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Cost Comparison of Protein Capture from Cultivation Broths by Expanded and Packed Bed Adsorption

机译:成本比较蛋白质的捕捉通过扩大和填充床培养的培养基配方吸附

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摘要

In the downstream processing of recombinant protein production, the reduction of unit operations required for product capture and purification, is of the utmost priority due to its cost diminishing effect. In this regard, target protein capture from cell suspensions in a fluidized bed of affinity particles with different sizes (expanded bed adsorption (EBA) with classified particles), presents an efficient tool since EBA may substitute cell disintegration, separation by centrifugation or filtration, and packed bed adsorption. However, as illustrated by experiments with the BSA/yeast cells system, the entire broth processing used in EBA also has detrimental influences due to the cell (or cell debris) binding on the affinity carrier. In particular, external mass transfer may become more dominant, and the lifetime of the affinity particles may reduce as a result of other cleaning procedures. Using simulations performed with a commercial software package, the cost superiority of alternate process routes (EBA or packed bed adsorption with preceding steps) can be evaluated. This elucidates the favorable application range for each route.
机译:在重组的下游加工蛋白质的生产,减少单位捕获和操作所需的产品净化,由于是最大的重点其成本递减效应。目标蛋白质从细胞悬浊液捕获粒子流化床的亲和力不同大小(膨胀床吸附(EBA)与分类粒子),提出了一种高效工具因为EBA可能替代细胞通过离心分离或解体,分离过滤和填充床吸附。说明了实验与BSA /酵母细胞系统,整个汤处理中使用由于EBA也有不利影响单元(或细胞碎片)绑定关联母舰。可能越来越占主导地位,的生命周期亲和力粒子可能会减少的结果其他清洁程序。商业软件包,执行成本优势的替代工艺路线(EBA或填充床吸附与前面的步骤)可以被评估。应用范围为每个路线。

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