Pfluger U N, Dahl J S, Lutz H U, Bachofen R
Arch Microbiol. 1975 Jun 22;104(2):179-84. doi: 10.1007/BF00447321.
A coupling factor necessary for the photophosphorylation and Mg2+-ATPase activities in Rhodospirillum rubrum chromatophores has been separated from these particles. Although the redox potential of coupling factor deficient chromatophores is slightly more oxidized than of the control, the addition of the coupling factor for reconstitution does not alter the redox potential. Phenazine methosulfate cannot restore or significantly enhance the photophosphorylation activities of uncoupled or reconstituted chromatophores compared to the control. The coupling factor can bind to coupling factor deficient membranes without addition of magnesium ions and thus restore the photophosphorylation and Mg2+-ATPase activities of these vesicles. The Ca2+-ATPase in the coupling factor preparation shows binding characteristics similar to those of the coupling factor.
一种参与红螺菌载色体中光磷酸化作用及Mg2 + -ATP酶活性的偶联因子已从这些颗粒中分离出来。尽管缺乏偶联因子的载色体的氧化还原电位比对照的略为氧化态,但加入用于重组的偶联因子并不会改变氧化还原电位。与对照相比,吩嗪硫酸甲酯不能恢复或显著增强解偶联或重组载色体的光磷酸化活性。偶联因子可以在不添加镁离子的情况下与缺乏偶联因子的膜结合,从而恢复这些囊泡的光磷酸化和Mg2 + -ATP酶活性。偶联因子制剂中的Ca2 + -ATP酶表现出与偶联因子相似的结合特性。