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表面电位和膜电位对与嗜硫红假单胞菌色素体膜结合的细胞色素c-555中点电位的影响。

Effects of surface potential and membrane potential on the midpoint potential of cytochrome c-555 bound to the chromatophore membrane of Chromatium vinosum.

作者信息

Itoh S

出版信息

Biochim Biophys Acta. 1980 Jul 8;591(2):346-55. doi: 10.1016/0005-2728(80)90165-6.

Abstract

The values of midpoint potential (Em) of cytochrome c-555 bound to the chromatophore membranes of a photosynthetic bacterium Chromatium vinosum was determined under various pH and salt conditions. After a long incubation at high ionic concentrations in the presence of carbonylcyanide m-chlorophenylhydrazone, which was added to abolish electrical potential difference between the inner and outer bulk phases of chromatophore, the Em value was almost constant at pH values between 4.0 and 8.4. With the decrease of salt concentration, the pH dependence of the Em value became more marked. Under low ionic conditions, Em became more positive with the decrease of pH. Addition of salt made the value more positive or negative at pH values higher or lower than 4.5, respectively. Divalent cation salts were more effective than monovalent cation salts in producing the positive shift of Em at pH 7.8. The Em value became more positive when the electrical potential of the inner side of the chromatophore was made more positive by the diffusion potential induced by the K+ concentration gradient in the presence of valinomycin. These results were explained by a change of redox potential at the inner surface of the chromatophore membrane, at which the cytochrome is assumed to be situated, due to the electrical potential difference with respect to the outer solution induced by the surface potential or membrane potential change. The values for the surface potential and the net surface charge density of the inner surface of the chromatophore membrane were estimated using the Gouy-Chapman diffuse double layer theory.

摘要

测定了光合细菌嗜硫小红卵菌(Chromatium vinosum)的色素体膜结合的细胞色素c - 555在不同pH和盐条件下的中点电位(Em)值。在羰基氰化物间氯苯腙存在下于高离子浓度下长时间孵育后(添加羰基氰化物间氯苯腙是为了消除色素体内外本体相之间的电势差),在pH值4.0至8.4之间,Em值几乎恒定。随着盐浓度降低,Em值对pH的依赖性变得更加明显。在低离子条件下,随着pH降低,Em变得更正。添加盐分别使pH高于或低于4.5时的值更正或更负。在pH 7.8时,二价阳离子盐比一价阳离子盐在使Em产生正向偏移方面更有效。当在缬氨霉素存在下由K +浓度梯度诱导的扩散电位使色素体内侧的电势更正时,Em值变得更正。这些结果可以通过色素体膜内表面(假定细胞色素位于此处)的氧化还原电位变化来解释,这种变化是由表面电位或膜电位变化引起的相对于外部溶液的电势差导致的。使用古依 - 查普曼扩散双电层理论估算了色素体膜内表面的表面电位和净表面电荷密度值。

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