Yeast synthetic biology for designed cell factories producing secretory recombinant proteins

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초록

Yeasts are prominent hosts for the production of recombinant proteins from industrial enzymes to therapeutic proteins. Particularly, the similarity of protein secretion pathways between these unicellular eukaryotic microorganisms and higher eukaryotic organisms has made them a preferential host to produce secretory recombinant proteins. However, there are several bottlenecks, in terms of quality and quantity, restricting their use as secretory recombinant protein production hosts. In this mini-review, we discuss recent developments in synthetic biology approaches to constructing yeast cell factories endowed with enhanced capacities of protein folding and secretion as well as designed targeted post-translational modification process functions. We focus on the new genetic tools for optimizing secretory protein expression, such as codon-optimized synthetic genes, combinatory synthetic signal peptides and copy number-controllable integration systems, and the advanced cellular engineering strategies, including endoplasmic reticulum and protein trafficking pathway engineering, synthetic glycosylation, and cell wall engineering, for improving the quality and yield of secretory recombinant proteins. © 2020 FEMS 2020.

키워드

protein trafficking pathway engineeringsecretory recombinant proteinssynthetic glycosylation pathwayyeast cell factorycell proteinmannose 6 phosphaterecombinant proteinsecretory proteinsignal peptidesynthetic DNAcell engineeringcomputer modelendoplasmic reticulumendoplasmic reticulum associated degradationfungal cell wallgene dosagegene expressionglycosylationnonhumanproduct recoveryprotein expressionprotein glycosylationprotein secretionReviewsynthetic biologyunfolded protein responseyeast cell
제목
Yeast synthetic biology for designed cell factories producing secretory recombinant proteins
저자
Thak, Eun JungYoo, Su JinMoon, Hye YunKang, Hyun Ah
DOI
10.1093/femsyr/foaa009
발행일
2020-03
유형
Review
저널명
FEMS Yeast Research
20
2

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