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RRNPP-type quorum sensing affects solvent formation and sporulation in Clostridium acetobutylicum

机译:RRNPP型致法感测量影响<斜体>乙酸梭菌酸梭菌性的溶剂形成和孢子率

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The strictly anaerobic bacterium Clostridium acetobutylicum is well known for its ability to convert sugars into organic acids and solvents, most notably the potential biofuel butanol. However, the regulation of its fermentation metabolism, in particular the shift from acid to solvent production, remains poorly understood. The aim of this study was to investigate whether cell–cell communication plays a role in controlling the timing of this shift or the extent of solvent formation. Analysis of the available C. acetobutylicum genome sequences revealed the presence of eight putative RRNPP-type quorum-sensing systems, here designated qssA to qssH , each consisting of an RRNPP-type regulator gene followed by a small open reading frame encoding a putative signalling peptide precursor. The identified regulator and signal peptide precursor genes were designated qsrA to qsrH and qspA to qspH , respectively. Triplicate regulator mutants were generated in strain ATCC 824 for each of the eight systems and screened for phenotypic changes. The qsrB mutants showed increased solvent formation during early solventogenesis and hence the QssB system was selected for further characterization. Overexpression of qsrB severely reduced solvent and endospore formation and this effect could be overcome by adding short synthetic peptides to the culture medium representing a specific region of the QspB signalling peptide precursor. In addition, overexpression of qspB increased the production of acetone and butanol and the initial (48?h) titre of heat-resistant endospores. Together, these findings establish a role for QssB quorum sensing in the regulation of early solventogenesis and sporulation in C. acetobutylicum .
机译:严格的厌氧细菌酸血糖氧化术是众所周知的,其能够将糖转化为有机酸和溶剂,最符念潜在的生物燃料丁醇。然而,对其发酵代谢的调节,特别是从酸性转变为溶剂产生,仍然是较差的理解。本研究的目的是研究细胞 - 细胞通信是否在控制这种偏移的时间或溶剂形成程度方面发挥作用。可用的C.乙酰丁基基因组序列的分析显示出八个推定的RRNPP型批量传感系统的存在,这里将QSSA指定为QSSH,每个QSSH组成,每个QSSH组成,其次由编码推定的信号传导肽的小开放式读取框架组成前体。将鉴定的调节剂和信号肽前体基因分别指定QSRH和QSPA至QSPH。对于八种系统中的每一个,在菌株ATCC 824中产生三份调节剂突变体并筛选表型变化。 QSRB突变体在早期溶剂发生期间表现出增加的溶剂形成,因此选择QSSB系统以进一步表征。 QSRB的过度表达严重降低溶剂和腹腔形成,可以通过向表示QSPB信号肽前体的特定区域的培养基中添加短合成肽来克服这种效果。此外,QSPB的过度表达增加了丙酮和丁醇的产生,初始(48·H)滴注的耐热性肠孢子。这些发现在一起,对乙酸乙酰丁基的早期溶剂发生和孢子瘤进行了QSSB法定感测的作用。

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