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  Enantioselective oxidation of racemic 1,2-propanediol to -(−)-lactic acid by Gluconobacter oxydans

W, S., Z, C., K, G., & D, W. (2004). Enantioselective oxidation of racemic 1,2-propanediol to -(−)-lactic acid by Gluconobacter oxydans. Tetrahedron: Asymmetry, Volume 15(Issue 8,), 1275-1277. Retrieved from Tetrahedron: Asymmetry.

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Item Permalink: https://hdl.handle.net/11858/00-001M-0000-0013-D975-3 Version Permalink: https://hdl.handle.net/11858/00-001M-0000-0013-D976-1
Genre: Journal Article

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 Creators:
W, Su1, Author
Z, Chang, Author
K, Gao, Author
D, Wei, Author
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1External Organizations, ou_persistent22              

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 Abstract: Gluconobacter oxydans DSM 2003 was firstly used in the production of (R)-2-hydroxy-propionic acid through microbial oxidation of racemic 1,2-propanediol. The biotransformation was processed with high enantiomeric excess (>99) and near theoretical yield (48 of racemic 1,2-propanediol) when the substrate concentration was lower than 20 g/L. When the substrate concentration was increased, maintaining the pH at 6.0 helped to improve the enantioselectivity.

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 Dates: 2004-04
 Publication Status: Issued
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 Identifiers: URI: Tetrahedron: Asymmetry
BibTex Citekey: 3211
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Title: Tetrahedron: Asymmetry
Source Genre: Journal
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Pages: - Volume / Issue: Volume 15 (Issue 8 ,) Sequence Number: - Start / End Page: 1275 - 1277 Identifier: -