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Use of Bioluminescence Markers To Detect Pseudomonas spp. in the Rhizosphere

机译:使用生物发光标记物检测假单胞菌。在根际

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摘要

The use of bioluminescence as a sensitive marker for detection of Pseudomonas spp. in the rhizosphere was investigated. Continuous expression of the luxCDABE genes, required for bioluminescence, was not detectable in the rhizosphere. However, when either a naphthalene-inducible luxCDABE construct or a constitutive luxAB construct (coding only for the luciferase) was introduced into the Pseudomonas cells, light emission could be initiated just prior to measurement by the addition of naphthalene or the substrate for luciferase, n-decyl aldehyde, respectively. These Pseudomonas cells could successfully be detected in the rhizosphere by using autophotography or optical fiber light measurement techniques. Detection required the presence of 103 to 104 CFU/cm of root, showing that the bioluminescence technique is at least 1,000-fold more sensitive than β-galactosidase-based systems.
机译:使用生物发光作为检测假单胞菌的敏感标记。在根际进行了调查。生物发光所需的luxCDABE基因的连续表达在根际中无法检测到。但是,当将萘诱导的luxCDABE构建体或组成型luxAB构建体(仅编码萤光素酶)引入假单胞菌细胞时,就可以在测量之前通过添加萘或萤光素酶n的底物来启动发光。 -癸醛。这些假单胞菌细胞可以通过使用自动摄影或光纤光测量技术在根际中成功检测到。检测需要存在103至104 CFU / cm的根,这表明生物发光技术的灵敏度至少比基于β-半乳糖苷酶的系统高1,000倍。

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