol 13 (01) ◽  
pp. 155-175 ◽  
Author(s):  
H. C Hemker ◽  
P.W Hemker ◽  
E. A Loeliger
Keyword(s):  
Kinetic Analysis ◽  
Enzyme Kinetics ◽  
Blood Clotting ◽  
Enzyme System ◽  
Enzyme Kinetic ◽  
Clotting Time ◽  
Standard Methods

SummaryApplication of the methods of enzyme-kinetic analysis to the results of clotting tests is feasible and can yield useful results. However, the standard methods of enzyme kinetics are not applicable without modifications imposed by the peculiarities of the blood-clotting enzyme system. The influence of the following complicating circumstances is calculated :1. Substrate is not present in excess.2. Only relative measures exist for concentrations of substrate or enzymes.3. Enzymes and substrates are often added together.4. Reagents are not pure.5. Clotting-time is our only measure for clotting-velocity.Formulas are deduced, which makes it possible to recognize the effect of these complications.

Kinin-Forming Enzyme System in DIC

1979 ◽  
Vol 10 (1) ◽  
pp. 98-101
Author(s):  
Masahiro MAKI ◽  
Kenji SOGA
Keyword(s):  
Enzyme System
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