第94回日本細菌学会総会

講演情報

オンデマンド口頭発表(ODP)

6 病原因子と生体防御

[ODP6A] a. 接着因子・定着因子

[ODP-117] ウェルシュ菌由来オートリシンの分子量変化と溶菌活性

○青野 りよ1,松永 望1,玉井 栄治2,片山 誠一1,櫃本 泰雄1 (1岡山理科大・理・臨床生命科学,2松山大・薬・感染症)

Autolysin of Clostridium perfringens (Acp, CPE1231), a single polypeptide with a molecular weight of 122 kDa, is composed of 10 N-terminal cell wall binding (CWB) domains (CWB) and a C-terminal catalytic domain (CD) which exerts an N-acethylglucosaminidase activity. In previous study, the apparent molecular weight of Acp was reported to be 95 kDa. However, the result of our experiment indicated the presence of 122 kDa Acp as well as 95 kDa Acp. Here, we investigated the expression of these Acps in the different stages of growth and their peptidoglycan-hydrolysing activity (lytic activity). In addition, the lytic activity of several recombinant Acp fragments (rAcp) were also examined. The result of Western blot analysis using anti-Acp polyclonal antibody revealed that both 122 kDa and 95 kDa were expressed during the vegetative growth, whereas only 95 kDa Acp was expressed during the stationary phase. Both 122 kDa Acp and 95 kDa Acp showed lytic activity by renaturing SDS-PAGE containing Micrococcus luteus cells. Autoclaved M. luteus cells were used for the measurement of lytic activity by various rAcps. rAcpCWB3-10+CD having 8 CWB domains and CD showed a significant higher lytic activity than that of rAcpCWB7-10+CD having 4 CWB domains and CD. These results suggest the biological significance of CWB domains in the peptidoglycanase activity of Acp.