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The hanR/hanI quorum-sensing system of Halomonas anticariensis, a moderately halophilic bacterium

机译:Halomonas Antiariensis的Hanr / Hani法定传感系统,一种适度嗜盐细菌

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Quorum sensing is a cell density-dependent gene expression mechanism found in many Gram-negative bacteria which involves the production of signal molecules such as N-acylhomoserine lactones (AHLs). One significant group of micro-organisms in which quorum sensing has not been previously studied, however, are the moderate halophiles. We describe here the results of our studies of the quorum-sensing system in Halomonas anticariensis FP35T, which is composed of luxR/luxI homologues: hanR (the putative transcriptional regulator gene) and hanI (the autoinducer synthase gene). To understand how the hanR/hanI system is organized and regulated we conducted RT-PCR and quantitative real-time PCR assays. Transcriptional analysis indicated that the hanR and hanI genes are on the same transcript and that their transcription is growth phase-dependent. HanI seems to be the only autoinducer synthase responsible for the synthesis of AHLs by the bacterium, since the inactivation of hanI resulted in the complete loss of its AHLs. We also found that the hanI gene appears to be transcribed from its own promoter and that its expression does not depend upon HanR. This finding was supported by the fact that the FP35hanR mutant showed AHL-producing activity and hanI expression similar to that of the wild-type strain, the latter being measured by RT-PCR. Moreover, hanR is expressed from its own promoter and appears to be independent of the AHL signalling molecules produced by HanI.
机译:致法感测是一种细胞密度依赖性基因表达机制,其在许多革兰氏阴性细菌中发现,涉及产生信号分子,例如N-酰基骨晶内酯内酯(AHL)。然而,预先研究了令人难以解决的一部分微生物的一组很大组微生物是中等嗜盐剂。我们在这里描述了我们对哈洛姆纳斯反应的批量传感系统的研究结果,它由Luxr / Luxi同源物组成:HANR(推定转录调节剂基因)和HANI(Auto ucher Synthase基因)。要了解如何组织和调节HANR / HANI系统,我们进行了RT-PCR和定量实时PCR测定。转录分析表明HANR和HANI基因在相同的转录物上,其转录是生长相位依赖性。汉尼似乎是唯一负责细菌合成AHL的唯一的自动挤力体合成酶,因为哈尼的失活导致其AHL的完全丧失。我们还发现Hani基因似乎从其自身的启动子转录,并且其表达不依赖于HANR。这种发现得到了FP35HANR突变体显示出类似于野生型菌株的产生的AHL-产生的活性和哈尼表达,后者通过RT-PCR测量。此外,HANR从其自身的启动子表达,并且似乎与Hani产生的AHL信号传导分子无关。

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