O-ADP-Ribosylation in the NAD/NADase System : 2-Alkanols as Efficient Substrates
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概要
- 論文の詳細を見る
Several 2-alkanols(2-propanol, 2-butanol, 2-pentanol, etc.)were examined as substrates for ADP-ribosylation in the NAD/NADase enzymatic system. Even though these secondary alcohols have hydroxy groups that are subject to the steric influence of a methyl group, they were shown to be efficiently ADP-ribosylated. However, in the case of 3-alkanol(3-butanol), only slight ADP-ribosylation was observed. In this enzymatic reaction, 1, 2-propanediol provided both 1-O- and 2-O-ADP-ribosylation products in the ratio 1:1 as determined by ^1H-NMR spectrometry. On the other hand, an equimolar mixture system of 1- and 2-propanols provided major 1-O- and minor 2-O-ribosylation products in the ratio 4:1. This is the first report of O-ADP-ribosylation of terminal secondary alcohols with the NAD/NADase enzymatic system.
- 公益社団法人日本薬学会の論文
- 2001-01-01
著者
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Hatakeyama M
Hokkaido Univ. Sapporo Jpn
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Hatakeyama Masanori
Division Of Molecular Oncology Institute For Genetic Medicine Hokkaido University
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Hatakeyama Masanori
Division Of Molecular Oncology Institute For Genetic Medicine And Division Of Chemistry Graduate Sch
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TONO-OKA Shuichi
Division of Molecular Oncology, Institute for Genetic Medicine, Hokkaido University
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Tonooka S
Hokkaido Univ. Sapporo Jpn
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Tono-oka Shuichi
Division Of Molecular Oncology Institute For Genetic Medicine Hokkaido University
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