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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 

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Enzymatic Synthesis of L-Pipecolic Acid by Delta(1)-Piperideine-2-carboxylate Reductase from Pseudomonas putida.

L-Pipecolic acid is a chiral pharmaceutical intermediate. An enzymatic system for the synthesis of L-pipecolic acid from L-lysine by commercial L-lysine alpha-oxidase from Trichoderma viride and an extract of recombinant Escherichia coli cells coexpressing Delta(1)-piperideine-2-carboxylate reductase from Pseudomonas putida and glucose dehydrogenase from Bacillus subtilis is described. A laboratory-scale process provided 27 g/l of L-pipecolic acid in 99.7% e.e.[1]

References

  1. Enzymatic Synthesis of L-Pipecolic Acid by Delta(1)-Piperideine-2-carboxylate Reductase from Pseudomonas putida. Muramatsu, H., Mihara, H., Yasuda, M., Ueda, M., Kurihara, T., Esaki, N. Biosci. Biotechnol. Biochem. (2006) [Pubmed]
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