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BMC Genomics  2009 

Snapshot of iron response in Shewanella oneidensis by gene network reconstruction

DOI: 10.1186/1471-2164-10-131

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Abstract:

We show that the iron response in S. oneidensis is a rapid process. Temporal gene expression profiles were examined for iron depletion and repletion, and a gene co-expression network was reconstructed. Modules of iron acquisition systems, anaerobic energy metabolism and protein degradation were the most noteworthy in the gene network. Bioinformatics analyses suggested that genes in each of the modules might be regulated by DNA-binding proteins Fur, CRP and RpoH, respectively. Closer inspection of these modules revealed a transcriptional regulator (SO2426) involved in iron acquisition and ten transcriptional factors involved in anaerobic energy metabolism. Selected genes in the network were analyzed by genetic studies. Disruption of genes encoding a putative alcaligin biosynthesis protein (SO3032) and a gene previously implicated in protein degradation (SO2017) led to severe growth deficiency under iron depletion conditions. Disruption of a novel transcriptional factor (SO1415) caused deficiency in both anaerobic iron reduction and growth with thiosulfate or TMAO as an electronic acceptor, suggesting that SO1415 is required for specific branches of anaerobic energy metabolism pathways.Using a reconstructed gene network, we identified major biological pathways that were differentially expressed during iron depletion and repletion. Genetic studies not only demonstrated the importance of iron acquisition and protein degradation for iron depletion, but also characterized a novel transcriptional factor (SO1415) with a role in anaerobic energy metabolism.Iron is an important nutrient for bacteria, serving as a co-factor for proteins involved in respiration, the tricarboxylic acid (TCA) cycle, enzyme catalysis, gene regulation, photosynthesis, N2 fixation, methanogenesis, H2 production and consumption, oxygen transport, and DNA biosynthesis [1-3]. Iron exists in two redox states under physiological conditions: the insoluble Fe(III) ferric form and the relatively soluble Fe(

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