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首页> 外文期刊>Journal of Biotechnology >A transcriptional study of acidogenic chemostat cells of Clostridium acetobutylicum-Solvent stress caused by a transient n-butanol pulse
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A transcriptional study of acidogenic chemostat cells of Clostridium acetobutylicum-Solvent stress caused by a transient n-butanol pulse

机译:正丁醇瞬时脉冲引起的丙酮丁醇梭菌产酸化学稳定细胞的转录研究

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摘要

The main product of the anaerobic fermentative bacterium Clostridium acetobutylicum is n-butanol, an organic solvent with severe toxic effects on the cells. Therefore, the identification of the molecular factors related to n-butanol stress constitutes a major strategy for furthering the understanding of the biotechnological production of n-butanol, an important industrial biofuel. Previous reports concerning n-butanol stress in C. acetobutylicum dealt exclusively with batch cultures. In this study, for the first time a comprehensive transcriptional analysis of n-butanol-stressed C. acetobutylicum was conducted using stable steady state acidogenic chemostat cultures. A total of 358 differentially expressed genes were significantly affected by n-butanol stress. Similarities, such as the upregulation of general stress genes, and differences in gene expression were compared in detail with earlier DNA microarrays performed in batch cultivation experiments. The main result of this analysis was the observation that genes involved in amino acid and nucleotide biosynthesis, as well as genes for specific transport systems were upregulated by n-butanol. Our results exclude any transcriptional response triggered by exogenous pH changes or solventogenic n-butanol formation. Finally, our data suggest that metabolic flux through the glycerolipid biosynthetic pathway increases, confirming that C. acetobutylicum modifies the cytoplasmic membrane composition in response to n-butanol stress
机译:厌氧发酵细菌丙酮丁醇梭菌的主要产品是正丁醇,这是一种对细胞具有严重毒性作用的有机溶剂。因此,鉴定与正丁醇胁迫有关的分子因素是进一步理解重要的工业生物燃料正丁醇的生物技术生产的主要策略。先前有关丙酮丁醇梭菌中正丁醇胁迫的报道仅涉及分批培养。在这项研究中,第一次使用稳定的稳态产酸化学恒温培养进行了正丁醇胁迫的丙酮丁醇梭菌的全面转录分析。总共358个差异表达基因受到正丁醇胁迫的显着影响。将相似之处(如一般胁迫基因的上调和基因表达的差异)与批量培养实验中进行的早期DNA微阵列进行了详细比较。该分析的主要结果是观察到正丁醇上调了氨基酸和核苷酸生物合成相关基因以及特定运输系统的基因。我们的结果不包括由外源pH值变化或溶剂型正丁醇形成引发的任何转录反应。最后,我们的数据表明,通过甘油脂类生物合成途径的代谢通量增加,从而证实丙酮丁醇梭菌响应于正丁醇胁迫而修饰了细胞质膜成分。

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