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Screening, identification and degrading gene assignment of a chrysene-degrading strain

机译:ry降解菌的筛选,鉴定和降解基因分配

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A predominant chrysene-degrading strain named CT?was isolated from the activated sludge of Zhenjiang coking plant. The strain was initially identified asParacoccus aminovorans?by the results of morphological observation, physio-biochemical test and 16S rDNA gene sequence analysis. Under the conditions of initial chrysene concentration of 40 mg/l, inoculation amount of 10% (V/V) at pH 7.0 and temperature of 35°C, the degradation efficiency of chrysene by the strain CT reached 85.2% within 8 days. Alkaline lysis was applied to the extract plasmids from strain CT to confirm the location of chrysene-degrading genes. A plasmid, greater than 15 kb, was detected. The transformants obtained the ability to degrade chrysene when the plasmid of strain CT was transformed to competent cell ofEscherichia coli?DH10B, and could remove 43% of chrysene in the solutions with concentration of 30 mg/l within 8 days. But the mutation lost the ability to degrade chrysene when its plasmid was eliminated by sodium dodecyl sulfonate (SDS) and high temperature. This indicated that the plasmid of strain CT carried chrysene-degrading genes.
机译:从镇江焦化厂的活性污泥中分离出一种主要的降解甲烷的菌株,称为CT ?。通过形态观察,生理生化试验和16S rDNA基因序列分析,初步鉴定该菌株为氨基amino。在初始浓度为40 mg / l,pH 7.0接种量为10%(V / V),温度为35°C的条件下,菌株CT降解of的降解效率在8天内达到85.2%。将碱性裂解应用于菌株CT的提取质粒中,以确认降解菊花的基因的位置。检测到大于15 kb的质粒。当将菌株CT的质粒转化到大肠杆菌DH10B感受态细胞中时,转化子具有降解甲烷的能力,并且在8天内可以去除溶液中浓度为30 mg / l的43%的菊花。但是,当十二烷基磺酸钠(SDS)和高温消除了其质粒后,该突变体便失去了降解的能力。这表明CT菌株的质粒带有降解丙烯的基因。

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