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. 2019 Jan 9;9:3276. doi: 10.3389/fmicb.2018.03276

Table 1.

Yarrowia lipolytica strains and plasmids.

Strain, plasmids, or constructs Description: (strain genotype and phenotype; cloned genes and MW of encoded proteins) Source
Parent and derivative strains
Po1f Genotype: MatA, leu2-270, ura3-302, xpr2-322, axp-2; Phenotype: Leu-, Ura-, ΔAEP, ΔAXP, Suc+ Madzak et al., 2000
Po1g Genotype: MatA, leu2-270, ura3-302::URA3, xpr2-332, axp-2; Phenotype: Leu-, ΔAEP, ΔAXP, Suc+, pBR platform Madzak et al., 2000
YL101 Previously named as Yl (EG II); expressing Tr eg2 (P07982; 42 kDa) with a hybrid promoter (hp4d) in parent strain Po1g. Wei et al., 2014
YL102 Previously named as Yl (CBH II); expressing Tr cbh2 (P07987; 47 kDa) with a hybrid promoter (hp4d) in parent strain Po1g. Wei et al., 2014
YL151 Previously named as Yl (chimeric CBH I); expressing chimeric cbh1 (Te CBH1 catalytic domain-Tr Linker-Tr CBM1; AAL89553 and P62694; 53 kDa) with a hybrid promoter (hp4d) in parent strain Po1g. Wei et al., 2014
HA1 Genotype: Po1f Δpex10 Δmfe1 leu- ura+ DGA1; Phenotype: prevent peroxisome biogenesis and β-oxidation by Δpex10 and Δmfe1, respectively; enhance lipid synthesis by DGA1 overexpression. Blazeck et al., 2014
YL165-1 Genotype: Po1f Δpex10 Δmfe1 leu- ura+ DGA1 chimeric cbh1 cbh2 eg2; Phenotype: prevent peroxisome biogenesis and β-oxidation by Δpex10 and Δmfe1, respectively; enhance lipid synthesis by DGA1 overexpression; co-express CBH I (with TEFin promoter) – CBH II (with GPD promoter) – EG II (with EXP1 promoter). This study
Plasmids and the cloned genes
pYLEX1 (i.e., pINA1269) hybrid promoter (hp4d); selection marker gene (LEU2). Madzak et al., 2000
pYLSC1 (i.e., pINA1296) hybrid promoter (hp4d); secretion signal (XPR2 pre-region); selection marker gene (LEU2). Madzak et al., 2000
pNREL151 Chimeric cbh1 (Te CBH1 catalytic domain-Tr Linker-Tr CBM1; AAL89553 and P62694; 53 kDa) in SfiI/Xbal cut pYLSC1. Wei et al., 2014
pNREL162 Chimeric cbh1-cbh2-eg2 cassette; cloned in vector pUC57. This work
pNREL165 Chimeric cbh1-cbh2-eg2 cassette; cloned in vector pYLEX1. This work

The theoretical molecular weight (MW) was calculated based on amino acid sequence (without a signal peptide). CBH, cellobiohydrolase; EG, endoglucanase; Te, Talaromyces emersonii; Tr, T. reesei.