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Purification and characterization of alkaline soda-bleach stable protease from Bacillus sp. APP-07 isolated from Laundromat soil

机译:芽孢杆菌属碱性苏打漂白稳定蛋白酶的纯化和鉴定。从洗衣店土壤中分离出来的APP-07

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摘要

The detergent-compatible alkaline protease was produced from the bacterial strain Bacillus sp. APP-07 isolated from Laundromat soil of Solapur, Maharashtra, India. The culture was grown in 1000 ml capacity baffled flask with a working volume of 100 ml and incubated at 55 °C for 33 h on a rotary shaker. After incubation, alkaline protease was partially purified by the sequential method of acetone precipitation followed by nominal molecular weight limit (NMWL) cut-off ultrafiltration using 50 K and 10 K filters. Finally, Sephadex G-100 gel filtration chromatographic purification was performed to obtain 3.12 fold purified alkaline protease enzyme with a 66.67% final yield. The purified enzyme showed 31907.269 units (U) of enzyme activity containing 8741.718 U/mg of specific enzyme activity. The molecular weight of the enzyme was confirmed about 33.0 kDa (kDa) by the SDS-PAGE analysis. The purified enzyme was stable at higher pH and temperature range, with an optimum pH 10.5 and temperature 55 °C. The enzyme showed excellent stability and compatibility in various detergents, surfactants, bleach, and oxidizing agents. The enzyme activity enhanced in the presence of Ca2+, Cu2+, and surfactants, whereas; the phenylmethylsulphonyl fluoride (PMSF) and Diisopropyl fluorophosphate (DFP) completely inhibit the enzymatic activity, which pointed out that the enzyme affiliated to serine-centered metalloproteases family.In conclusion, the remarkable tolerance and stability of the enzyme explored the promising candidature for the several potential applications in the laundry detergents. The sustainability of the enzyme might serve several possible applications in the laundry detergents, leather industries, and other harsh industrial processes.
机译:洗涤剂相容的碱性蛋白酶由细菌菌株芽孢杆菌属(Bacillus sp。)产生。 APP-07从印度马哈拉施特拉邦索拉普的自助洗衣店土壤中分离出来。将培养物在1000毫升容量的带挡板烧瓶中培养,该烧瓶的工作体积为100毫升,并在55℃下在旋转摇床上孵育33个小时。温育后,碱性蛋白酶通过丙酮沉淀的顺序方法部分纯化,然后使用50 K和10 K过滤器进行标称分子量极限(NMWL)截止超滤。最后,进行Sephadex G-100凝胶过滤层析纯化,获得3.12倍纯化的碱性蛋白酶,最终收率66.67%。纯化的酶显示31907.269单位(U)的酶活性,其中包含8741.718 U / mg的比酶活性。通过SDS-PAGE分析确认该酶的分子量为约33.0 kDa(kDa)。纯化的酶在较高的pH和温度范围内稳定,最佳pH为10.5,温度为55°C。该酶在各种洗涤剂,表面活性剂,漂白剂和氧化剂中均显示出极好的稳定性和相容性。在Ca 2 + ,Cu 2 + 和表面活性剂存在下,酶活性增强。苯甲基磺酰氟(PMSF)和氟磷酸二异丙酯(DFP)完全抑制了酶的活性,这表明该酶属于丝氨酸为中心的金属蛋白酶家族。总之,该酶的显着耐受性和稳定性为这几种酶探索了有希望的候选条件。在洗衣粉中的潜在应用。酶的可持续性可能会在洗衣粉,皮革工业和其他苛刻的工业过程中提供多种可能的应用。

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