Chen Rachel
School of Chemical and Biomolecular Engineering, Georgia Institute of Technology, 311 Ferst Drive, NW, Atlanta, GA, 30332-0100, USA.
Microb Cell Fact. 2015 Dec 9;14:197. doi: 10.1186/s12934-015-0389-z.
In the first science review on the then nascent Metabolic Engineering field in 1991, Dr. James E. Bailey described how improving erythropoietin (EPO) glycosylation can be achieved via metabolic engineering of Chinese hamster ovary (CHO) cells. In the intervening decades, metabolic engineering has brought sweet successes in glycoprotein engineering, including antibodies, vaccines, and other human therapeutics. Today, not only eukaryotes (CHO, plant, insect, yeast) are being used for manufacturing protein therapeutics with human-like glycosylation, newly elucidated bacterial glycosylation systems are enthusiastically embraced as potential breakthrough to revolutionize the biopharmaceutical industry. Notwithstanding these excitement in glycoprotein, the sweet metabolic engineering reaches far beyond glycoproteins. Many different types of oligo- and poly-saccharides are synthesized with metabolically engineered cells. For example, several recombinant hyaluronan bioprocesses are now in commercial production, and the titer of 2'-fucosyllactose, the most abundant fucosylated trisaccharide in human milk, reaches over 20 g/L with engineered E. coli cells. These successes represent only the first low hanging fruits, which have been appreciated scientifically, medically and fortunately, commercially as well. As one of the four building blocks of life, sugar molecules permeate almost all aspects of life. They are also unique in being intimately associated with all major types of biopolymers (including DNA/RNA, proteins, lipids) meanwhile they stand alone as bioactive polysaccharides, or free soluble oligosaccharides. As such, all sugar moieties in biological components, small or big and free or bound, are important targets for metabolic engineering. Opportunities abound at the interface of glycosciences and metabolic engineering. Continued investment and successes in this branch of metabolic engineering will make vastly diverse sugar-containing molecules (a.k.a. glycoconjugates) available for biomedical applications, sustainable technology development, and as invaluable tools for basic scientific research. This short review focuses on the most recent development in the field, with emphasis on the synthesis technology for glycoprotein, polysaccharide, and oligosaccharide.
在1991年对当时新兴的代谢工程领域的首次科学综述中,詹姆斯·E·贝利博士描述了如何通过对中国仓鼠卵巢(CHO)细胞进行代谢工程来改善促红细胞生成素(EPO)的糖基化。在随后的几十年里,代谢工程在糖蛋白工程方面取得了巨大成功,包括抗体、疫苗和其他人类治疗药物。如今,不仅真核生物(CHO、植物、昆虫、酵母)被用于生产具有类人糖基化的蛋白质治疗药物,新发现的细菌糖基化系统也被积极视为可能彻底改变生物制药行业的潜在突破。尽管糖蛋白领域有这些令人兴奋的进展,但甜蜜的代谢工程远远超出了糖蛋白的范畴。许多不同类型的寡糖和多糖都是用代谢工程改造的细胞合成的。例如,几种重组透明质酸生物工艺现已投入商业生产,用工程化大肠杆菌细胞生产的2'-岩藻糖基乳糖(人乳中最丰富的岩藻糖基化三糖)的产量超过20 g/L。这些成功仅仅代表了最初的低垂果实,它们在科学、医学以及幸运的是在商业上都得到了认可。作为生命的四大基本组成部分之一,糖分子几乎渗透到生命的各个方面。它们还具有独特之处,即与所有主要类型的生物聚合物(包括DNA/RNA、蛋白质、脂质)密切相关,同时又作为生物活性多糖或游离可溶性寡糖独立存在。因此,生物成分中所有大小、游离或结合的糖部分都是代谢工程的重要目标。糖科学与代谢工程的交叉领域机遇众多。在这一代谢工程分支上持续的投入和成功将使大量不同的含糖分子(即糖缀合物)可用于生物医学应用、可持续技术开发,并作为基础科学研究的宝贵工具。本简短综述聚焦于该领域的最新进展,重点介绍糖蛋白、多糖和寡糖的合成技术。