Hamada S, Okahashi N, Kimura S, Imanishi H, Koga T, Kawata S, Michalek S M, McGhee J R
Jpn J Med Sci Biol. 1982 Aug;35(4):171-81. doi: 10.7883/yoken1952.35.171.
Purified cell walls of Actinomyces viscosus and Actinomyces naeslundii were solubilized by the enzymatic action of Ml N-acetylmuramidase. Soluble cell wall carbohydrate antigens were purified by column chromatography. A purified antigen preparation (fraction C) from A. viscosus ATCC 19246 was found to contain deoxyhexoses (rhamnose and 6-deoxytalose), hexosse (galactose, glucose and mannose), and a peptidoglycan component. This preparation gave a single precipitin band against antiserum to homologous whole cells. Similar antigen preparations were purified from Ml enzyme lysate of A. viscosus SK4 and A. naeslundii ATCC 12104 cell walls.
粘性放线菌和内氏放线菌的纯化细胞壁通过Ml N - 乙酰胞壁酸酶的酶促作用溶解。可溶性细胞壁碳水化合物抗原通过柱色谱法纯化。发现来自粘性放线菌ATCC 19246的纯化抗原制剂(C级分)含有脱氧己糖(鼠李糖和6 - 脱氧塔罗糖)、己糖(半乳糖、葡萄糖和甘露糖)以及肽聚糖成分。该制剂针对同源全细胞抗血清产生单一沉淀带。从粘性放线菌SK4和内氏放线菌ATCC 12104细胞壁的Ml酶裂解物中纯化出了类似的抗原制剂。