In silico and experimental characterization of a new polyextremophilic subtilisin-like protease from Microbacterium metallidurans and its application as a laundry detergent additive

IF 2.6 4区 生物学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY 3 Biotech Pub Date : 2024-08-12 DOI:10.1007/s13205-024-04043-1
Afwa Gorrab, Rania Ouertani, Khouloud Hammami, Amal Souii, Fatma Kallel, Ahmed Slaheddine Masmoudi, Ameur Cherif, Mohamed Neifar
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Abstract

Considering the current growing interest in new and improved enzymes for use in a variety of applications, the present study aimed to characterize a novel detergent-stable serine alkaline protease from the extremophilic actinobacterium Microbacterium metallidurans TL13 (MmSP) using a combined in silico and experimental approach. The MmSP showed a close phylogenetic relationship with high molecular weight S8 peptidases of Microbacterium species. Moreover, its physical and chemical parameters computed using Expasy’s ProtParam tool revealed that MmSP is hydrophilic, halophilic and thermo-alkali stable. 3D structure modelling and functional prediction of TL13 serine protease resulted in the detection of five characteristic domains: [catalytic subtilase domain, fibronectin (Fn) type-III domain, peptidase inhibitor I9, protease-associated (PA) domain and bacterial Ig-like domain (group 3)], as well as the three amino acid residues [aspartate (D182), histidine (H272) and serine (S604)] in the catalytic subtilase domain. The extremophilic strain TL13 was tested for protease production using agricultural wastes/by-products as carbon substrates. Maximum enzyme activity (390 U/gds) was obtained at 8th day fermentation on potato peel medium. Extracellular extract was concentrated and partially purified using ammonium sulfate precipitation methodology (1.58 folds purification fold). The optimal pH, temperature and salinity of MmSP were 9, 60 °C and 1 M NaCl, respectively. The MmSP protease showed broad pH stability, thermal stability, salt tolerance and detergent compatibility. In order to achieve the maximum stain removal efficacy by the TL 13 serine protease, the operation conditions were optimized using a Box–Behnken Design (BBD) with four variables, namely, time (15–75 min), temperature (30–60 °C), MmSP enzyme concentration (5–10 U/mL) and pH (7–11). The maximum stain removal yield (95 ± 4%) obtained under the optimal enzymatic operation conditions (treatment with 7.5 U/mL of MmSP during 30 min at 32 °C and pH9) was in good agreement with the value predicted by the regression model (98 ± %), which prove the validity of the fitted model. In conclusion, MmSP appears to be a good candidate for industrial applications, particularly in laundry detergent formulations, due to its high hydrophilicity, alkali-halo-stability, detergent compatibility and stain removal efficiency.

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冶金微细菌中一种新型多嗜极性枯草蛋白酶的硅学和实验表征及其在洗衣粉添加剂中的应用
考虑到目前人们对用于各种应用的新型和改良酶的兴趣日益浓厚,本研究旨在采用硅学和实验相结合的方法,对来自嗜极放线菌金属微细菌 TL13(MmSP)的新型去污剂稳定型丝氨酸碱性蛋白酶进行表征。该蛋白酶与微杆菌中的高分子量 S8 肽酶有着密切的系统发育关系。此外,利用 Expasy 的 ProtParam 工具计算的物理和化学参数显示,MmSP 具有亲水性、亲卤性和热碱稳定性。通过对 TL13 丝氨酸蛋白酶的三维结构建模和功能预测,发现了五个特征结构域:[催化亚基酶结构域、纤连蛋白(Fn)III 型结构域、肽酶抑制剂 I9、蛋白酶相关(PA)结构域和细菌 Ig 样结构域(第 3 组)],以及催化亚基酶结构域中的三个氨基酸残基[天冬氨酸(D182)、组氨酸(H272)和丝氨酸(S604)]。以农业废弃物/副产品为碳底物,对嗜极菌株 TL13 进行了蛋白酶生产测试。在马铃薯皮培养基上发酵第 8 天时,获得了最大酶活性(390 U/gds )。利用硫酸铵沉淀法浓缩并部分纯化了胞外提取物(纯化倍数为 1.58 倍)。MmSP 的最佳 pH 值、温度和盐度分别为 9、60 °C 和 1 M NaCl。MmSP 蛋白酶具有广泛的 pH 稳定性、热稳定性、耐盐性和洗涤剂兼容性。为了使 TL 13 丝氨酸蛋白酶达到最大的去污效果,采用盒-贝肯设计(BBD)法对操作条件进行了优化,包括时间(15-75 分钟)、温度(30-60 ℃)、MmSP 酶浓度(5-10 U/mL)和 pH 值(7-11)四个变量。在最佳酶解操作条件下(32 ℃、pH9 条件下,30 分钟内使用 7.5 U/mL的 MmSP 处理)获得的最大去污率(95 ± 4%)与回归模型预测值(98 ± %)非常吻合,证明了拟合模型的有效性。总之,由于 MmSP 具有高亲水性、碱-卤稳定性、洗涤剂兼容性和去污效率,它似乎是工业应用(尤其是洗衣粉配方)的理想候选物质。
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来源期刊
3 Biotech
3 Biotech Agricultural and Biological Sciences-Agricultural and Biological Sciences (miscellaneous)
CiteScore
6.00
自引率
0.00%
发文量
314
期刊介绍: 3 Biotech publishes the results of the latest research related to the study and application of biotechnology to: - Medicine and Biomedical Sciences - Agriculture - The Environment The focus on these three technology sectors recognizes that complete Biotechnology applications often require a combination of techniques. 3 Biotech not only presents the latest developments in biotechnology but also addresses the problems and benefits of integrating a variety of techniques for a particular application. 3 Biotech will appeal to scientists and engineers in both academia and industry focused on the safe and efficient application of Biotechnology to Medicine, Agriculture and the Environment.
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