Kats L N, Konstantinova N D, Kharat'ian E F
Zh Mikrobiol Epidemiol Immunobiol. 1976 Feb(2):67-9.
A study was made of deposition of diformazan TNBT and TCNBT in the presence of succinate and without it in stable L-forms of Str. pyogenes group A, St. aureus and L. monocytogenes. Diformazan proved to deposit on the cytoplasmic membrane, in the lamellar mesosomes and myelin-like structures and also on individual intracellulor membranes not forming special membrane organoids. Diformazan was localized on the membranes mostly asymmetrically, on the cytoplasmic membrane-on its internal side, and on the ring-like intracellulor membranes- externally. Localization of diformazan on the ring-like membranes is atributed to the fact that ring-like membranous structures in the L-forms formed as a result of invagination of the cytoplasmic membrane in the same way as bacterial mesosomes. Since L-form cells could not be released of endogenous substrates by the methods elaborated for bacteria, cytological data did not permit to ascertain dehydrogenases, responsible for asymmetrical localization of diformazan on the L-form membranes. On the basis of these data one can judge only the sum total activity of dehydrogenases in different membranes.
对化脓性链球菌A群、金黄色葡萄球菌和单核细胞增生李斯特菌的稳定L型在琥珀酸盐存在和不存在的情况下二亚甲蓝TNBT和TCNBT的沉积进行了研究。结果证明,二亚甲蓝沉积在细胞质膜、板层中体和髓磷脂样结构上,也沉积在未形成特殊膜细胞器的单个细胞内膜上。二亚甲蓝主要不对称地定位在膜上,在细胞质膜上——位于其内侧,在环状细胞内膜上——位于外侧。二亚甲蓝在环状膜上的定位归因于这样一个事实,即L型中的环状膜结构是由于细胞质膜内陷形成的,其方式与细菌中体相同。由于用为细菌设计的方法无法使L型细胞释放内源性底物,细胞学数据无法确定负责二亚甲蓝在L型膜上不对称定位的脱氢酶。基于这些数据,只能判断不同膜中脱氢酶的总活性。