详细信息
粘质沙雷氏菌脂肪酶的固定化及催化拆分反式3-(4’-甲氧苯基)缩水甘油酸甲酯
Immobilization of Serratia marcescens Lipase and Catalytic Resolution of Trans-3-(4’-methoxyphenyl)glycidic Acid Methyl Ester
文献类型:期刊文献
中文题名:粘质沙雷氏菌脂肪酶的固定化及催化拆分反式3-(4’-甲氧苯基)缩水甘油酸甲酯
英文题名:Immobilization of Serratia marcescens Lipase and Catalytic Resolution of Trans-3-(4’-methoxyphenyl)glycidic Acid Methyl Ester
作者:龙章德[1];许建和[1];潘江[1]
机构:[1]华东理工大学生物反应器工程国家重点实验室
年份:2007
卷号:28
期号:2
起止页码:175
中文期刊名:催化学报
收录:CSTPCD;;Scopus;北大核心:【北大核心2004】;CSCD:【CSCD2011_2012】;
基金:国家自然科学基金(20506037;203900506);上海市重大科技攻关项目(05DZ19350).
语种:中文
中文关键词:粘质沙雷氏菌;脂肪酶;固定化;对映选择性水解;反式3-(4’-甲氧苯基)缩水甘油酸甲酯;硅藻土;环氧树脂;Eupergit;C
外文关键词:Serratia marcescens; lipase; immobilization; enantioselective hydrolysis; 3-(4'-methoxyphenyl)
摘要:对粘质沙雷氏菌脂肪酶进行了固定化研究,确定硅藻土和环氧树脂EupergitC是较好的固定化载体.固定化后酶的热稳定性、pH稳定性及储存稳定性均明显提高.以EupergitC共价固定的脂肪酶,其操作稳定性比硅藻土吸附酶好,重复使用10批次后,剩余酶活力还有50%左右,戊二醛交联对EupergitC固定化酶稳定性的提高没有明显效果,而硅藻土吸附酶经戊二醛交联后稳定性有所提高,经5批次反应后剩余酶活力还有50%.使用交联后的硅藻土固定化酶(1g,200U),在两相搅拌反应器(工作体积200ml,甲苯∶水体积比=1)中对地尔硫卓手性前体(±)-反式3-(4’-甲氧苯基)缩水甘油酸甲酯((±)-MPGM)(有机相浓度为0.5mol/L)进行了催化拆分,经5批次反应后,共得纯(2R,3S)-(-)-MPGM18.6g,产品光学纯度(对映体过量)>99%,总收率为37.2%.
Seven carriers were investigated for immobilization of the lipase from Serratia marcescens ECU1010, and diatomite and Eupergit C were found to be ideal supports. The thermal and storage stability of the lipase was significantly improved after being immobilized onto these two supports. After heating at 50 ℃ for 6 h, only a small decrease in the activity was observed for the diatomite-adsorbed lipase. About 50 % of the initial activity was retained when the two immobilized enzyme samples were storaged at 4 ℃ for 180 days. Operational stability tests indicated that the half-life of the lipase immobilized on Eupergit C was about 2-fold longer than that of the diatomite-immobilized lipase. The crosslinking with glutaraldehyde had no significant effect on the activity of the Eupergit C-immobilized lipase, whereas the reusability of the crosslinked diatomite-immobilized enzyme was slightly improved. Using the crosslinked diatomite-immobilized lipase, an up-scaled bioresolution of ( ± )-3-(4' methoxyphenyl)glycidic acid methyl ester (( ± )-MPGM) was performed in a 500-ml emulsion reactor with 200 ml biphasic solution (toluene:water = 1:1) at 30 ℃ and 0.5 mol/L of ( ± )-MPGM in toluene. After 5 batches of reaction, crystalline (2R, 3S)-(-)-MPGM with a chemical purity of 100 % and optical purity of 〉 99% enantiomeric excess was obtained in a yield of 37.2 %.
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