Beveridge T J, Schultze-Lam S
Department of Microbiology, College of Biological Science, University of Guelph, Ontario, Canada.
Microbiology (Reading). 1996 Oct;142 ( Pt 10):2887-95. doi: 10.1099/13500872-142-10-2887.
Archaea possess a broader range of cell envelope structural formats than eubacteria and their cell walls do not contain peptidoglycan. Some archaea have only a single S-layer as their cell wall (e.g. Methanococcus jannaschii and Sulfolobus acidocaldarius), whereas others have multiple layers (e.g. Methanospirillum hungatei). Sometimes there can also be a high proportion of tetraether lipids in membranes to make the envelope more resilient to environmental stress (e.g. Methanococcus jannaschii and Sulfolobus acidocaldarius grown at 70 degrees C). Since the Gram reaction depends on both the structural format and the chemical composition of the cell envelope of eubacteria, it was important to determine if the same is true for archaea. Methanospirillum hungatei, Methanosarcina mazei, Methanobacterium formicicum, Methanococcus jannaschii and Sulfolobus acidocaldarius, chosen because of their different envelope formats and chemistries, were subjected to a Gram stain that can be used for transmission electron microscopy. In this staining regimen, the iodine is replaced by potassium trichloro(eta 2-ethylene)platinate(II) as the mordant, and the platinum of the new compound is the electron-scattering agent for electron microscopy. Of all these archaea, only Methanobacterium formicicum stained Gram-positive since its pseudomurein wall remained intact; the platinum compound formed large electron-dense aggregates with the crystal violet that were located in the vicinity of the cell wall and the plasma membrane. All but the terminal filament cells of Methanospirillum hungatei stained Gram-negative because the limiting porosity of its external sheath was so small that the Gram reagents could not enter the cells. The terminal cells of filaments stained Gram-positive because the staining reagents gained entry through the terminal plugs. All other archaea stained Gram-negative because their cell walls were so disrupted during staining that the crystal violet-platinum complex could not be retained by the cells. Methanococcus jannaschii was grown at both 50 degrees C and 70 degrees C so that the tetraether lipids in its plasma membrane could be increased from 20% (50 degrees C) to 45% (70 degrees C) of the total lipids; in both cases the cells stained Gram-negative.
古菌拥有比真细菌更广泛的细胞包膜结构形式,并且它们的细胞壁不含肽聚糖。一些古菌仅具有单层S层作为其细胞壁(例如詹氏甲烷球菌和嗜酸热硫化叶菌),而其他古菌则具有多层(例如亨氏甲烷螺菌)。有时,膜中也可能含有高比例的四醚脂质,以使包膜对环境压力更具弹性(例如在70摄氏度下生长的詹氏甲烷球菌和嗜酸热硫化叶菌)。由于革兰氏反应取决于真细菌细胞包膜的结构形式和化学成分,因此确定古菌是否也是如此很重要。选择亨氏甲烷螺菌、马氏甲烷八叠球菌、甲酸甲烷杆菌、詹氏甲烷球菌和嗜酸热硫化叶菌,因其具有不同的包膜形式和化学组成,对它们进行可用于透射电子显微镜的革兰氏染色。在这种染色方法中,碘被三氯(η2-乙烯)铂酸钾(II)取代作为媒染剂,新化合物中的铂是电子显微镜的电子散射剂。在所有这些古菌中,只有甲酸甲烷杆菌染成革兰氏阳性,因为其假肽聚糖壁保持完整;铂化合物与结晶紫形成大的电子致密聚集体,位于细胞壁和质膜附近。除亨氏甲烷螺菌的末端丝状细胞外,所有细胞均染成革兰氏阴性,因为其外部鞘的限制孔隙率非常小,以至于革兰氏试剂无法进入细胞。丝状细胞的末端细胞染成革兰氏阳性,因为染色试剂通过末端塞进入细胞。所有其他古菌均染成革兰氏阴性,因为它们的细胞壁在染色过程中被破坏,以至于结晶紫-铂复合物无法被细胞保留。詹氏甲烷球菌在50摄氏度和70摄氏度下生长,以便其质膜中的四醚脂质可以从总脂质的20%(50摄氏度)增加到45%(70摄氏度);在这两种情况下,细胞均染成革兰氏阴性。