HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Enzymatic and nonenzymatic dehydration reactions of L-arogenate.

Abstract
L-Arogenate, an immediate precursor of either L-tyrosine, L-phenylalanine, or both in many microorganisms and plants, may undergo two types of dehydration reactions that yield products of increased stability. Under acidic conditions, a facile aromatization attended by loss of the C-4 hydroxyl and the C-1 carboxyl moieties results in quantitative conversion to L-phenylalanine. When aromatization was largely prevented by maintaining pH in the range of 7.5-12, a second dehydration reaction occurred in which the alanyl side chain and the carboxyl group at C-1 formed a lactam ring to yield spiro-arogenate. The latter reaction occurs at 100 degrees C, roughly 50% conversion being obtained in 2 h. The product formed from L-arogenate was authentic spiro-arogenate, as demonstrated by high-performance liquid chromatography and thin-layer chromatography identification procedures. Further confirmation was obtained by 1H nuclear magnetic resonance, ultraviolet spectroscopy, and mass spectrometry. Thus far, the conversion of L-arogenate to spiro-arogenate is not known to be enzyme catalyzed. The other dehydratase reaction, however, is catalyzed in nature by an enzyme denoted arogenate dehydratase. An improved assay is described for this in which [3H]dansyl derivatives of L-arogenate (substrate) and L-phenylalanine (product) are separated by using bidimensional thin-layer chromatography. The radioactive reaction product is then quantitated. This assay was used to study partially purified arogenate dehydratase from Pseudomonas diminuta, an organism that depends upon the arogenate pathway for L-phenylalanine biosynthesis.(ABSTRACT TRUNCATED AT 250 WORDS)
AuthorsL O Zamir, R Tiberio, M Fiske, A Berry, R A Jensen
JournalBiochemistry (Biochemistry) Vol. 24 Issue 7 Pg. 1607-12 (Mar 26 1985) ISSN: 0006-2960 [Print] United States
PMID3924095 (Publication Type: Comparative Study, Journal Article, Research Support, U.S. Gov't, P.H.S.)
Chemical References
  • Amino Acids, Dicarboxylic
  • Cyclohexenes
  • Tyrosine
  • Phenylalanine
  • pretyrosine
  • delta-(spiro-4-hydroxy-2,5-cyclohexadienyl)pyroglutamate
  • Hydro-Lyases
  • pretyrosine dehydratase
  • Pyrrolidonecarboxylic Acid
Topics
  • Amino Acids, Dicarboxylic (metabolism)
  • Cyclohexenes
  • Hydro-Lyases (antagonists & inhibitors, metabolism)
  • Phenylalanine (pharmacology)
  • Pseudomonas (metabolism)
  • Pseudomonas aeruginosa (metabolism)
  • Pyrrolidonecarboxylic Acid (analogs & derivatives, metabolism)
  • Species Specificity
  • Tyrosine (analogs & derivatives, metabolism)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: