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首页> 外文期刊>Bioprocess and Biosystems Engineering >Plasmid DNA primary recovery from E-coli lysates by depth bed microfiltration
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Plasmid DNA primary recovery from E-coli lysates by depth bed microfiltration

机译:通过深度床微滤从大肠杆菌裂解物中初步回收质粒DNA

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Recently, several studies have been published on the application of plasmid DNA (pDNA) in gene therapy and vaccine production. The bioprocess to obtain pDNA involves the steps of fermentation, primary recovery, secondary recovery and final purification. The pDNA primary recovery, which is the key step to the rest of the process, includes biomass separation, alkaline lysis and clarification of the lysate. In this work, the clarification by depth bed microfiltration of lysates of E. coli DH5 alpha containing the plasmid pVAX1-NH36 was investigated. The studies were conducted using filter capsules with nominal 8.0 A mu m pore size using fluxes of 0.0027 and 0.004 cm(3)/(cm(2)-s). The results were compared with the conventional clarification by centrifugation. A fiber coating model was used to describe the behavior of the microfiltration system. A 99 % of solids elimination of the lysates was achieved with depth bed filtration method. The removed solids occupied 23 and 43 % (for 4 and 6 cm(3)/min, respectively) of the void volume of the depth bed microfiltration capsule since an early breakthrough curve is characteristic of these processes. The depth bed microfiltration process for removal of solids from the cell lysate showed competitive results compared to clarification by centrifugation.
机译:最近,已经发表了一些关于质粒DNA(pDNA)在基因治疗和疫苗生产中的应用的研究。获得pDNA的生物过程涉及发酵,一级回收,二级回收和最终纯化的步骤。 pDNA的初步回收是其余过程的关键步骤,包括生物质分离,碱裂解和裂解物的澄清。在这项工作中,研究了通过深床微滤对含有质粒pVAX1-NH36的大肠杆菌DH5α裂解物的澄清。该研究使用孔径为8.0 Aμm的滤膜胶囊进行,通量为0.0027和0.004 cm(3)/(cm(2)-s)。通过离心将结果与常规澄清进行比较。纤维涂层模型用于描述微滤系统的行为。用深度床过滤方法可实现99%的固体消除裂解物。由于早期穿透曲线是这些过程的特征,因此去除的固体占据了深床微滤胶囊的空隙体积的23%和43%(分别为4和6 cm(3)/ min)。与通过离心澄清相比,用于从细胞裂解物中去除固体的深床微滤工艺显示出竞争性结果。

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