Introduction and expression of genes for metabolic engineering applications in Saccharomyces cerevisiae

被引:204
作者
Da Silva, Nancy A. [1 ]
Srikrishnan, Sneha [1 ]
机构
[1] Univ Calif Irvine, Dept Chem Engn & Mat Sci, Irvine, CA 92697 USA
关键词
yeast; plasmids; genomic integration; promoters; HIGH-COPY-NUMBER; GLYCERALDEHYDE-3-PHOSPHATE DEHYDROGENASE GENES; ANTIMALARIAL-DRUG PRECURSOR; ALPHA-AMYLASE PRODUCTION; HIGH-LEVEL EXPRESSION; PYRUVATE-KINASE GENE; HETEROLOGOUS PROTEINS; DELTA-INTEGRATION; SHUTTLE VECTORS; HOMOLOGOUS RECOMBINATION;
D O I
10.1111/j.1567-1364.2011.00769.x
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Metabolic pathway engineering in the yeast Saccharomyces cerevisiae leads to improved production of a wide range of compounds, ranging from ethanol (from biomass) to natural products such as sesquiterpenes. The introduction of multienzyme pathways requires precise control over the level and timing of expression of the associated genes. Gene number and promoter strength/regulation are two critical control points, and multiple studies have focused on modulating these in yeast. This MiniReview focuses on methods for introducing genes and controlling their copy number and on the many promoters (both constitutive and inducible) that have been successfully employed. The advantages and disadvantages of the methods will be presented, and applications to pathway engineering will be highlighted.
引用
收藏
页码:197 / 214
页数:18
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