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Open AccessJournal ArticleDOI

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

TLDR
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 Pichia pastoris toward optimizing biop rocesses based on the results obtained in chemostat cultures.
Abstract
The methylotrophic yeast Pichia pastoris (Komagataella phaffii) 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 13C-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 Pichia pastoris 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.

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Citations
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Systems-level organization of yeast methylotrophic lifestyle

TL;DR: It is found that the entire methanol assimilation pathway is localized to peroxisomes rather than employing part of the cytosolic pentose phosphate pathway for xylulose-5-phosphate regeneration, illustrating how concerted interpretation of multiple levels of systems biology data can contribute to elucidation of yet unknown cellular pathways and revolutionize the understanding of cellular biology.

Effect of Plasmid design and type of integration event on recombinant protein expression in Pichia pastoris

TL;DR: In this paper, the influence of ectopic integration by high throughput screening of >700 transformants and whole-genome sequencing of 27 transformants was investigated by different vector designs and linearization approaches.
Journal ArticleDOI

Pichia pastoris ( Komagataella phaffii ) as a Cost-Effective Tool for Vaccine Production for Low- and Middle-Income Countries (LMICs).

TL;DR: A review of the latest developments in Pichia pastoris from cell engineering and design to industrial production systems with focus on vaccine development and with reference to specific key case studies is presented in this paper.
Journal ArticleDOI

Strategies for Heterologous Expression, Synthesis, and Purification of Animal Venom Toxins

TL;DR: This review presents the strategies that can be used to express toxins in bacteria, yeast, insect cells, or mammalian cells, as well as synthetic approaches that do not involve cells, such as cell-free biosynthesis and peptide synthesis.
References
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Journal ArticleDOI

Absolute protein expression profiling estimates the relative contributions of transcriptional and translational regulation

TL;DR: Using APEX, it is demonstrated that 73% of the variance in yeast protein abundance is explained by mRNA abundance, with the number of proteins per mRNA log-normally distributed about ∼5,600 (∼540 in E. coli) protein molecules/mRNA.
Journal ArticleDOI

Recent advances in the expression of foreign genes in Pichia pastoris

TL;DR: The Pichia pastoris heterologous gene expression system has been utilized to produce attractive levels of a variety of intracellular and extracellular proteins of interest and improvements in understanding and application have improved its utility even further.
Journal ArticleDOI

Protein expression in Pichia pastoris: recent achievements and perspectives for heterologous protein production.

TL;DR: This review refers to established tools in protein expression in P. pastoris and highlights novel developments in the areas of expression vector design, host strain engineering and screening for high-level expression strains.
Journal ArticleDOI

BiGG Models: A platform for integrating, standardizing and sharing genome-scale models.

TL;DR: BiGG Models is presented, a completely redesigned Biochemical, Genetic and Genomic knowledge base that contains more than 75 high-quality, manually-curated genome-scale metabolic models that will facilitate diverse systems biology studies and support knowledge-based analysis of diverse experimental data.
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