A systems-level approach for metabolic engineering of yeast cell factories
Review article, 2012

The generation of novel yeast cell factories for production of high-value industrial biotechnological products relies on three metabolic engineering principles: design, construction, and analysis. In the last two decades, strong efforts have been put on developing faster and more efficient strategies and/or technologies for each one of these principles. For design and construction, three major strategies are described in this review: (1) rational metabolic engineering; (2) inverse metabolic engineering; and (3) evolutionary strategies. Independent of the selected strategy, the process of designing yeast strains involves five decision points: (1) choice of product, (2) choice of chassis, (3) identification of target genes, (4) regulating the expression level of target genes, and (5) network balancing of the target genes. At the construction level, several molecular biology tools have been developed through the concept of synthetic biology and applied for the generation of novel, engineered yeast strains. For comprehensive and quantitative analysis of constructed strains, systems biology tools are commonly used and using a multi-omics approach. Key information about the biological system can be revealed, for example, identification of genetic regulatory mechanisms and competitive pathways, thereby assisting the in silico design of metabolic engineering strategies for improving strain performance. Examples on how systems and synthetic biology brought yeast metabolic engineering closer to industrial biotechnology are described in this review, and these examples should demonstrate the potential of a systems-level approach for fast and efficient generation of yeast cell factories.

in silico strain optimization

glucose repression

technologies

ethanol-production

omics'

synthetic biology

metabolic engineering

directed evolution

saccharomyces-cerevisiae strains

fermentation

Saccharomyces cerevisiae

functional genomics

systems biology

in-vivo kinetics

ribosome entry site

xylose

synthetic biology

gene-expression

Author

Il-Kwon Kim

Chalmers, Chemical and Biological Engineering, Life Sciences

Antonio Roldao

Chalmers, Chemical and Biological Engineering, Life Sciences

Verena Siewers

Chalmers, Chemical and Biological Engineering, Life Sciences

Jens B Nielsen

Chalmers, Chemical and Biological Engineering, Life Sciences

FEMS Yeast Research

1567-1356 (ISSN) 1567-1364 (eISSN)

Vol. 12 2 228-248

Subject Categories

Industrial Biotechnology

Areas of Advance

Energy

Life Science Engineering (2010-2018)

DOI

10.1111/j.1567-1364.2011.00779.x

More information

Latest update

7/21/2021