Guan Ningzi, Chen Rachel
School of Chemical and Biomolecular Engineering, Georgia Institute of Technology, Atlanta-30332, GA, United States.
Recent Pat Biotechnol. 2018;12(2):92-100. doi: 10.2174/1872208311666170531110721.
Human milk oligosaccharide (HMO) is a third most abundant component in breast milk. HMOs are molecules naturally tailored to the need of an infant. They protect infants from diseases, foster healthy gastrointestinal systems, reinforce fledgling immune function, and promote early brain development. Supplement HMOs to infant formula, which lack this critical element, would substantially improve the function of formula. Overwhelming evidence also indicate that HMOs can be used for the treatment of arthritis and related autoimmune disease, and inhibition of bacteria adhesion or as potential prebiotics. The prospect of using HMO in these applications has stimulated worldwide interest in developing synthesis technology for these valuable products.
As the quantities extracted from human milk are limited, and chemical synthesis methods are time-consuming, costly, and complex, biotechnological approach, involving either enzyme catalysis or metabolically engineered bacteria is preferred. In this review, we highlight the most recent advances in the synthesis technologies, as disclosed in patents and patent applications, and analyze these technologies against those reported in literatures.
Significant progress has been made over the past decade, especially in whole-cell biocatalysis for smaller HMOs. Significant challenges remain for larger and more complex HMOs.
人乳寡糖(HMO)是母乳中第三丰富的成分。HMO是天然适应婴儿需求的分子。它们保护婴儿免受疾病侵害,促进健康的胃肠道系统,增强初建的免疫功能,并促进早期大脑发育。在缺乏这种关键成分的婴儿配方奶粉中添加HMO将显著改善配方奶粉的功能。大量证据还表明,HMO可用于治疗关节炎和相关自身免疫性疾病,抑制细菌粘附或作为潜在的益生元。在这些应用中使用HMO的前景激发了全球对开发这些有价值产品合成技术的兴趣。
由于从人乳中提取的量有限,且化学合成方法耗时、成本高且复杂,因此涉及酶催化或代谢工程细菌的生物技术方法更受青睐。在本综述中,我们重点介绍了专利和专利申请中披露的合成技术的最新进展,并将这些技术与文献中报道的技术进行了分析。
在过去十年中取得了重大进展,特别是在较小HMO的全细胞生物催化方面。对于更大、更复杂的HMO,仍然存在重大挑战。