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核黄素的鉴定:揭示大肠杆菌BL21(DE3)和MG1655之间不同的代谢特征。

Identification of riboflavin: revealing different metabolic characteristics between Escherichia coli BL21(DE3) and MG1655.

作者信息

Wang Xinran, Wang Qian, Qi Qingsheng

机构信息

National Glycoengineering Research Center, State Key Laboratory of Microbial Technology, Shandong University, Jinan 250100, P. R. China.

National Glycoengineering Research Center, State Key Laboratory of Microbial Technology, Shandong University, Jinan 250100, P. R. China

出版信息

FEMS Microbiol Lett. 2015 Jun;362(11). doi: 10.1093/femsle/fnv071. Epub 2015 Apr 28.

Abstract

There are many physiological differences between Escherichia coli B and K-12 strains, owing to their different origins. Deeper insight into the metabolic and regulative mechanisms of these strains will inform improved usage of these industrial workhorses. In the present study, we observed that BL21 fermentation broth gradually turned yellow during cultivation. By spectral analysis and liquid chromatography-mass spectrometry identification, we confirmed for the first time that the yellow substance accumulated in the fermentation broth is riboflavin. Comparing the enzyme sequences involved in riboflavin metabolism between BL21 and MG1655, we identified a site mutation on the 115 residue of bifunctional riboflavin kinase/FMN adenylyltransferase (RibF) in BL21. This His115Leu mutation was found to reduce enzyme activity to 55% of that of MG1655, which is probably one reason for riboflavin accumulation in BL21. Quantitative PCR analysis showed that genes of the entire branch of the riboflavin and FAD biosynthesis pathways in BL21 were up-regulated. Several physiological and metabolic characteristics of BL21 and MG1655 were found to be different, and may also be related to the riboflavin accumulation.

摘要

由于起源不同,大肠杆菌B株和K - 12株之间存在许多生理差异。深入了解这些菌株的代谢和调控机制将有助于更好地利用这些工业主力军。在本研究中,我们观察到BL21发酵液在培养过程中逐渐变黄。通过光谱分析和液相色谱 - 质谱鉴定,我们首次证实发酵液中积累的黄色物质是核黄素。比较BL21和MG1655中参与核黄素代谢的酶序列,我们在BL21的双功能核黄素激酶/FMN腺苷酸转移酶(RibF)的第115个残基上鉴定出一个位点突变。发现这种His115Leu突变使酶活性降低至MG1655的55%,这可能是BL21中核黄素积累的原因之一。定量PCR分析表明,BL21中核黄素和FAD生物合成途径的整个分支的基因上调。发现BL21和MG1655的几个生理和代谢特征不同,也可能与核黄素积累有关。

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