Klein Tobias, Niklas Jens, Heinzle Elmar
Research Area Biochemical Engineering, Institute of Chemical Engineering, Vienna University of Technology, Gumpendorfer Strasse 1a, 1060, Vienna, Austria.
J Ind Microbiol Biotechnol. 2015 Mar;42(3):453-64. doi: 10.1007/s10295-014-1569-2. Epub 2015 Jan 6.
Metabolic bottlenecks play an increasing role in yeasts and mammalian cells applied for high-performance production of proteins, particularly of pharmaceutical ones that require complex posttranslational modifications. We review the present status and developments focusing on the rational metabolic engineering of such cells to optimize the supply chain for building blocks and energy. Methods comprise selection of beneficial genetic modifications, rational design of media and feeding strategies. Design of better producer cells based on whole genome-wide metabolic network analysis becomes increasingly possible. High-resolution methods of metabolic flux analysis for the complex networks in these compartmented cells are increasingly available. We discuss phenomena that are common to both types of organisms but also those that are different with respect to the supply chain for the production and secretion of pharmaceutical proteins.
代谢瓶颈在用于高效生产蛋白质(尤其是需要复杂翻译后修饰的药用蛋白质)的酵母和哺乳动物细胞中发挥着越来越重要的作用。我们综述了当前的研究现状和进展,重点关注对此类细胞进行合理的代谢工程改造,以优化构建模块和能量的供应链。方法包括选择有益的基因修饰、合理设计培养基和补料策略。基于全基因组代谢网络分析来设计更好的生产细胞变得越来越可行。用于这些具有区室化结构细胞中复杂网络的高分辨率代谢通量分析方法也越来越多。我们讨论了这两类生物体共有的现象,以及在药用蛋白质生产和分泌的供应链方面存在差异的现象。