Zhang Jinyou, Reddy Jayanthi, Buckland Barry, Greasham Randolph
Bioprocess R&D, Merck Research Laboratories, PO Box 2000, Rahway, New Jersey 07065, USA.
Biotechnol Bioeng. 2003 Jun 20;82(6):640-52. doi: 10.1002/bit.10608.
Yeast extract (YE) is commonly used as a key component in the complex media for industrial fermentations. However, the lot-to-lot variation of this raw material frequently requires extensive "use testing" of many lots to identify only the few that support desired fermentation performance. Through extensive fermentation studies and chemical analyses, we have identified adenine and two metabolizable carbon sources, trehalose and lactate, as the principle components in YE that affect the production of a recombinant protein antigen by a yeast strain. Adenine is required for culture growth and the relationship between biomass and measured adenine can be expressed by a Michaelis-Menten model, while the slowly metabolized trehalose serves to maintain the energy supply to the continued antigen synthesis. The rapidly utilized lactate exerts an indirect positive effect by sparing some of the accumulated ethanol from being consumed for growth to being utilized in the product formation. The effects of these YE components are mutually dependent. Based on the database generated from 40 lots at laboratory scale, a relatively high level of carbon sources in YE (trehalose plus lactate, >9.5% w/w) and an intermediate level of adenine (0.14-0.24% w/w) appear to be the minimal requirement of a good lot for this recombinant yeast fermentation. Many poor lots were improved in lab fermenters by rational supplementation of trehalose, lactate, or adenine to compensate for their insufficiencies. At the large production scale, predictions based on adenine and trehalose/lactate contents in various YE lots used correlated reasonably well with culture growth and antigen yield, illustrating the feasibility of such a simple chemical/biochemical analysis as a rapid and reliable initial screening tool. Without incurring any compositional change to an established manufacturing medium, this study demonstrates an effective approach to achieve consistency in fermentations employing complex nutrients and to improve fermentation productivities supported by suboptimal lots of raw material.
酵母提取物(YE)通常用作工业发酵复合培养基中的关键成分。然而,这种原材料的批次间差异常常需要对许多批次进行广泛的“使用测试”,以找出仅有的少数能支持理想发酵性能的批次。通过广泛的发酵研究和化学分析,我们已确定腺嘌呤以及两种可代谢碳源海藻糖和乳酸,是YE中影响酵母菌株生产重组蛋白抗原的主要成分。培养生长需要腺嘌呤,生物量与测得的腺嘌呤之间的关系可用米氏模型表示,而代谢缓慢的海藻糖则用于维持持续抗原合成的能量供应。快速利用的乳酸通过节省部分积累的乙醇来发挥间接的积极作用,否则这些乙醇会用于生长而非产物形成。这些YE成分的作用相互依赖。基于实验室规模40个批次的数据,YE中相对较高水平的碳源(海藻糖加乳酸,>9.5% w/w)和中等水平的腺嘌呤(0.14 - 0.24% w/w)似乎是该重组酵母发酵优质批次的最低要求。许多质量差的批次在实验室发酵罐中通过合理补充海藻糖、乳酸或腺嘌呤来弥补其不足而得到改善。在大规模生产中,基于所用各种YE批次中腺嘌呤和海藻糖/乳酸含量的预测与培养生长和抗原产量具有合理的相关性,这说明了这种简单的化学/生化分析作为快速可靠的初步筛选工具的可行性。在不对既定生产培养基进行任何成分改变的情况下,本研究展示了一种有效方法,可实现使用复杂营养物发酵的一致性,并提高由次优原材料批次支持的发酵生产率。