Kobayashi H, Tonokawa H, Fukasawa S, Yamakura F
Department of Chemistry, Faculty of Science, Josai University, Saitama, Japan.
Free Radic Res Commun. 1991;12-13 Pt 1:437-41. doi: 10.3109/10715769109145814.
We investigated the induction of Cu,Zn-SOD (bacteriocuprein) and Fe-SOD in Photobacterium leiognathi DK-A1 which was isolated from the light organ of the squid, Droteuthis kensaki. The induction of superoxide dismutases depended on the addition of paraquat to the medium. Induction of SOD by paraquat was attributed mostly to the bacteriocuprein by measuring of the activities of both SODs by using densitometry of isoelectrofocusing gel. When paraquat was added to the culture at various times in the early log phase of growth, the most efficient induction of the SODs, which was measured at the time of harvesting the cells (17 hours after inoculation), was observed when paraquat was added at 60 min after the inoculation. Catalase was not significantly induced by the addition of paraquat or increasing of oxygen concentration. We developed an assay of SOD by modification of a cytochrome c-xanthine oxidase method using a computer equipped absorption spectrophotometer.
我们研究了从剑尖柔鱼(Droteuthis kensaki)发光器官分离出的发光杆菌(Photobacterium leiognathi)DK-A1中铜锌超氧化物歧化酶(细菌铜蛋白)和铁超氧化物歧化酶的诱导情况。超氧化物歧化酶的诱导取决于向培养基中添加百草枯。通过等电聚焦凝胶密度测定法测量两种超氧化物歧化酶的活性,发现百草枯对超氧化物歧化酶的诱导主要归因于细菌铜蛋白。当在生长对数早期的不同时间向培养物中添加百草枯时,在收获细胞时(接种后17小时)测量发现,在接种后60分钟添加百草枯时,超氧化物歧化酶的诱导效果最佳。添加百草枯或提高氧气浓度均未显著诱导过氧化氢酶。我们利用配备计算机的吸收分光光度计,通过改良细胞色素c-黄嘌呤氧化酶法开发了一种超氧化物歧化酶检测方法。