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. 2020 Oct 6;8:585935. doi: 10.3389/fbioe.2020.585935

TABLE 2.

Comparison of reported ALK production titers in yeast.

Host ALK pathway enzymes Remarks ALK titer (mg/L)a References
Saccharomyces cerevisiae Engineered FACR and cADO Wild-type S. cerevisiae 1.496 This work
Engineered FACR and cADO Four ADHs were deleted. Fatty acyl-CoA biosynthesis was upregulated by deleting OPI1. 1.54
S. cerevisiae Cyanobacterial FAAR and cADO HFD1 aldehyde dehydrogenase gene was deleted. 0.14 Zhou et al., 2016b
CAR and cADO POX1 was deleted to inactivate beta-oxidation. HFD1 and ADH5 were deleted to inactivate competing pathways. 0.8
S. cerevisiae Cyanobacterial FAAR and cADO Cytosolic ALK pathway in wild-type S. cerevisiae. 0.035 Zhou et al., 2016a
CAR and cADO Cytosolic ALK pathway in wild-type S. cerevisiae. 0.06
CAR and cADO Cytosolic ALK pathway. POX1 was deleted to inactivate beta-oxidation. HFD1, ADH5, and SFA1 were deleted to inactivate competing pathways. 0.7
CAR and cADO Peroxisomal ALK pathway. POX1 was deleted to inactivate beta-oxidation. HFD1 was deleted to inactivate competing pathway. 1.2
CAR and cADO Peroxisomal ALK pathway. POX1 was deleted to inactivate beta-oxidation. HFD1 was deleted to inactivate competing pathway. Peroxisome biogenesis was increased by deleting PEX31–32 and overexpressing PEX34. 3.55
S. cerevisiae DOX and cADO FAA1 and FAA4 were deleted to accumulate FFAs. 0.074 Foo et al., 2017
Yarrowia lipolytica Bacterial FACR and cADO Cytosolic ALK pathway in an oleaginous yeast host. 3.2 Xu et al., 2016
Bacterial FACR and cADO The ALK pathway was targeted to the endoplasmic reticulum of the oleaginous yeast. 16.8
CAR and cADO Cytosolic ALK pathway in an oleaginous yeast host. 23.3
S. cerevisiae Fatty acid decarboxylase, UndA The host was engineered to produce medium-chain fatty acids and inactivate the beta-oxidation pathway. The highest titer was achieved with 20 g/L of glucose. 3.35 Zhu et al., 2017
S. cerevisiae Fatty acid decarboxylase, OleT FAA1 and FAA4 were deleted to accumulate FFAs. HEM3 was overexpressed to increase the heme co-factor. CCP1 was deleted to accumulate H2O2. The highest titer was achieved upon gene expression tuning and bioreactor process optimization. 3.7 Chen et al., 2015

ALK, alkane and alkene; FACR, fatty acyl-CoA reductase; FAAR, fatty acyl-(acyl-carrier-protein) reductase; cADO, cyanobacterial aldehyde deformylating oxygenase; FFA, free fatty acid.aTiters of fatty acyl-CoA-dependent ALK pathway are shown in bold. Otherwise, the titers were from FFA-dependent ALK pathways.