A new approach using multiplex long accurate PCR and yeast artificial chromosomes for bacterial chromosome mapping and sequencing.

    • Laboratoire de Génétique Microbienne, Institut National de la Recherche Agronomique, Jouy en Josas, France. [email protected]
Published May 1, 1996. Vol 6 Issue 5, pp. 448-453. https://doi.org/10.1101/gr.6.5.448
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Abstract

An efficient approach for structural studies on bacterial chromosomes is presented. It is based on high-resolution PCR map construction by using a multiplex long accurate PCR (MLA PCR) protocol and a YAC clone carrying the region to be mapped as indicator. The high-resolution PCR map of the bacillus subtilis rrnB-dnaB region is presented as an example. Data are also presented on the use of DNA generated by LA PCR for sequencing; they are relevant to LA PCR induced mutations and justify the application of such mapping for sequencing long stretches of bacterial chromosomes.

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