Danon A, Brith-Lindner M, Caplan S R
Biophys Struct Mech. 1977 Apr 21;3(1):1-17. doi: 10.1007/BF00536449.
A protein closely resembling the purple membrane protein pre-exists in the cell membrane of H. halobium prior to the appearance of functional bacteriorhodopsin. It is associated with a differentiated membranous structure which has been isolated on a sucrose gradient and appears to be a precursor of the purple membrane. The identity of the precursor protein as a form of the purple membrane protein was established in different ways: (1) The cell proteins were labelled in vivo with 14C-proline during dark aerobic growth, the label was "chased", and the cells transferred to the illuminated near-anaerobic conditions under which purple membrane is optimally synthesised (induction conditions). Cell lysates were fractionated on sucrose gradients at different times after induction. Label first found in the precursor fraction appeared within 24 h in the purple membrane fraction. (2) SDS-urea-acrylamide gel electrophoresis of the purple membrane protein and the precursor showed only one protein band whose migration coincided with that of the purple membrane band. (3) The amino-acid analysis of the purified precursor was very similar to that of the purple membrane. The absorption spectrum of the precursor showed little of the characteristic absorption of bacteriorhodopsin at 570 nm. A major band appears at 412 nm, the exact nature of which is not known. The difference spectrum (reduced versus oxidised) of a purified fraction showed only traces of cytochrome. Thin-layer chromatography of an acetone-soluble lipid extract indicated the presence of retinal and beta-carotene. Cells grown in the presence of nicotine did not develop purple membrane after induction: the species absorbing at 412 nm was much less abundant than in non-inhibited cells, but a new fraction was present with a sharp peak at 345 nm consisting mainly of lycopene.
在功能性细菌视紫红质出现之前,一种与紫膜蛋白极为相似的蛋白质就已预先存在于嗜盐菌的细胞膜中。它与一种已在蔗糖梯度上分离出来的分化膜结构相关联,这种膜结构似乎是紫膜的前体。通过不同方式确定了前体蛋白作为紫膜蛋白的一种形式:(1)在黑暗需氧生长期间,用¹⁴C - 脯氨酸在体内标记细胞蛋白,进行“追踪”,然后将细胞转移到光照近厌氧条件下,在此条件下紫膜能最佳合成(诱导条件)。在诱导后的不同时间,将细胞裂解物在蔗糖梯度上进行分级分离。最初在前体组分中发现的标记在24小时内出现在紫膜组分中。(2)紫膜蛋白和前体的SDS - 尿素 - 丙烯酰胺凝胶电泳仅显示一条蛋白带,其迁移与紫膜带一致。(3)纯化前体的氨基酸分析与紫膜的非常相似。前体的吸收光谱在570nm处几乎没有细菌视紫红质的特征吸收。在412nm处出现一条主要谱带,其确切性质尚不清楚。纯化组分的差示光谱(还原态与氧化态)仅显示微量细胞色素。丙酮可溶性脂质提取物的薄层色谱表明存在视黄醛和β - 胡萝卜素。在尼古丁存在下生长的细胞在诱导后未形成紫膜:在412nm处吸收的物质比未受抑制的细胞中少得多,但出现了一个新的组分,在345nm处有一个尖锐峰,主要由番茄红素组成。