Hunter D J, Brown K R, Pettigrew G W
Department of Preclinical Veterinary Sciences, University of Edinburgh, U.K.
Biochem J. 1989 Aug 15;262(1):233-40. doi: 10.1042/bj2620233.
The cellular location of cytochrome c4 in Pseudomonas stutzeri and Azotobacter vinelandii was investigated by the production of spheroplasts. Soluble cytochrome c4 was found to be located in the periplasm in both organisms. The remaining cytochrome c4 was membrane-bound. The orientation of this membrane-bound cytochrome c4 fraction was investigated by proteolysis of the cytochrome on intact spheroplasts. In P. stutzeri, 78% of the membrane-bound cytochrome c4 could be proteolysed, whilst 82% of the spheroplasts remained intact, suggesting that the membrane-bound cytochrome c4 is on the periplasmic face of the membrane in this organism. Cytochrome c4 was not susceptible to proteolysis on A. vinelandii spheroplasts, in spite of being digestible in the purified state. Cytochrome c5 was shown to have a similar cellular distribution to cytochrome c4. Selective removal of cytochrome c4 from membranes of P. stutzeri was accomplished by the use of sodium iodide and propan-2-ol, with the retention of most of the ascorbate-TMPD (NNN'N'-tetramethylbenzene-1,4-diamine) oxidase activity associated with the membrane. Sodium iodide removed most of the cytochrome c4 from A. vinelandii membranes with retention of 62% of the ascorbate-TMPD oxidase activity. Cytochrome c4 could be returned to the washed membranes, but with no recovery of this enzyme activity. We conclude that cytochrome c4 is not involved in the ascorbate-TMPD oxidase activity associated with the membranes of these two organisms.
通过制备原生质球研究了施氏假单胞菌和棕色固氮菌中细胞色素c4的细胞定位。发现可溶性细胞色素c4在这两种生物体中均位于周质中。其余的细胞色素c4与膜结合。通过对完整原生质球上的细胞色素进行蛋白水解来研究这种膜结合细胞色素c4部分的取向。在施氏假单胞菌中,78%的膜结合细胞色素c4可被蛋白水解,而82%的原生质球保持完整,这表明在该生物体中膜结合细胞色素c4位于膜的周质面。尽管纯化状态下的细胞色素c4可被消化,但在棕色固氮菌原生质球上它不易被蛋白水解。细胞色素c5显示出与细胞色素c4相似的细胞分布。通过使用碘化钠和丙-2-醇从施氏假单胞菌的膜中选择性去除细胞色素c4,同时保留了与膜相关的大部分抗坏血酸-TMPD(NNN'N'-四甲基苯-1,4-二胺)氧化酶活性。碘化钠从棕色固氮菌膜中去除了大部分细胞色素c4,同时保留了62%的抗坏血酸-TMPD氧化酶活性。细胞色素c4可以重新回到洗涤过的膜上,但这种酶活性没有恢复。我们得出结论,细胞色素c4不参与这两种生物体膜相关的抗坏血酸-TMPD氧化酶活性。