Literature DB >> 5584009

The dimerization of delta-1-piperidine-2-carboxylic acid.

D B Hope, K C Horncastle, R T Aplin.   

Abstract

The l-amino acid oxidase of Mytilus edulis has been used to oxidize l-lysine on a large scale in the presence of catalase. The alpha-oxo acid derived from lysine cyclizes to a Schiff base, which readily dimerizes. The dimer undergoes spontaneous dehydration and decarboxylation to form 1,2,3,4,5,6,7,8-octahydropyrido[3,2-a]-indolizin-10(4bH)-one. This structure was established by a study of its molecular weight and infrared, nuclear-magnetic-resonance and mass spectra.

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Year:  1967        PMID: 5584009      PMCID: PMC1198360          DOI: 10.1042/bj1050663

Source DB:  PubMed          Journal:  Biochem J        ISSN: 0264-6021            Impact factor:   3.857


  3 in total

1.  [Reaction product of the enzymatic oxidation of putrescine and cadaverine].

Authors:  K HASSE; H MAISACK
Journal:  Biochem Z       Date:  1955

2.  The alpha-keto analogues of arginine, ornithine, and lysine.

Authors:  A MEISTER
Journal:  J Biol Chem       Date:  1954-02       Impact factor: 5.157

3.  The oxidation of lysine and oxalysine by Mytilus edulis: Identification of the products formed in the presence and the absence of catalase.

Authors:  D B Hope; K C Horncastle
Journal:  Biochem J       Date:  1967-03       Impact factor: 3.857

  3 in total
  1 in total

1.  Biochemical Principles and Functional Aspects of Pipecolic Acid Biosynthesis in Plant Immunity.

Authors:  Michael Hartmann; Denis Kim; Friederike Bernsdorff; Ziba Ajami-Rashidi; Nicola Scholten; Stefan Schreiber; Tatyana Zeier; Stefan Schuck; Vanessa Reichel-Deland; Jürgen Zeier
Journal:  Plant Physiol       Date:  2017-03-22       Impact factor: 8.340

  1 in total

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