首页> 外文期刊>Microbiological Research >Quorum quenching activity in cell-free lysate of endophytic bacteria isolated from Pterocarpus santalinus Linn., and its effect on quorum sensing regulated biofilm in Pseudornonas aeruginosa PAO1
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Quorum quenching activity in cell-free lysate of endophytic bacteria isolated from Pterocarpus santalinus Linn., and its effect on quorum sensing regulated biofilm in Pseudornonas aeruginosa PAO1

机译:分离自紫檀木的内生细菌的无细胞裂解物中的群体猝灭活性及其对铜绿假单胞菌PAO1群体感应调控的生物膜的影响

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Quorum sensing mechanism allows the microorganisms to resist the antibiotic treatment by forming biofilms. Quorum quenching is one of the mechanisms to control the development of drug resistance in microbes. Endophyte bacteria are beneficial to plant growth as they support the immune system against the pathogen attack. The endophytic bacteria present in Pterocmpus santalinus were screened for the presence of N-acyl homoserine lactones (AHLs) degrading bacteria using biosensor strains and further confirmed by quantifying the violacein production. Cell-free lysate of endophytic bacteria, Bacillus firmus PT18 and Enterobacter asburiae PT39 exhibited potent AHL degrading ability by inhibiting about 80% violacein production in biosensor strain. Furthermore, when the cell-free lysate was applied to Pseudomonas aeruginosa PAO1 and PAO1-JP2 biofilm it resulted in significant (p <0.01) inhibition of biofilm formation. The biofilm inhibition was confirmed by visualization of biofilm slides under fluorescence microscopy, which showed decrease in total biomass formation in treated slides. Isolation and amplification of the gene (aiiA) indicated that the presence of AHL lactonase in cell-free lysate and sequence alignment indicated that AiiA contains a "HXHXDH" zinc-binding motif that is being conserved in several groups of metallohydrolases. Therefore, the study shows the potential of AHLs degradation by AHL lactonase present in cell-free lysate of isolated endophytic bacteria and inhibition of quorum sensing regulated biofilm formation in P. aeruginosa PAO1
机译:群体感应机制使微生物能够通过形成生物膜来抵抗抗生素治疗。群体猝灭是控制微生物耐药性发展的机制之一。内生细菌对植物生长有益,因为它们支持抵抗病原体侵袭的免疫系统。使用生物传感器菌株筛选存在于檀香对虾中的内生细菌是否存在降解N-酰基高丝氨酸内酯(AHL)的细菌,并通过定量紫胶素的产生进一步确认。内生细菌,芽孢杆菌PT18和白僵菌肠杆菌PT39的无细胞裂解物通过抑制生物传感器菌株中约80%的紫胶素产生表现出有效的AHL降解能力。此外,将无细胞裂解液应用于铜绿假单胞菌PAO1和PAO1-JP2生物膜时,会显着(p <0.01)抑制生物膜的形成。通过在荧光显微镜下观察生物膜载玻片,证实了生物膜抑制作用,这表明处理过的载玻片中总生物量形成减少。基因(aiiA)的分离和扩增表明,AHL内酯酶在无细胞裂解物中的存在和序列比对表明,AiiA包含一个“ HXHXDH”锌结合基序,该基序在几组金属水解酶中均得到保守。因此,该研究表明分离的内生细菌的无细胞裂解物中存在的AHL内酯酶可降解AHLs,并抑制铜绿假单胞菌PAO1中群体感应调节的生物膜形成。

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