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Laccase-induced derivatization of unprotected amino acid L-tryptophan by coupling with p-hydroquinone 2,5-dihydroxy-N-(2-hydroxyethyl)-benzamide.

Laccase-induced derivatization of unprotected amino acid L-tryptophan by coupling with p-hydroquinone 2,5-dihydroxy-N-(2-hydroxyethyl)-benzamide. Research Abstract Details 

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  • Laccase-induced derivatization of unprotected amino acid L-tryptophan by coupling with p-hydroquinone 2,5-dihydroxy-N-(2-hydroxyethyl)-benzamide. Abstract Text:

    k mandaK Manda,e hammerE Hammer,a mikolaschA Mikolasch,d D ,k thurowK Thurow,f schauerF Schauer,k mandaK Manda,e hammerE Hammer,a mikolaschA Mikolasch,d D ,k thurowK Thurow,f schauerF Schauer,k mandaK Manda,e hammerE Hammer,a mikolaschA Mikolasch,d gördesD Gördes,k thurowK Thurow,f schauerF Schauer,

    We have studied the enzymatic derivatization of amino acids by use of the polyphenol oxidase laccase. Derivatization of L-tryptophan was achieved by enzymatic crosslinking with the laccase substrate 2,5-dihydroxy-N-(2-hydroxyethyl)-benzamide. The main product (yield up to 70%) was identified as the quinoid compound 2-[2-(2-hydroxy-ethylcarbamoyl)-3,6-dioxo-cyclohexa-1,4-dienylamino]-3-(1H-indol-3-yl)- propionic acid and demonstrates that laccase-catalyzed C-N-coupling occurred on the amino group of the aliphatic side chain. These enzyme based reactions provide a simple and fast method for the derivatization of unprotected amino acids.

    Laccase-induced derivatization of unprotected amino acid L-tryptophan by coupling with p-hydroquinone 2,5-dihydroxy-N-(2-hydroxyethyl)-benzamide. Publishing Authors By Initials

    k mandaK Manda,e hammerE Hammer,a mikolaschA Mikolasch,d D ,k thurowK Thurow,f schauerF Schauer,k mandaK Manda,e hammerE Hammer,a mikolaschA Mikolasch,d D ,k thurowK Thurow,f schauerF Schauer,k mandaK Manda,e hammerE Hammer,a mikolaschA Mikolasch,d gördesD Gördes,k thurowK Thurow,f schauerF Schauer,

    For similar abstracts research abstracts see: abstracts research

    PUBMED ID PMID:

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    Laccase-induced derivatization of unprotected amino acid L-tryptophan by coupling with p-hydroquinone 2,5-dihydroxy-N-(2-hydroxyethyl)-benzamide. Journal Published:

    PUBLICATION TYPE: Journal Article

    Journal: Amino acids

    VOLUME: 31

    Page Numbers: 409-19

    Journal Abbreviation: Amino Acids

    ISSN: 0939-4451

    DAY: 4

    MONTH: 04

    YEAR: 2006

    Laccase-induced derivatization of unprotected amino acid L-tryptophan by coupling with p-hydroquinone 2,5-dihydroxy-N-(2-hydroxyethyl)-benzamide. Information

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    LANGUAGE: eng

    NlmUniqueID: 9200312

    Laccase-induced derivatization of unprotected amino acid L-tryptophan by coupling with p-hydroquinone 2,5-dihydroxy-N-(2-hydroxyethyl)-benzamide. Keywords Mesh Terms:

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    Grant and Affiliation Information for Laccase-induced derivatization of unprotected amino acid L-tryptophan by coupling with p-hydroquinone 2,5-dihydroxy-N-(2-hydroxyethyl)-benzamide.

    AFFILIATION: Institut für Mikrobiologie, Ernst-Moritz-Arndt-Universität Greifswald, Greifswald, Germany.

    Country: Austria

    Austria Research PublicationAustria Research Publication

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    MEDLINETA: Amino Acids

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