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Table 2 Plasmids used in this work

From: Coupling gene regulatory patterns to bioprocess conditions to optimize synthetic metabolic modules for improved sesquiterpene production in yeast

Plasmid

Features

Reference

pRS423

E. coli/S. cerevisiae shuttle plasmid; 2 μ, HIS3

[45]

pRS424

E. coli/S. cerevisiae shuttle plasmid; 2 μ, TRP1

[45]

pRS425

E. coli/S. cerevisiae shuttle plasmid; 2 μ, LEU2

[45]

pPMVAu8

pRS423: P RPL4A >EfmvaS>T EFM1 –P RPL15A >EfmvaE>T EBS1

[23]

pPMVAd3

pRS424: P RPL8B >ERG12>T NAT5 –P SSB1 >ERG8>T IDP1 –P RPL3 >MVD1>T PRM9 –P YEF3 >IDI1>T RPL15A

[23]

pJT1

pRS425: P TEF2 >ERG20>T RPL3 –P TEF1 –AcNES1-T RPL41B

[23]

pPMVAugw

pRS423: T EFM1 <EfmvaS<P CUP1 –P CUP1 >EfmvaE>T EBS1

This work

pIMVAu1

pRS423: HMG2 (−309, −153)-HIS3-T EFM1 <EfmvaS<P GAL1 –P GAL10 >ACS2>T ACS2 –P GAL2 >EfmvaE>T EBS1 –P GAL7 >HMG2 K6R(1, 292)

This work

pPMVAd36

pRS424: P CUP1 >ERG12>T NAT5 –P TEF2 >ERG8>T IDP1 –T PRM9 <MVD1<P TEF2 –T RPL15A <IDI1<P TEF1

This work

pIMVAd39T

pUC19: pdc5 (−277, −32)-P GAL2 >ERG12>T NAT5 –P TEF2 >ERG8>T IDP1 –T PRM9 <MVD1<P ADH2 –T RPL15A <IDI1<P TEF1 -TRP1-pdc5 (95,373)

This work

pJT3

pRS425: T RPL3 <ScERG20<P CUP1 –P CUP1 >AcNES1>T RPL41B

This work

pJT9R

pRS425: T RPL3 <ScERG20<P GAL1 –P GAL2 >AcNES1>T RPL41B

This work

pILGFP3

Yeast integration plasmid; yEGFP without promoter

[33]

pILGH4

pILGFP3: with yEGFP removed

[33]

pILGB5A

pILGFP3: P GAL1 -yEGFP

[33]

pILGB6

pILGFP3: P GAL10 -yEGFP

This work

pILGFPQ3

pILGFP3: P GAL2 -yEGFP

This work

pITGFPQ4

pILGFP3: P GAL7 -yEGFP

This work

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