Skip to main content
. 2021 Sep 8;6(5):e00654-21. doi: 10.1128/mSphere.00654-21

TABLE 4.

Effect of fdrA variation on anaerobic allantoin degradation

Strain Allantoin consumed (mM) Production (mM)
Glycerol consumed (mM) Production (mM)
Growth pH
Oxamate Oxalate Succinate Formate Acetate Ethanol
MG1655 (ancestor) 21.1 ± 1.0a 16.6 ± 1.2 3.2 ± 1.4 29.4 ± 1.2 6.2 ± 0.7 26.8 ± 0.4 15.3 ± 1.0 12.6 ± 0.6 0.7 ± 0 6.2 ± 0.1
MG1655 ΔfdrA 21.0 ± 0.9 0 10.9 ± 0.8 28.6 ± 1.2 5.4 ± 0.8 27.2 ± 1.8 14.4 ± 0.6 13.7 ± 0.6 0.6 ± 0 6.1 ± 0.1
MG1655 ΔfdrA pNTR-SD::fdrA 20.2 ± 0.2 5.6 ± 1.3 7.9 ± 0.2 28.5 ± 0.7 6.3 ± 0.1 20.3 ± 0.6 7.5 ± 0.2 12.0 ± 0.1 0.6 ± 0 6.0 ± 0
MG1655 fdrAD296Y 20.8 ± 0.8 20.9 ± 1.7 0.4 ± 0.8 36.3 ± 2.0 10.0 ± 0.3 30.0 ± 1.6 20.3 ± 0.4 11.9 ± 0.6 0.6 ± 0 5.9 ± 0
a

Bacterial strains (wild type, FdrAD296Y, ΔfdrA, and ΔfdrA containing pNTR-SD::fdrA) were anaerobically grown in M9 containing glycerol (50 mM), DMSO (50 mM), and allantoin (20 mM) for 72 h, whereby allantoin was used as a sole nitrogen source. Values are averages and SD for 3 replicates.