Suppr超能文献

从卷曲魏斯氏菌MBFCNC-2(1)中克隆ftfCNC-2(1)基因并在枯草芽孢杆菌中作为胞外活性果聚糖蔗糖酶进行异源表达。

Cloning and heterologous expression of the ftfCNC-2(1) gene from Weissella confusa MBFCNC-2(1) as an extracellular active fructansucrase in Bacillus subtilis.

作者信息

Malik Amarila, Hapsari Maria Tyas, Ohtsu Iwao, Ishikawa Shu, Takagi Hiroshi

机构信息

Pharmaceutical Biotechnology Research Group, Faculty of Pharmacy, Universitas Indonesia, Kampus UI Depok, Depok 16424, Indonesia.

Pharmaceutical Biotechnology Research Group, Faculty of Pharmacy, Universitas Indonesia, Kampus UI Depok, Depok 16424, Indonesia.

出版信息

J Biosci Bioeng. 2015 May;119(5):515-20. doi: 10.1016/j.jbiosc.2014.09.024. Epub 2014 Oct 29.

Abstract

Fructan-exopolysaccharides (fructan-EPS) (inulin and levan) and their oligosaccharides (fructooligosaccharides, FOS) have drawn considerable interest in the food and pharmaceutical industries. EPS-producing lactic acid bacteria have been reported to produce β-fructans (inulin and levan), as well as α-glucans, by the function of sucrase enzymes, i.e., fructansucrase and glucansucrase. A fructansucrase ftfCNC-2(1) gene from Weissella confusa strain MBFCNC-2(1) was previously cloned in Escherichia coli. In this study, we aimed to express the ftf[CNC-2(1)] gene in Bacillus subtilis to obtain the active form of the extracellular recombinant protein FTF[CNC-2(1)]. This cloning was achieved by inserting the gene in-fusion with the signal sequence of the B. subtilis subtilisin E. SDS-polyacrylamide gel electrophoresis analysis and in situ activity assay with Periodic Acid-Schiff staining revealed that the recombinant FTF[CNC-2(1)] was successfully expressed as an extracellular protein from B. subtilis DB403 in its active form, which was confirmed using sucrose and raffinose.

摘要

果聚糖胞外多糖(果聚糖-EPS)(菊粉和左聚糖)及其低聚糖(低聚果糖,FOS)在食品和制药行业引起了广泛关注。据报道,产生EPS的乳酸菌通过蔗糖酶(即果聚糖蔗糖酶和葡聚糖蔗糖酶)的作用产生β-果聚糖(菊粉和左聚糖)以及α-葡聚糖。先前已将来自困惑魏斯氏菌MBFCNC-2(1)菌株的果聚糖蔗糖酶ftfCNC-2(1)基因克隆到大肠杆菌中。在本研究中,我们旨在将ftf[CNC-2(1)]基因在枯草芽孢杆菌中表达,以获得细胞外重组蛋白FTF[CNC-2(1)]的活性形式。通过将该基因与枯草芽孢杆菌枯草杆菌蛋白酶E的信号序列融合插入来实现这种克隆。十二烷基硫酸钠-聚丙烯酰胺凝胶电泳分析和高碘酸-席夫染色原位活性测定表明,重组FTF[CNC-2(1)]以活性形式成功地作为枯草芽孢杆菌DB403的细胞外蛋白表达,这通过使用蔗糖和棉子糖得到了证实。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验