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新型且高效的大肠杆菌重组人胰岛素纯化工艺。

New and efficient purification process for recombinant human insulin produced in Escherichia coli.

机构信息

Downstream Processing Group, Bioprocessing Technology Institute, A*STAR Research Entities, Singapore, Singapore.

Microbial Cell Bioprocessing Group, Bioprocessing Technology Institute, A*STAR Research Entities, Singapore, Singapore.

出版信息

Appl Microbiol Biotechnol. 2021 Dec;105(24):9137-9151. doi: 10.1007/s00253-021-11697-x. Epub 2021 Nov 25.

Abstract

A new and efficient purification process for recombinant human insulin production was developed by exploring new resins and optimizing purification steps from E. coli inclusion body washing to insulin polishing. A combined additives inclusion body wash protocol drastically improved efficiency in clarifying ZZ-proinsulin samples. ZZ-proinsulin recovery increased three-fold under optimized solubilization and sulfitolysis incubation temperature and duration. Desalting with Bio-Gel P4 and P6 resulted in higher sample loading and product recovery compared to conventional resins. A higher recovery (96%) and purity (81%) of ZZ-proinsulin were achievable with the Nuvia S cation exchanger for proinsulin purification compared to a reported process using expensive affinity chromatography resin. As the first step for insulin purification, process scale-up is more economical and practical when Nuvia HR-S cation exchanger was used instead of commonly used reversed-phase chromatography. Nuvia HR-S was highly effective in removing ZZ fusion protein (90% removal) after enzymatic cleavage, although ZZ fusion protein has a very close theoretical pI to human insulin, which was supposedly challenging to be removed by cation exchange chromatography. Also, insulin can be eluted at a lower ethanol % using Nuvia HR-S compared to other reported processes and is thus more environmentally sustainable. Recombinant human insulin was obtained with over 98% purity in just a single reversed-phase polishing step, which is comparable to the reference standard. The process workflow presented here can be potentially applied for the development of purification workflow for insulin analogs or other peptide products derived from E. coli inclusion body.Key points• Drastic efficiency improvement for inclusion body wash with combined additives.• High recovery of proinsulin purification with high capacity cation exchange resin.• Effective removal of fusion tag at lower ethanol % with high-resolution resin.

摘要

一种新的、高效的重组人胰岛素生产纯化工艺,通过探索新型树脂和优化从大肠杆菌包涵体洗涤到胰岛素精制剂的纯化步骤来开发。一种组合添加剂包涵体洗涤方案极大地提高了 ZZ-胰岛素样品的澄清效率。在优化的溶解和亚硫酸氢盐酶解孵育温度和时间下,ZZ-胰岛素回收率提高了三倍。与传统树脂相比,使用 Bio-Gel P4 和 P6 进行脱盐可实现更高的样品加载和产物回收率。与使用昂贵的亲和层析树脂的报道工艺相比,Nuvia S 阳离子交换剂可实现更高的 ZZ-胰岛素回收率(96%)和纯度(81%)用于胰岛素前体的纯化。作为胰岛素纯化的第一步,当使用 Nuvia HR-S 阳离子交换剂代替常用的反相色谱法时,工艺放大更经济实用。Nuvia HR-S 在后酶切时非常有效地去除 ZZ 融合蛋白(去除 90%),尽管 ZZ 融合蛋白与人胰岛素的理论等电点非常接近,这按理说是难以通过阳离子交换色谱去除的。此外,与其他报道的工艺相比,Nuvia HR-S 可以在较低的乙醇%下洗脱胰岛素,因此更具环境可持续性。仅通过单一的反相抛光步骤即可获得纯度超过 98%的重组人胰岛素,与参比标准相当。本文提出的工艺流程可潜在地应用于胰岛素类似物或其他源自大肠杆菌包涵体的肽产品的纯化流程开发。

关键点

• 组合添加剂包涵体洗涤效率大幅提高。

• 高容量阳离子交换树脂实现高胰岛素前体回收率。

• 使用高分辨率树脂在较低乙醇%下有效去除融合标签。

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New and efficient purification process for recombinant human insulin produced in Escherichia coli.
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