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Immobilization of fungal nitrilase and bacterial amidase ? two enzymes working in accord

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388971%3A_____%2F06%3A00051108" target="_blank" >RIV/61388971:_____/06:00051108 - isvavai.cz</a>

  • Result on the web

  • DOI - Digital Object Identifier

Alternative languages

  • Result language

    angličtina

  • Original language name

    Immobilization of fungal nitrilase and bacterial amidase ? two enzymes working in accord

  • Original language description

    A nitrilase from Aspergillus niger and an amidase from Rhodococcus erythropolis co-immobilized on a 1-mL Butyl Sepharose column were used for the hydrolysis of 4-cyanopyridine into isonicotinic acid. The former enzyme converted the nitrile into the acid: amide mixture (molar ratio ca. 3 : 1), while the latter enzyme hydrolyzed the by-product amide. Therefore, the ratio of amide in the total product decreased to about 5 %. Sodium sulfate was used as a component of the elution buffer, as the commonly used ammonium sulfate (0.8 M) acted as an amidase inhibitor. The hydrolysis of 4-cyanopyridine by a nitrilase from F. solani gave isonicotinic acid and isonicotinamide at a molar ratio of about 98 : 2. When using this enzyme and the amidase immobilized on two columns operated in tandem, the percentage of isonicotinamide in total product decreased to < 0.2 %kdi

  • Czech name

    Imobilizace houbové nitrilasy a bakteriální amidasy ? součinnost dvou enzymů

  • Czech description

    Nitrilasa z vláknité houby Aspergillus niger a amidasa z baktérie Rhodococcus erythropolis byly koimobilizovány na 1-mL koloně s Butyl Sepharosou a použity pro hydrolýzu 4-kyanopyridinu na kyselinu isonikotinovou. Nitrilasa transformovala nitril na směskyseliny a amidu (mol. poměr ca. 3 : 1), zatímco amidasa hydrolyzovala vedlejší produkt amid. Zastoupení amidu v celkovém produktu se tak snížilo na asi 5%. Síran sodný byl použit jako součást elučního pufru, protože obvykle používaný síran amonný (0,8 M) působil jako inhibitor amidasy. Hydrolýza 4-kyanopyridinu nitrilasou z F. solani poskytla kyselinu isonikotinovou a isonikotinamid v mol. poměru ca. 98 : 2. Když byly nitrilasa a amidasa imobilizovány na dvou kolonách spojených sériově, zastoupení isonikotinamidu v celkovém produktu se snížilo na < 0.2 %

Classification

  • Type

    J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

  • CEP classification

    EE - Microbiology, virology

  • OECD FORD branch

Result continuities

  • Project

    Result was created during the realization of more than one project. More information in the Projects tab.

  • Continuities

    Z - Vyzkumny zamer (s odkazem do CEZ)

Others

  • Publication year

    2006

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Biocatalysis and Biotransformation

  • ISSN

    1024-2422

  • e-ISSN

  • Volume of the periodical

    24

  • Issue of the periodical within the volume

    6

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    5

  • Pages from-to

    414-418

  • UT code for WoS article

  • EID of the result in the Scopus database