Granum P E, Skjelkvåle R
Appl Environ Microbiol. 1981 Oct;42(4):596-8. doi: 10.1128/aem.42.4.596-598.1981.
Four enterotoxin-positive strains of Clostridium perfringens were tested for sporulation and enterotoxin production on defined media. The medium described by Sacks and Thompson (Appl. Environ. Microbiol. 35:405-409, 1978) gave the highest enterotoxin production and was selected for the production of endogenously labeled enterotoxin. The specific radioactivity of the enterotoxin was 16,000 dpm/microgram when the tritiated amino acids were added to the growth medium just before the inoculum. Addition of the radioactive amino acids during the growth period gave consistently lower specific radioactivity. When the enterotoxin was produced on the medium described by Duncan and Strong (Appl. Microbiol. 16:82-89, 1968), the highest specific radioactivity of the enterotoxin was found when the radioactive amino acids were added to the growth medium 4 h after inoculation. In this case, the specific activity of the enterotoxin was 10,000 dpm/microgram.
对四株产气荚膜梭菌肠毒素阳性菌株进行了检测,以确定其在特定培养基上的芽孢形成和肠毒素产生情况。萨克斯和汤普森(《应用与环境微生物学》35:405 - 409, 1978)描述的培养基产生的肠毒素产量最高,因此被选用于产生内源性标记的肠毒素。当在接种前将氚标记的氨基酸添加到生长培养基中时,肠毒素的比放射性为16,000 dpm/微克。在生长期间添加放射性氨基酸会使比放射性持续降低。当在邓肯和斯特朗(《应用微生物学》16:82 - 89, 1968)描述的培养基上产生肠毒素时,在接种后4小时将放射性氨基酸添加到生长培养基中时,发现肠毒素的比放射性最高。在这种情况下,肠毒素的比活性为10,000 dpm/微克。