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Image Search Results
Journal: Applied and Environmental Microbiology
Article Title: Transposase-Mediated Chromosomal Integration of Exogenous Genes in Acidithiobacillus ferrooxidans
doi: 10.1128/AEM.01381-18
Figure Lengend Snippet: The transposon integration sites were confirmed by amplification of the region of the genome flanking the insertion sites. Panel A shows the genomic PCR amplification scheme for the AFKI1 strain. The primers flanking the insertion site were designed from the published genome sequence for ATCC 23270. In the wild-type genome, the PCR amplicon is of a known size. In the transposon-integrated strains, the same PCR primers were used to amplify the transposon region as well, resulting in a 3.5-kb increase in amplicon size. Panel B shows the results of the method applied to the three transposon locations identified in the mutant strains and visualized on an agarose gel, confirming the successful identification of integration sites.
Article Snippet: Using the NCBI Nucleotide blastx program, sequences were compared against the published
Techniques: Amplification, Sequencing, Mutagenesis, Agarose Gel Electrophoresis
Journal: Applied and Environmental Microbiology
Article Title: Transposase-Mediated Chromosomal Integration of Exogenous Genes in Acidithiobacillus ferrooxidans
doi: 10.1128/AEM.01381-18
Figure Lengend Snippet: Location of the chromosomal integration sites. Panel A shows the integration loci for KDC-integrated strains. The insertion locus identifies the 9-bp sequence duplicated by the transposase to insert the transposon. Panel B shows the approximate locations of the transposon insertions for the mutant strains in relation to the whole A. ferrooxidans 23270 genome.
Article Snippet: Using the NCBI Nucleotide blastx program, sequences were compared against the published
Techniques: Sequencing, Mutagenesis