[Efficiency of Escherichia coli and Bacillus subtilis Expression Systems for Production of Binase Mutants].

Q3 Medicine
A I Nadyrova, A S Kosnyrev, V V Ulyanova, E V Dudkina, V I Vershinina, O N Ilinskaya
{"title":"[Efficiency of Escherichia coli and Bacillus subtilis Expression Systems for Production of Binase Mutants].","authors":"A I Nadyrova,&nbsp;A S Kosnyrev,&nbsp;V V Ulyanova,&nbsp;E V Dudkina,&nbsp;V I Vershinina,&nbsp;O N Ilinskaya","doi":"10.31857/S0026898423050154, EDN: YXONYN","DOIUrl":null,"url":null,"abstract":"<p><p>Bacillus pumilus ribonuclease (binase) exhibits cytotoxic and oncolytic properties, while causing genotoxic effects at high concentrations. Mutants that have reduced catalytic activity and preserve the antitumor properties of the native enzyme could exert lower toxic side effects. Mutant binase forms with the Lys26Ala and His101Glu single substitutions were obtained by site-directed mutagenesis. A comparative analysis of Escherichia coli- and Bacillus subtilis-based expression systems demonstrated that the latter is better to use to produce the binase mutants. The binase mutants with reduced catalytic activity were isolated and purified to homogeneity by ion exchange chromatography; the maximum yield was 25 mg/L. Catalytic activities of the mutants toward natural RNA-substrates in comparison with those for native binase were estimated at 11% and 0.02%, respectively. Like native binase, the Lys26Ala mutant was found to be cytotoxic to the A549, BT-20, and HuTu 80 tumor cell lines, but did not substantially affect normal WI-38 cells. The His101Glu mutant did not show cytotoxicity.</p>","PeriodicalId":39818,"journal":{"name":"Molekulyarnaya Biologiya","volume":"57 5","pages":"807-818"},"PeriodicalIF":0.0000,"publicationDate":"2023-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Molekulyarnaya Biologiya","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.31857/S0026898423050154, EDN: YXONYN","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0

Abstract

Bacillus pumilus ribonuclease (binase) exhibits cytotoxic and oncolytic properties, while causing genotoxic effects at high concentrations. Mutants that have reduced catalytic activity and preserve the antitumor properties of the native enzyme could exert lower toxic side effects. Mutant binase forms with the Lys26Ala and His101Glu single substitutions were obtained by site-directed mutagenesis. A comparative analysis of Escherichia coli- and Bacillus subtilis-based expression systems demonstrated that the latter is better to use to produce the binase mutants. The binase mutants with reduced catalytic activity were isolated and purified to homogeneity by ion exchange chromatography; the maximum yield was 25 mg/L. Catalytic activities of the mutants toward natural RNA-substrates in comparison with those for native binase were estimated at 11% and 0.02%, respectively. Like native binase, the Lys26Ala mutant was found to be cytotoxic to the A549, BT-20, and HuTu 80 tumor cell lines, but did not substantially affect normal WI-38 cells. The His101Glu mutant did not show cytotoxicity.

[大肠杆菌和枯草芽孢杆菌表达系统生产Binase突变体的效率]。
短小芽孢杆菌核糖核酸酶(binase)表现出细胞毒性和溶瘤特性,同时在高浓度下引起遗传毒性作用。催化活性降低并保持天然酶抗肿瘤特性的突变体可以发挥较低的毒副作用。通过定点诱变获得具有Lys26Ala和His101Glu单取代的突变二元酶形式。对基于大肠杆菌和枯草芽孢杆菌的表达系统的比较分析表明,后者更适合用于生产二元酶突变体。分离催化活性降低的二元酶突变体,并通过离子交换色谱纯化至均一;最大产量为25mg/L。与天然二进制酶相比,突变体对天然RNA底物的催化活性估计分别为11%和0.02%。与天然二进制酶一样,发现Lys26Ala突变体对A549、BT-20和HuTu 80肿瘤细胞系具有细胞毒性,但基本上不影响正常的WI-38细胞。His101Glu突变体没有表现出细胞毒性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Molekulyarnaya Biologiya
Molekulyarnaya Biologiya Medicine-Medicine (all)
CiteScore
0.70
自引率
0.00%
发文量
131
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信