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AmtR,谷氨酸棒杆菌氮调节系统中的一种全局阻遏物。

AmtR, a global repressor in the nitrogen regulation system of Corynebacterium glutamicum.

作者信息

Jakoby M, Nolden L, Meier-Wagner J, Krämer R, Burkovski A

机构信息

Institut für Biochemie der Universität zu Köln, Germany.

出版信息

Mol Microbiol. 2000 Aug;37(4):964-77. doi: 10.1046/j.1365-2958.2000.02073.x.

Abstract

The uptake and assimilation of nitrogen sources is effectively regulated in bacteria. In the Gram-negative enterobacterium Escherichia coli, the NtrB/C two-component system is responsible for the activation of transcription of different enzymes and transporters, depending on the nitrogen status of the cell. In this study, we investigated regulation of ammonium uptake in Corynebacterium glutamicum, a Gram-positive soil bacterium closely related to Mycobacterium tuberculosis. As shown by Northern blot hybridizations, regulation occurs on the level of transcription upon nitrogen starvation. In contrast to enterobacteria, a repressor protein is involved in regulation, as revealed by measurements of methylammonium uptake and beta-galactosidase activity in reporter strains. The repressor-encoding gene, designated amtR, was isolated and sequenced. Deletion of amtR led to deregulation of transcription of amt coding for the C. glutamicum (methyl)ammonium uptake system. E. coli extracts from amtR-expressing cells were applied in gel retardation experiments, and binding of AmtR to the amt upstream region was observed. By deletion analyses, a target motif for AmtR binding was identified, and binding of purified AmtR protein to this motif, ATCTATAGN1-4ATAG, was shown. Furthermore, the binding of AmtR to this sequence was proven in vivo using a yeast one-hybrid system. Subsequent studies showed that AmtR not only regulates transcription of the amt gene but also of the amtB-glnK-glnD operon encoding an amt paralogue, the signal transduction protein PII and the uridylyltransferase/uridylyl-removing enzyme, key components of the nitrogen regulatory cascade. In summary, regulation of ammonium uptake and assimilation in the high G+C content Gram-positive bacterium C. glutamicum differs significantly from the mechanism found in the low G+C content Gram-positive model organism Bacillus subtilis and from the paradigm of nitrogen control in the Gram-negative enterobacteria.

摘要

细菌中氮源的摄取和同化受到有效调控。在革兰氏阴性肠道细菌大肠杆菌中,NtrB/C双组分系统负责根据细胞的氮状态激活不同酶和转运蛋白的转录。在本研究中,我们调查了谷氨酸棒杆菌(一种与结核分枝杆菌密切相关的革兰氏阳性土壤细菌)中铵摄取的调控。如Northern印迹杂交所示,在氮饥饿时,调控发生在转录水平。与肠道细菌不同,通过对报告菌株中甲基铵摄取和β-半乳糖苷酶活性的测量发现,一种阻遏蛋白参与了调控。分离并测序了编码该阻遏蛋白的基因,命名为amtR。amtR的缺失导致编码谷氨酸棒杆菌(甲基)铵摄取系统的amt转录失控。将表达amtR的大肠杆菌提取物用于凝胶阻滞实验,观察到AmtR与amt上游区域的结合。通过缺失分析,确定了AmtR结合的靶基序,并证明纯化的AmtR蛋白与该基序ATCTATAGN1 - 4ATAG结合。此外,使用酵母单杂交系统在体内证明了AmtR与该序列的结合。随后的研究表明,AmtR不仅调控amt基因的转录,还调控编码amt旁系同源物、信号转导蛋白PII以及尿苷酰转移酶/尿苷酰去除酶(氮调控级联反应的关键组分)的amtB - glnK - glnD操纵子的转录。总之,高G + C含量的革兰氏阳性细菌谷氨酸棒杆菌中铵摄取和同化的调控与低G + C含量的革兰氏阳性模式生物枯草芽孢杆菌中的机制以及革兰氏阴性肠道细菌中的氮控制范式有显著差异。

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