Literature summary extracted from

Li, Z.; Li, F.; Cai, L.; Chen, Z.; Qin, L.; Gao, X.D.
One-pot multienzyme synthesis of rare ketoses from glycerol (2020), J. Agric. Food Chem., 68, 1347-1353 .

Application

EC Number	Application	Comment	Organism
1.1.3.41	synthesis	synthesis of rare ketoses from glycerol and D-/L-glyceraldehyde in a one-pot multienzyme fashion in which the only carbon source is glycerol. Glycerol is phosphorylated and then oxidized at C2 to afford dihydroxyacetone phosphate. The primary alcohol of glycerol is also oxidized to give the acceptor molecule glycerol aldehyde in situ (D- or L-isomer can be formed stereospecifically with either alditol oxidase or horse liver alcohol dehydrogenase). Different dihydroxyacetone phosphate-dependent aldolases are used to generate the aldol adducts (rare ketohexose phosphates) with various stereoconfigurations and diastereomeric ratios	Streptomyces coelicolor

Organism

EC Number	Organism	UniProt	Comment	Textmining
1.1.3.41	Streptomyces coelicolor	-	-	-
1.1.3.41	Streptomyces coelicolor A3(2)	-	-	-

Synonyms

EC Number	Synonyms	Comment	Organism
1.1.3.41	AldO	-	Streptomyces coelicolor

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Release 2023.1 (January 2023)