首页> 外文OA文献 >The Global Nitrogen Regulator NtcA Regulates Transcription of the Signal Transducer P II (GlnB) and Influences Its Phosphorylation Level in Response to Nitrogen and Carbon Supplies in the Cyanobacterium Synechococcus sp. Strain PCC 7942
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The Global Nitrogen Regulator NtcA Regulates Transcription of the Signal Transducer P II (GlnB) and Influences Its Phosphorylation Level in Response to Nitrogen and Carbon Supplies in the Cyanobacterium Synechococcus sp. Strain PCC 7942

机译:全局氮稳压剂NTCA调节信号传感器P II(GLNB)的转录,并影响其Cyanobacterium SyneChococcus SP中的氮和碳供应的磷酸化水平。菌株PCC 7942

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摘要

The P(II) protein is encoded by a unique glnB gene in Synechococcus sp. strain PCC 7942. Its expression has been analyzed in the wild type and in NtcA-null mutant cells grown under different conditions of nitrogen and carbon supply. RNA-DNA hybridization experiments revealed the presence of one transcript species 680 nucleotides long, whatever the nutrient conditions tested. A second transcript species, 620 nucleotides long, absent in the NtcA null mutant, was observed in wild-type cells that were nitrogen starved for 2 h under both high and low CO2 and in the presence of nitrate under a high CO2 concentration. Primer extension analysis indicated that the two transcript species are generated from two tandem promoters, a σ70 Escherichia coli-type promoter and an NtcA-dependent promoter, located 120 and 53 nucleotides, respectively, from the glnB initiation codon. The NtcA- dependent promoter is up-regulated under the conditions mentioned above, while the σ70 E. coli-type promoter displays constitutive levels of transcripts in the NtcA null mutant and slightly different levels in the wild-type cells, depending on the nitrogen and carbon supplies. In general, a good correlation between the amounts of the two transcript species and that of the P(II) protein was observed, as revealed by immunodetection with specific antibodies. The phosphorylation level of P(II) in the wild type is inversely correlated with nitrogen availability and directly correlated with higher CO2 concentration. This regulation is correspondingly less stringent in the NtcA null mutant cells. In contrast, the dephosphorylation of P(II) is NtcA independent.
机译:P(II)蛋白由SyneChocccus Sp中的独特Glnb基因编码。菌株PCC 7942.在野生型和NTCA-NULL突变体中分析其表达在不同的氮气和碳供应条件下生长。 RNA-DNA杂交实验揭示了一种转录物种680核苷酸的存在,无论是否测试了任何营养条件。在NTCA无突变体中,在NTCA无突变体中不存在的第二个转录物种620核苷酸在野生型细胞中观察到在高和低CO 2下含氮,并且在高CO 2浓度下在硝酸盐存在下。引物延伸分析表明,两种转录物物种分别由两种串联启动子,分别由GLNB引发密码子分别从GLNB引发剂和NTCA依赖性启动子,位于120和53个核苷酸的NTCA依赖性启动子产生。在上述条件下,NTCA依赖启动子上调,而σ70大肠杆菌型启动子在NTCA空突变体中显示组成型转录物和野生型细胞中略微不同的水平,这取决于氮气和碳源。通常,观察到两种转录物种的量与P(II)蛋白的量之间的良好相关性,如具有特异性抗体的免疫检测所揭示的那样。野生型P(II)的磷酸化水平与氮可用性相反,并与较高的CO 2浓度直接相关。该调节在NTCA无突变体细胞中相应地相应地严格。相反,P(II)的去磷酸化是NTCA独立的。

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