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Table 1 Plasmids used in this study

From: Metabolic engineering of the l-serine biosynthetic pathway improves glutathione production in Saccharomyces cerevisiae

Plasmid

Description

pATP405

Intact vector

pATP405-SER2

PTDH3-SER2-TTDH3, LEU2 marker

pATP405-SER1

PTDH3-SER1-TTDH3, LEU2 marker

pATP405-SER3

PTDH3-SER3-TTDH3, LEU2 marker

pATP405-SER33

PTDH3-SER33-TTDH3, LEU2 marker

pATP405-SER33/SER2/SER1

PTDH3-SER33-TTDH3/PADH1-SER2-TADH1/PPGK1-SER1-TPGK1, LEU2 marker

pATP406

Intact vector

pATP406-SER3

PPGK1-SER3-TPGK1, URA3 marker

pATP406-SHM2

PPGK1-SHM2-TPGK1, URA3 marker

pATP406-CYS4

PADH1-CYS4-TADH1, URA3 marker

pATP406-SHM2/CYS4

PTDH3-SHM2-TTDH3/PADH1-CYS4-TADH1, URA3 marker

pATP406-SHM2/SER3

PTDH3-SHM2-TTDH3/PPGK1-SER3-TPGK1, URA3 marker

pATP406-CYS4/SER3

PTDH3-CYS4-TTDH3/PPGK1-SER3-TPGK1, URA3 marker

pATP406-SHM2/CYS4/SER3

PTDH3-SHM2-TTDH3/PADH1-CYS4-TADH1/PPGK1-SER3-TPGK1, URA3 marker