Table 1.
Target higher alcohols | Number of proper strains Total (single/double/triple/quadruple deletion mutants) |
|||
---|---|---|---|---|
iBKEco52 | iBKSce50 | iBKSce50Δmit | iBKSce50+7 | |
1-propanol from OAA | 458 (0/11/85/362) |
40 (2/16/14/8) |
108 (4/27/50/27) |
467 (4/23/128/312) |
1-Butanol from AcCoA | 347 (1/17/87/242) |
1 (1/0/0/0) |
49 (2/7/17/23) |
192 (33/22/44/93) |
1-Butanol from OAA | 501 (0/10/89/402) |
71 (0/10/30/31) |
120 (3/25/59/33) |
373 (2/17/116/238) |
Isobutanol from PYR | 501 (1/14/83/403) |
38 (2/15/21/0) |
85 (4/25/30/26) |
276 (2/18/81/175) |
3-Methyl-1-butanol from PYR | 208 (2/13/51/142) |
46 (1/15/21/9) |
98 (4/25/46/23) |
94 (2/5/33/54) |
Isopentenol from AcCoA | 330 (0/5/55/270) |
0 (0/0/0/0) |
104 (0/12/51/41) |
166 (2/10/54/100) |
The "proper" strains were defined as viable target-producing strains in which all deletions contributed to the improvement of product yields. The growth rates and product yields were determined by FBA-based metabolic simulations. iBKSce50Δmit is an hypothetical S. cerevisiae model derived by merging the cytosolic and mitochondrial networks into one compartment. iBKSce50+7 is a model of iBKSce50 expanded by the addition of 7 E. coli reactions.