Ozone production by amino acids contributes to killing of bacteria

被引:44
作者
Yamashita, Kouhei [1 ]
Miyoshi, Takashi [1 ]
Arai, Toshiyuki [2 ]
Endo, Nobuyuki [3 ]
Itoh, Hiroshi [4 ]
Makino, Keisuke [5 ]
Mizugishi, Kiyomi [6 ]
Uchiyama, Takashi [1 ]
Sasada, Masataka [4 ]
机构
[1] Kyoto Univ Hosp, Dept Hematol & Oncol, Kyoto 6068507, Japan
[2] Kyoto Univ Hosp, Dept Anesthesia, Kyoto 6068507, Japan
[3] Wakasa Wan Energy Res Ctr, Fukui 9140129, Japan
[4] Kyoto Univ, Grad Sch Med, Dept Human Hlth Sci, Kyoto 6068507, Japan
[5] Kyoto Univ, Inst Adv Energy, Kyoto 6110011, Japan
[6] Kanazawa Univ, Grad Sch Med Sci, Dept Physiol, Kanazawa, Ishikawa 9208640, Japan
关键词
host defense; singlet oxygen; neutrophil; chronic granulomatous disease;
D O I
10.1073/pnas.0807952105
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Reactive oxygen species produced by phagocytosing neutrophils are essential for innate host defense against invading microbes. Previous observations revealed that anti body-catalyzed ozone formation by human neutrophils contributed to the killing of bacteria. In this study, we discovered that 4 amino acids themselves were able to catalyze the production of an oxidant with the chemical signature of ozone from singlet oxygen in the water-oxidation pathway, at comparable level to antibodies. The resultant oxidant with the chemical signature of ozone exhibited significant bactericidal activity in our distinct cell-free system and in human neutrophils. The results also suggest that an oxidant with the chemical signature of ozone produced by neutrophils might potentiate a host defense system, when the host is challenged by high doses of infectious agents. Our findings provide biological insights into the killing of bacteria by neutrophils.
引用
收藏
页码:16912 / 16917
页数:6
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