Chen Su-Ching, Duan Kow-Jen
Department of Bioengineering, Tatung University, Taipei 104, Taiwan.
Int J Mol Sci. 2015 Jun 3;16(6):12499-512. doi: 10.3390/ijms160612499.
β-Galactosidase was immobilized on chitosan-coated magnetic Fe3O4 nanoparticles and was used to produce galactooligosaccharides (GOS) from lactose. Immobilized enzyme was prepared with or without the coupling agent, tris(hydroxymethyl)phosphine (THP). The two immobilized systems and the free enzyme achieved their maximum activity at pH 6.0 with an optimal temperature of 50 °C. The immobilized enzymes showed higher activities at a wider range of temperatures and pH. Furthermore, the immobilized enzyme coupled with THP showed higher thermal stability than that without THP. However, activity retention of batchwise reactions was similar for both immobilized systems. All the three enzyme systems produced GOS compound with similar concentration profiles, with a maximum GOS yield of 50.5% from 36% (w · v(-1)) lactose on a dry weight basis. The chitosan-coated magnetic Fe3O4 nanoparticles can be regenerated using a desorption/re-adsorption process described in this study.
β-半乳糖苷酶固定在壳聚糖包被的磁性Fe3O4纳米颗粒上,并用于从乳糖生产低聚半乳糖(GOS)。固定化酶的制备使用或不使用偶联剂三(羟甲基)膦(THP)。两种固定化体系和游离酶在pH 6.0、最佳温度50°C时达到最大活性。固定化酶在更宽的温度和pH范围内表现出更高的活性。此外,与未使用THP的固定化酶相比,使用THP的固定化酶表现出更高的热稳定性。然而,两种固定化体系在分批反应中的活性保留率相似。所有这三种酶系统产生的GOS化合物具有相似的浓度分布,以干重计,从36%(w·v(-1))乳糖中获得的最大GOS产率为50.5%。壳聚糖包被的磁性Fe3O4纳米颗粒可以使用本研究中描述的解吸/再吸附过程进行再生。