Tsuzuki K, Kimura K, Fujii N, Yokosawa N, Indoh T, Murakami T, Oguma K
Department of Microbiology, Sapporo Medical College, Japan.
Infect Immun. 1990 Oct;58(10):3173-7. doi: 10.1128/iai.58.10.3173-3177.1990.
In Clostridium botulinum types C and D, phage conversion to toxin and hemagglutinin (HA) production has been reported. DNA was extracted from a converting type C Stockholm phage, c-st, and a fragment (7.8 kilobase pairs) coding for the parts of both toxin and HA was cloned. The gene for HA was recloned, and the complete nucleotide sequence was determined. The molecular mass of this gene product was 33 kilodaltons, and it showed HA activity. The HA preparation partially purified from a type C Stockholm culture demonstrated two major bands (33 and 53 kilodaltons) on sodium dodecyl sulfate-polyacrylamide gel electrophoresis with or without reducing agent. The amino acid sequence of the N terminus of the 33-kilodalton component of the native HA preparation, which was determined by a direct protein microsequencing procedure, was identical to that deduced from the nucleotide sequence of cloned HA gene. These data indicate that the cloned gene product (33 kilodaltons) is an important component of HA.
在C型和D型肉毒梭菌中,已有噬菌体转化产生毒素和血凝素(HA)的报道。从一种转化型C型斯德哥尔摩噬菌体c-st中提取DNA,并克隆了一个编码毒素和HA部分的片段(7.8千碱基对)。对HA基因进行了重新克隆,并确定了其完整的核苷酸序列。该基因产物的分子量为33千道尔顿,具有HA活性。从C型斯德哥尔摩培养物中部分纯化得到的HA制剂,在有无还原剂的情况下,在十二烷基硫酸钠-聚丙烯酰胺凝胶电泳上显示出两条主要条带(33和53千道尔顿)。通过直接蛋白质微量测序法确定的天然HA制剂中33千道尔顿成分N端的氨基酸序列,与从克隆的HA基因核苷酸序列推导的序列相同。这些数据表明,克隆的基因产物(33千道尔顿)是HA的重要组成部分。