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Literature summary for 3.5.1.75 extracted from

  • Lu, X.; Zhou, N.; Tian, Y.
    Spectrophotometric determination of ethyl carbamate through bi-enzymatic cascade reactions (2015), Anal. Methods, 7, 1261-1264 .
No PubMed abstract available

Application

Application Comment Organism
analysis the enzyme is used in spectrophotometric determination of ethyl carbamate through bi-enzymatic cascade reactions, method, overview. Detection of ethyl carbamate (urethane) in Chinese rice wine. Urethane is known as a genotoxic carcinogen1 that widely exists in fermented foods and alcoholic beverages, such as bread, yogurt, cheese, brandy, Chinese rice wine, sake, and wine, due to the natural biochemical processes in the fermentation process Talaromyces variabilis

Natural Substrates/ Products (Substrates)

Natural Substrates Organism Comment (Nat. Sub.) Natural Products Comment (Nat. Pro.) Rev. Reac.
urethane + H2O Talaromyces variabilis
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ethanol + CO2 + NH3
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?
urethane + H2O Talaromyces variabilis JN-A525
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ethanol + CO2 + NH3
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?

Organism

Organism UniProt Comment Textmining
Talaromyces variabilis
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-
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Talaromyces variabilis JN-A525
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-
-

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
additional information a highly sensitive spectrophotometric method for ethyl carbamate (EC) determination is established through glutamate dehydrogenase/urethanase cascade reactions and the corresponding change in NADH concentration. The absorbance at 340 nm is linearly related to the EC concentration within the range of 300-5000 nM, with a low detection limit of 9.28 nM. Method optimization. The absorbance declines slowly at either pH 4.5 or pH 8.0, which is around the optimal pH of one of the enzymes. But the absorbance decreases with the fastest rate at pH 6.0 Talaromyces variabilis ?
-
?
additional information a highly sensitive spectrophotometric method for ethyl carbamate (EC) determination is established through glutamate dehydrogenase/urethanase cascade reactions and the corresponding change in NADH concentration. The absorbance at 340 nm is linearly related to the EC concentration within the range of 300-5000 nM, with a low detection limit of 9.28 nM. Method optimization. The absorbance declines slowly at either pH 4.5 or pH 8.0, which is around the optimal pH of one of the enzymes. But the absorbance decreases with the fastest rate at pH 6.0 Talaromyces variabilis JN-A525 ?
-
?
urethane + H2O
-
Talaromyces variabilis ethanol + CO2 + NH3
-
?
urethane + H2O
-
Talaromyces variabilis JN-A525 ethanol + CO2 + NH3
-
?

pH Optimum

pH Optimum Minimum pH Optimum Maximum Comment Organism
4.5
-
-
Talaromyces variabilis