Mechanism of strong resistance of Helicobacter pylori respiration to nitric oxide

被引:8
作者
Park, AM
Nagata, K
Sato, EF
Tamura, T
Shimono, K
Inoue, M
机构
[1] Osaka City Univ, Sch Med, Dept Biochem & Mol Pathol, Osaka 5458585, Japan
[2] Hyogo Med Univ, Dept Bacteriol, Nishinomiya, Hyogo 6638501, Japan
[3] Hinode En Elder Hlth Ctr, Kobe, Hyogo 6570852, Japan
关键词
Helicobacter pylori; respiration; nitric oxide; cytochrome c oxidase; oxidative stress; superoxide; mitochondria; gastric ulcer;
D O I
10.1016/S0003-9861(02)00691-4
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
The aim of the present work is to elucidate the mechanism by which the respiration of Helicobacter pylori but not of Escherichia coli shows a strong resistance to nitric oxide (NO). Nitric oxide strongly but reversibly inhibited the oxygen consumption by sonicated membranes from H. pylori and Triton X-100-treated cells. Although the sensitivity of the H. pylori respiration to cyanide was low, it also increased after the treatment with Triton X-100. Kinetic analyses revealed that NO was rapidly degraded by E coli and the Triton X-100-treated H. pylori, but not by the intact H. pylori. Thus, the low sensitivity to NO might reflect the low affinity of the cytochrome c oxidase for this radical within the membrane/lipid bilayers of H. pylori. Such properties of the oxidase in H. pylori membranes may, at least in part, underlie the mechanism by which this bacterium thrives in NO-enriched gastric juice. (C) 2002 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:129 / 135
页数:7
相关论文
共 33 条
[21]   RAPID REACTION BETWEEN PEROXONITRITE ION AND CARBON-DIOXIDE - IMPLICATIONS FOR BIOLOGICAL-ACTIVITY [J].
LYMAR, SV ;
HURST, JK .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1995, 117 (34) :8867-8868
[22]   HELICOBACTER-PYLORI - THE ETIOLOGIC AGENT FOR PEPTIC-ULCER [J].
MARSHALL, BJ .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1995, 274 (13) :1064-1066
[23]   Characteristics of the aerobic respiratory chains of the microaerophiles Campylobacter jejuni and Helicobacter pylori [J].
Mendz, GL ;
Smith, MA ;
Finel, M ;
Korolik, V .
ARCHIVES OF MICROBIOLOGY, 2000, 174 (1-2) :1-10
[24]   KINETIC AND STRUCTURAL DIFFERENCES BETWEEN CYTOCHROME-C OXIDASES FROM BEEF-LIVER AND HEART [J].
MERLE, P ;
KADENBACH, B .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1982, 125 (01) :239-244
[25]   Helicobacter pylori generates superoxide radicals and modulates nitric oxide metabolism [J].
Nagata, K ;
Yu, H ;
Nishikawa, M ;
Kashiba, M ;
Nakamura, A ;
Sato, EF ;
Tamura, T ;
Inoue, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (23) :14071-14073
[26]   A cb-type cytochrome-c oxidase terminates the respiratory chain in Helicobacter pylori [J].
Nagata, K ;
Tsukita, S ;
Tamura, T ;
Sone, N .
MICROBIOLOGY-UK, 1996, 142 :1757-1763
[27]   Flavohemoglobin hmp affords inducible protection for Escherichia coli respiration, catalyzed by cytochromes bo′ or bd, from nitric oxide [J].
Stevanin, TM ;
Ioannidis, N ;
Mills, CE ;
Kim, SO ;
Hughes, MN ;
Poole, RK .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (46) :35868-35875
[28]   OXYGEN-DEPENDENT REGULATION OF MITOCHONDRIAL ENERGY-METABOLISM BY NITRIC-OXIDE [J].
TAKEHARA, Y ;
KANNO, T ;
YOSHIOKA, T ;
INOUE, M ;
UTSUMI, K .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1995, 323 (01) :27-32
[29]   Oxygen concentration regulates NO-dependent relaxation of aortic smooth muscles [J].
Takehara, Y ;
Nakahara, H ;
Okada, S ;
Yamaoka, K ;
Hamazaki, K ;
Yamazato, A ;
Inoue, M ;
Utsumi, K .
FREE RADICAL RESEARCH, 1999, 30 (04) :287-294
[30]   Importance of guanine nitration and hydroxylation in DNA in vitro and in vivo [J].
Tuo, J ;
Liu, L ;
Poulsen, HE ;
Weimann, A ;
Svendsen, O ;
Loft, S .
FREE RADICAL BIOLOGY AND MEDICINE, 2000, 29 (02) :147-155