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作 者:张萌[1,2] 张晓梅 窦文芳 许泓瑜 许正宏[1,2]
机构地区:[1]江南大学医药学院制药工程研究室,江苏无锡214122 [2]江南大学工业生物技术教育部重点实验室,江苏无锡214122
出 处:《微生物学通报》2009年第1期14-19,共6页Microbiology China
基 金:江苏省博士后基金(No.SY20061019);国家"973计划"项目(No.2007CB707804);国家"863计划"重点项目资助(No.2006AA020104);教育部新世纪优秀人才支持计划(No.NCET-07-0380)资助
摘 要:从内蒙古锡林浩特地区盐湖菌种样品分离获得一株嗜盐脂肪酶高产菌,结合生理生化试验和16SrDNA序列分析结果,鉴定并命名为Haloterrigena thermotoleransZ4。该菌最适生长NaCI浓度为3.5mol/L,最高生长温度为60℃,属于嗜盐耐热古生菌。粗酶性质研究表明,金属离子(Ba^2+、Fe^2+、Cu^2+)对酶有激活作用,酶活不同程度的提高了20%~30%;该酶受EDTA的抑制,酶活下降了20%,受PMSF的完全抑制。该酶对NaCl有较高的依赖专一性,至少需要0.5mol/LNaCl维持活性并且高浓度NaCl可以提高其耐热水平。醇类物质对于提高酶的热稳定性有一定作用,丙三醇效果最好。该酶对短链底物对硝基苯酚丁酸酯(p—NPB)的最适水解条件为:pH8.0、70℃、3.5mol/LNaCl:而对长链底物对硝基苯酚十六酸酯协NPP)的最适水解条件为:oH8.0、80℃、2.5mol/LNaCl。A halobacteria strain Z4 producing extracellular halophilic lipase screened from Hypersaline lakes of Inner Mongolia was identified as Haloterrigena thermotolerans. The crude lipase from Z4 was partially characterized using p-NPB. The activity of crude lipase was markedly increased 20%-30% by metal ions (Ba^2+,Fe^2+,Cu^2+), but was obviously decreased 20% by EDTA. The lipase was completely inhibited by PMSF. The activity and heat resistance of enzyme was increased by NaCl, suggesting that the enzyme has strong dependence and specificity on NaCl. The thermostability of the crude enzyme was increased by alcohols, the glycerin is the best one. The optimum conditions for the crude lipase hydrolyzing p-NPB were followed: 3.5 mol/L NaC1, 70℃ and pH 8.0, and the optimum conditions for the crude lipase hydrolyzing p-NPP were followed: 2.5 mol/L NaCl, 80℃ and pH 8.0.
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