首页> 美国卫生研究院文献>Journal of Bacteriology >The Global Nitrogen Regulator NtcA Regulates Transcription of the Signal Transducer PII (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 PII (GlnB) and Influences Its Phosphorylation Level in Response to Nitrogen and Carbon Supplies in the Cyanobacterium Synechococcus sp. Strain PCC 7942

机译:全球氮调节剂NtcA调节信号转导子PII(GlnB)的转录并影响其对蓝藻Synechococcus sp。中氮和碳供应的响应的磷酸化水平。应变PCC 7942

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摘要

The PII 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 PII protein was observed, as revealed by immunodetection with specific antibodies. The phosphorylation level of PII 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 PII is NtcA independent.
机译:PII蛋白由Synechococcus sp。中的独特glnB基因编码。菌株PCC7942。已经在野生型和在不同氮和碳供应条件下生长的NtcA-null突变细胞中分析了其表达。 RNA-DNA杂交实验表明,无论所测试的营养条件如何,一种转录物的长度都为680个核苷酸。在野生型细胞中观察到第二个转录本物种,长620个核苷酸,在NtcA无效突变体中缺失,该野生型细胞在高和低CO2下以及在高CO2浓度下存在硝酸盐的情况下都挨饿了2小时。引物延伸分析表明,这两个转录物是由两个串联启动子产生的,分别是来自glnB起始的120 53>核苷酸和一个 70 大肠杆菌型启动子以及一个依赖NtcA的启动子。密码子。 NtcA依赖性启动子在上述条件下上调,而ς 70 大肠杆菌型启动子在NtcA无效突变体中显示转录本的组成水平,而野生型中则略有不同。类型的电池,具体取决于氮和碳的供应。通常,如通过特异性抗体的免疫检测所揭示的,观察到两个转录物种类的量与PII蛋白的量之间的良好相关性。野生型中PII的磷酸化水平与氮的利用率成反比,与较高的CO2浓度成正比。该调节相应地在NtcA无效突变细胞中不那么严格。相反,PII的去磷酸化是非NtcA依赖性的。

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