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Results 1 - 7 of 7
EC Number Substrates Commentary Substrates Organism Products Commentary (Products) Reversibility
Display the reaction diagram Show all sequences 1.13.11.644-nitro-6-oxohepta-2,4-dienedioate - Bradyrhizobium sp. 2-oxo-3-(5-oxofuran-2-ylidene)propanoate + nitrite 2nd step of reaction, spontaneous ?
Display the reaction diagram Show all sequences 1.13.11.645-chlorosalicylate + O2 - Bradyrhizobium sp. 2-oxo-3-(5-oxofuran-2-ylidene)propanoate + chloride overall reaction ?
Display the reaction diagram Show all sequences 1.13.11.645-nitrosalicylate + O2 oxidation catalyzed by cell extracts requires 0.97 mol O2/mol 5-nitrosalicylate Bradyrhizobium sp. 2-oxo-3-(5-oxofuran-2-ylidene)propanoate + nitrite overall reaction ?
Display the reaction diagram Show all sequences 1.13.11.645-nitrosalicylate + O2 results are consistent with a dioxygenase-catalyzed ring opening followed by spontaneous lactonization and nitrite elimination and enzyme-catalyzed hydrolysis of the lactone to produce maleylpyruvate Bradyrhizobium sp. 2-oxo-3-(5-oxofuran-2-ylidene)propanoate + nitrite overall reaction. The initial ring fission product of 5-nitrosalicylate dioxygenation is spontaneously and rapidly cyclized to form lactones, accompanied by the release of NO2- ?
Display the reaction diagram Show all sequences 1.13.11.645-nitrosalicylate + O2 - Bradyrhizobium sp. 4-nitro-6-oxohepta-2,4-dienedioate 1st step of reaction ?
Display the reaction diagram Show all sequences 1.13.11.64more no substrates: 4-chlorocatechol, 4-nitrocatechol Bradyrhizobium sp. ? - ?
Display the reaction diagram Show all sequences 1.13.11.64salicylate + O2 - Bradyrhizobium sp. ? - ?
Results 1 - 7 of 7