Food Process Engineering Group, Wageningen University, P.O. Box 8129, 6700 EV, Wageningen, The Netherlands.
Appl Biochem Biotechnol. 2013 May;170(2):340-58. doi: 10.1007/s12010-013-0181-7. Epub 2013 Mar 23.
A β-galactosidase preparation from Bacillus circulans consists of four isoforms called β-gal-A, β-gal-B, β-gal-C, and β-gal-D. These isoforms differ in lactose hydrolysis and galacto-oligosaccharide (GOS) synthesis at low substrate concentrations. For this reason, using a selection of the isoforms may be relevant for GOS production, which is typically done at high substrate concentrations. At initial lactose concentrations in between 0.44 % and 0.68 % (w/w), β-gal-A showed the least oligosaccharide formation, followed by β-gal-B and β-gal-C; most oligosaccharides were formed by β-gal-D. The differences in behavior were confirmed by studying the thermodynamics of lactose conversion with isothermal titration calorimetry since especially β-gal-A showed a different profile than the other isoforms. Also during the conversion of allolactose and 4-galactosyllactose at 0.44 % and 0.61 % (w/w), respectively, β-gal-A and β-gal-D showed clear differences. In contrast to above findings, the selectivity of the isoforms did hardly differ at an initial lactose concentration of 30 % (w/w), except for a slightly higher production of galactose with β-gal-A. These differences were hypothesized to be related to the different accessibility of the active sites of the isoforms for different-sized reactants. The initial GOS formation rates of the isoforms indicate that β-gal-A and β-gal-B are the best isoforms for GOS production at high lactose concentrations.
一种来自环状芽孢杆菌的β-半乳糖苷酶制剂由四种同工酶组成,分别称为β-半乳糖苷酶-A、β-半乳糖苷酶-B、β-半乳糖苷酶-C 和 β-半乳糖苷酶-D。这些同工酶在低底物浓度下的乳糖水解和半乳糖低聚糖(GOS)合成方面存在差异。因此,选择使用这些同工酶中的一种可能与 GOS 的生产有关,GOS 的生产通常在高底物浓度下进行。在初始乳糖浓度在 0.44%和 0.68%(w/w)之间时,β-半乳糖苷酶-A 显示出最少的寡糖形成,其次是β-半乳糖苷酶-B 和β-半乳糖苷酶-C;β-半乳糖苷酶-D 形成最多的寡糖。通过等温滴定微量热法研究乳糖转化的热力学,证实了这些同工酶之间的行为差异,因为β-半乳糖苷酶-A 与其他同工酶的表现不同。此外,在分别为 0.44%和 0.61%(w/w)的别乳糖和 4-半乳糖基乳糖的转化过程中,β-半乳糖苷酶-A 和β-半乳糖苷酶-D 也表现出明显的差异。与上述发现相反,除了β-半乳糖苷酶-A 产生的半乳糖量略高外,同工酶的选择性在初始乳糖浓度为 30%(w/w)时几乎没有差异。这些差异被假设与同工酶的不同活性位点对不同大小的反应物的不同可及性有关。同工酶的初始 GOS 形成速率表明,β-半乳糖苷酶-A 和β-半乳糖苷酶-B 是高乳糖浓度下生产 GOS 的最佳同工酶。