P. aeruginosa EMS1의 mutagen 처리를 통한 고기능 유화재 균주의 개발

This study was performed to improve the efficency of production of biosudactant which were produced by newly screened MNNGCN-Methyl-N-Nitro- Nitrosoguanidine) mutagenized P. aeruginosa EMS1. A culture grown exponentially for $30^{\circ}C$ in trypic soy brotb is adjusted to pH. MNNG is added and incubated in water bath shaker at about 250 ${\sim}$300rpm. After 20 min, is dilutecl into colded trypic soy broth and centrifugation. The cell pellet is resuspended in 50$m{\ell}$ of trypic soy broth. Cultures are grown at $30^{\circ}C$ overnight. cetyltrimethylammonium bromide-metbylene blue agar plate selected dark blue halo colony. Peanut oil, Castor oil, Olive oil, and so on were compared as carbon source of surface tension and emulsifying activity.

생물 계면활성제의 개발을 위해 MNNG(N-Methyl-N-Nitro- NitrMoguanidjne), EMS, UV radiator 등 random mutation을 유도하여 가장 고기능 유화제 생산 균주를 선별하여 다양한 탄소원에 따른 생육도와 유화활성, 유화 활성에 미치는 pH 등 생물 계면활성제의 생산에 관한 조사를 한 결과 Bunker A에서는 유화활성이 원래 균주보다 최고 약 6배까지 증가했으며 표면장력 또한 40.3dyne/cm 에서 34.0dyne/cm 으로 크게 감소되었다.