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General colorimetric method for DNA diagnostics allowing direct solid-phase genomic sequencing of the positive samples.

机译:用于DNA诊断的通用比色方法,可对阳性样品进行直接固相基因组测序。

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摘要

A system for rapid colorimetric detection of specific genome DNA fragments amplified by the polymerase chain reaction (PCR) is described that has been designed to allow direct solid-phase sequencing of positive samples. The amplified material is immobilized on magnetic beads by using the biotin streptavidin system. An Escherichia coli lac operator DNA sequence is incorporated in the amplified material during the second step of a nested primer procedure. This 21-base-pair sequence is used for a general colorimetric detection with a fusion protein consisting of the E. coli Lac repressor and beta-galactosidase. Positive samples can be treated subsequently with alkali to obtain a single-stranded DNA template suitable for direct genomic sequencing. This method to detect immobilized amplified nucleic acids (DIANA) is well adapted for automated or semiautomated clinical assays. Here, we show that it can be used to detect and sequence Chlamydia trachomatis genomic DNA in clinical samples.
机译:描述了一种用于快速比色检测通过聚合酶链反应(PCR)扩增的特定基因组DNA片段的系统,该系统已设计为允许对阳性样品进行直接固相测序。通过使用生物素链霉亲和素系统将扩增的材料固定在磁珠上。在巢式引物方法的第二步中,将大肠杆菌lac操纵基因DNA序列掺入扩增的材料中。此21个碱基对的序列用于由大肠杆菌Lac阻遏物和β-半乳糖苷酶组成的融合蛋白进行比色检测。阳性样品可以随后用碱处理,以获得适合直接基因组测序的单链DNA模板。这种检测固定的扩增核酸(DIANA)的方法非常适合于自动化或半自动化的临床检测。在这里,我们证明了它可用于检测临床样品中的沙眼衣原体基因组DNA并对其进行测序。

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