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Preparation of ACE-inhibitory peptides from milk protein in continuous enzyme membrane reactor with gradient dilution feeding substrate

机译:梯度稀释进料底物在连续酶膜反应器中由乳蛋白制备ACE抑制肽

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In this study, a novel method of gradient dilution feeding substrate (GDFS) was established to improve the yield of angiotensin-converting enzyme (ACE) inhibitory peptides from milk protein. The hydrolysis process stability, enzymatic efficiency and kinetics of the method were studied and compared with traditional feeding modes, viz., adding water after feeding substrate or constant concentration feeding substrate. Results showed that the GDFS mode achieved the highest membrane flux and lowest fluctuation of protein concentration in the reactor. Moreover, the GDFS maximized protein conversion rate, yield of peptides, and ACE-inhibitory activity, with their values of 67.58 %, 138.51 g/(g*Neutrase), and 0.74 mg/mL (IC50), respectively. In further study, the kinetic model of GDFS mode was successfully established with K m of 69.481 g/L and V-max of 0.752 g.L-1 min(-1). Based on the optimum condition of the kinetic model, the practical longest runtime was 720 min. Obtained results suggested that GDFS mode could be used as an alternative method in the preparation of high-yield bioactive peptides.
机译:在这项研究中,建立了一种新的梯度稀释进料底物(GDFS)方法,以提高牛奶蛋白中血管紧张素转化酶(ACE)抑制肽的产量。研究了该方法的水解过程稳定性,酶效率和动力学,并与传统的进料方式进行了比较,即在进料底物或恒浓度进料底物后加水。结果表明,GDFS模式在反应器中获得了最高的膜通量和最低的蛋白质浓度波动。此外,GDFS使蛋白质转化率,肽产量和ACE抑制活性最大化,其值分别为67.58%,138.51 g /(g * Neutrase)和0.74 mg / mL(IC50)。在进一步研究中,成功​​建立了GDFS模式的动力学模型,K m为69.481 g / L,V-max为0.752 g.L-1 min(-1)。根据动力学模型的最佳条件,实际最长运行时间为720分钟。所得结果表明,GDFS模式可以用作制备高产生物活性肽的替代方法。

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