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Chinese Academy of Sciences Institutional Repositories Grid
Biochemical characterization and molecular docking of cloned xylanase gene from Bacillus subtilis RTS expressed in E. coli

文献类型:期刊论文

作者Saleem, Aimen2,5; Waris, Saboora1,4; Ahmed, Toheed3; Tabassum, Romana2,5
刊名INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES
出版日期2021-01-31
卷号168页码:310-321
关键词Cloning Sequencing Genetic characterization AutoDock Vina
ISSN号0141-8130
DOI10.1016/j.ijbiomac.2020.12.001
英文摘要This study employed mesophilic Bacillus subtilis RTS strain isolated from soil with high xylanolytic activity. A 642 bp (xyn) xylanase gene (GenBank accession number MT677937) was extracted from Bacillus subtilis RTS and cloned in Escherichia coli BL21 cells using pET21c expression system. The cloned gene belongs to glycoside hydrolase family 11 with protein size of approximately 23 KDa. The recombinant xylanase showed optimal enzymeactivity at 60 degrees C and at pH6.5. Thermostability of recombinant xylanase was observed between the temperature range of 30-60 degrees C. Xylanase also remained stable in different concentration of various organic solvents (ethanol, butanol). This might be due to the formation of protein/organic solvent interface which prevents stripping of essential water molecules from enzyme, thus enzyme conformation and activity remained stable. Finally, the molecular docking analysis through AutoDock Vina showed the involvement of Tyr 108, Arg140 and Pro144 in protein-ligand interaction, which stabilizes this complex. The observed stability of recombinant xylanase at higher temperature and in the presence of organic solvent (ethanol, butanol) suggested possible application of this enzyme in biofuel and other industrial applications. (C) 2020 Elsevier B.V. All rights reserved.
WOS关键词CELLULASE-FREE XYLANASE ; THERMOSTABLE XYLANASE ; PURIFICATION ; CLONING ; LICHENIFORMIS
资助项目Higher Education Commission (HEC), H9 Islamabad, Pakista[PAK-US/HEC/2011/144]
WOS研究方向Biochemistry & Molecular Biology ; Chemistry ; Polymer Science
语种英语
WOS记录号WOS:000608018200032
出版者ELSEVIER
资助机构Higher Education Commission (HEC), H9 Islamabad, Pakista
源URL[http://ir.ipe.ac.cn/handle/122111/43261]  
专题中国科学院过程工程研究所
通讯作者Tabassum, Romana
作者单位1.Shaheed Zulfiqar Ali Bhutto Med Univ, Dept Mol Biol, Islamabad, Pakistan
2.Natl Inst Biotechnol & Genet Engn NIBGE, PO Box577,Jhang Rd 3800, Faisalabad, Pakistan
3.Chinese Acad Sci, Key Lab Green Proc & Engn, Inst Proc Engn, Beijing 100190, Peoples R China
4.Quaid i Azam Univ, Dept Biol Sci, Islamabad, Pakistan
5.Pakistan Inst Engn & Appl Sci PIEAS, Islamabad, Pakistan
推荐引用方式
GB/T 7714
Saleem, Aimen,Waris, Saboora,Ahmed, Toheed,et al. Biochemical characterization and molecular docking of cloned xylanase gene from Bacillus subtilis RTS expressed in E. coli[J]. INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,2021,168:310-321.
APA Saleem, Aimen,Waris, Saboora,Ahmed, Toheed,&Tabassum, Romana.(2021).Biochemical characterization and molecular docking of cloned xylanase gene from Bacillus subtilis RTS expressed in E. coli.INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,168,310-321.
MLA Saleem, Aimen,et al."Biochemical characterization and molecular docking of cloned xylanase gene from Bacillus subtilis RTS expressed in E. coli".INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES 168(2021):310-321.

入库方式: OAI收割

来源:过程工程研究所

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