Institute of Microbiology, University of Stuttgart, Allmandring 31, D-70569 Stuttgart, Germany.
Institute of Microbiology, University of Stuttgart, Allmandring 31, D-70569 Stuttgart, Germany.
J Biotechnol. 2017 Sep 20;258:79-91. doi: 10.1016/j.jbiotec.2017.07.030. Epub 2017 Jul 29.
Human milk oligosaccharides (HMO) are almost unique constituents of breast milk and are not found in appreciable amounts in cow milk. Due to several positive aspects of HMO for the development, health, and wellbeing of infants, production of HMO would be desirable. As a result, scientists from different disciplines have developed methods for the preparation of single HMO compounds. Here, we review approaches to HMO preparation by (chemo-)enzymatic syntheses or by whole-cell biotransformation with recombinant bacterial cells. With lactose as acceptor (in vitro or in vivo), fucosyltransferases can be used for the production of 2'-fucosyllactose, 3-fucosyllactose, or more complex fucosylated core structures. Sialylated HMO can be produced by sialyltransferases and trans-sialidases. Core structures as lacto-N-tetraose can be obtained by glycosyltransferases from chemical donor compounds or by multi-enzyme cascades; recent publications also show production of lacto-N-tetraose by recombinant Escherichia coli bacteria and approaches to obtain fucosylated core structures. In view of an industrial production of HMOs, the whole cell biotransformation is at this stage the most promising option to provide human milk oligosaccharides as food additive.
人乳寡糖(HMO)是母乳中几乎独一无二的成分,在牛奶中含量很少。由于 HMO 对婴儿的发育、健康和幸福有几个积极的方面,因此希望生产 HMO。为此,来自不同学科的科学家已经开发出了用于制备单一 HMO 化合物的方法。在这里,我们回顾了通过(化学)酶合成或使用重组细菌细胞进行全细胞生物转化来制备 HMO 的方法。以乳糖为受体(体外或体内),可以使用岩藻糖基转移酶生产 2'-岩藻糖基乳糖、3-岩藻糖基乳糖或更复杂的岩藻糖基核心结构。唾液酸转移酶和转唾液酸酶可产生唾液酸化的 HMO。通过糖苷转移酶可以从化学供体化合物或多酶级联获得核心结构如乳-N-四糖;最近的出版物还展示了通过重组大肠杆菌生产乳-N-四糖的方法以及获得岩藻糖基核心结构的方法。鉴于 HMO 的工业化生产,在现阶段,全细胞生物转化是提供人乳寡糖作为食品添加剂的最有前途的选择。