THE ROTENONE-INSENSITIVE REDUCTION OF QUINONES AND NITROCOMPOUNDS BY MITOCHONDRIAL NADH-UBIQUINONE REDUCTASE

被引:34
作者
BIRONAITE, DA
CENAS, NK
KULYS, JJ
机构
[1] Institute of Biochemistry, Lithuanian Academy of Scienes
关键词
NADH; UBIQUINONE REDUCTASE; ELECTRON TRANSFER; QUINONE; NITROCOMPOUND;
D O I
10.1016/S0005-2728(09)91008-8
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 rotenone-insensitive reduction of quinones and aromatic nitrocompounds by mitochondrial NADH: ubiquinone reductase (complex I, EC 1.6.99.3) has been studied. It was found that these reactions proceed via a mixed one- and two-electron transfer. The logarithms of the bimolecular rate constants of oxidation (TN/K(m)) are proportional to the one-electron-reduction potentials of oxidizers. The reactivities of nitrocompounds are close to those of quinones. Unlike the reduction of ferricyanide, these reactions are not inhibited by NADH. However, they are inhibited by NAD+ and ADP-ribose, which also act as the mixed-type inhibitors for ferricyanide. TN/K(m) of quinones and nitrocompounds depend on the NAD+/NADH ratio, but not on NAD+ concentration. They are diminished by the limiting factors of 2.5-3.5 at NAD+/NADH > 200. It seems that rotenone-insensitive reduction of quinones and nitrocompounds takes place near the NAD+/NADH and ferricyanide binding site, and the inhibition is caused by induced conformational changes after the binding of NAD+ or ADP-ribose.
引用
收藏
页码:203 / 209
页数:7
相关论文
共 35 条
  • [1] MAMMALIAN-CELL TOXICITY OF NITRO-COMPOUNDS - DEPENDENCE UPON REDUCTION POTENTIAL
    ADAMS, GE
    CLARKE, ED
    JACOBS, RS
    STRATFORD, IJ
    WALLACE, RG
    WARDMAN, P
    WATTS, ME
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1976, 72 (03) : 824 - 829
  • [2] EVIDENCE FOR 2 INDEPENDENT PATHWAYS OF ELECTRON-TRANSFER IN MITOCHONDRIAL NADH-Q OXIDOREDUCTASE .2. KINETICS OF REOXIDATION OF THE REDUCED ENZYME
    ALBRACHT, SPJ
    BAKKER, PTA
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA, 1986, 850 (03) : 423 - 428
  • [3] REACTIONS OF THE SEMIQUINONE FREE-RADICALS OF ANTI-TUMOR AGENTS WITH OXYGEN AND IRON COMPLEXES
    BUTLER, J
    HOEY, BM
    SWALLOW, AJ
    [J]. FEBS LETTERS, 1985, 182 (01) : 95 - 98
  • [4] BUTLER J, 1986, Journal of Free Radicals in Biology and Medicine, V2, P77, DOI 10.1016/0748-5514(86)90127-3
  • [5] CENAS NK, 1989, UKR BIOKHIM ZH+, V61, P23
  • [6] MUTAGENICITY OF QUINONES - PATHWAYS OF METABOLIC-ACTIVATION AND DETOXIFICATION
    CHESIS, PL
    LEVIN, DE
    SMITH, MT
    ERNSTER, L
    AMES, BN
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (06): : 1696 - 1700
  • [7] CLELAND WW, 1963, BIOCHIM BIOPHYS ACTA, V67, P188
  • [8] DAVIES KJA, 1986, J BIOL CHEM, V261, P3060
  • [9] CONSIDERATIONS FOR THE DESIGN OF NITROPHENYL MUSTARDS AS AGENTS WITH SELECTIVE TOXICITY FOR HYPOXIC TUMOR-CELLS
    DENNY, WA
    WILSON, WR
    [J]. JOURNAL OF MEDICINAL CHEMISTRY, 1986, 29 (06) : 879 - 887
  • [10] STEADY-STATE KINETICS OF HIGH MOLECULAR-WEIGHT (TYPE-I) NADH DEHYDROGENASE
    DOOIJEWAARD, G
    SLATER, EC
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA, 1976, 440 (01) : 1 - 15