Gallis H A, Miller S E, Wheat R W
Infect Immun. 1976 May;13(5):1459-66. doi: 10.1128/iai.13.5.1459-1466.1976.
The resistance of native and trypsin-treated [14C] glucose-labeled cell walls to degradation by lysozyme and human lysosomal enzymes was confirmed. In contrast, chemically N-acetylated cell walls undergo significant degradation by these enzymes in the pH range of 4.5 to 5.5 without prior removal of the group-specific carbohydrate. N-acetylation after removal of the group A carbohydrate by formamide extraction renders the cell walls considerably more susceptible to these enzymes than by formamaide extraction alone. It appears, therefore, that unless N-acetylation can occur in vivo, streptococcal cell walls are minimally degraded, if at all, by human peripheral blood leukocytes or lysozyme. Examination of leukocyte extracts from normal subjects and patients with post-streptococcal syndromes revealed no qualitative differences in ability to dissolve streptococcal cell walls.
天然的和经胰蛋白酶处理的[14C]葡萄糖标记的细胞壁对溶菌酶和人溶酶体酶降解的抗性得到了证实。相比之下,化学N-乙酰化的细胞壁在4.5至5.5的pH范围内会被这些酶显著降解,且无需事先去除基团特异性碳水化合物。通过甲酰胺萃取去除A组碳水化合物后进行N-乙酰化,使细胞壁比仅通过甲酰胺萃取更容易受到这些酶的作用。因此,除非N-乙酰化能在体内发生,否则链球菌细胞壁即使有降解,也会被人外周血白细胞或溶菌酶降至最低程度。对正常受试者和链球菌感染后综合征患者的白细胞提取物进行检查,发现溶解链球菌细胞壁的能力没有质的差异。