![]()
|
|
||||||||
J. Biol. Chem., Vol. 255, Issue 24, 11694-11697, 12, 1980
T Yubisui, S Matsukawa and Y Yoneyama
The nonenzymatic reduction of methemoglobin by the reduced form of flavin
mononucleotide was studied under various conditions by following the
reaction with a stopped flow apparatus. The reaction was very fast,
compared with the reduction of the flavin by NADPH-flavin reductase of
human erythrocytes, and followed a second order rate law: the rate constant
(K) for the reduction of methemoglobin by reduced flavin mononucleotide was
determined to be 5.5 X 10(6) M-1 S-1 in 50 mM phosphate buffer (pH 7.0) at
25 degrees C. The reaction was not influenced by changing phosphate buffer
concentration from 10 to 100 mM. The rate of reduction at the physiological
pH, 7.0, was about 95% of the maximal value that observed at around pH 6.4.
Formation of deoxyhemoglobin and oxidized form of flavin mononucleotide by
the reaction proceeded stoichiometrically in a ratio of unity. These
results apparently indicate that the limiting step for the reduction of
methemoglobin by the NADPH-flavin reductase system in human erythrocytes is
the enzymatic reduction of flavin.
Stopped flow studies on the nonenzymatic reduction of methemoglobin by reduced flavin mononucleotide
![]()
CiteULike
Complore
Connotea
Del.icio.us
Digg
Reddit
Technorati What's this?
This article has been cited by other articles:
![]() |
S. Kitamura, K. Takekawa, K. Sugihara, K. Tatsumi, and S. Ohta Pseudoenzymatic reduction of N-hydroxy-2-acetylaminofluorene to 2-acetylaminofluorene mediated by cytochrome P450 Carcinogenesis, February 1, 1999; 20(2): 347 - 350. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| All ASBMB Journals | Molecular and Cellular Proteomics |
| Journal of Lipid Research | ASBMB Today |