Recent Patents on Biotechnology

Rongling Wu
Departments of Public Health Sciences and Statistics
Pennsylvania State College of Medicine
Hershey, PA
USA

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Optically Pure α-Amino Acids Production by the “Hydantoinase Process”

Author(s): Francisco J.L. Heras-Vazquez, Josefa M. Clemente-Jimenez, Sergio Martinez-Rodriguez and Felipe Rodriguez-Vico

Affiliation: University of Almeria,Department of Biochemistry and Molecular Biology, CITE I, La Canada,s/n, 04120 Almeria, Spain.

Keywords: D- and L-amino acids, “Hydantoinase Process”, hydantoinase, D- and L-N-carbamoyl-amidohydolase, hydantoin racemase, polycistronic messenger, fermentation, recombinant system

Abstract:

Optically pure D- or L-amino acids are used as intermediates in several industries. D-amino acids are involved in the synthesis of antibiotics, pesticides, sweeteners and other biologically active peptides. L-amino acids are used as feed and food additives, as intermediates for pharmaceuticals, cosmetics, pesticides and as chiral synthons in organic synthesis. The specific activity of these optically pure amino acids depends on their structure, chirality and purity. There are two main approaches to obtain optically pure amino acids, namely chemical and enzymatic synthesis. Chemical synthesis gives racemic mixtures of amino acids of low yield and is not environment friendly. One of the most widely-used enzymatic method is the “Hydantoinase Process”. In this cascade of reactions, the chemically synthesized D,L-5-monosubstituted hydantoin ring is first hydrolyzed by a stereoselective hydantoinase enzyme to give the corresponding N-carbamoyl α-amino acid that is hydrolyzed by highly enantiospecific N-carbamoyl α-amino acid amidohydrolase (Ncarbamoylase) to yield the free amino acid. At the same time, the remaining non-hydrolyzed 5-monosubstituted hydantoin is racemized by the hydantion racemase enzyme. This process has evolved over the years from the isolation of microorganisms with one or several of these enzymes to the construction of recombinant systems for industrial application.

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Article Details

VOLUME: 2
ISSUE: 1
Page: [35 - 46]
Pages: 12
DOI: 10.2174/187220808783330947