首页> 美国卫生研究院文献>Journal of Bacteriology >The Heat Shock Genes dnaK dnaJ and grpE Are Involved in Regulation of Putisolvin Biosynthesis in Pseudomonas putida PCL1445
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The Heat Shock Genes dnaK dnaJ and grpE Are Involved in Regulation of Putisolvin Biosynthesis in Pseudomonas putida PCL1445

机译:热休克基因dnaKdnaJ和grpE参与恶臭假单胞菌PCL1445的腐殖酚生物合成的调控。

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摘要

Pseudomonas putida PCL1445 produces two cyclic lipopeptides, putisolvins I and II, which possess surfactant activity and play an important role in biofilm formation and degradation. In order to identify genes and traits that are involved in the regulation of putisolvin production of PCL1445, a Tn5luxAB library was generated and mutants were selected for the lack of biosurfactant production using a drop-collapsing assay. Sequence analysis of the Tn5luxAB flanking region of one biosurfactant mutant, strain PCL1627, showed that the transposon had inserted in a dnaK homologue which is located downstream of grpE and upstream of dnaJ. Analysis of putisolvin production and expression studies indicate that dnaK, together with the dnaJ and grpE heat shock genes, takes part in the positive regulation (directly or indirectly) of putisolvin biosynthesis at the transcriptional level. Growth of PCL1445 at low temperature resulted in an increased level of putisolvins, and mutant analyses showed that this requires dnaK and dnaJ but not grpE. In addition, putisolvin biosynthesis of PCL1445 was found to be dependent on the GacA/GacS two-component signaling system. Expression analysis indicated that dnaK is positively regulated by GacA/GacS.
机译:恶臭假单胞菌PCL1445产生两个环状脂肽,恶臭素I和II,它们具有表面活性剂活性,并在生物膜形成和降解中起重要作用。为了鉴定参与PCL1445的putisolvin生产调控的基因和性状,生成了一个Tn5luxAB文库,并使用滴落-折叠分析法选择了缺乏生物表面活性剂生产的突变体。一个生物表面活性剂突变体PCL1627的Tn5luxAB侧翼区的序列分析表明,该转座子已插入到位于grpE下游和dnaJ上游的dnaK同源物中。对putisolvin产生和表达研究的分析表明,dnaK与dnaJ和grpE热休克基因一起在转录水平上参与了putisolvin生物合成的正调控(直接或间接)。 PCL1445在低温下的生长导致腐殖素水平提高,突变分析表明这需要dnaK和dnaJ,但不需要grpE。此外,发现PCL1445的腐固酚生物合成依赖于GacA / GacS两组分信号系统。表达分析表明,dnaK受GacA / GacS正调控。

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