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J. Biol. Chem., Vol. 261, Issue 25, 11444-11447, Sep, 1986
Stoichiometric conversion of oxygen to superoxide anion during the respiratory burst in neutrophils. Direct evidence by a new method for measurement of superoxide anion with diacetyldeuteroheme-substituted horseradish peroxidase
R Makino, T Tanaka, T Iizuka, Y Ishimura and S Kanegasaki
Extracellular release of superoxide anion (O-2) and hydrogen peroxide
(H2O2) during the respiratory burst of porcine and human neutrophils was
studied by using diacetyldeuteroheme-substituted horseradish peroxidase as
a trapping agent for these oxygen derivatives. The method permitted
simultaneous measurement of oxygen consumption and formation of both O-2
and H2O2 in a single reaction mixture. When neutrophils were stimulated
with phorbol myristate acetate in the presence of the heme-substituted
peroxidase, a rapid accumulation of compound III, a complex of the enzyme
with O-2, was observed accompanying an increase in oxygen consumption.
During the process, amounts of compound III formed and oxygen consumed were
stoichiometric, and no compound II, an indicator of H2O2 formation, was
observed. These results establish that neutrophils stimulated with the
phorbol ester produce exclusively O-2 as the primary oxygen metabolite and
release it into the extracellular medium. When a limited amount of
opsonized zymosan was used as the stimulus, compound III formation was also
observed but it ceased at an early stage of oxygen consumption. When a
sufficient amount of azide was included in the system, however, formation
of compound II was noted in the later stage of oxygen consumption. The
findings suggest that O- 2, formed during phagocytosis, is converted to
H2O2 within phagosomes and then diffuses out into the extracellular medium
when its decomposition by catalase and/or peroxidases is blocked by azide.

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Copyright © 1986 by the American Society for Biochemistry and Molecular Biology.
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