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Substrate specificity of phospholipase A2 isozyme from the pyloric ceca of the starfish Asterina pectinifera
イトマキヒトデ幽門盲のう由来ホスホリパーゼA2アイソザイムの基質特異性
2004
Nippon Suisan Gakkaishi
イトマキヒトデ幽門盲のう由来ホスホリパーゼA2アイソザイムの基質特異性
Phospholipase A 2 isozyme (PLA 2 II), which showed diŠerent mobility on native PAGE from that of the PLA 2 (PLA 2 I) puriˆed previously, was isolated from the pyloric ceca of the starˆsh Asterina pectinifera. The PLA 2 II was mainly oleic acid released from 1 palmitoyl 2 oleoyl sn glycero 3 phosphocholine. The N terminal amino acid sequence of the PLA 2 II was SVYQF. For hydrolysis of egg yolk phosphatidylcholine, the optimum pH and temperature of the PLA 2 II were at around pH 9.0 and
doi:10.2331/suisan.70.54
fatcat:ehbga5ogjnba5i3jf4mnm3yibu