Chen W, Ohmiya K, Shimizu S
Appl Environ Microbiol. 1986 Oct;52(4):612-6. doi: 10.1128/aem.52.4.612-616.1986.
Two strains of rumen anaerobes isolated from dehydrodivanillin-degrading cultures were identified as Fusobacterium varium and Enterococcus faecium. These organisms degraded dehydrodivanillin synergistically to 5-carboxymethylvanillin and vanillic acid. Specific conditions for protoplast formation and cell wall regeneration for both bacteria were determined, under strictly anaerobic conditions, to be as follows. The cell wall of each bacterium in yeast extract medium was loosened by adding penicillin G during early log-phase growth. The cell wall of F. varium was lysed by lysozyme (1 mg/ml) in glycerol (0.2 M)-phosphate buffer (0.05 M; pH 7.0). The addition of NaCl (0.08 M) with lysozyme was necessary for lysis of E. faecium in this solution. Almost all cells were converted to protoplasts after 2 h of incubation at 37 degrees C. Regeneration of both protoplasts was 20 to 30% on an agar-containing yeast extract medium.
从降解脱氢双香草醛的培养物中分离出的两株瘤胃厌氧菌被鉴定为多变梭杆菌和粪肠球菌。这些微生物协同将脱氢双香草醛降解为5-羧甲基香草醛和香草酸。在严格厌氧条件下,确定两种细菌原生质体形成和细胞壁再生的具体条件如下。在对数生长期早期,通过添加青霉素G使酵母提取物培养基中每种细菌的细胞壁松弛。多变梭杆菌的细胞壁在甘油(0.2M)-磷酸盐缓冲液(0.05M;pH7.0)中用溶菌酶(1mg/ml)裂解。在此溶液中,粪肠球菌的裂解需要添加NaCl(0.08M)和溶菌酶。在37℃孵育2小时后,几乎所有细胞都转化为原生质体。在含琼脂的酵母提取物培养基上,两种原生质体的再生率为20%至30%。