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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1165116Generated: November 1, 2026

Urea → Malic Acid

https://huagongshe.com/reaction/1165116

Reaction equation

Participants

RoleNameHCIDCharge
ReactantUreaHCID 1176—
Reactant(2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanalHCID 107526—
ReactantMonobasic potassium phosphateHCID 516951—
ReactantDisodium fumarateHCID 6364607—
SolventPhosphateHCID 1061—
ProductMalic AcidHCID 525—
ProductFumaric AcidHCID 444972—

Reaction Steps

Washed cells of Brevibacterium ammoniagenes (IAM 1645) deposited at and obtained from the Institute of Applied Microbiology, University of Tokyo, was prepared by aerobically culturing the strain in a medium (pH 7.2) comprising glucose 2%, sodium fumarate 0.5%, urea 0.2%, monopotassium dihydrogen phosphate 0.2%, magnesium sulfate·7 hydrate 0.05% and corn steep liquor 1%. The cells were dispersed in 0.05 M phosphate buffer (pH 7.7) at a dark place to prepare a suspension of cells having a concentration of 30.0 OD630 μm. The bacterial liquor was divided into two portions. One portion thereof was allowed to stand at 30° C. for 1 hour at a distance of 20 cm apart from a 150 W "Cool Beam" light (supplied from Tokyo Shibaura Denki K. K., Japan) at light energy of 7×102 μE/g cells·second (light-standing). The other portion thereof was allowed to stand at 30° C. for 1 hour at a dark place (dark-standing). By using these bacterial liquor in the following formulations, malic acid was produced from fumaric acid. The reaction velocity was studied in comparison with the amounts of malic acid thus produced.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04908313
Source datasetuspto-grants-1990_03
ORD IDord-af6f9a5bd76046ceba5ae4edaa373154
Source noteuspto-grants-1990_03