Department of Microbiology, University of Karachi, Karachi, 75270, Pakistan.
Department of Pharmaceutical Sciences, College of Pharmacy, Oregon State University, Corvallis, 97331, USA.
Appl Biochem Biotechnol. 2024 Aug;196(8):5045-5063. doi: 10.1007/s12010-023-04790-6. Epub 2023 Nov 24.
Microbial alkaline proteases are dominating the global enzyme market with a share of over 65% due to their multifarious catalytic potentials. Hence, production of proteases with novel properties of commercial significance is highly desirable to meet the global enzyme demand. Here, we report the purification, characterization, and pilot-scale application of a serine protease from the desert soil bacterium Bacillus subtilis ZMS-2 with novel properties as dehairing agent in leather processing. The enzyme was purified 16.5-fold with a specific activity of 1543.5 U mg and recovery percentage of 33.6% using ammonium sulfate precipitation, ion exchange, and gel filtration chromatography. The purified enzyme was characterized as a metal ion-, surfactant-, and denaturant-compatible alkaline serine protease having a molecular weight of 36.1 kDa with an optimum activity at pH 8.5 and 60 °C. The catalytic activity of the enzyme was enhanced by Zn (204%), Ag (110%), HO (123%), Triton X-100 (110%), iso-octane (109%), chloroform (110%), ethanol (105%), ethyl acetate (110%), and acetonitrile (128%). During pilot-scale applications, the optimum condition was found to be a combination of enzyme (1.5%, 460 U mL), sodium sulfide (2%), and calcium hydroxide (lime) (3%). Under this condition, the time required for complete dehairing was 90 min. Chemoenzymatically processed skins exhibited better physical properties than chemically processed skin, including tensile strength (16.35 ± 6.68 N/mm), ball burst (452.88 ± 6.06 N/mm), percent elongation (38.85 ± 1.06 N), tear strength (50.16 ± 4.42 N/mm), and softness (6.5 mm). Electron microscopy analysis of the treated skin showed complete removal of hairs with roots, confirming the keratin specificity of the enzyme. Moreover, the enzyme-assisted dehairing process reduced chemical oxygen demand (COD), biochemical oxygen demand (BOD), total dissolved solids (TDS), and total suspended solids (TSS) by 68, 77, 34, and 39%, respectively. Thus, the alkaline serine protease from B. subtilis ZMS-2 is a potential dehairing agent for the eco-friendly processing of animal skins on industrial scales.
微生物碱性蛋白酶因其多样的催化潜力而占据了全球酶市场 65%以上的份额。因此,生产具有商业意义的新型特性的蛋白酶以满足全球酶的需求是非常理想的。在这里,我们报告了一种来自沙漠土壤芽孢杆菌枯草芽孢杆菌 ZMS-2 的丝氨酸蛋白酶的纯化、表征和中试规模应用,该蛋白酶具有新型的毛发处理剂特性,可用于皮革加工。该酶使用硫酸铵沉淀、离子交换和凝胶过滤层析法纯化 16.5 倍,比活为 1543.5 U mg,回收率为 33.6%。纯化后的酶被表征为一种金属离子、表面活性剂和变性剂兼容的碱性丝氨酸蛋白酶,分子量为 36.1 kDa,最适 pH 为 8.5,最适温度为 60°C。该酶的催化活性可通过 Zn(204%)、Ag(110%)、HO(123%)、Triton X-100(110%)、异辛烷(109%)、氯仿(110%)、乙醇(105%)、乙酸乙酯(110%)和乙腈(128%)增强。在中试规模应用中,发现最佳条件是酶(1.5%,460 U mL)、硫化钠(2%)和氢氧化钙(石灰)(3%)的组合。在此条件下,完全脱毛所需的时间为 90 分钟。通过化学酶法处理的皮具有比化学处理皮更好的物理性能,包括拉伸强度(16.35 ± 6.68 N/mm)、球爆裂(452.88 ± 6.06 N/mm)、伸长率(38.85 ± 1.06%)、撕裂强度(50.16 ± 4.42 N/mm)和柔软度(6.5 mm)。处理过的皮肤的电子显微镜分析表明毛发和根部已完全去除,证实了酶对角蛋白的特异性。此外,酶辅助脱毛工艺可使化学需氧量(COD)、生化需氧量(BOD)、总溶解固体(TDS)和总悬浮固体(TSS)分别减少 68%、77%、34%和 39%。因此,枯草芽孢杆菌 ZMS-2 的碱性丝氨酸蛋白酶是一种用于动物皮在工业规模上进行环保处理的潜在毛发处理剂。