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Description
| - V práci je studována reakce rostlinných aminoxidas s N6-aminoalkylderiváty adeninu. (cs)
- Plant copper-containing amine oxidases (CAOs, EC 1.4.3.6) catalyze the oxidation of various amines. Once there was a hypothesis that the enzymes could oxidize cytokinins - plant hormones derived from adenine1, however, it has been shown that they rather cause inhibition2. Here we report a study on the reactions of three plant CAOs from grass pea (Lathyrus sativus), lentil (Lens esculenta) and a Mediterranean shrub (Euphorbia characias) with synthetic N6-aminoalkyl derivatives of adenine representing combined analogues of cytokinins and polyamines. The following compounds were prepared using an established method: N6-(3-aminopropyl)adenine, APAD; N6-(4-aminobutyl)adenine, ABAD; N6-(4-amino-trans-but-2-enyl)adenine, ATBAD; N6-(4-amino-cis-but-2-enyl)adenine, ACBAD and N6-(4-aminobut-2-ynyl)adenine, ABYAD. First, reaction rates of enzymatic oxidation were measured to decide between substrate and inhibitory properties. Two of the studied adenine derivatives were found to be substrates (ABAD, ATBAD) and th
- Plant copper-containing amine oxidases (CAOs, EC 1.4.3.6) catalyze the oxidation of various amines. Once there was a hypothesis that the enzymes could oxidize cytokinins - plant hormones derived from adenine1, however, it has been shown that they rather cause inhibition2. Here we report a study on the reactions of three plant CAOs from grass pea (Lathyrus sativus), lentil (Lens esculenta) and a Mediterranean shrub (Euphorbia characias) with synthetic N6-aminoalkyl derivatives of adenine representing combined analogues of cytokinins and polyamines. The following compounds were prepared using an established method: N6-(3-aminopropyl)adenine, APAD; N6-(4-aminobutyl)adenine, ABAD; N6-(4-amino-trans-but-2-enyl)adenine, ATBAD; N6-(4-amino-cis-but-2-enyl)adenine, ACBAD and N6-(4-aminobut-2-ynyl)adenine, ABYAD. First, reaction rates of enzymatic oxidation were measured to decide between substrate and inhibitory properties. Two of the studied adenine derivatives were found to be substrates (ABAD, ATBAD) and th (en)
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Title
| - Reakce rostlinných aminoxidas s N6-aminoalkylderiváty adeninu (cs)
- Reactions of plant amine oxidases with N6-aminoalkyl derivatives of adenine
- Reactions of plant amine oxidases with N6-aminoalkyl derivatives of adenine (en)
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skos:prefLabel
| - Reakce rostlinných aminoxidas s N6-aminoalkylderiváty adeninu (cs)
- Reactions of plant amine oxidases with N6-aminoalkyl derivatives of adenine
- Reactions of plant amine oxidases with N6-aminoalkyl derivatives of adenine (en)
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skos:notation
| - RIV/61989592:15310/04:00002168!RIV/2005/MSM/153105/N
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http://linked.open.../vavai/riv/strany
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http://linked.open...avai/riv/aktivita
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http://linked.open...avai/riv/aktivity
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http://linked.open...iv/cisloPeriodika
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http://linked.open...vai/riv/dodaniDat
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http://linked.open...aciTvurceVysledku
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http://linked.open.../riv/druhVysledku
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http://linked.open...iv/duvernostUdaju
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http://linked.open...titaPredkladatele
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http://linked.open...dnocenehoVysledku
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http://linked.open...ai/riv/idVysledku
| - RIV/61989592:15310/04:00002168
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http://linked.open...riv/jazykVysledku
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http://linked.open.../riv/klicovaSlova
| - amine oxidase;adenine;cytokinin;cytokinin oxidase/dehydrogenase;polyamine (en)
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http://linked.open.../riv/klicoveSlovo
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http://linked.open...odStatuVydavatele
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http://linked.open...ontrolniKodProRIV
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http://linked.open...i/riv/nazevZdroje
| - Acta Universitatis Palackianae Olomucensis, Facultas Rerum Naturalium, Chemica
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http://linked.open...in/vavai/riv/obor
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http://linked.open...ichTvurcuVysledku
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http://linked.open...cetTvurcuVysledku
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http://linked.open...UplatneniVysledku
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http://linked.open...v/svazekPeriodika
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http://linked.open...iv/tvurceVysledku
| - Šebela, Marek
- Maloň, Michal
- Fryčák, Petr
- Floris, Giovanni
- Medda, Rosaria
- Peč, Pavel
- Lamplot, Zbyněk
- Longu, Silvia
- Padiglia, Alessandra
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http://linked.open...n/vavai/riv/zamer
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issn
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number of pages
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http://localhost/t...ganizacniJednotka
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