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首页> 外文期刊>Applied and Environmental Microbiology >Assay for detection and enumeration of genetically engineered microorganisms which is based on the activity of a deregulated 2,4-dichlorophenoxyacetate monooxygenase.
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Assay for detection and enumeration of genetically engineered microorganisms which is based on the activity of a deregulated 2,4-dichlorophenoxyacetate monooxygenase.

机译:用于检测和枚举基因工程微生物的测定方法,该方法基于失调的2,4-二氯苯氧基乙酸酯单加氧酶的活性。

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An assay system was developed for the enumeration of genetically engineered microorganisms expressing a deregulated 2,4-dichlorophenoxyacetate (TFD) monooxygenase, which converts phenoxyacetate (PAA) to phenol. In PAA-amended cultures of Pseudomonas aeruginosa PAO1C(pRO103) and Pseudomonas putida PPO301(pRO103), strains which express a deregulated TFD monooxygenase, phenol production was proportional to cell number. Phenol was reacted, under specific conditions, with a 4-aminoantipyrine dye to form an intensely colored dye-phenol complex (AAPPC), which when measured spectrophotometrically could detect as few as 10(3) cells per ml. This assay was corroborated by monitoring the disappearance of PAA and the accumulation of phenol by high-performance liquid chromatography and gas chromatography. The AAPPC assay was modified for use with plate cultures and clearly distinguished colonies of PPO301(pRO103) and PAO1C(pRO103) from a strain expressing a regulated TFD monooxygenase. Colonies of P. putida PPO301(pRO101) remained cream colored, while colonies of PPO301(pRO103) and PAO1C(pRO103) turned a distinct red.
机译:开发了一种检测系统,用于枚举表达失控的2,4-二氯苯氧乙酸酯(TFD)单加氧酶的基因工程微生物,该酶将苯氧乙酸酯(PAA)转化为苯酚。在PAA改良的铜绿假单胞菌PAO1C(pRO103)和恶臭假单胞菌PPO301(pRO103)的培养物中,表达失调的TFD单加氧酶的菌株,苯酚的产生与细胞数成正比。在特定条件下,苯酚与4-氨基安替比林染料反应,形成深色染料-酚复合物(AAPPC),用分光光度法测量时,每毫升可检测到10(3)个细胞。通过高效液相色谱和气相色谱监测PAA的消失和苯酚的积累,从而证实了该测定方法。修改了AAPPC测定法以用于平板培养,并从表达受调节的TFD单加氧酶的菌株中清楚地区分了PPO301(pRO103)和PAO1C(pRO103)菌落。恶臭假单胞菌PPO301(pRO101)的菌落保持乳白色,而PPO301(pRO103)和PAO1C(pRO103)的菌落变成明显的红色。

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