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Genomic survey of cAMP and cGMP signalling components in the cyanobacterium Synechocystis PCC 6803

机译:CAM CAMCACTIUMSICECHOCYSTIS PCC 6803中CAM的基因组调查和CGMP信号传导组分

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Cyanobacteria modulate intracellular levels of cAMP and cGMP in response to environmental conditions (light, nutrients and pH). In an attempt to identify components of the cAMP and cGMP signalling pathways in Synechocystis PCC 6803, the authors screened its complete genome sequence by using bioinformatic tools and data from sequence–function studies performed on both eukaryotic and prokaryotic cAMP/cGMP-dependent proteins. Sll1624 and Slr2100 were tentatively assigned as being two putative cyclic nucleotide phosphodiesterases. Five proteins were identified as having all the determinants required to be cyclic nucleotide receptors, two of them being probably more specific for cGMP (an element of two-component regulatory systems – Slr2104 – and a putative cyclic-nucleotide-gated cation channel – Slr1575), the three others being probably more specific for cAMP: (i) a protein of unidentified function (Slr0842); (ii) a putative cyclic-nucleotide-modulated permease (Slr0593), previously annotated as a kinase A regulatory subunit; and (iii) a putative transcription factor (CRP-Syn =Sll1371), which possesses cAMP- and DNA-binding determinants homologous to those of the cAMP receptor protein of Escherichia coli (CRP-Ec). This homology, together with the presence in Synechocystis of CRP-Ec-like binding sites upstream of crp, cya1, slr1575, and several genes encoding enzymes involved in transport and metabolism, strongly suggests that CRP-Syn is a global regulator.
机译:Cyanobacteria在响应环境条件下调节细胞内营地和CGMP(光,营养素和pH)。为了识别SyneChocystis PCC 6803中CAMP和CGMP信号传导途径的组分,作者通过使用在真核和原核营/ CGMP依赖性蛋白质上进行的序列函数研究的生物信息工具和数据来筛选其完整的基因组序列。 SLL1624和SLR2100暂时分配为两个推定的循环核苷酸磷酸二酯酶。将五种蛋白质鉴定为具有循环核苷酸受体所需的所有决定因素,其中两种可能更具体对CGMP(双组分调节系统的元素 - SLR2104 - 以及推定的环核苷酸门控通道 - SLR1575) ,三个其他可能更具体地对营地更具体:(i)未识别功能的蛋白质(SLR0842); (ii)推定的环核苷酸调节允许(SLR0593),以前作为激酶是调节亚基的调整; (iii)推定的转录因子(CRP-SYN = SLL1371),其具有与大肠杆菌(CRP-EC)的CAMP受体蛋白质同源的营养和DNA结合的决定簇。这种同源性与CRP,CyA1,SLR1575的CRP-EC样结合位点的SneCeChocystis的存在一起强烈表明CRP-SYN是全球调节器的CRP-EC的结合位点和若干酶。

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