Kröncke K D, Golecki J R, Jann K
Max-Planck-Institut für Immunbiologie, Universität Freiburg, Federal Republic of Germany.
J Bacteriol. 1990 Jun;172(6):3469-72. doi: 10.1128/jb.172.6.3469-3472.1990.
The de novo expression of Escherichia coli K1, K5, and K12 capsules was analyzed with immunoelectron microscopy in temperature upshift experiments, with upshift from 18 degrees C (capsule restrictive) to 37 degrees C (capsule permissive). Newly produced capsular polysaccharides appeared at the cell surface atop membrane adhesion sites (Bayer's junctions). After plasmolysis of the bacteria at an early expression stage, the capsular polysaccharides were labeled at discrete sites in the periplasm by the immunogold technique. After temperature upshift in the presence of carbonyl cyanide m-chlorophenylhydrazone (CCCP) or chloramphenicol, the polysaccharides were labeled in the cytoplasm.
在温度升高实验中,利用免疫电子显微镜分析了大肠杆菌K1、K5和K12荚膜的从头表达情况,温度从18℃(荚膜限制温度)升高到37℃(荚膜允许温度)。新产生的荚膜多糖出现在细胞膜粘附位点(拜尔结)上方的细胞表面。在早期表达阶段对细菌进行质壁分离后,通过免疫金技术在周质中的离散位点标记荚膜多糖。在存在羰基氰化物间氯苯腙(CCCP)或氯霉素的情况下进行温度升高后,多糖在细胞质中被标记。