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Table 4 Strains, plasmids and primers used in this study

From: Xylose fermentation efficiency of industrial Saccharomyces cerevisiae yeast with separate or combined xylose reductase/xylitol dehydrogenase and xylose isomerase pathways

 

Relevant features

Source

S. cerevisiae strains

 PE-2∆GRE3

S. cerevisiae PE-2 (isolated from Brazilian first generation bioethanol plants [44, 46], gre3::natMX4/gre3::kanMX4

Romaní et al. [13]

 PE-XR/XDH

PE-2∆GRE3, pMEC1049

Romaní et al. [13]

 PE-XR/XDH + XI

PE-2∆GRE3, pMEC1049 + XI

This work

 PE-XI

PE-2∆GRE3, pMEC_XI

This work

 CA11

S. cerevisiae strain isolated from Brazilian “cachaça” fermentation processes

Pereira et al. and Schwan et al. [43, 44]

 CA11-XR/XDH

CA11, pMEC1049

Costa et al. [14]

 CA11-XR/XDH + XI

CA11, pMEC1049 + XI

This work

 CA11-XI

CA11, pMEC_XI

This work

Plasmids

 pMEC1049

pYPK4-TEF1tp-XR(N272D)-TDH3tp-XDH-PGI1tp-XKS1-FBA1tp-TAL1- PDC1tp, HphMX4

Romaní et al. [13]

 pBED-CpXI-NATMX

Plasmid containing the xylA gene from Clostridium phytofermentans with HXT7 promoter and CYC terminator

Brat et al. [20]

 pMEC1049 + XI

pMEC1049 containing the xylA gene from C. phytofermentans with HXT7 promoter and CYC terminator

This work

 pYPKa_Z_PGI1tp

 

Pereira et al. [47]

 pMEC_XI

pMEC1049 + XI after removal of XR and XDH coding sequences

This work

Primers

Sequence (5′– > 3′)

 

XI_FW

ACGATTTAGGTGACACTATAGAACGCGGCCGCCAGGAGCTCGTAGGAACAA

 

XI_RV

GGGGATCCGTCGACCTGCAGCGTACGAAGCTTCAGCCGATCTCCAGCCGAC

 

577

GTTCTGATCCTCGAGCATCTTAAGAATTC

 

567

GTCGGCTGCAGGTCACTAGTGAG