2019
DOI: 10.3390/microorganisms8010045
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Cupriavidus sp. HN-2, a Novel Quorum Quenching Bacterial Isolate, is a Potent Biocontrol Agent Against Xanthomonas campestris pv. campestris

Abstract: Diffusible signal factor (DSF) represents a family of widely conserved quorum sensing (QS) signals involved in the regulation of virulence factor production in many Gram-negative bacterial pathogens. Quorum quenching, which disrupts QS either by degradation of QS signals or interference of signal generation or perception, is a promising strategy for prevention and control of QS-mediated bacterial infections. In this study, a novel DSF-degrading strain, HN-2, was isolated from contaminated soil and identified a… Show more

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Cited by 29 publications
(33 citation statements)
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“…The first-order kinetic equation was followed to fit experimental data of cypermethrin degradation kinetics as follows [40]:…”
Section: Kinetic Analysis Of Cypermethrinmentioning
confidence: 99%
“…The first-order kinetic equation was followed to fit experimental data of cypermethrin degradation kinetics as follows [40]:…”
Section: Kinetic Analysis Of Cypermethrinmentioning
confidence: 99%
“…Microbial consortiums communicated with each other via the mechanism known as quorum sensing (Ye et al, 2019(Ye et al, , 2020. Due to this communication in the lindane-contaminated sites, the metabolic burden is divided into various members and the consortium perform complex functions.…”
Section: Microbial Consortiummentioning
confidence: 99%
“…The prevention and control of black rot disease have become important concerns, due to the hugely destructive impacts of block rot disease on the productivity and quality of cruciferous plants [ 11 ]. In recent years, QQ has been increasingly interested in the development of a biocontrol method based on QS of microorganisms as an alternative and effective way to control plant diseases [ 16 , 17 , 47 , 48 ]. Among all of the methods of QQ, biocontrol bacteria with degrading signal molecule activity have appeared as efficient tools in plant disease management [ 49 ].…”
Section: Discussionmentioning
confidence: 99%
“…The cultures were incubated at 30 °C and 200 rpm, and the same volume of cultures was taken out and centrifuged to obtain the supernatant, where the residual DSF was extracted from different intervals [ 46 ]. HPLC was performed to determine the amount of residual DSF under the following conditions: C 18 reverse chromatographic column, flow rate of 1 mL·min −1 , column temperature of 35 °C, mobile phase of methanol/water = 80:20 ( ν : ν ), detection wavelength of 210 nm, and injection quantity of 20 μL [ 47 ]. Each treatment was replicated three times.…”
Section: Methodsmentioning
confidence: 99%
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