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连续培养作为一种实现细胞工厂合理生物工艺开发的工具。

Continuous Cultivation as a Tool Toward the Rational Bioprocess Development With Cell Factory.

作者信息

Nieto-Taype Miguel Angel, Garcia-Ortega Xavier, Albiol Joan, Montesinos-Seguí José Luis, Valero Francisco

机构信息

Department of Chemical, Biological and Environmental Engineering, School of Engineering, Universitat Autònoma de Barcelona, Bellaterra, Spain.

出版信息

Front Bioeng Biotechnol. 2020 Jun 25;8:632. doi: 10.3389/fbioe.2020.00632. eCollection 2020.

Abstract

The methylotrophic yeast () is currently considered one of the most promising hosts for recombinant protein production (RPP) and metabolites due to the availability of several tools to efficiently regulate the recombinant expression, its ability to perform eukaryotic post-translational modifications and to secrete the product in the extracellular media. The challenge of improving the bioprocess efficiency can be faced from two main approaches: the strain engineering, which includes enhancements in the recombinant expression regulation as well as overcoming potential cell capacity bottlenecks; and the bioprocess engineering, focused on the development of rational-based efficient operational strategies. Understanding the effect of strain and operational improvements in bioprocess efficiency requires to attain a robust knowledge about the metabolic and physiological changes triggered into the cells. For this purpose, a number of studies have revealed chemostat cultures to provide a robust tool for accurate, reliable, and reproducible bioprocess characterization. It should involve the determination of key specific rates, productivities, and yields for different C and N sources, as well as optimizing media formulation and operating conditions. Furthermore, studies along the different levels of systems biology are usually performed also in chemostat cultures. Transcriptomic, proteomic and metabolic flux analysis, using different techniques like differential target gene expression, protein description and C-based metabolic flux analysis, are widely described as valued examples in the literature. In this scenario, the main advantage of a continuous operation relies on the quality of the homogeneous samples obtained under steady-state conditions, where both the metabolic and physiological status of the cells remain unaltered in an all-encompassing picture of the cell environment. This contribution aims to provide the state of the art of the different approaches that allow the design of rational strain and bioprocess engineering improvements in toward optimizing bioprocesses based on the results obtained in chemostat cultures. Interestingly, continuous cultivation is also currently emerging as an alternative operational mode in industrial biotechnology for implementing continuous process operations.

摘要

由于有多种工具可有效调控重组表达,且具有进行真核生物翻译后修饰以及在细胞外培养基中分泌产物的能力,甲基营养型酵母目前被认为是重组蛋白生产(RPP)和代谢物最有前景的宿主之一。提高生物过程效率面临的挑战可以从两个主要途径来应对:菌株工程,包括增强重组表达调控以及克服潜在的细胞容量瓶颈;以及生物过程工程,专注于开发基于理性的高效操作策略。要理解菌株和操作改进对生物过程效率的影响,需要深入了解细胞内引发的代谢和生理变化。为此,许多研究表明恒化器培养为准确、可靠和可重复的生物过程表征提供了一个强大的工具。这应包括确定不同碳源和氮源的关键比速率、生产率和产量,以及优化培养基配方和操作条件。此外,通常也在恒化器培养中进行不同系统生物学水平的研究。转录组学、蛋白质组学和代谢通量分析,使用诸如差异靶基因表达、蛋白质描述和基于碳的代谢通量分析等不同技术,在文献中被广泛描述为有价值的例子。在这种情况下,连续操作的主要优点在于在稳态条件下获得的均匀样品的质量,此时细胞的代谢和生理状态在细胞环境的全面图景中保持不变。本论文旨在提供不同方法的最新进展,这些方法能够基于在恒化器培养中获得的结果,设计合理的菌株和生物过程工程改进措施,以优化毕赤酵母的生物过程。有趣的是,连续培养目前也正在成为工业生物技术中实施连续过程操作的一种替代操作模式。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f917/7330098/34d4720b2743/fbioe-08-00632-g0001.jpg

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