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深红红螺菌载色体中的闪光诱导光合磷酸化。I. 细胞色素c - 420含量与光合磷酸化之间的关系。

Flash-induced photophosphorylation in Rhodospirillum rubrum chromatophores. I. The relationship between cytochrome c-420 content and photophosphorylation.

作者信息

del Valle-Tascon S, van Grondelle R, Duysens L N

出版信息

Biochim Biophys Acta. 1978 Oct 11;504(1):26-39. doi: 10.1016/0005-2728(78)90004-x.

Abstract

The content of cytochrome c-420 in Rhodospirillum rubrum chromatophores prepared by grinding with alumina is 5--10% of that in whole cells, and 20--40% in chromatophores by 'French' pressing. Flash-induced phosphorylation of various chromatophores which varied in cytochrome content from 7 to 40% is proportional to the cytochrome content. Extrapolating the cytochrome c-420 content to that observed in whole cells, a ratio ATP/P+X- near 1 is calculated. At low flash intensity the phosphorylation per flash is proportional to flash energy. Photophosphorylation in flashes given after a time of several minutes is only slightly dependent on the number of flashes. If the flashes are spaced from 0.1 to 10 s, relative phosphorylation in the first flash is about 70% and in the second 90+ of that observed in the following flashes. Proton binding is not affected by the cytochrome c-420 content and a ratio of H+/P+x- of 2.3 was found. These results can be explained by a working hypothesis in which charge separation occurring at one reaction centre and the resulting electron transport mediated amongst others by c-420, results in the injection of two protons into an ATPase, this in contrast to a chemiosmotic mechanism, where the protons are released in the chromatophore inner space.

摘要

通过用氧化铝研磨制备的红螺菌载色体中细胞色素c - 420的含量是全细胞中的5 - 10%,而通过“法式”压榨制备的载色体中该含量为20 - 40%。对细胞色素含量在7%至40%之间变化的各种载色体进行闪光诱导磷酸化,其与细胞色素含量成正比。将细胞色素c - 420的含量外推至全细胞中观察到的含量,计算出ATP/P⁺ + X⁻的比率接近1。在低闪光强度下,每次闪光的磷酸化与闪光能量成正比。在几分钟后给予的闪光中的光合磷酸化仅略微依赖于闪光次数。如果闪光间隔为0.1至10秒,第一次闪光中的相对磷酸化约为后续闪光中观察到的70%,第二次为90%以上。质子结合不受细胞色素c - 420含量的影响,并且发现H⁺/P⁺ + X⁻的比率为2.3。这些结果可以用一个工作假说来解释,即在一个反应中心发生电荷分离,以及由此产生的电子传递(其中包括由c - 420介导)导致向ATP酶中注入两个质子,这与化学渗透机制相反,在化学渗透机制中质子在载色体内部空间中释放。

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