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首页> 外文期刊>Applied and Environmental Microbiology >Unlabeled Helper Oligonucleotides Increase the In Situ Accessibility to 16S rRNA of Fluorescently Labeled Oligonucleotide Probes
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Unlabeled Helper Oligonucleotides Increase the In Situ Accessibility to 16S rRNA of Fluorescently Labeled Oligonucleotide Probes

机译:未标记的辅助寡核苷酸增加了荧光标记的寡核苷酸探针对16S rRNA的原位可达性

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摘要

Target site inaccessibility represents a significant problem for fluorescence in situ hybridization (FISH) of 16S rRNA with oligonucleotide probes. Here, unlabeled oligonucleotides (helpers) that bind adjacent to the probe target site were evaluated for their potential to increase weak probe hybridization signals inEscherichia coli DSM 30083T. The use of helpers enhanced the fluorescence signal of all six probes examined at least fourfold. In one case, the signal of probe Eco474 was increased 25-fold with the use of a single helper probe, H440-2. In another case, four unlabeled helpers raised the FISH signal of a formerly weak probe, Eco585, to the level of the brightest monolabeled oligonucleotide probes available for E. coli. The temperature of dissociation and the mismatch discrimination of probes were not significantly influenced by the addition of helpers. Therefore, using helpers should not cause labeling of additional nontarget organisms at a defined stringency of hybridization. However, the helper action is based on sequence-specific binding, and there is thus a potential for narrowing the target group which must be considered when designing helpers. We conclude that helpers can open inaccessible rRNA regions for FISH with oligonucleotide probes and will thereby further improve the applicability of this technique for in situ identification of microorganisms.
机译:靶位点难以接近代表了16S rRNA与寡核苷酸探针的荧光原位杂交(FISH)的重大问题。在此,评估了与探针靶位点相邻结合的未标记寡核苷酸(辅助物)在大肠杆菌DSM 30083T中增加弱探针杂交信号的潜力。使用辅助剂增强了所检查的所有六个探针的荧光信号至少四倍。在一种情况下,使用单个辅助探针H440-2可使探针Eco474的信号增加25倍。在另一种情况下,四个未标记的辅助分子将以前较弱的探针Eco585的FISH信号提高到可用于大肠杆菌的最亮的单标记寡核苷酸探针的水平。解离的温度和探针的错配判别不受辅助物的添加的显着影响。因此,使用辅助物不应导致在定义的严格杂交条件下标记其他非靶标生物。但是,辅助作用是基于序列特异性结合的,因此有可能缩小目标组的范围,这在设计辅助物时必须加以考虑。我们得出的结论是,辅助分子可以用寡核苷酸探针打开FISH难以接近的rRNA区域,从而进一步提高该技术在微生物原位鉴定中的适用性。

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