Novo Nordisk Center for Biosustainability, Department of Chemical & Biological Engineering, Chalmers University of Technology, SE412 96 Gothenburg, Sweden.
Curr Opin Biotechnol. 2012 Dec;23(6):965-71. doi: 10.1016/j.copbio.2012.03.011. Epub 2012 Apr 13.
Since the approval of recombinant insulin from Escherichia coli for its clinical use in the early 1980s, the amount of recombinant pharmaceutical proteins obtained by microbial fermentations has significantly increased. The recent advances in genomics together with high throughput analysis techniques (the so-called-omics approaches) and integrative approaches (systems biology) allow the development of novel microbial cell factories as valuable platforms for large scale production of therapeutic proteins. This review summarizes the main achievements and the current situation in the field of recombinant therapeutics using yeast Saccharomyces cerevisiae as a model platform, and discusses the future potential of this platform for production of blood proteins and substitutes.
自 20 世纪 80 年代初批准大肠杆菌重组胰岛素用于临床以来,通过微生物发酵获得的重组药物蛋白的数量显著增加。基因组学的最新进展以及高通量分析技术(所谓的“组学”方法)和综合方法(系统生物学)使得新型微生物细胞工厂的开发成为治疗性蛋白大规模生产的有价值的平台。本文综述了利用酿酒酵母作为模型平台进行重组治疗的主要成就和现状,并讨论了该平台生产血液蛋白和替代品的未来潜力。