首页> 美国卫生研究院文献>Saudi Journal of Biological Sciences >Isolation and screening of Streptomyces sp. Al-Dhabi-49 from the environment of Saudi Arabia with concomitant production of lipase and protease in submerged fermentation
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Isolation and screening of Streptomyces sp. Al-Dhabi-49 from the environment of Saudi Arabia with concomitant production of lipase and protease in submerged fermentation

机译:链霉菌的分离和筛选。来自沙特阿拉伯环境的Al-Dhabi-49在水下发酵中伴随产生脂肪酶和蛋白酶

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摘要

In this study, sp. Al-Dhabi-49 was isolated from the soil sample of Saudi Arabian environment for the simultaneous production of lipase and protease in submerged fermentation. The process parameters were optimized to enhance enzymes production. The production of protease and lipase was found to be maximum after 5 days of incubation (139.2 ± 2.1 U/ml, 253 ± 4.4 U/ml). Proteolytic enzyme increases with the increase in pH up to 9.0 (147.2 ± 3.6 U/ml) and enzyme production depleted significantly at higher pH values. In the case of lipase, production was maximum in the culture medium containing pH 8.0 (166 ± 1.3 U/ml). The maximum production of protease was observed at 40 °C (174 ± 12.1 U/ml) by sp. Lipase activity was found to be optimum at the range of temperatures (30–50 °C) and maximum production was achieved at 35 °C (168 ± 7.8 U/ml). Among the evaluated carbon sources, maltose significantly influenced on protease production (218 ± 12.8 U/ml). Lipase production was maximum when sp. was cultured in the presence of glucose (162 ± 10.8U/ml). Among various concentrations of peptone, 1.0% (w/v) significantly enhanced protease production. The lipase production was very high in the culture medium containing malt extract as nitrogen source (86 ± 10.2 U/ml). Protease production was maximum in the presence of Ca as ionic source (212 ± 3.8 U/ml) and lipase production was enhanced by the addition of Mg with the fermentation medium (163.7 ± 6.2 U/ml).
机译:在这项研究中,sp。从沙特阿拉伯环境的土壤样品中分离出Al-Dhabi-49,以在水下发酵中同时生产脂肪酶和蛋白酶。优化工艺参数以提高酶的产生。孵育5天后发现蛋白酶和脂肪酶的产量最高(139.2±2.1 U / ml,253±4.4 U / ml)。蛋白水解酶随着pH值的增加而增加,最高可达9.0(147.2±3.6 U / ml),并且在更高的pH值下酶的产量显着减少。在脂肪酶的情况下,在含pH 8.0(166±1.3 U / ml)的培养基中产量最高。通过sp在40°C(174±12.1 U / ml)观察到蛋白酶的最大产量。发现脂肪酶活性在温度范围(30–50°C)时最佳,在35°C(168±7.8 U / ml)时达到最大产量。在评估的碳源中,麦芽糖显着影响蛋白酶的产生(218±12.8 U / ml)。当sp时脂肪酶的产量最高。在葡萄糖(162±10.8U / ml)存在下培养。在各种浓度的蛋白ept中,1.0%(w / v)显着提高了蛋白酶的产量。在含有麦芽提取物作为氮源的培养基中,脂肪酶的产量很高(86±10.2 U / ml)。在有Ca作为离子源的情况下,蛋白酶的产量最高(212±3.8 U / ml),通过在发酵培养基中添加Mg(163.7±6.2 U / ml)可提高脂肪酶的产量。

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