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沈抚灌区广宿主石油烃代谢质粒的分离及鉴定
引用本文:王亚菲,李慧,李小彬.沈抚灌区广宿主石油烃代谢质粒的分离及鉴定[J].生态学杂志,2013,24(11):3289-3299.
作者姓名:王亚菲  李慧  李小彬
作者单位:(;1.中国科学院沈阳应用生态研究所森林与土壤生态国家重点实验室, 沈阳 110164; ;2.中国科学院大学, 北京 100049)
摘    要:本研究采用“三亲配对外源分离法”,从沈抚灌区土壤、底泥和水样中共计分离得到8个广宿主(BHR)石油烃代谢质粒,并通过对其进行抗生素抗性检测和抗性遗传标记,将其转移至大肠杆菌(Escherichia coli)EC100宿主中进行操作.不相容性群分析结果表明: pS3-2C、pS4-6G为Inc P质粒;pS3-2G、pW22-3G、pA15-7G为Inc N质粒;pS7-2G 为Inc W质粒;pA23-1G和 pA10-1C为Inc Q质粒.采用PCR扩增已报道的石油烃污染物降解基因的方法初步分析其石油烃代谢功能,质粒pS3-2G、pS7-2G、pA23-1G、pW22-3G和pA10-1C上含有编码芳香环羟化双加氧酶基因(phdA)和甲苯单加氧酶基因(touA)的片段;pA15-7G含有编码甲苯双加氧酶和甲苯单加氧酶基因片段;pS3-2C含有编码芳香环羟化双加氧酶、苯双加氧酶和甲苯双加氧酶基因片段;pS4-6G仅含有编码芳香环羟化双加氧酶基因片段.通过宿主范围检测,除质粒pS3-2C外,其余7个质粒均可在变形菌纲(Proteobacteria)α-、β-、γ-亚纲的代表性菌株根瘤农杆菌(Agrobacterium tumefaciens)C58、钩虫贪铜菌(Cupriavidus necator)JMP228、大肠杆菌EC100间进行转移并稳定传代.

关 键 词:水平基因转移  三亲配对外源质粒分离  广宿主质粒  石油烃降解  生物修复

Isolation and characterization of petroleum catabolic broad host range plasmids from Shen Fu wastewater irrigation zone.
WANG Ya-fei,LI Hui,LI Xiao-bin.Isolation and characterization of petroleum catabolic broad host range plasmids from Shen Fu wastewater irrigation zone.[J].Chinese Journal of Ecology,2013,24(11):3289-3299.
Authors:WANG Ya-fei  LI Hui  LI Xiao-bin
Institution:(;1.State Key Laboratory of Forest and Soil Ecology, Institute of Applied Ecology, Chinese Academy of Sciences, Shenyang 110164, China; ;University of Chinese Academy of Sciences, Beijing 100049, China)
Abstract:Based on triparental mating, we isolated a total of eight broad host range (BHR) petroleum hydrocarbon catabolic plasmids from the soils, sediments, and wastewater samples in the Shen Fu irrigation zone. The antibiotic resistance of the plasmids was tested, and then, the plasmids were transferred to Escherichia coli EC100. The plasmids carrying no antibiotic resistance were tagged by miniTn5 transposon consisting of antibiotic resistant genes. The PCR based incompatibility test revealed that the pS3-2C and pS4-6G belonged to Inc P group, the pS3-2G, pW22-3G, and pA15-7G belonged to Inc N group, the pS7-2G was identified as Inc W plasmid, and the pA23-1G and pA10-1C were placed into Inc Q group. By adopting the reported PCR amplification methods of petroleum hydrocarbon degrading catabolic genes, the petroleum degrading capability of these BHR plasmids were preliminarily analyzed. The plasmids pS3-2G, pS7-2G, pA23-1G, pW22-3G, and pA10-1C carried aromatic ring- hydroxylating dioxygenase gene phdA and toluene monooxygenase gene touA; the plasmid pA15-7G carried  touA and toluene dioxygenase gene tod; the plasmid pS3-2C carried ben, phdA, and tod; whereas the pS4-6G only carried ben. The host range test showed that all the isolated plasmids except pS3-2C could be transferred and maintained stably in the representative strains Agrobacterium tumefaciens C58, Cupriavidus necator JMP228, and E. coli EC100 of the α-, β-, and γ-Proteobacteria, respectively.
Keywords:horizontal gene transfer  exogenous plasmid isolation by triparental mating  broad host range plasmid  degradation of petroleum hydrocarbon  bioremediation  
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