Results 251 to 260 of about 55,716 (280)
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1975
Publisher Summary Pyrocatechase was isolated from cells of a pseudomonad, which catalyzed oxidative ring cleavage of the benzene ring of catechol forming cis, cis-muconic acid as the reaction product. This enzyme exhibited properties unlike those of an oxidase or dehydrogenase because it was not associated with any of the previously known coenzymes ...
Mitchel T. Abbott+2 more
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Publisher Summary Pyrocatechase was isolated from cells of a pseudomonad, which catalyzed oxidative ring cleavage of the benzene ring of catechol forming cis, cis-muconic acid as the reaction product. This enzyme exhibited properties unlike those of an oxidase or dehydrogenase because it was not associated with any of the previously known coenzymes ...
Mitchel T. Abbott+2 more
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2-Oxoglutarate-dependent dioxygenases in cancer
Nature Reviews. Cancer, 2020J. Losman, P. Koivunen, W. Kaelin
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2004
Pseudomonads have an exceptional ability to utilize aromatic compounds as sole source of energy and carbon. This capability is critical to maintaining the global carbon cycle. Aromatic compounds are planar, fully conjugated, ring-shaped molecules possessing (4n + 2)π electrons where n is a nonnegative integer (Huckel’s rule)93.
Jeffrey T. Bolin+2 more
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Pseudomonads have an exceptional ability to utilize aromatic compounds as sole source of energy and carbon. This capability is critical to maintaining the global carbon cycle. Aromatic compounds are planar, fully conjugated, ring-shaped molecules possessing (4n + 2)π electrons where n is a nonnegative integer (Huckel’s rule)93.
Jeffrey T. Bolin+2 more
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Aromatic Hydrocarbon Dioxygenases
2004Since the initial discovery of toluene dioxygenase (TDO) by David Gibson and coworkers (Yeh et al. 1977; Subramanian et al. 1979), aromatic hydrocarbon dioxygenases have been reported to catalyze the initial reaction in the bacterial biodegradation of a diverse array of aromatic and polyaromatic hydrocarbons, aromatic acids, chlorinated aromatic, and ...
Rebecca E. Parales, Sol M. Resnick
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Indoleamine 2,3-dioxygenases, or IDOs, are the main enzymes responsible for the metabolism of l-Tryptophan (Trp), and the open gate of the kynurenine pathway, where the majority of the intake of the essential amino acid is conveyed. The kynurenine pathway produces a great variety of molecules, involved in a great spectrum of physio-pathological ...
Coluccia, Michele+2 more
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Coluccia, Michele+2 more
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Proanthocyanidin subunit composition determined by functionally diverged dioxygenases
Nature Plants, 2018J. Jun+3 more
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