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Validation of a more sensitive method for using spotted oligonucleotide DNA microarrays for functional genomics studies on bacterial communities

机译:验证使用斑点寡核苷酸DNA微阵列进行细菌群落功能基因组学研究的更灵敏方法

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Spotted oligonucleotide microarrays potentially offer a wide scope of applications for microbial ecology, especially as they improve the flexibility of design and the specificity of detection compared to PCR product based microarrays. Sensitivity, however, was expected to be problematic, as studies with the more sensitive PCR-based cDNA microarrays indicate that only genes from populations contributing to more than 5% of the community DNA can be detected. We evaluated several parameters to increase sensitivity and then tested applicability for bacterial functional genomics. The optimal parameters were the use of 5'-C6-amino-modified 70-mers printed on CMT-GAPS II substrates at a 40 μM concentration combined with the use of Tyramide Signal Amplification labelling. This protocol allowed detection of single copy genes belonging to an organism contributing to 1% or more of the total community. To demonstrate its application, we detected the specific aromatic oxygenase genes in a soil community degrading polychlorinated biphenyls (PCBs). This increase in sensitivity is important if oligonucleotide microarrays are to be used for simultaneous monitoring of a range of functions performed by different microorganisms in the environment.
机译:斑点寡核苷酸微阵列可能为微生物生态学提供广泛的应用,尤其是与基于PCR产物的微阵列相比,它们提高了设计的灵活性和检测的特异性。但是,由于使用基于PCR的更敏感的cDNA微阵列进行的研究表明,只能检测到来自群体中占社区DNA 5%以上的基因,因此灵敏度可能会出现问题。我们评估了几个参数以提高灵敏度,然后测试了细菌功能基因组学的适用性。最佳参数是使用在CMT-GAPS II底物上以40μM的浓度印刷5'-C6-氨基修饰的70-mers,并结合使用酪酰胺信号放大标记。该方案允许检测属于生物体的单拷贝基因,该生物体占总群落的1%或更多。为了证明其应用,我们在降解多氯联苯(PCB)的土壤群落中检测到特定的芳香氧化酶基因。如果将寡核苷酸微阵列用于同时监测环境中不同微生物所执行的一系列功能,那么灵敏度的提高非常重要。

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