Usui Kimihito, Miyazaki Shinya, Kaito Chikara, Sekimizu Kazuhisa
Laboratory of Microbiology, Graduate School of Pharmaceutical Sciences, The University of Tokyo, 3-1, 7-Chome, Hongo, Bunkyo-ku, Tokyo 113-0033, Japan.
Microb Pathog. 2009 Feb;46(2):59-62. doi: 10.1016/j.micpath.2008.10.010. Epub 2008 Nov 12.
Overnight cultures of 16 of 25 species of soil bacterium injected into silkworm hemolymph killed the silkworms. Injection of culture supernatants of five of these 16 bacterial species into the hemolymph also killed silkworms. Analysis of 16S rRNA indicated that the toxic species were Bacillus species. We purified an exotoxin produced by one of the Bacillus species by measuring the specific activity based on silkworm toxicity. The final step of purification revealed that the silkworm-killing activity was due to a 34-kDa protein. LC/MS/MS analysis revealed that the 34-kDa protein is sphingomyelinase C of Bacillus cereus. We propose that the silkworm infection model is useful for identifying pathogenic bacteria from soil and purifying bacterial toxins.
将25种土壤细菌中的16种的过夜培养物注射到家蚕血淋巴中会杀死家蚕。将这16种细菌中的5种的培养上清液注射到血淋巴中也会杀死家蚕。对16S rRNA的分析表明,有毒菌种为芽孢杆菌属菌种。我们通过基于家蚕毒性测量比活性,纯化了一种芽孢杆菌属菌种产生的外毒素。纯化的最后一步表明,家蚕致死活性归因于一种34 kDa的蛋白质。液相色谱/串联质谱分析表明,这种34 kDa的蛋白质是蜡样芽孢杆菌的鞘磷脂酶C。我们认为家蚕感染模型有助于从土壤中鉴定病原菌并纯化细菌毒素。