Maluszynska G M, Magnusson K E, Stendahl O, Lock R, Kniola B
Department of Medical Microbiology, Faculty of Health Sciences, University of Linköping, Sweden.
APMIS. 1988 Sep;96(9):773-82.
When cultivated at reduced redox potential the physico-chemical surface properties were altered in strains of E. coli, Salmonella and Yersinia bacteria. In particular, strains which showed hydrophilic surface properties under normal aerobic cultivation became more hydrophobic when exposed to anaerobic conditions (e.g. E. coli K12, E. coli K12D21, E. coli K12D22, S. minnesota S99, S. typhimurium 395MS, S. braenderup 2828 and Yersinia enterocolitica). Moreover, there were qualitative as well as quantitative differences in the protein profiles of whole bacterial lysates and membrane preparations analysed in SDS-PAGE. There were no qualitative differences in the lipopolysaccharide (LPS) bands. However, when E. coli K12D22 were cultivated aerobically, remarkably more high molecular temperature-sensitive (70 degrees C for 45 min) carbohydrate material was produced (weight about 360 KD and 660 KD). Interaction between polymorphonuclear leukocytes (PMNL) and the E. coli K12D22 strain, measured as chemiluminescence, showed that the anaerobically cultivated bacteria induced a chemiluminescence that was mainly of intracellular origin, while the aerobically cultivated induced an extracellular response. Phagocytosis and killing-studies showed that only anaerobically-grown E. coli were effectively inactivated by the PMNL.
当在降低的氧化还原电位下培养时,大肠杆菌、沙门氏菌和耶尔森氏菌菌株的物理化学表面性质会发生改变。特别是,在正常需氧培养条件下表现出亲水性表面性质的菌株,在暴露于厌氧条件时会变得更疏水(例如大肠杆菌K12、大肠杆菌K12D21、大肠杆菌K12D22、明尼苏达沙门氏菌S99、鼠伤寒沙门氏菌395MS、布伦德鲁普沙门氏菌2828和小肠结肠炎耶尔森氏菌)。此外,在SDS-PAGE分析的全细菌裂解物和膜制剂的蛋白质谱中存在定性和定量差异。脂多糖(LPS)条带没有定性差异。然而,当大肠杆菌K12D22进行需氧培养时,会产生显著更多的高分子量温度敏感型(70摄氏度,45分钟)碳水化合物物质(重量约为360KD和660KD)。以化学发光测量的多形核白细胞(PMNL)与大肠杆菌K12D22菌株之间的相互作用表明,厌氧培养的细菌诱导的化学发光主要源于细胞内,而需氧培养的细菌诱导的是细胞外反应。吞噬和杀伤研究表明,只有厌氧生长的大肠杆菌能被PMNL有效灭活。