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Production and partial characterization of two types of phytase from Aspergillus niger NCIM 563 under submerged fermentation conditions

机译:在水下发酵条件下黑曲霉NCIM 563两种植酸酶的生产和部分表征

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Novel extracellular phytase was produced by Aspergillus niger NCIM 563 under submerged fermentation conditions at 30 °C in medium containing dextrin and glucose as carbon sources along with sodium nitrate as nitrogen source. Maximum phytase activity (41.47 IU/mL at pH 2.5 and 10.71 IU/mL at pH 4.0) was obtained when dextrin was used as carbon source along with glucose and sodium nitrate as nitrogen source. Nearly 13 times increase in phytase activity was observed when phosphate in the form of KH2PO4 (0.004 g/100 mL) was added in the fermentation medium. Physic-chemical properties of partially purified enzyme indicate the possibility of two distinct forms of phytases, Phy I and Phy II. Optimum pH and temperature for Phy I was 2.5 and 60 °C while Phy II was 4.0 and 60 °C, respectively. Phy I was stable in the pH range 1.5–3.5 while Phy II was stable in the wider pH range, 2.0–7.0. Molecular weight of Phy I and Phy II on Sephacryl S-200 was approximately 304 kDa and 183 kDa, respectively. Phy I activity was moderately stimulated in the presence of 1 mM Mg2+, Mn2+, Ca2+ and Fe3+ ions and inhibited by Zn2+ and Cd2+ ions while Phy II activity was moderately stimulated by Fe3+ ions and was inhibited by Hg2+, Mn2+ and Zn2+ ions at 1 mM concentration in reaction mixture. The Km for Phy I and II was 3.18 and 0.514 mM while Vmax was 331.16 and 59.47 μmols/min/mg protein, respectively.
机译:由黑曲霉NCIM 563在30°C的深层发酵条件下,在含有糊精和葡萄糖作为碳源以及硝酸钠作为氮源的培养基中,生产新型胞外植酸酶。当使用糊精作为碳源以及葡萄糖和硝酸钠作为氮源时,可获得最大的植酸酶活性(pH 2.5时41.47 IU / mL,pH 4.0时10.71 IU / mL)。当在发酵培养基中添加磷酸钾(0.004 g / 100 mL)形式的植酸酶时,植酸酶活性提高了近13倍。部分纯化的酶的物理化学性质表明存在两种不同形式的肌醇六磷酸酶Phy I和Phy II的可能性。 Phy I的最佳pH和温度分别为2.5和60°C,而Phy II的最佳pH和温度分别为4.0和60°C。 Phy I在1.5-3.5的pH范围内稳定,而Phy II在2.0-7.0的较宽pH范围内稳定。 Sephacryl S-200上Phy I和Phy II的分子量分别约为304 kDa和183 kDa。在存在1 mM Mg2 + ,Mn2 + ,Ca2 + 和Fe3 + 离子的情况下,可适度刺激Phy I的活性,并受到Zn2 + 和Cd2 + 的抑制。浓度为1 mM的Fe3 +离子可适度刺激Phy II活性,而Hg2 +,Mn2 +和Zn2 +离子可抑制Phy II活性。 Phy I和II的Km分别为3.18和0.514 mM,而Vmax分别为331.16和59.47μmol/ min / mg蛋白质。

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