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Table 1 Strains and plasmids used in this study

From: Metabolic engineering of Saccharomyces cerevisiae for efficient production of glucaric acid at high titer

Strains and plasmids

Relevant genotype

Reference

E. coli JM109

 

Stored in author’s laboratory

S. cerevisiae BY4741

MATa, his3Δ1, leu2Δ0, met15Δ0, ura3Δ0

Stored in author’s laboratory

BY4741 opi1∆

Bga-0

MATa, his3Δ1, leu2Δ0, met15Δ0, ura3Δ0, opi1∆0

BY474 carrying pY26GPD-TEF-miox4-udh

Stored in author’s laboratory

This study

Bga-1

BY474 opi1∆ carrying pY26GPD-TEF-miox4-udh

This study

Bga-2

BY474 opi1∆ carrying pY26GPD-TEF-miox4-histag

This study

Bga-3

BY474 opi1∆ carrying miox4 and udh

This study

E. coli pUG6

E. coli plasmid with segment LoxP-KanMX4-LoxP

Stored in author’s laboratory

E. coli pSH65

pY26-GPD-TEF

pY26-miox4-udh

pY26-miox4-histag

Shuttle plasmid for E. coli and S. cerevisiae, Cre gene under GAL2 regulative regulation

Integrating plasmid, URA3 marker, MCS derived from

pBLUESCRIPT (ColE1 (derivative) ori, f1 ori, AmpR)

pY26GPD-TEF carrying miox4 and udh

pY26GPD-TEF carrying miox4-histag

Stored in author’s laboratory

Stored in author’s laboratory

This study

This study