Spitznagel J K
J Bacteriol. 1966 Jan;91(1):401-8. doi: 10.1128/jb.91.1.401-408.1966.
Spitznagel, John K. (University of North Carolina School of Medicine, Chapel Hill). Normal serum cytotoxicity for P(32)-labeled smooth Enterobacteriaceae. III. Isolation of a gammaG normal antibody and characterization of other serum factors causing P(32) loss. J. Bacteriol. 91:401-408. 1966.-Gram-negative bacteria lost metabolically incorporated P(32) when suspended in serum only if the serum contained heat-labile in addition to heat-stable factors. Gram-positive bacteria labeled with P(32) and included for comparison lost P(32) in heat-inactivated as well as in fresh normal serum. Further investigation of gram-negative bacteria showed that a smooth Escherichia coli (O117:H27) lost P(32) only if suspended in serum containing complement fractions C'1, C'2, C'3, and C'4 "normal" antibody and lysozyme. The normal antibody was recovered by absorption on and subsequent elution from E. coli O117:H27 cell walls. Immunoelectrophoresis showed that it was a gammaG-globulin. Its P(32)-releasing activity was destroyed by 2-mercaptoethanol. Lysozyme was found to potentiate the P(32)-releasing action of normal antibody plus complement. Evidence was obtained suggesting that beta(1C) globulin was the component absorbed to zymosan during serum absorption at 15 C. Reduction of the beta(1C) level evidently upsets an important balance that exists in normal serum among complement, antibody, and lysozyme. This balance is essential for maximal P(32) release from labeled bacteria, or possibly for a maximal antibacterial effect from normal serum. The possible relationships of bactericidal, bacteriolytic, and opsonic action of normal serum are discussed.
斯皮茨纳格尔,约翰·K.(北卡罗来纳大学医学院,教堂山)。正常血清对P(32)标记的光滑肠杆菌科细菌的细胞毒性。III.γG正常抗体的分离及其他导致P(32)丢失的血清因子的特性。《细菌学杂志》91:401 - 408。1966年。-革兰氏阴性菌仅当血清中除了热稳定因子外还含有热不稳定因子时,悬浮于血清中才会失去代谢掺入的P(32)。为作比较而标记有P(32)的革兰氏阳性菌在热灭活血清和新鲜正常血清中都会丢失P(32)。对革兰氏阴性菌的进一步研究表明,光滑型大肠杆菌(O117:H27)仅当悬浮于含有补体成分C'1、C'2、C'3和C'4、“正常”抗体及溶菌酶的血清中时才会丢失P(32)。正常抗体通过吸附于大肠杆菌O117:H27细胞壁并随后洗脱而得以回收。免疫电泳显示它是一种γG球蛋白。其释放P(32)的活性被2 - 巯基乙醇破坏。发现溶菌酶可增强正常抗体加补体的P(32)释放作用。有证据表明,β(1C)球蛋白是15℃血清吸收过程中被吸附到酵母聚糖上的成分。β(1C)水平的降低显然打破了正常血清中补体、抗体和溶菌酶之间存在的重要平衡。这种平衡对于从标记细菌中最大程度释放P(32)至关重要,或者可能对于正常血清的最大抗菌作用至关重要。文中讨论了正常血清的杀菌、溶菌和调理作用之间的可能关系。