首页> 外文期刊>Biotechnology Letters >Specific detection of an oil-degrading bacterium, Corynebacerium sp. IC10, in sand microcosms by PCR using species-specific primers based on 16S rRNA gene sequences
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Specific detection of an oil-degrading bacterium, Corynebacerium sp. IC10, in sand microcosms by PCR using species-specific primers based on 16S rRNA gene sequences

机译:石油降解细菌Corynebacerium sp。的特异性检测。使用基于16S rRNA基因序列的物种特异性引物通过PCR在沙子微观世界中检测IC10

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摘要

A species-specific PCR technique to detect an oil-degrading bacterium, Corynebacterium sp. IC10, released into sand microcosms is described. PCR primers, specific to strain IC10, were designed based on 16S rRNA gene sequences and tested against both closely and distantly related bacterial strains using four primer combinations involving two forward and two reverse primers. Two sets of them were specific to the strain IC10 and Corynebacterium variabilis and one set was selected for further analysis. The PCR amplification was able to detect 1 pg template DNA of strain IC10 and 1.2X10~(-4) c.f.u. of IC10ml wet sand~(-1) in the presence of 3X10~8 Escherichia coli cells. In non-sterile sand microcosms seeded with the strain IC 10, the sensitivity of detection decreased to 9.6X10~5 c.f.u. ml wet sand~(-1) . The detection sensitivity thus depends on the complexity of background heterogeneous DNA of environmental samples. The assay is suitable for detection f Corynebacterium sp. IC 10 in laboratory microcosms, however, cross reaction with non-oil degrading coryneforms may prohibit its use in uncharacterized systems
机译:一种特定物种的PCR技术,用于检测油降解细菌Corynebacterium sp.。描述了释放到沙子微观世界中的IC10。基于16S rRNA基因序列设计了针对IC10菌株的PCR引物,并使用涉及两个正向和两个反向引物的四种引物组合针对紧密和远距离相关的细菌菌株进行了测试。其中有两套对菌株IC10和变异棒状杆菌具有特异性,并选择了一套用于进一步分析。 PCR扩增能够检测IC10株和1.2X10〜(-4)c.f.u的1 pg模板DNA。 3X10〜8大肠杆菌细胞存在下,IC10ml湿沙〜(-1)的浓度。在用IC 10菌株播种的非无菌砂微观世界中,检测的灵敏度降至9.6X10〜5c.f.u。 ml湿沙〜(-1)。因此,检测灵敏度取决于环境样品的背景异质DNA的复杂性。该测定法适合于棒状杆菌属种的检测。实验室缩微中的IC 10,但是与非降油性棒状杆菌的交叉反应可能会禁止在未表征的系统中使用

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