Lee Sang-Cheol, Lee Seung-Jin, Kim Sun-Hee, Park In-Hye, Lee Yong-Seok, Chung Soo-Yeol, Choi Yong-Lark
Department of Biotechnology, Faculty of Natural Resources and Life Science, Dong-A University, Busan 604-714, Republic of Korea.
Bioresour Technol. 2008 May;99(7):2288-92. doi: 10.1016/j.biortech.2007.05.020. Epub 2007 Jun 26.
To obtain predominant bacteria degrading crude oil, we isolated some bacteria from waste soybean oil. Isolated bacterial strain had a marked tributyrin (C4:0) degrading activity as developed clear zone around the colony after incubation for 24h at 37 degrees C. It was identified as Klebsiella sp. Y6-1 by analysis of 16S rRNA gene. Crude biosurfactant was extracted from the culture supernatant of Klebsiella sp. Y6-1 by organic solvent (methanol:chloroform:1-butanol) after vacuum freeze drying and the extracted biosurfactant was purified by silica gel column chromatography. When the purified biosurfactant dropped, it formed degrading zone on crude oil plate. When a constituent element of the purified biosurfactant was analyzed by TLC and SDS-PAGE, it was composed of peptides and lipid. The emulsification activity and stability of biosurfactant was measured by using hydrocarbons and crude oil. The emulsification activity and stability of the biosurfactant showed better than the chemically synthesized surfactant. It reduced the surface tension of water from 72 to 32 mN/m at a concentration of 40 mg/l.
为了获得降解原油的优势细菌,我们从废弃大豆油中分离出了一些细菌。分离出的菌株具有显著的三丁酸甘油酯(C4:0)降解活性,在37℃下培养24小时后,菌落周围出现了清晰的降解圈。通过16S rRNA基因分析,它被鉴定为克雷伯氏菌属Y6-1。在真空冷冻干燥后,通过有机溶剂(甲醇:氯仿:正丁醇)从克雷伯氏菌属Y6-1的培养上清液中提取粗生物表面活性剂,并通过硅胶柱色谱法对提取的生物表面活性剂进行纯化。当纯化的生物表面活性剂滴下时,在原油平板上形成了降解圈。通过TLC和SDS-PAGE对纯化的生物表面活性剂的组成成分进行分析时,发现它由肽和脂质组成。使用碳氢化合物和原油测量了生物表面活性剂的乳化活性和稳定性。该生物表面活性剂的乳化活性和稳定性优于化学合成表面活性剂。在浓度为40mg/l时,它将水的表面张力从72降低到了32mN/m。