Literature DB >> 1326533

Reconstitution of superoxide-forming NADPH oxidase activity with cytochrome b558 purified from porcine neutrophils. Requirement of a membrane-bound flavin enzyme for reconstitution of activity.

T Miki1, L S Yoshida, K Kakinuma.   

Abstract

Cytochrome b558 of pig blood neutrophils was purified from the membranes of resting cells to examine its ability to reconstitute superoxide (O2-)-forming NADPH oxidase activity in a cell-free assay system containing cytosol and fatty acid. The membrane-associated cytochrome b558 was solubilized with a detergent, n-heptyl beta-thioglucoside, and purified by DEAE-Sepharose, heparin-Sepharose, and Mono Q column chromatography. The final preparation of cytochrome containing 11.5 nmol of protoheme/mg of protein gave bands of the large and small subunits on immunoblotted gel. The cell-free system with the purified cytochrome alone as a membrane component showed little O2(-)-generating activity in the absence of exogenous FAD. However, the system showed high O2(-)-generating activity of 31.8 mol/s/mol of cytochrome b558 (52.5% of the original O2(-)-generating activity of the solubilized membranes) in the presence of a nitro blue tetrazolium (NBT) reductase fraction that was separated from the cytochrome b fraction by heparin-Sepharose chromatography. Heat treatment of the NBT reductase fraction resulted in loss of the O2(-)-generating activity in the reconstituted system. The O2(-)-forming activity of the reconstituted system was markedly decreased by removal of FAD from the NBT reductase fraction and was restored by readdition of FAD to the FAD-depleted reductase. The reconstituted system containing purified cytochrome b558 plus the NBT reductase showed approximately 100 times higher O2(-)-generating activity than a system containing rabbit liver NADPH-cytochrome P-450 reductase instead. These results suggest that both the FAD-dependent NBT reductase and cytochrome b558 are required as membrane redox components for O2(-)-forming NADPH oxidase activity. The present data are discussed in comparison with previously reported results on reconstituted systems containing added free FAD.

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Year:  1992        PMID: 1326533

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  5 in total

1.  Fungal metabolite gliotoxin targets flavocytochrome b558 in the activation of the human neutrophil NADPH oxidase.

Authors:  Satoshi Nishida; Lucia S Yoshida; Takashi Shimoyama; Hiroyuki Nunoi; Toshihiro Kobayashi; Shohko Tsunawaki
Journal:  Infect Immun       Date:  2005-01       Impact factor: 3.441

2.  NADPH-cytochrome c reductase from human neutrophil membranes: purification, characterization and localization.

Authors:  Y Nisimoto; H Otsuka-Murakami; S Iwata
Journal:  Biochem J       Date:  1994-02-01       Impact factor: 3.857

Review 3.  SH3-dependent assembly of the phagocyte NADPH oxidase.

Authors:  L C McPhail
Journal:  J Exp Med       Date:  1994-12-01       Impact factor: 14.307

4.  Evaluation of radical scavenging properties of shikonin.

Authors:  Lucia S Yoshida; Shunji Kohri; Shohko Tsunawaki; Tomohito Kakegawa; Taizo Taniguchi; Hiromi Takano-Ohmuro; Hirotada Fujii
Journal:  J Clin Biochem Nutr       Date:  2014-08-05       Impact factor: 3.114

5.  NADPH-binding component of the respiratory burst oxidase system: studies using neutrophil membranes from patients with chronic granulomatous disease lacking the beta-subunit of cytochrome b558.

Authors:  S Tsunawaki; H Mizunari; H Namiki; T Kuratsuji
Journal:  J Exp Med       Date:  1994-01-01       Impact factor: 14.307

  5 in total

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