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Transcriptional Program of Early Sporulation and Stationary-Phase Events in Clostridium acetobutylicum

机译:丙酮丁醇梭菌的早期孢子形成和平稳阶段的转录程序。

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摘要

DNA microarray analysis of Clostridium acetobutylicum was used to examine the genomic-scale gene expression changes during the shift from exponential-phase growth and acidogenesis to stationary phase and solventogenesis. Self-organizing maps were used to identify novel expression patterns of functional gene classes, including aromatic and branched-chain amino acid synthesis, ribosomal proteins, cobalt and iron transporters, cobalamin biosynthesis, and lipid biosynthesis. The majority of pSOL1 megaplasmid genes (in addition to the solventogenic genes aad-ctfA-ctfB and adc) had increased expression at the onset of solventogenesis, suggesting that other megaplasmid genes may play a role in stationary-phase phenomena. Analysis of sporulation genes and comparison with published Bacillus subtilis results indicated conserved expression patterns of early sporulation genes, including spo0A, the sigF operon, and putative canonical genes of the σH and σF regulons. However, sigE expression could not be detected within 7.5 h of initial spo0A expression, consistent with the observed extended time between the appearance of clostridial forms and endospore formation. The results were compared with microarray comparisons of the wild-type strain and the nonsolventogenic, asporogenous M5 strain, which lacks the pSOL1 megaplasmid. While some results were similar, the expression of primary metabolism genes and heat shock proteins was higher in M5, suggesting a difference in metabolic regulation or a butyrate stress response in M5. The results of this microarray platform and analysis were further validated by comparing gene expression patterns to previously published Northern analyses, reporter assays, and two-dimensional protein electrophoresis data of metabolic genes (including all major solventogenesis genes), sporulation genes, heat shock proteins, and other solventogenesis-induced gene expression.
机译:丙酮丁醇梭菌的DNA芯片分析用于检查从指数相生长和酸生成到固定相和溶剂生成转变过程中基因组规模的基因表达变化。自组织图用于鉴定功能基因类别的新型表达模式,包括芳香族和支链氨基酸合成,核糖体蛋白,钴和铁转运蛋白,钴胺素生物合成和脂质生物合成。大多数pSOL1大质粒基因(除了产溶剂基因aad-ctfA-ctfB和adc)在溶剂生成开始时就具有增加的表达,这表明其他大质粒基因可能在固定相现象中起作用。孢子形成基因的分析和与枯草芽孢杆菌结果的比较表明,早期孢子形成基因的保守表达模式,包括spo0A,sigF操纵子以及σ H 和σ F的推定规范基因 regulons。但是,在最初的spo0A表达的7.5小时内未检测到sigE表达,这与观察到的梭菌形式出现和孢子形成之间的延长时间一致。将结果与野生型菌株和缺乏pSOL1大质粒的非溶剂型,产孢子性M5菌株的微阵列比较进行了比较。虽然一些结果相似,但M5中的主要代谢基因和热休克蛋白的表达较高,表明M5的代谢调节或丁酸应激反应有所不同。通过将基因表达模式与先前发表的Northern分析,报告基因分析以及代谢基因(包括所有主要溶剂生成基因),孢子形成基因,热激蛋白,蛋白质,蛋白质,蛋白质,蛋白质,蛋白质等的二维蛋白质电泳数据进行比较,进一步验证了该微阵列平台和分析的结果和其他溶剂生成诱导的基因表达。

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