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在酵母中表达耐盐假溶菌酶以在高盐条件下高效进行蛋白质水解。

Expression of a Salt-Tolerant Pseudolysin in Yeast for Efficient Protein Hydrolysis under High-Salt Conditions.

机构信息

School of Food Science and Engineering, South China University of Technology, Guangzhou 510641, China.

Guangdong Food Green Processing and Nutrition Regulation Technologies Research Center, Guangzhou 510650, China.

出版信息

Biomolecules. 2022 Dec 30;13(1):83. doi: 10.3390/biom13010083.

Abstract

Protease biocatalysis in a high-salt environment is very attractive for applications in the detergent industry, the production of diagnostic kits, and traditional food fermentation. However, high-salt conditions can reduce protease activity or even inactivate enzymes. Herein, in order to explore new protease sources, we expressed a salt-tolerant pseudolysin of SWJSS3 isolated from deep-sea mud in . After optimizing the concentration of ion cofactors in yeast peptone dextrose (YPD) medium, the proteolytic activity in the supernatant was 2.41 times more than that in the control group when supplemented with 5 mM CaCl and 0.4 mM ZnCl. The extracellular proteolytic activity of pseudolysin reached 258.95 U/mL with optimized expression cassettes. In addition, the expression system increased the salt tolerance of pseudolysin to sodium chloride (NaCl)and sodium dodecyl sulfate (SDS) and the recombinant pseudolysin retained 15.19% activity when stored in 3 M NaCl for 7 days. The recombinant pseudolysin was able to efficiently degrade the β-conglycinin from low-denatured soy protein isolates and glycinin from high-denatured soy protein isolates under high temperatures (60 °C) and high-salt (3 M NaCl) conditions. Our study provides a salt-tolerant recombinant protease with promising applications in protein hydrolysis under high-salt conditions.

摘要

在高盐环境中进行蛋白酶生物催化对于应用于洗涤剂工业、诊断试剂盒生产和传统食品发酵非常有吸引力。然而,高盐条件会降低蛋白酶的活性,甚至使酶失活。在此,为了探索新的蛋白酶来源,我们在 中表达了从深海泥中分离到的耐盐假溶菌酶 SWJSS3。在优化酵母蛋白胨葡萄糖(YPD)培养基中离子辅助因子的浓度后,当补充 5 mM CaCl2 和 0.4 mM ZnCl2 时,上清液中的酶解活性比对照组高 2.41 倍。优化表达盒后,假溶菌酶的细胞外酶解活性达到 258.95 U/mL。此外,表达系统提高了假溶菌酶对氯化钠(NaCl)和十二烷基硫酸钠(SDS)的耐盐性,重组假溶菌酶在 3 M NaCl 中储存 7 天仍保留 15.19%的活性。重组假溶菌酶能够在高温(60°C)和高盐(3 M NaCl)条件下有效地降解低变性大豆蛋白分离物中的β-伴大豆球蛋白和高变性大豆蛋白分离物中的大豆球蛋白。我们的研究提供了一种耐盐重组蛋白酶,有望在高盐条件下用于蛋白质水解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e46/9855795/6541596649be/biomolecules-13-00083-g001.jpg

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