4.7 Article

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

期刊

APPLIED MICROBIOLOGY AND BIOTECHNOLOGY
卷 105, 期 24, 页码 9137-9151

出版社

SPRINGER
DOI: 10.1007/s00253-021-11697-x

关键词

Recombinant human insulin; Inclusion body; Proinsulin recovery and purification; Insulin purification; Cation exchange chromatography; Desalting

资金

  1. Bio-Rad Laboratories (USA)
  2. Agency for Science, Technology and Research (A*STAR)

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The new and efficient purification process for recombinant human insulin production significantly improved efficiency and achieved higher recovery and purity by exploring new resins and optimizing purification steps. The process is more economical and practical than conventional methods, especially when using Nuvia HR-S cation exchanger.
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.

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