Table 3 |
||||
|
Deletion phenotypes predicted differently under raffinose conditions by iLL672 builds with and without α-galactosidase activity |
||||
|
Gene |
Experimental phenotype of deletion under YPRaff |
Predicted phenotype of deletion mutant made by iLL672 build with α-galctosidase |
Predicted phenotype of deletion mutant made by iLL672 build without α-galctosidase |
Reason for incorrect prediction made by iLL672 build with α-galactosidase activity |
|
|
||||
|
Gal1 |
Viable |
Unviable |
Viable |
Galactose is produced when α-galactosidic bond in raffinose is cleaved. Therefore, in build with α-galactosidase, Gal genes are required to metabolize galactose produced during raffinose catabolism |
|
Gal7 |
Viable |
Unviable |
Viable |
See explanation for Gal1 |
|
Gal10 |
Viable |
Unviable |
Viable |
See explanation for Gal1 |
|
YBR184W |
Viable |
Unviable |
Viable |
YBR184W is the putative α-galactosidase and is essential by definition of the model build |
|
Suc2 |
Unviable |
Viable |
Unviable |
The galactose produced when the α-galactosidic bond is cleaved can be used as the primary carbon source, with the remaining sucrose unit being excreted |
|
Pgi1 |
Unviable |
Viable |
Unviable |
Pgi1 catalyzes the reversible conversion of glucose-6-phosphate to fructose-6-phosphate in glycolysis and gluconeogenesis. The pentose phosphate pathway can be used to bypass the deletion of this gene to maintain glycolytic function Without the α-galactosidase only the fructose unit of raffinose is usable, making Pgi1 essential for its role in gluconeogenesis |
|
|
||||
|
Snitkin et al. Genome Biology 2008 9:R140 doi:10.1186/gb-2008-9-9-r140 |
||||