Direct Genome Transfer from Acholeplasma laidlawii to Yeast

Abstract

Cloning bacterial genomes in yeast or other hosts is a crucial step in workflows for creating highly engineered strains. The genome of Acholeplasma laidlawii can be cloned in yeast if a toxic gene is removed, but this deletion has not been tested in live bacteria. Here, we demonstrate cloning the 1.46 Mb genome of A. laidlawii strain DN-E by integrating a yeast vector into the toxic gene and transferring the genome directly to yeast using cell fusion. Genomic integration was only possible when A. laidlawii was complemented with a functional recA gene. Following cell fusion, 13 out of 20 screened yeast colonies contained the A. laidlawii genome, as determined by multiplex PCR. This is the first demonstration showing cloning entire A. laidlawii genomes by simply mixing donor and recipient cells in fusion buffer, bringing us one step closer to creating fully synthetic Acholeplasma strains. GRAPHICAL ABSTRACT O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=83 SRC="FIGDIR/small/683135v1_ufig1.gif" ALT="Figure 1"> View larger version (24K): org.highwire.dtl.DTLVardef@1429a68org.highwire.dtl.DTLVardef@1a754c1org.highwire.dtl.DTLVardef@ad6044org.highwire.dtl.DTLVardef@8b2539_HPS_FORMAT_FIGEXP M_FIG C_FIG