Two isolates (JNM56C1 and JNM60C2) were subcultured in the presence of 30 μg/mL CTX. Total DNA from both were purified using the QIAamp DNA extraction mini kit (Qiagen, Hilden, Germany) and were subjected to paired end whole genome sequencing (2 × 300 bp) on an Illumina HiSeq2500 platform (Illumina, San Diego, CA, USA). Both de novo and reference guided assembly was carried out using Velvet and Bowtie2, respectively [49 (link),50 (link)], to build genomes as described previously [51 (link)].
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