Table 1. Saccharomyces cerevisiae strains used in this study.
Strain | Relevant genotype/description | Reference |
---|---|---|
CEN.PK 113-7D | MATa MAL2-8c SUC2 | 55 |
IMX581 | MATa ura3-52 MAL2-8c SUC2 can1Δ::cas9-natNT2 | 33 |
IMX696 | MATa ura3-52 MAL2-8c SUC2 CAN1::cas9-natNT2 gre3:: [pTDH3_RPE1- pPGK1_TKL1- pTEF1_TAL1- pPGI1_NQM - pTPI1_RKI1- pPYK1_TKL2- (pTPI1_xylA_tCYC1)*36 pTEF1_XKS1] pUDE335 | This study |
IMS0488 | Single-cell line isolated after adaptation of IMX696 to anaerobic growth on xylose (reactor 1) | This study |
IMS0489 | Single-cell line isolated after adaptation of IMX696 to anaerobic growth on xylose (reactor 2) | This study |
IMX906 | MATa ura3-52 MAL2-8c SUC2 CAN1::cas9-natNT2 gre3:: [pTDH3_RPE1- pPGK1_TKL1- pTEF1_TAL1- pPGI1_ NQM1-pTPI1_RKI1- pPYK1_TKL2- (pTPI1_xylA_tCYC1)*36 pTEF1_XKS1] pmr1Δ::amdSYM pUDE335 | This study |
IMX979 | IMX906 with PMR1 reintegrated at PMR1 locus | This study |
IMK692 | MATa MAL2-8c SUC2 pmr1Δ::amdSYM | This study |
Native gene terminator sequences were used for expression of RPE1, TKL1, TAL1, NQM1, RKI1, TKL2 and XKS1.