温度和pH对粪藻P2蛋白酶稳定性的影响

E. A. Obichi, V. Ezebuiro
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摘要

背景:细菌蛋白酶是一类非常重要的工业酶。它们参与蛋白质中肽键的水解。细菌蛋白酶的工业应用一直受到产率低和生物工艺条件不稳定的限制。本实验旨在研究温度和pH对粪Alcaligene faecalis P2菌株蛋白酶稳定性的影响。方法:从大豆废水影响的土壤中分离出蛋白酶产菌,在酪蛋白琼脂平板上筛选蛋白酶产菌。按照蛋白酶测定的标准方法进行蛋白酶测定,并在20 ~ 90℃的温度范围和3 ~ 12的pH范围内考察蛋白酶的稳定性。利用蛋白酶产生菌的分子特征对其进行了鉴定。结果:蛋白酶测定结果显示,1单位粗酶释放酪氨酸量为0.176µmol/mL,蛋白酶活性为0.19 U/mL。稳定性研究表明,该蛋白酶具有较宽的pH谱和温度稳定性。在pH为9、温度为40℃条件下,蛋白酶在30min后最稳定,在pH为9条件下,蛋白酶活性最高,为1.259 U/mL。根据其16S基因的系统发育分析,将该蛋白酶产生菌归类为Alcaligene faecalis P2。序列已提交给GenBank,注册号为MZ477004。结论:本研究表明,大豆废水影响的土壤中蕴藏着具有较高工业潜力的蛋白酶产菌。此外,研究表明,本研究产生的蛋白酶在较宽的温度和pH下都能保持其活性。
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Effects of Temperature and pH on the Stability of Protease Produced by Alcaligenes faecalis P2
Background: Bacterial proteases represent a group of very important industrial enzymes. They are involved in the hydrolysis of peptide bond found in protein. Industrial application of bacterial proteases has been limited by low yield and instability at biotechnological process conditions. This study was design to investigate the effect of temperature and pH on the stability of protease produced by Alcaligene faecalis strain P2. Methodology: Protease-producing bacteria were isolated from beans effluent-impacted soil and screened for protease production on Casein agar plate. Protease assay was carried out following standard method for protease determination and the stability of the protease produced was investigated over temperature range of 20 to 90 oC and pH range of 3 to 12. The protease-producing bacterium was identified using its molecular characteristics. Results: Protease assay result showed that the amount of tyrosine released by one unit of the crude enzyme was 0.176 µmol/mL resulting in 0.19 U/mL protease activity. Stability studies showed that the protease had wide spectrum of pH and temperature stability. The protease was most stable at pH 9 and temperature of 40 oC after 30 min. Maximum protease activity of 1.259 U/mL was recorded with pH 9 after 30 min. The protease-producing bacterium was classified as Alcaligene faecalis P2 based on phylogenetic analysis of its 16S gene analysis. The sequences have been submitted to GenBank under the accession number MZ477004. Conclusion: This study therefore has demonstrated that beans effluent-impacted soil harbours protease producing bacteria with high industrial potentials. In addition, the study revealed that the protease produced in this study can retain its activity over wide temperature and pH.
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