Pelletier C, Bourlioux P, van Heijenoort J
Département de Microbiologie et Immunologie, Faculté de Pharmacie, Châtenay-Malabry, France.
FEMS Microbiol Lett. 1994 Apr 1;117(2):203-6. doi: 10.1111/j.1574-6968.1994.tb06765.x.
Release of lipopolysaccharide from E. coli was studied in the presence of sub-minimal inhibitory concentrations of ethylenediaminetetraacetic acid (EDTA). In untreated cells no release was detected with 50 mM Mg2+ in the medium, but a steady release of over 50% of the synthesized lipopolysaccharide was observed with 0.1 mM Mg2+. EDTA at MIC/8 led to a 2- to 3-fold higher release, presumably by an adjustment of the concentration of unchelated Mg2+ to a value still sustaining normal growth but giving rise to a highly unstable outer membrane. No structural difference was observed between cell-bound and released lipopolysaccharide.
在亚最小抑菌浓度的乙二胺四乙酸(EDTA)存在下,研究了大肠杆菌中脂多糖的释放情况。在未处理的细胞中,培养基中含有50 mM Mg2+时未检测到释放,但在含有0.1 mM Mg2+时,观察到超过50%的合成脂多糖持续释放。MIC/8的EDTA导致释放量增加2至3倍,推测是通过将未螯合的Mg2+浓度调整到仍能维持正常生长但会导致外膜高度不稳定的值。细胞结合的脂多糖和释放的脂多糖之间未观察到结构差异。