Faraday communications. Application of iodine-laser temperature jump to an irreversible enzyme reaction. Reaction of ascorbic acid with hydrogen peroxide catalysed by peroxidase

1994 ◽  
Vol 90 (20) ◽  
pp. 3201 ◽  
Author(s):  
Joachim Frank ◽  
Josef F. Holzwarth ◽  
H. Brian Dunford
Langmuir ◽  
2000 ◽  
Vol 16 (14) ◽  
pp. 5892-5899 ◽  
Author(s):  
Luís M. M. Nazário ◽  
João P. S. G. Crespo ◽  
Josef F. Holzwarth ◽  
T. Alan Hatton

Langmuir ◽  
1995 ◽  
Vol 11 (7) ◽  
pp. 2405-2409 ◽  
Author(s):  
C. Petit ◽  
J. F. Holzwarth ◽  
M. P. Pileni

Biochemistry ◽  
1988 ◽  
Vol 27 (17) ◽  
pp. 6628-6633 ◽  
Author(s):  
Josef F. Holzwarth ◽  
Frank Meyer ◽  
Michael Pickard ◽  
H. Brian Dunford

1985 ◽  
Vol 18 (10) ◽  
pp. 833-836 ◽  
Author(s):  
J Gormally ◽  
D M Bloor ◽  
S Higson

2019 ◽  
Vol 29 (3) ◽  
Author(s):  
Mai Ngọc Tuan Anh

Silver nanoplates (SNPs) having different size were synthesized by a seed-mediated method. The seeds -silver nanoparticles with 4 – 6 nm diameters were synthesized first by reducing silver nitrate with sodium borohydride in the present of Trisodium Citrate and Hydrogen peroxide. Then these seeds were developed by continue reducing Ag\(^+\) ions with various amount of L-Ascorbic acid to form SNPs. Our analysis showed that the concentratrion of L-Ascorbic acid, a secondary reducing agent, played an important role to form SNPs. In addition, the size and in-plane dipole plasmon resonance wavelenght of silver nanoplates were increased when the concentration of added silver nitrate increased. The characterization of SNPs were studied by UV-Vis, FE-SEM, EDS and TEM methods.


1991 ◽  
Vol 56 (4) ◽  
pp. 923-932
Author(s):  
Jana Stejskalová ◽  
Pavel Stopka ◽  
Zdeněk Pavlíček

The ESR spectra of peroxidase systems of methaemoglobin-ascorbic acid-hydrogen peroxide and methaemoglobin-haptoglobin complex-ascorbic acid-hydrogen peroxide have been measured in the acetate buffer of pH 4.5. For the system with methaemoglobin an asymmetrical signal with g ~ 2 has been observed which is interpreted as the perpendicular region of anisotropic spectrum of superoxide radical. On the other hand, for the system with methaemoglobin-haptoglobin complex the observed signal with g ~ 2 is symmetrical and is interpreted as a signal of delocalized electron. After realization of three repeatedly induced peroxidase processes the ESR signal of the perpendicular part of anisotropic spectrum of superoxide radical is distinctly diminished, whereas the signal of delocalized electron remains practically unchanged. An amino acid analysis of methaemoglobin along with results of the ESR measurements make it possible to derive a hypothesis about the role of haptoglobin in increasing of the peroxidase activity of methaemoglobin.


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