Appl Environ Microbiol. 1995 Jan;61(1):130-7. doi: 10.1128/aem.61.1.130-137.1995.
A green Chlorobium sp. with spinae, strain JSB1, was isolated from an enrichment culture previously obtained from Fayetteville Green Lake, N.Y. (J. S. Brooke, J. B. Thompson, T. J. Beveridge, and S. F. Koval, Arch. Microbiol. 157:319-322, 1992). Cells were gram-negative, nonmotile rods which contained bacteriochlorophyll c and chlorosomes. Spinae were best seen by transmission electron microscopy in thin sections of cells fixed in the presence of tannic acid. High-resolution scanning electron microscopy showed the spinae randomly distributed at the cell surface and at the junctions between cells. Spinae were physically sheared from cells and isolated from the culture supernatant by ultrafiltration. As observed by electron microscopy, spinae demonstrated unusual structural stability when exposed for 1 h at 37 deg C to chemical treatments such as hydrogen bond-breaking agents, detergents, metal-chelating agents, proteases, and organic solvents. They were stable for 1 h at 37 deg C over the pH range 2.3 to 9.9 and in 1 M HCl and 1 M NaOH. The structural integrity of the spinae was also maintained when spinae were subjected to harsher treatments of autoclaving in 2% (wt/vol) sodium dodecyl sulfate and exposure to dithiothreitol at pH 9 for 1 h at 100 deg C. Partially dissociated spinae were obtained after 5 h at 100 deg C in 1 M HCl and 1 M NaOH. In acid, the tubular spinae became amorphous structures, with no helical striations visible. In alkali, the spinae had dissociated into irregular aggregates of disks. Since both high temperature and extremes of pH were required to achieve partial dissociation of the spinae, the strength of the structure presumably comes from covalent bonding.
一株带刺的绿色绿硫菌(Chlorobium sp.),JSB1 菌株,从纽约州费耶特维尔绿湖(Fayetteville Green Lake)的富集培养物中分离得到(J. S. Brooke、J. B. Thompson、T. J. Beveridge 和 S. F. Koval,Arch. Microbiol. 157:319-322, 1992)。细胞呈革兰氏阴性,无运动性的杆状,含有菌绿素 c 和类菌叶绿素体。在含有单宁酸的固定细胞的薄切片中,通过透射电子显微镜可以最好地观察到刺。高分辨率扫描电子显微镜显示刺随机分布在细胞表面和细胞之间的连接处。刺从细胞上物理剪切下来,并通过超滤从培养上清液中分离出来。正如电子显微镜观察到的,刺在 37°C 下暴露于氢键破坏剂、清洁剂、金属螯合剂、蛋白酶和有机溶剂等化学处理 1 小时后,表现出异常的结构稳定性。它们在 pH 值为 2.3 至 9.9 的范围内在 37°C 下稳定 1 小时,并且在 1 M HCl 和 1 M NaOH 中稳定。当刺在 2%(重量/体积)十二烷基硫酸钠中进行高压灭菌处理,并在 pH 9 下在 100°C 下暴露于二硫苏糖醇 1 小时时,刺的结构完整性也得到了保持。在 1 M HCl 和 1 M NaOH 中于 100°C 下孵育 5 小时后,获得部分解离的刺。在酸性条件下,管状刺变成无可见螺旋条纹的无定形结构。在碱性条件下,刺已解离成不规则的圆盘聚集物。由于高温和极端 pH 值都需要实现刺的部分解离,因此结构的强度可能来自于共价键。