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首页> 外文期刊>World Journal of Microbiology & Biotechnology >Purification and characterization of a cold active alkaline protease from Stenotrophomonas sp., isolated from Kashmir, India
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Purification and characterization of a cold active alkaline protease from Stenotrophomonas sp., isolated from Kashmir, India

机译:分离自印度克什米尔的拟单胞菌属的冷活性碱性蛋白酶的纯化和表征

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摘要

A Psychrotolerant alkaline protease producing bacterium IIIM-ST045 was isolated from a soil sample collected from the Thajiwas glacier of Kashmir, India and identified as Stenotrophomonas sp. on the basis of its biochemical properties and 16S ribosomal gene sequencing. The strain could grow well within a temperature range of 4-37A degrees C however, showed optimum growth at 15A degrees C. The strain was found to over-produce proteases when it was grown in media containing lactose as carbon source (157.50 U mg(-1)). The maximum specific enzyme activity (398 U mg(-1)) was obtained using soya oil as nitrogen source, however, the inorganic nitrogen sources urea, ammonium chloride and ammonium sulphate showed the lowest production of 38.9, 62.2 and 57.9 U mg(-1). The enzyme was purified to 18.45 folds and the molecular weight of the partially purified protease was estimated to be similar to 55 kDa by SDS-PAGE analysis. The protease activity increased as the increase in enzyme concentration while as the optimum enzyme activity was found when casein (1% w/v) was used as substrate. The enzyme was highly active over a wide range of pH from 6.5 to 12.0 showing optimum activity at pH 10.0. The optimum temperature for the enzyme was 15A degrees C. Proteolytic activity reduced gradually with higher temperatures with a decrease of 56% at 40A degrees C. The purified enzyme was checked for the removal of protein containing tea stains using a silk cloth within a temperature range of 10-60A degrees C. The best washing efficiency results obtained at low temperatures indicate that the enzyme may be used for cold washing purposes of delicate fabrics that otherwise are vulnerable to high temperatures.
机译:从从印度克什米尔的塔吉瓦斯冰川收集的土壤样品中分离出产生抗精神病碱性蛋白酶的细菌IIIM-ST045,并将其鉴定为嗜碱菌。根据其生化特性和16S核糖体基因测序。该菌株在4-37A摄氏度的温度范围内可以很好地生长,但是在15A摄氏度下表现出最佳的生长。当该菌株在以乳糖为碳源(157.50 U mg( -1))。以大豆油为氮源可获得最大的比酶活性(398 U mg(-1)),而无机氮源尿素,氯化铵和硫酸铵的最低酶活度分别为38.9、62.2和57.9 U mg(- 1)。将该酶纯化至18.45倍,并且通过SDS-PAGE分析估计部分纯化的蛋白酶的分子量类似于55kDa。当使用酪蛋白(1%w / v)作为底物时,蛋白酶活性随着酶浓度的增加而增加,而发现了最佳酶活性。该酶在6.5至12.0的宽pH范围内均具有高活性,在pH 10.0时显示最佳活性。酶的最适温度为15A摄氏度。蛋白水解活性随着温度的升高而逐渐降低,在40A摄氏度下降低了56%。在一定温度范围内,用丝布检查纯化的酶是否去除了茶渍中的蛋白质。在低温下获得的最佳洗涤效率为10-60A。在低温下获得的最佳洗涤效率结果表明,该酶可用于脆弱织物的冷洗涤目的,否则易受高温的影响。

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