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Purification and Characterization of Agarase PV-1 from Pseudomonas vesicularis MA103

Pseudomonas vesicularis MA103所產洋菜酶(Agarase)PV-1之純化與特性

摘要


液化洋菜菌株Pseudomonas vesicularis所產MA103-agarases經超濃縮、DE-52離子交換樹脂、與Bio-Gel P-100層析後可得純化洋菜黴(Agarase)PV-1。Agarase PV-1最適pH和溫度分別為6.0和40℃;然而其活性在50℃下15分鐘後減少80.0%。Agarase PV-1的分子量為62.9 kDa,且在鈉離子環境中可以提高20%的相對活性。Agarase PV-1以HIMEDIA(上標 TM) agar為基質時有最佳之基質特異性活性,相對agarose為基質分解活性分別為1.4倍。Agarase PV-1水解中性洋菜之水解產物經HPLC分析,所得產物為一群介於新洋菜二糖(neoagarobiose)與新洋菜六糖(neoagarohexose)間之寡醣。利用Agarases PV-1與新洋菜六糖混合反應,經HPLC分析,所得產物為數個大於新洋菜六糖之寡醣。

並列摘要


The agarases producing strain Pseudomonas (P.) vesicularis MA103 is an agar-liquefying strain. The crude MA103-agarases is concentrated by ultrafiltration, chromatography by ion-exchange, and Bio-Gel P-100 to obtained Agarase PV-1. The optimum pH and temperature for Agarase PV-1 were 6.0 and 40℃; however 80.0% of the enzyme activity was inactivated in 15 min under 50℃. The molecular mass of Agarase PV-1 was 62.9 kDa and under sodium ion could enhance 20% relative agarase activity. The best substrate specific activities of Agarase PV-1 toward brand Himedia(superscript TM) agar were 1.4-time digestion activity compare to agarose, respectively. Hydrolytic products of agarose digested by Agarase PV-1 were analyzed by HPLC, and the results showed that they were oligosaccharides, withe molecular size between neoagarohexaose and neoagarobiose. Products of neoagarohexaose reacted with Agarase PV-1 analyzed by HPLC were oligosaccharides, with molecular size larger than neoagarohexaose.

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