<p>(A) PCR verification of gene deletion. Lane 1, a 42,725 bp fragment was amplified using primers ZB287/ZB288. The size of the fragment was too large and could not be PCR-amplified, thus no band was seen in lane 1. Lane 2, a 1981 bp fragment was amplified using primers ZB287/ZB288. The CDA biosynthetic gene cluster was replaced with the <i>aac(3)IV</i> gene. Lane3, a 927 bp fragment was amplified using primers ZB287/ZB288, and the resistance gene was removed. Lane 4, a 4073 bp fragment was amplified with primers ZB289/ZB290. Lanes 5 and 6 showed the bands before and after removing the <i>aphII</i> resistance gene. Lane 7, a 928 bp fragment was amplified with primers ZB285/ZB286. Lanes 8 and 9 showed thebands before and after removing the <...
Lane M: DNA molecular weight standard. (a) The fusion PCR result from the upstream and downstream ho...
<p>A: <i>Foc-SIX1</i> gene deletion and replacement with an intact selectable marker gene (<i>hph</i...
<p>(A) PCR verification of expected 199 bp target length amplicon. Lane M, 50 bp DNA ladder (Molecul...
<p><b>A)</b> PCR verification of <i>vdCYC8</i> deletion mutants with primer CYC8test-F/R. Lanes 1–6 ...
<p>In presence of K103N-AAC (A1) and K103-AAT (A2) mutants, only the specific mutant amplicons will ...
<p>Primers BPSL2179-up and BPSL2179-down were used to generate a 3108 bp fragment from strains carry...
<p>(A) PCR products amplified from primers, TofI(H)F and TofI(H)R, to confirm the <i>tofI</i> deleti...
<p>(A) Diagram of the primers used to screen for homozygous strains in the <i>acsA</i> locus. Primer...
<div><p>(A) Verification of <i>ddrA</i> and <i>recA</i> gene deletions by PCR analysis. Purified PCR...
<p>Strains are listed in <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.01427...
<p>A. Schematic overview of the Pop-In-Pop-Out method for mutant construction. The uracil auxotrophi...
<p>(A) The genes <i>ehx</i> and <i>ecf</i> were detected in EDL933 but not in ΔpO157. Lane M: marker...
(A) Schematic representation of the bb0562-bb0564 region of the B. burgdorferi chromosome (Chr). The...
<p>The PCR product from three mutated isolates <i>ssaS</i>::Km (lanes 1–3) and the wild type gene <i...
Panel A shows a PCR analysis of genomic DNA isolated from the parental (WT) and Δfbpase cell lines. ...
Lane M: DNA molecular weight standard. (a) The fusion PCR result from the upstream and downstream ho...
<p>A: <i>Foc-SIX1</i> gene deletion and replacement with an intact selectable marker gene (<i>hph</i...
<p>(A) PCR verification of expected 199 bp target length amplicon. Lane M, 50 bp DNA ladder (Molecul...
<p><b>A)</b> PCR verification of <i>vdCYC8</i> deletion mutants with primer CYC8test-F/R. Lanes 1–6 ...
<p>In presence of K103N-AAC (A1) and K103-AAT (A2) mutants, only the specific mutant amplicons will ...
<p>Primers BPSL2179-up and BPSL2179-down were used to generate a 3108 bp fragment from strains carry...
<p>(A) PCR products amplified from primers, TofI(H)F and TofI(H)R, to confirm the <i>tofI</i> deleti...
<p>(A) Diagram of the primers used to screen for homozygous strains in the <i>acsA</i> locus. Primer...
<div><p>(A) Verification of <i>ddrA</i> and <i>recA</i> gene deletions by PCR analysis. Purified PCR...
<p>Strains are listed in <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.01427...
<p>A. Schematic overview of the Pop-In-Pop-Out method for mutant construction. The uracil auxotrophi...
<p>(A) The genes <i>ehx</i> and <i>ecf</i> were detected in EDL933 but not in ΔpO157. Lane M: marker...
(A) Schematic representation of the bb0562-bb0564 region of the B. burgdorferi chromosome (Chr). The...
<p>The PCR product from three mutated isolates <i>ssaS</i>::Km (lanes 1–3) and the wild type gene <i...
Panel A shows a PCR analysis of genomic DNA isolated from the parental (WT) and Δfbpase cell lines. ...
Lane M: DNA molecular weight standard. (a) The fusion PCR result from the upstream and downstream ho...
<p>A: <i>Foc-SIX1</i> gene deletion and replacement with an intact selectable marker gene (<i>hph</i...
<p>(A) PCR verification of expected 199 bp target length amplicon. Lane M, 50 bp DNA ladder (Molecul...