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Table 2 Plasmids used in this study

From: Metabolic engineering strategies for optimizing acetate reduction, ethanol yield and osmotolerance in Saccharomyces cerevisiae

Plasmid

Characteristics

Origin

p426-TEF (empty)

2 μ, URA3, TEF1p-CYC1t

[75]

pMEL10

2 μ, KlURA3, SNR52p-gRNA.CAN1.Y-SUP4t

[48]

pMEL11

2 μ, amdS, SNR52p-gRNA.CAN1.Y-SUP4t

[48]

pROS10

KlURA3-gRNA.CAN1-2mu-gRNA.ADE2

[48]

pUDI076

pRS406-TDH3p-eutE-CYC1t

[29]

pUDR103

2 μ, KlURA3, SNR52p-gRNA.SGA1.Y-SUP4t

This work

pUDR119

2 μ, amdS, SNR52p-gRNA.SGA1.Y-SUP4t

[76]

pUDR240

KlURA3-gRNA.GPD1-2mu-gRNA.GPD2

This work

pUDR264

2 μ, amdS, SNR52p-gRNA.ALD6.Y-SUP4t

This work

pMK-RQ-gpsA

Delivery vector, codon-optimized gpsA ORF

GeneArt, Germany