从嗜盐环境中分离的一种新微生物的碱性蛋白酶的酶学特性。

IF 2 4区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
R P Rejisha, M Murugan
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引用次数: 0

摘要

微生物酶,尤其是细菌碱性蛋白酶,在许多工业过程中都是必不可少的,包括洗涤剂制造、食品加工、生物修复、药品和制革。由于其可能的工业效益,本研究重点研究了芽孢杆菌spi -4菌株产生的嗜盐碱性蛋白酶的纯化和特性。方法:对细菌SPII-4的16S rRNA基因进行测序并进行系统发育分析。以酪蛋白为底物测定细胞外粗酶的蛋白水解活性。温度、pH、盐度、金属离子和化学溶剂都被用来评估酶的活性。每个实验都进行三次重复,并使用Microsoft Excel中具有不等方差的学生t检验来评估统计显著性。结果:16S rRNA测序结果与Bacillus sp.菌株2S4的同源性为100%,覆盖率为99%。该蛋白酶在40°C、碱性pH值9-11、NaCl浓度高达5%的条件下活性最强。当存在BaCl2时,该酶在金属离子中活性最高(14.64 U/mg)。此外,它在表面活性剂Triton-X和各种化学溶剂中都能保持活性。讨论:芽孢杆菌SPII-4蛋白酶在表面活性剂和溶剂的存在下,以及在极高和极低的盐度和碱度条件下,都表现出优异的稳定性和活性。这些特征表明该蛋白酶具有广泛工业应用的潜力,并且与相关嗜盐细菌酶的研究一致。为了最大限度地提高其商业用途,需要进行更多的净化和规模化研究。结论:芽孢杆菌SPII-4的碱性蛋白酶在高盐、高碱度和高溶剂条件下具有稳定性,具有相当大的工业应用前景。这些特性使其成为食品、洗涤剂和制药行业以及生物修复领域的可行选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Enzymatic Characterization of Alkaline Protease from a Novel Microorganism Isolated from a Halophilic Environment.

Introduction: Microbial enzymes, especially bacterial alkaline proteases, are essential to many industrial processes, including the manufacturing of detergents, food processing, bioremediation, medicines, and tanneries. Because of its possible industrial benefits, this study focuses on the purification and characterisation of a halophilic alkaline protease generated by Bacillus sp. strain SPII-4.

Methods: The bacteria SPII-4's 16S rRNA gene was sequenced and subjected to phylogenetic analysis. Casein was used as a substrate to measure the extracellular crude enzyme's proteolytic activity. Temperature, pH, salinity, metal ions, and chemical solvents were all used to assess enzymatic activity. Every experiment was run in triplicate, and Student's t-tests with unequal variances in Microsoft Excel were used to assess statistical significance.

Results: The 16S rRNA sequencing matched Bacillus sp. strain 2S4 with 100% identity and 99% coverage. The protease was most active at 40°C, in the alkaline pH range of 9-11, and at concentrations of up to 5% NaCl. The enzyme had the maximum activity (14.64 U/mg) among the metal ions examined when BaCl2 was present. Additionally, it maintained its activity in the presence of the surfactant Triton-X and in a variety of chemical solvents. The observed differences were statistically significant (p < 0.001)

Discussion: The Bacillus SPII-4 protease showed exceptional stability and activity in the presence of surfactants and solvents, as well as in extremely high and low salinity and alkalinity conditions. These characteristics point to the protease's potential for widespread industrial use and are in line with research on related halophilic bacterial enzymes. To maximize its commercial usage, more purification and scale-up research are necessary.

Conclusion: Bacillus sp. SPII-4's halo-alkaline protease exhibits considerable industrial promise because of its stability in conditions that are high in salt, alkalinity, and solvents. These qualities make it a viable option for use in the food, detergent, and pharmaceutical sectors as well as in bioremediation.

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来源期刊
Current protein & peptide science
Current protein & peptide science 生物-生化与分子生物学
CiteScore
5.20
自引率
0.00%
发文量
73
审稿时长
6 months
期刊介绍: Current Protein & Peptide Science publishes full-length/mini review articles on specific aspects involving proteins, peptides, and interactions between the enzymes, the binding interactions of hormones and their receptors; the properties of transcription factors and other molecules that regulate gene expression; the reactions leading to the immune response; the process of signal transduction; the structure and function of proteins involved in the cytoskeleton and molecular motors; the properties of membrane channels and transporters; and the generation and storage of metabolic energy. In addition, reviews of experimental studies of protein folding and design are given special emphasis. Manuscripts submitted to Current Protein and Peptide Science should cover a field by discussing research from the leading laboratories in a field and should pose questions for future studies. Original papers, research articles and letter articles/short communications are not considered for publication in Current Protein & Peptide Science.
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