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自循环操作提高大肠杆菌中重组蛋白的产量。

Self-cycling operation increases productivity of recombinant protein in Escherichia coli.

机构信息

Department of Chemical Engineering, McGill University, Montreal, Quebec, Canada.

出版信息

Biotechnol Bioeng. 2012 Sep;109(9):2262-70. doi: 10.1002/bit.24492. Epub 2012 Mar 30.

Abstract

Self-cycling fermentation (SCF), a cyclical, semi-continuous process that induces cell synchrony, was incorporated into a recombinant protein production scheme. Escherichia coli CY15050, a lac(-) mutant lysogenized with temperature-sensitive phage λ modified to over-express β-galactosidase, was used as a model system. The production scheme was divided into two de-coupled stages. The host cells were cultured under SCF operation in the first stage before being brought to a second stage where protein production was induced. In the first stage, the host strain demonstrated a stable cycling pattern immediately following the first cycle. This reproducible pattern was maintained over the course of the experiments and a significant degree of cell synchrony was obtained. By growing cells using SCF, productivity increased 50% and production time decreased by 40% compared to a batch culture under similar conditions. In addition, synchronized cultures induced from the end of a SCF cycle displayed shorter lysis times and a more complete culture-wide lysis than unsynchronized cultures. Finally, protein synthesis was influenced by the time at which the lytic phase was induced in the cell life cycle. For example, induction of a synchronized culture immediately prior to cell division resulted in the maximum protein productivity, suggesting protein production can be optimized with respect to the cell life cycle using SCF.

摘要

自循环发酵(SCF)是一种周期性的半连续过程,可诱导细胞同步,被纳入重组蛋白生产方案中。大肠杆菌 CY15050 是一种带有温度敏感噬菌体 λ 的 lac(-)突变体溶原菌,该噬菌体经过修饰后可以过表达β-半乳糖苷酶,被用作模型系统。生产方案分为两个解耦阶段。在第一阶段,在进行蛋白质生产诱导之前,采用 SCF 操作对宿主细胞进行培养。在第一阶段,宿主菌株在第一轮之后立即表现出稳定的循环模式。这种可重复的模式在实验过程中得以维持,并获得了相当程度的细胞同步性。与在类似条件下进行批式培养相比,通过使用 SCF 培养细胞,生产力提高了 50%,生产时间减少了 40%。此外,与非同步培养物相比,从 SCF 周期结束时诱导的同步培养物显示出更短的裂解时间和更完整的全培养物裂解。最后,蛋白质合成受到细胞生命周期中诱导裂解阶段的时间的影响。例如,在细胞分裂前立即诱导同步培养物,可获得最大的蛋白质生产力,表明可以使用 SCF 根据细胞生命周期对蛋白质生产进行优化。

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