Mechanism of superoxide anion generation in the toxic red tide phytoplankton Chattonella marina:: possible involvement of NAD(P)H oxidase

被引:85
作者
Kim, D
Nakamura, A
Okamoto, T
Komatsu, N
Oda, T
Iida, T
Ishimatsu, A
Muramatsu, T
机构
[1] Nagasaki Univ, Fac Fisheries, Div Biochem, Nagasaki 8528521, Japan
[2] Miyazaki Univ, Fac Agr, Dept Anim Grassland & Fishery Sci, Miyazaki 88921, Japan
[3] Nagasaki Univ, Inst Marine Res, Nagasaki 8512213, Japan
来源
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS | 2000年 / 1524卷 / 2-3期
基金
日本学术振兴会;
关键词
reactive oxygen species; toxic phytoplankton; NADPH oxidase; hybridization; DNA probe; Chattonella marina;
D O I
10.1016/S0304-4165(00)00161-6
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Red tide phytoplankton Chattonella marina is known to produce reactive oxygen species (ROS), such as superoxide anion (O-2(-)), hydrogen peroxide (H2O2) and hydroxyl radical (.OH), under normal physiological conditions. Although several lines of evidence suggest that ROS are involved in the mortality of fish exposed to C. marina, the mechanism of ROS generation in C. marina remains to be clarified. In this study, we found that the cell-free supernatant prepared from C. marina cells showed NAD(P)H-dependent O-2(-) generation, and this response was inhibited by diphenyleneiodonium, an inhibitor of mammalian NADPH oxidase. When the cell-free supernatant of C. marina was analyzed by immunoblotting using antibody raised against the human neutrophil cytochrome b558 large subunit (gp91phox), a main band of approximately 110 kDa was detected. The cell. surface localization of the epitope recognized with this antibody was also demonstrated in C. marina by indirect immunofluorescence. Furthermore, Southern blot analysis performed on genomic DNA of C. marina with a probe covering the C-terminal region of gp91phox suggested the presence of a single-copy gene coding for gp91phox homologous protein in C. marina. These results provide evidence for the involvement of an enzymatic system analogous to the neutrophil NADPH oxidase as a source of O-2(-) production in C. marina. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:220 / 227
页数:8
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