EC Number | Protein Variants | Comment | Organism |
---|---|---|---|
4.2.1.91 | additional information | construction of knockout mutant adt3/4/5/6, as well as ADT knockout mutants adt1, adt3, adt4, adt5, adt4/5, adt1/4/5, and adt3/4/5, phenotypes, detailed overview | Arabidopsis thaliana |
EC Number | Localization | Comment | Organism | GeneOntology No. | Textmining |
---|---|---|---|---|---|
4.2.1.91 | chloroplast | - |
Arabidopsis thaliana | 9507 | - |
EC Number | Natural Substrates | Organism | Comment (Nat. Sub.) | Natural Products | Comment (Nat. Pro.) | Rev. | Reac. |
---|---|---|---|---|---|---|---|
4.2.1.91 | L-arogenate | Arabidopsis thaliana | - |
L-phenylalanine + H2O + CO2 | - |
? |
EC Number | Organism | UniProt | Comment | Textmining |
---|---|---|---|---|
4.2.1.91 | Arabidopsis thaliana | O22241 | - |
- |
4.2.1.91 | Arabidopsis thaliana | Q9FNJ8 | - |
- |
4.2.1.91 | Arabidopsis thaliana | Q9SA96 | - |
- |
4.2.1.91 | Arabidopsis thaliana | Q9SGD6 | - |
- |
4.2.1.91 | Arabidopsis thaliana | Q9ZUY3 | - |
- |
EC Number | Source Tissue | Comment | Organism | Textmining |
---|---|---|---|---|
4.2.1.91 | rosette leaf | - |
Arabidopsis thaliana | - |
4.2.1.91 | seedling | - |
Arabidopsis thaliana | - |
EC Number | Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
---|---|---|---|---|---|---|---|
4.2.1.91 | L-arogenate | - |
Arabidopsis thaliana | L-phenylalanine + H2O + CO2 | - |
? |
EC Number | Synonyms | Comment | Organism |
---|---|---|---|
4.2.1.91 | AdT | - |
Arabidopsis thaliana |
4.2.1.91 | ADT1 | - |
Arabidopsis thaliana |
4.2.1.91 | ADT3 | - |
Arabidopsis thaliana |
4.2.1.91 | ADT4 | - |
Arabidopsis thaliana |
4.2.1.91 | ADT5 | - |
Arabidopsis thaliana |
4.2.1.91 | ADT6 | - |
Arabidopsis thaliana |
EC Number | General Information | Comment | Organism |
---|---|---|---|
4.2.1.91 | malfunction | ADT-deficient Arabidopsis thaliana mutants have significantly reduced lignin contents, with stronger reductions in lines that have deficiencies in more ADT isoforms, effects of the modulation of ADT on photosynthetic parameters and secondary metabolism, metabolomics, overview. A reduced carbon flux into L-Phe biosynthesis in ADT mutants impairs the consumption of photosynthetically produced ATP, leading to an increased ATP/ADP ratio, overaccumulation of transitory starch, and lower electron transport rates. The effect on electron transport rates is caused by an increase in proton motive force across the thylakoid membrane that downregulates photosystem II activity by the high-energy quenching mechanism. ADT mutants show reduced flavonoid, phenylpropanoid, lignan, and glucosinolate contents, including glucosinolates that are not derived from aromatic amino acids, and significantly increased contents of putative galactolipids and apocarotenoids. Concerning respiration and carbon fixation rates, ADT knockout mutant adt3/4/5/6 does reveal no significant difference in both night- and day-adapted plants. Transitory starch in chloroplasts might serve, at least in part, as an alternative carbon sink in ADT-deficient plants. In the adt3/4/5/6 knockout, the starch content is increased by more than 60%. Phenomics analysis with the adt3/4/5/6 mutant and metabolic analysis of rosette leaves | Arabidopsis thaliana |
4.2.1.91 | malfunction | ADT-deficient Arabidopsis thaliana mutants have significantly reduced lignin contents, with stronger reductions in lines that have deficiencies in more ADT isoforms, effects of the modulation of ADT on photosynthetic parameters and secondary metabolism, metabolomics, overview. A reduced carbon flux into Phe biosynthesis in ADT mutants impairs the consumption of photosynthetically produced ATP, leading to an increased ATP/ADP ratio, overaccumulation of transitory starch, and lower electron transport rates. The effect on electron transport rates is caused by an increase in proton motive force across the thylakoid membrane that downregulates photosystem II activity by the high-energy quenching mechanism. ADT mutants show reduced flavonoid, phenylpropanoid, lignan, and glucosinolate contents, including glucosinolates that are not derived from aromatic amino acids, and significantly increased contents of putative galactolipids and apocarotenoids. Concerning respiration and carbon fixation rates, ADT knockout mutant adt3/4/5/6 does reveal no significant difference in both night- and day-adapted plants. Transitory starch in chloroplasts might serve, at least in part, as an alternative carbon sink in ADT-deficient plants. In the adt3/4/5/6 knockout, the starch content is increased by more than 60%. Phenomics analysis with the adt3/4/5/6 mutant and metabolic analysis of rosette leaves | Arabidopsis thaliana |
4.2.1.91 | metabolism | arogenate dehydratase (ADT) catalyzes the final step of phenylalanine (Phe) biosynthesis, effects of the modulation of ADT on photosynthetic parameters and secondary metabolism, metabolomics, overview | Arabidopsis thaliana |