卤代烷烃脱卤酶LinB在枯草芽孢杆菌孢子表面的首次展示。

IF 1 4区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY Protein and Peptide Letters Pub Date : 2023-01-01 DOI:10.2174/0109298665238177231020044054
Fuli Wang, Xiujie Liu, Tianyu Song, Chengxin Pei, Qibin Huang, Hui Jiang, Hailing Xi
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引用次数: 0

摘要

背景:作为一种卤代烷烃脱卤酶,林B对许多剧毒难降解化合物具有良好的催化活性,可以以绿色无毒的方式实现化学武器HD的消除。目的:在枯草芽孢杆菌孢子表面展示卤代烷脱卤酶LinB。方法:通过基因重组构建了卤代烷烃脱卤酶LinB的枯草芽孢杆菌孢子表面展示系统。结果:LinB能成功地在孢子表面显示。所展示的LinB孢子对HD类似物2-氯乙基乙基硫醚(2-CEES)的水解活性为4.30±0.09U/mL,比活性为0.78±0.03U/mg。本研究获得了LinB(日本飞燕草UT26)的枯草芽孢杆菌孢子,该孢子具有以前未报道的酶活性。结论:孢子表面展示技术以抗性孢子为载体,保证了LinB的活性,提高了其稳定性,降低了生产成本,扩大了其应用范围。
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First Display of Haloalkane Dehalogenase LinB on the Surface of Bacillus subtilis Spore.

Background: LinB, as a Haloalkane dehalogenase, has good catalytic activity for many highly toxic and recalcitrant compounds, and can realize the elimination of chemical weapons HD in a green non-toxic mode.

Objectives: In order to display Haloalkane dehalogenase LinB on the surface of Bacillus subtilis spore.

Methods: We have constituted the B. subtilis spore surface display system of halogenated alkanes dehalogenase LinB by gene recombination.

Results: Data revealed that LinB can display on spore surface successfully. The hydrolyzing HD analogue 2-chloroethyl ethylsulfide (2-CEES) activity of displayed LinB spores was 4.30±0.09 U/mL, and its specific activity was 0.78±0.03U/mg. Meanwhile, LinB spores showed a stronger stress resistance activity on 2-CEES than free LinB. This study obtained B. subtilis spores of LinB (phingobium japonicum UT26) with enzyme activity that was not reported before.

Conclusion: Spore surface display technology uses resistance spore as the carrier to guarantee LinB activity, enhances its stability, and reduces the production cost, thus expanding the range of its application.

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来源期刊
Protein and Peptide Letters
Protein and Peptide Letters 生物-生化与分子生物学
CiteScore
2.90
自引率
0.00%
发文量
98
审稿时长
2 months
期刊介绍: Protein & Peptide Letters publishes letters, original research papers, mini-reviews and guest edited issues in all important aspects of protein and peptide research, including structural studies, advances in recombinant expression, function, synthesis, enzymology, immunology, molecular modeling, and drug design. Manuscripts must have a significant element of novelty, timeliness and urgency that merit rapid publication. Reports of crystallization and preliminary structure determination of biologically important proteins are considered only if they include significant new approaches or deal with proteins of immediate importance, and preliminary structure determinations of biologically important proteins. Purely theoretical/review papers should provide new insight into the principles of protein/peptide structure and function. Manuscripts describing computational work should include some experimental data to provide confirmation of the results of calculations. Protein & Peptide Letters focuses on: Structure Studies Advances in Recombinant Expression Drug Design Chemical Synthesis Function Pharmacology Enzymology Conformational Analysis Immunology Biotechnology Protein Engineering Protein Folding Sequencing Molecular Recognition Purification and Analysis
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