Suppr超能文献

在大肠杆菌BL21中,在T7启动子控制下的芽孢杆菌属WLY78菌株固氮基因操纵子的表达

Expression of the N2 fixation gene operon of Paenibacillus sp. WLY78 under the control of the T7 promoter in Escherichia coli BL21.

作者信息

Zhang Lihong, Liu Xiaomeng, Li Xinxin, Chen Sanfeng

机构信息

State Key Laboratory for Agrobiotechnology and College of Biological Sciences, China Agricultural University, Yuanmingyuan West Road No. 2, Haidian District, Beijing, 100193, People's Republic of China.

College of Life Science, Shanxi Normal University, Linfen, 041000, Shanxi, China.

出版信息

Biotechnol Lett. 2015 Oct;37(10):1999-2004. doi: 10.1007/s10529-015-1874-5. Epub 2015 Jun 9.

Abstract

OBJECTIVE

To investigate the transcription and translation and nitrogenase activity of the nine N2-fixing-gene (nif) operon (nifBHDKENXhesAnifX) of Paenibacillus sp. WLY78 under the control of the T7 promoter in Escherichia coli BL21 under different conditions.

RESULTS

The Paenibacillus nif operon under the control of the T7 promoter is significantly transcribed and effectively translated in E. coli BL21 when grown in medium containing organic N compounds (yeast extract and Tryptone) or NH4+ by using RT-PCR and Western blot analysis. Transcription and translation of foreign nif genes in E. coli are not inhibited by environmental organic or inorganic N compounds or O2. However, contrary to transcription and translation, nitrogenase activity is 4% lower in the recombinant E. coli 78-32 compared to the native Paenibacillus sp. WLY78.

CONCLUSION

The Paenibacillus nif operon under the control of T7 promoter enables E. coli BL21 to synthesize active nitrogenase. This study shows how the nif gene operon can be transferred to non-N2-fixing bacteria or to eukaryotic organelles.

摘要

目的

研究在不同条件下,芽孢杆菌属WLY78的九个固氮基因(nif)操纵子(nifBHDKENXhesAnifX)在T7启动子控制下于大肠杆菌BL21中的转录、翻译及固氮酶活性。

结果

通过逆转录聚合酶链式反应(RT-PCR)和蛋白质免疫印迹分析表明,当在含有有机氮化合物(酵母提取物和胰蛋白胨)或NH4+的培养基中生长时,受T7启动子控制的芽孢杆菌nif操纵子在大肠杆菌BL21中能显著转录并有效翻译。环境中的有机或无机氮化合物以及O2均不会抑制大肠杆菌中外源nif基因的转录和翻译。然而,与转录和翻译情况相反,重组大肠杆菌78-32中的固氮酶活性比天然芽孢杆菌属WLY78低4%。

结论

受T7启动子控制的芽孢杆菌nif操纵子能使大肠杆菌BL21合成有活性的固氮酶。本研究展示了nif基因操纵子如何转移至非固氮细菌或真核细胞器中。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验