| Cloned (Comment) | Organism |
|---|---|
| gene atzF, qualitative and quantitative RT-PCR enzyme expression analysis | Pantoea piersonii |
| Protein Variants | Comment | Organism |
|---|---|---|
| additional information | significantly higher concentrations of extracellular NH4-N are detected in the cultures along with overexpression of urea carboxylase (UC) and allophanate hydrolase (AH) genes. The bacterium forms biofilm, and displays swimming and swarming motilities in presence of urea. Additional glucose supply to urea boosts the colonization but ameliorates the media alkalization and ammonification through suppression of gene expressions encoding UC and AH | Pantoea piersonii |
| Natural Substrates | Organism | Comment (Nat. Sub.) | Natural Products | Comment (Nat. Pro.) | Rev. | Reac. |
|---|---|---|---|---|---|---|
| urea-1-carboxylate + H2O | Pantoea piersonii | - |
2 CO2 + 2 NH3 | - |
? | |
| urea-1-carboxylate + H2O | Pantoea piersonii YU22 | - |
2 CO2 + 2 NH3 | - |
? |
| Organism | UniProt | Comment | Textmining |
|---|---|---|---|
| Pantoea piersonii | A0AAJ5UBK2 | Kalamiella piersonii strain YU22 / MCC3118 | - |
| Pantoea piersonii YU22 | A0AAJ5UBK2 | Kalamiella piersonii strain YU22 / MCC3118 | - |
| Source Tissue | Comment | Organism | Textmining |
|---|---|---|---|
| additional information | Growth kinetics of YU22 cells in M9 media containing urea, urea + glucose, L-asparagine, L-asparagine + glucose and glucose alone, overview | Pantoea piersonii | - |
| Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
|---|---|---|---|---|---|---|
| urea-1-carboxylate + H2O | - |
Pantoea piersonii | 2 CO2 + 2 NH3 | - |
? | |
| urea-1-carboxylate + H2O | - |
Pantoea piersonii YU22 | 2 CO2 + 2 NH3 | - |
? |
| Synonyms | Comment | Organism |
|---|---|---|
| AtzF | - |
Pantoea piersonii |
| General Information | Comment | Organism |
|---|---|---|
| metabolism | presence of an alternate enzyme system for urea breakdown namely urea carboxylase (UC, EC 6.3.4.6) and allophanate hydrolase (AH) in comparison to the major pathway through the activity of the enzyme urease. The urease-negative strain YU22 can utilize the UC and AH system for urea metabolism. Altered gene expression shows the evidence for active UC and AH pathway for urea degradation, overview. Significant higher expression of UC (7.6-26.7fold), and AH (18.7-39.3-old) genes are found in the presence of urea during 24-72 h of incubation, whereas, their expressions declines marginally at 96 h | Pantoea piersonii |
| physiological function | many urease-negative pathogenic bacteria may utilize the urea carboxylase (UC) and allophanate hydrolase (AH) enzyme system to gain advantages for their survival in different host conditions | Pantoea piersonii |