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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 487045Generated: October 26, 2026

DL-alanine → L-Lysine

https://huagongshe.com/reaction/487045

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDL-alanineHCID 602—
ReactantNicotinamideHCID 936—
ReactantThiamine HydrochlorideHCID 6202—
ReactantSulfuric acid magnesium salt (1:1)HCID 24083—
Reactant(2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanalHCID 107526—
ReactantBiotinHCID 171548—
ReactantPotassiumHCID 5462222—
ReactantAmmonium SulfateHCID 6097028—
ProductL-LysineHCID 5962—

Reaction Steps

An aqueous solution medium having a composition of 10% of glucose, 2% of ammonium sulfate, 0.1% of potassium primary phosphate, 0.04% of magnesium sulfate, 0.001% of ferrous sulfate, 200 μg/l of thiamine hydrochloride, 500 μg/l of biotin, 5 ml/dl of Aji-Eki®, 1 mg/dl of nicotinamide and 0.1% of DL-alanine, at pH 7.0, was charged in an amount of 300 ml into separate small sized glass jar fermenters. After sterilizing in a conventional manner, the various L-lysine-producing bacterial strains shown in Table 11, which had been previously grown in bouillon slants at 30° C. for 48 hours, were inoculated thereon. Then, incubation was carried out at 31.5° C. for 48 hours at 1200 rpm at an aeration rate of 1/2 volume per minute, while keeping the pH at 7.0 by the addition of ammonia gas. After completion of the fermentation, the yield of L-lysine produced and accumulated in the solution based on glucose was determined and is shown in Table 11.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05294547
Source datasetuspto-grants-1994_03
ORD IDord-b0238f302d32451580ab037873b18d0f
Source noteuspto-grants-1994_03