Photoacoustic Studies of the Photocycles of Bacteriorhodopsin at Low Temperatures

P. S. Bechthold, K. Kohl, W. Sperling
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Abstract

Halobacterium halobium is extremely halophilic and requires a high concentration of NaCl (CNaCl > 2M) for growth and maintenance of structure. It occurs in salt lakes (e.g. Dead Sea, salt ponds) and survives even in crystalline salt. Under conditions of limited oxygen supply, 1ight-energy-converting membrane patches, the so-called purple membranes, are synthesized within the outer membrane of the bacteria. The purple membrane contains practically only one protein, called bacteriorhodopsin (BR) (1), which is arranged in a two-dimensional lattice, whose structure is known within a resolution of 7Å (2). BR is a chromoprotein and the pigment of the purple membrane. The purple membrane can be isolated by lysis of the cells and following purification by different centrifugation steps. The chromophoric group of BR is retinal, alternatively either in the all-trans or 13-cis configuration (3). Other retinal isomers were not found in vivo. BR which contains all-trans retinal is called trans BR BRtrans568, BR which contains 13-cis retinal is called 13-cis BR BR13-cis548. The two BR isomers are interconvertible by means of several pathways (Fig. 1) (4). One pathway does not require light (‘dark adaptation’); the others are initiated by light. Each isomer forms its distinct primary photoproduct. In the case of trans BR, the photoproduct returns via dark reactions through a series of transients to its initial isomer, trans BR (trans BR cycle). The light-energy-converting process, i.e. the active transport of protons from one side of the purple membrane to the other, can be correlated to the trans BR cycle. The function of the 13-cis BR cycle is not yet known. In the case of 13-cis BR, the dark pathway is split: most of the molecules return to their initial isomer, 13-cis BR (13-cis BR cycle), but some, on an alter native path, go to trans BR. Both pathways are connected by light reaction pathways, which are occupied by photo-excitation of transients. The environmental light conditions determine the isomeric composition of BR. In the dark-adapted state, BR contains a mixture of 13-cis BR and trans BR in a ratio of 1:1. On illumination of a dark-adapted sample with moderate light (e.g. 1mW/cm2), nearly all BR molecules are found in the trans BR state within a few seconds. The photoproducts of each BR isomer can be identified by means of low temperature absorption spectroscopy. To overcome light scattering due to cracks forming in aqueous suspensions at low temperatures, the BR samples have to be suspended in a glycerol/water mixture (w:w = 2:1) for optical absorption measurements. Only photoacoustic spectroscopy enables us to examine the photoproducts and intermediates of the two BR photocycles in buffered aqueous suspensions at low temperatures. We thus obtained photoacoustic spectra of nearly the same quality as optical absorption spectra.
低温下细菌视紫红质光循环的光声研究
halobium halobium是极度嗜盐的,需要高浓度的NaCl (CNaCl > 2M)来生长和维持结构。它存在于盐湖(如死海、盐池)中,甚至存在于结晶盐中。在氧气供应有限的条件下,在细菌的外膜内合成了光能转换膜斑块,即所谓的紫色膜。紫色膜实际上只包含一种蛋白质,称为细菌视紫红质(BR)(1),它以二维晶格排列,其结构在7Å的分辨率内已知(2)。BR是紫色膜的一种色蛋白和色素。紫色膜可以通过细胞裂解和不同的离心步骤纯化得到。BR的显色基团是视网膜的,要么是全反式的,要么是13顺式的(3)。在体内没有发现其他视网膜异构体。含有全反式视网膜的BR称为反式BR BRtrans568,含有13顺式视网膜的BR称为13顺式BR BR13-cis548。这两种溴异构体可以通过几种途径相互转化(图1)(4)。一种途径不需要光(“暗适应”);其他的是由光发起的。每种异构体形成其独特的初级光产物。在反式BR的情况下,光产物通过一系列的暗反应返回到它的初始异构体,反式BR(反式BR循环)。光能转换过程,即质子从紫色膜的一侧主动传递到另一侧,可以与反式BR循环相关。13-顺式BR循环的功能尚不清楚。在13-顺式溴的情况下,暗途径是分裂的:大多数分子回到它们最初的同分异构体,13-顺式溴(13-顺式溴循环),但一些分子,在另一种途径上,变成反式溴。这两种途径由光反应途径连接,光反应途径由瞬态光激发占据。环境光照条件决定了BR的异构体组成。在暗适应状态下,BR含有13-顺式BR和反式BR的混合物,比例为1:1。在中等光照下(例如1mW/cm2),几乎所有BR分子在几秒钟内都处于反BR状态。各BR异构体的光产物均可通过低温吸收光谱法进行鉴定。为了克服在低温下水悬浮液中由于裂缝形成的光散射,BR样品必须悬浮在甘油/水混合物(w:w = 2:1)中进行光学吸收测量。只有光声光谱才能使我们在低温下研究缓冲水悬浮液中两个BR光循环的光产物和中间体。因此,我们获得了与光学吸收光谱质量几乎相同的光声光谱。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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