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使用嗜热栖热菌DNA聚合酶进行DNA测序以及对聚合酶链反应扩增的DNA进行直接测序。

DNA sequencing with Thermus aquaticus DNA polymerase and direct sequencing of polymerase chain reaction-amplified DNA.

作者信息

Innis M A, Myambo K B, Gelfand D H, Brow M A

机构信息

Department of Microbial Genetics, Cetus Corporation, Emeryville, CA 94608.

出版信息

Proc Natl Acad Sci U S A. 1988 Dec;85(24):9436-40. doi: 10.1073/pnas.85.24.9436.

Abstract

The highly thermostable DNA polymerase from Thermus aquaticus (Taq) is ideal for both manual and automated DNA sequencing because it is fast, highly processive, has little or no 3'-exonuclease activity, and is active over a broad range of temperatures. Sequencing protocols are presented that produce readable extension products greater than 1000 bases having uniform band intensities. A combination of high reaction temperatures and the base analog 7-deaza-2'-deoxyguanosine was used to sequence through G + C-rich DNA and to resolve gel compressions. We modified the polymerase chain reaction (PCR) conditions for direct DNA sequencing of asymmetric PCR products without intermediate purification by using Taq DNA polymerase. The coupling of template preparation by asymmetric PCR and direct sequencing should facilitate automation for large-scale sequencing projects.

摘要

来自嗜热水生栖热菌(Taq)的高度耐热DNA聚合酶对于手动和自动DNA测序而言都是理想之选,因为它速度快、持续合成能力强、几乎没有或完全没有3'外切核酸酶活性,并且在很宽的温度范围内都具有活性。本文介绍了一些测序方案,这些方案能产生大于1000个碱基且条带强度均匀的可读延伸产物。通过结合高反应温度和碱基类似物7-脱氮-2'-脱氧鸟苷来对富含G + C的DNA进行测序并解决凝胶压缩问题。我们修改了聚合酶链反应(PCR)条件,以便使用Taq DNA聚合酶对不对称PCR产物进行直接DNA测序而无需中间纯化。通过不对称PCR制备模板与直接测序相结合,应有助于大规模测序项目的自动化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a7c/282767/fe83b02d34c7/pnas00303-0073-a.jpg

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