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Criteria to design green enzymatic processes in ionic liquid/supercritical carbon dioxide systems

机译:在离子液体/超临界二氧化碳系统中设计绿色酶促工艺的标准

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Five different ionic liquids (ILs) based on quaternary ammonium cations, with functional side chains ((3-hydroxypropyl)-trimethyl-, (3-cyanopropyl)-trimethyl-, butyltrimethyl-, (5-cyanopentyl)-trimethyl- and hexyl-trimethyl-) associated with the same anion (bis(trifluoromethane)sulfonyl amide)), were synthesized, and their suitability for Candida antarctica lipase B (CALB)-catalyzed ester synthesis in IL/supercritical carbon dioxide (scCO(2)) biphasic systems was assayed. Catalytic efficiency of the system has been analyzed as a function of both enzyme properties and mass-transfer phenomena criteria. First, the suitability of these ILs as enzymic reaction media was tested for the kinetic resolution of rac-phenylethanol. All ILs were found to be suitable media for enzyme catalysis, the best catalytic parameter (5.3 U/mg specific activity, 94.9% selectivity) being obtained for the (5-cyanopentyl)-trimethylammonium. Second, enzyme stability in all of the ILs was studied at 50 degreesC over a period of 50 days, and data were analyzed by a two-step kinetic deactivation model. All of the ILs were shown to act as stabilizing agents with respect to hexane, producing an increase in the free energy of deactivation (to 25 kJ/mol protein) and an improvement in the half-life time of the enzyme (2000-fold), which agrees with the observed increased hydrophobicity of the cation alkyl side chain (measured by Hansen's solubility parameter, 6). By using two different CALB-IL systems with different hydrophobicity in the cation, continuous processes to synthesize six different short chain alkyl esters (butyl acetate, butyl propionate, butyl butyrate, hexyl propionate, hexyl butyrate, and octyl propionate) in scCO(2) at 10 MPa and 50 degreesC were carried out. Both rate-limiting parameters (synthetic activity and scCO(2)-ILs mass-transfer phenomena) were related with the delta-parameter of the ILs-alkyl chain and reagents.
机译:五种基于季铵阳离子的离子液体(IL),具有功能性侧链((3-羟丙基)-三甲基-,(3-氰基丙基)-三甲基-,丁基三甲基-,(5-氰基戊基)-三甲基和己基-合成与相同的阴离子(双(三氟甲烷)磺酰胺基)的三甲基),并适用于IL /超临界二氧化碳(scCO(2))双相系统中的南极假丝酵母脂肪酶B(CALB)催化的酯合成。被测定。系统的催化效率已被分析为酶性质和传质现象标准的函数。首先,测试了这些ILs作为酶促反应介质的适用性,用于外消旋苯乙醇的动力学拆分。发现所有IL都是适合酶催化的介质,对于(5-氰基戊基)-三甲基铵获得了最佳的催化参数(5.3U / mg比活性,94.9%的选择性)。其次,在50℃下于50天的时间内研究所有IL的酶稳定性,并通过两步动力学失活模型分析数据。已显示所有IL对己烷均起稳定剂的作用,使失活自由能增加(至25 kJ / mol蛋白),并延长了酶的半衰期(2000倍)。 ,与观察到的阳离子烷基侧链疏水性增加(通过Hansen溶解度参数6测得)一致。通过在阳离子中使用两个具有不同疏水性的不同​​CALB-IL系统,连续过程在scCO(2)中合成六种不同的短链烷基酯(乙酸丁酯,丙酸丁酯,丁酸丁酯,丙酸己酯,丁酸己酯和丙酸辛酯)在10MPa和50℃下进行。这两个速率限制参数(合成活性和scCO(2)-ILs传质现象)与ILs-烷基链和试剂的德尔塔参数有关。

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