Vikbjerg Anders F, Mu Huiling, Xu Xuebing
BioCentrum-DTU, Technical University of Denmark, DK 2800 Lyngby, Denmark.
Biotechnol Prog. 2005 Mar-Apr;21(2):397-404. doi: 10.1021/bp049633y.
Lipase-catalyzed acidolysis was examined for the production of structured phospholipids in a hexane system. In a practical operation of the reaction system, the formation of lyso-phospholipids from hydrolysis is often a serious problem, as demonstrated from previous studies. A clear elucidation of the issue and optimization of the system are essential for the practical applications in reality. The effects of enzyme dosage, reaction temperature, solvent amount, reaction time, and substrate ratio were optimized in terms of the acyl incorporation, which led to the products, and lyso-phospholipids formed by hydrolysis, which led to the low yields. The biocatalyst used was the commercial immobilized lipase Lipozyme TL IM and substrates used were phosphatidylcholine (PC) from soybean and caprylic acid. A response surface design was used to evaluate the influence of selected parameters and their relationships on the incorporation of caprylic acid and the corresponding recovery of PC. Incorporation of fatty acids increased with increasing enzyme dosage, reaction temperature, solvent amount, reaction time, and substrate ratio. Enzyme dosage had the most significant effect on the incorporation, followed by reaction time, reaction temperature, solvent amount, and substrate ratio. However the parameters had also a negative influence on the PC recovery. Solvent amount had the most negative effect on recovery, followed by enzyme dosage, temperature, and reaction time. Individually substrate ratio had no significant effect on the PC recovery. Interactions were observed between different parameters. On the basis of the models, the reaction was optimized for the maximum incorporation and maximum PC recovery. With all of the considerations, the optimal conditions are recommended as enzyme dosage 29%, reaction time 50 h, temperature 54 degrees C, substrate ratio 15 mol/mol caprylic acid/PC, and 5 mL of hexane per 3 g substrate. No additional water is necessary. Under these conditions, an incorporation of caprylic acid up to 46% and recovery of PC up to 60% can be obtained from the prediction. The prediction was confirmed from the verification experiments.
研究了脂肪酶催化酸解反应在己烷体系中生产结构化磷脂的过程。在反应体系的实际操作中,如先前研究所表明的,水解产生溶血磷脂通常是一个严重问题。明确阐明该问题并优化体系对于实际应用至关重要。从辛酸掺入量以及水解产生的溶血磷脂(导致产率较低)方面,对酶用量、反应温度、溶剂量、反应时间和底物比例的影响进行了优化。所使用的生物催化剂是商业固定化脂肪酶Lipozyme TL IM,所用底物是大豆磷脂酰胆碱(PC)和辛酸。采用响应面设计来评估所选参数及其相互关系对辛酸掺入量和相应PC回收率的影响。脂肪酸的掺入量随着酶用量、反应温度、溶剂量、反应时间和底物比例的增加而增加。酶用量对掺入量影响最为显著,其次是反应时间、反应温度、溶剂量和底物比例。然而,这些参数对PC回收率也有负面影响。溶剂量对回收率的负面影响最大,其次是酶用量、温度和反应时间。单独来看,底物比例对PC回收率没有显著影响。不同参数之间存在相互作用。基于这些模型,对反应进行了优化以实现最大掺入量和最大PC回收率。综合所有因素,推荐的最佳条件为:酶用量29%、反应时间50小时、温度54℃、底物比例为15摩尔/摩尔辛酸/PC,每3克底物使用5毫升己烷。无需额外加水。在这些条件下,根据预测可获得高达46%的辛酸掺入量和高达60% 的PC回收率。验证实验证实了该预测。