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- W1991139932 abstract "Tryptophan synthase catalyzes the nucleophilic replacement of the hydroxyl group at C-3 of L-serine. This enzyme can use benzyl mercaptan as a nucleophile in the conversion of serine to S-benzyl-L-cysteine which is deblocked by treatment with sodium in liquid ammonia to yield L-cysteine. A strain of E. coli engineered to overproduce tryptophan synthase was used in the conversion of L-serine to L-cysteine. Labeled serine was prepared biosynthetically as described previously." @default.
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- W1991139932 date "1991-11-01" @default.
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- W1991139932 title "Stereoselective synthesis of stable isotope-labeled L-α-amino acids: Chemomicrobiological synthesis of 13C- and 2H-labeled L-cysteine" @default.
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- W1991139932 doi "https://doi.org/10.1002/jlcr.2580291108" @default.
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