Landman O E, Ryter A, Fréhel C
J Bacteriol. 1968 Dec;96(6):2154-70. doi: 10.1128/jb.96.6.2154-2170.1968.
Protoplasts of Bacillus subtilis plated on SD medium form L colonies in quantitative yield and propagate in the L form indefinitely. L bodies or protoplasts placed in 25% gelatin medium form bacillary colonies. Details of the reversion of naked bodies to the walled form are reported. In 25% gelatin medium, reversion begins earlier (about 50% reversion in 4 hr) than the multiplication of bacilli. Thus, virtually all the observed bacillary forms are themselves revertants and not the offspring of a few growing clones. The optimal temperature for reversion is 26 C in 25% gelatin. When cells reverting at 26 C are warmed to 40 C for 3 min, reversion is delayed markedly, whereas viability is unaffected. For electron microscopy, a dense protoplast inoculum was placed on a gelatin surface, incubated, and then fixed in situ. There was no multiplication, but crowding delayed reversion markedly. Successive events of reversion are as follows. The loose nucleoid of the protoplasts condenses in response to the gelatin medium and condenses further and further as reversion proceeds. A thin coat of wall develops around the bodies of various sizes and shapes and then increases uniformly in thickness until a wall of normal aspect is formed. Rod-shaped cells grow out from these bodies-sometimes in several directions at once. A few mesosomes begin to appear only after a thin coat of wall has been formed. These are dense, atypical structures compartmented by membranes. They are located at the cell periphery and do not seem to be in contact with the nucleoids. Quantitative estimates showed that only 20 to 25% of revertant cells or cells grown on gelatin contain even a single mesosome. The others have no mesosome at all. Mesosomes thus do not appear to play a significant role in reversion, and normal mesosome functions must presumably be performed elsewhere in the cell in gelatin-grown bacilli. The role of cell wall, its synthesis, and its chemical nature in successive steps in reversion are discussed.
接种在SD培养基上的枯草芽孢杆菌原生质体可定量产生L菌落,并能以L型无限繁殖。置于25%明胶培养基中的L型小体或原生质体可形成杆菌菌落。本文报道了裸露小体回复为有壁形式的详细过程。在25%明胶培养基中,回复开始的时间(4小时内约50%回复)比杆菌繁殖的时间早。因此,几乎所有观察到的杆菌形式本身都是回复体,而不是少数生长克隆的后代。在25%明胶中回复的最适温度是26℃。当在26℃回复的细胞升温至40℃持续3分钟时,回复明显延迟,而活力不受影响。用于电子显微镜观察时,将密集的原生质体接种物置于明胶表面,进行培养,然后原位固定。没有繁殖现象,但拥挤明显延迟了回复。回复的连续过程如下。原生质体松散的类核因明胶培养基而浓缩,并随着回复的进行进一步浓缩。在各种大小和形状的小体周围形成一层薄的细胞壁,然后厚度均匀增加,直到形成正常外观的细胞壁。杆状细胞从这些小体中生长出来——有时同时向几个方向生长。只有在形成一层薄的细胞壁后才开始出现一些间体。这些是由膜分隔的密集、非典型结构。它们位于细胞周边,似乎不与类核接触。定量估计表明,只有20%至25%的回复细胞或在明胶上生长的细胞含有哪怕一个间体。其他细胞根本没有间体。因此,间体似乎在回复中不发挥重要作用,在明胶培养基中生长的杆菌中正常的间体功能大概在细胞的其他部位进行。本文讨论了细胞壁在回复的连续步骤中的作用、其合成及其化学性质。