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.
No takes yet. Share an insight, caveat, or question.
Akira Hiraishi (1992) studied this question.
Synapse has enriched 5 related papers. Consider them for comparative context: