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November 1, 1992Letters in Applied Microbiology379 citations

Direct automated sequencing of 16S rDNA amplified by polymerase chain reaction from bacterial cultures without DNA purification

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AHAkira Hiraishi

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Abstract

The 16S rRNA gene from various bacterial cultures was amplified by the polymerase chain reaction without DNA purification, and sequenced directly by using a laser fluorescent DNA sequencer and Tth polymerase with a cycle sequencing protocol. The described procedures provide almost complete 16S rDNA sequence data within a couple of days and facilitate systematic studies.

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Cite This Study

Akira Hiraishi (1992) studied this question.

synapsesocial.com/papers/6a1fe50a91899344c12e4aa2https://doi.org/10.1111/j.1472-765x.1992.tb00765.x
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Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1PCR amplification of 16S rDNA from lyophilized cell cultures facilitates studies in molecular systematics1990 · 63 citations
  2. 2Rapid determination of bacterial ribosomal RNA sequences by direct sequencing of enzymatically amplified DNA1989 · 129 citations
  3. 3Nucleic Acids Research2009 · 680 citations
  4. 4Direct amplication of DNA from colonies of Bacillus subtilis and Escherichia coli by the polymerase chain reaction1990 · 53 citations
  5. 5Rapid determination of 16S ribosomal RNA sequences for phylogenetic analyses.1985 · 3,076 citations