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Image Search Results
Journal: BMC microbiology
Article Title: Comparative genomics of Enterococcus spp. isolated from bovine feces.
doi: 10.1186/s12866-017-0962-1
Figure Lengend Snippet: Fig. 1 Phylogenetic tree constructed based on analysis of single-nucleotide polymorphisms (SNPs) of the core genes of 48 entercocci genomes, including the 21 isolates obtained from bovine feces in the present study. Entercoccus faecalis, Entercoccus faecium, Enterococcus hirae, Entercoccus durans, Entercoccus casseliflavus and Entercoccus gallinarum were compared using E. faecium strain T110 as a reference
Article Snippet: The 27 compete genomes from NCBI included: E. hirae (2 strains; ATCC 9790, R17),
Techniques: Construct
Journal: BMC microbiology
Article Title: Comparative genomics of Enterococcus spp. isolated from bovine feces.
doi: 10.1186/s12866-017-0962-1
Figure Lengend Snippet: Fig. 3 a Phylogenetic tree of Entercoccus faecium genome sequences from the present study and complete genome sequences from the NCBI database based on analysis of single-nucleotide varients (SNVs) of the core genes. b Relatedness tree of E. faecium genome sequences from present study and complete genome sequences from the NCBI database based on Pearson correlation similarity matrix analysis of accessory genes. Origin of isolates are as indicated in the figures
Article Snippet: The 27 compete genomes from NCBI included: E. hirae (2 strains; ATCC 9790, R17),
Techniques:
Journal: BMC microbiology
Article Title: Comparative genomics of Enterococcus spp. isolated from bovine feces.
doi: 10.1186/s12866-017-0962-1
Figure Lengend Snippet: Fig. 4 a Blast atlas of 10 Enterococcus hirae strains isolated from bovine feces and E. hirae strain R17 mapped against E. hirae ATCC9790. b Blast atlas of the genomes of 3 Entercoccus faecium isolates from bovine feces and 12 complete E. faecium genomes from the NCBI database mapped against reference sequence E. faecium DO. Blast atlases were generated by GView Java package software [28] using both alignment length and percent identity cut-off values of 80%. Based on the reference genomes, phage and transposon related regions/loci are indicated on the altas diagram
Article Snippet: The 27 compete genomes from NCBI included: E. hirae (2 strains; ATCC 9790, R17),
Techniques: Isolation, Sequencing, Generated, Software
Journal: Frontiers in Microbiology
Article Title: Insights in the Antimicrobial Potential of the Natural Nisin Variant Nisin H
doi: 10.3389/fmicb.2020.573614
Figure Lengend Snippet: Determination of purity, yield and cleavage efficiency of the pre-nisin variants. (A) Purity of the purified nisin A and the variants nisin H and nisin H F 1 I (Marker: Precision Plus Protein Dual Xtra standards Bio-Rad). (B) Yields after purification of nisin A and their corresponding variants via cation-exchange chromatography. (C) Quantification of the cleavage efficiency of NisP. (D) Chromatogram of nisin H. (E) Chromatogram of the nisin H F 1 I variant. The pre-nisin variants before NisP cleavage were shown by blue dashed lines and after NisP cleavage by black lines. Error bars represent the standard deviation of at least three biological replicates.
Article Snippet: All bacteria used for minimum inhibitory concentration (MIC) determination of
Techniques: Purification, Marker, Chromatography, Variant Assay, Standard Deviation
Journal: Frontiers in Microbiology
Article Title: Insights in the Antimicrobial Potential of the Natural Nisin Variant Nisin H
doi: 10.3389/fmicb.2020.573614
Figure Lengend Snippet: Nisin mediated pore formation, visualized with the SYTOX green assay. The NZ9000Cm strain incubated with the SYTOX dye. After a stable baseline (∼200 s), one of the nisin variants (100 nM) was added (indicated with an arrow). The fluorescence signal was measured using a fluorolog (Horiba III). The rapid increase in fluorescence indicates pore formation. The black line represents the addition of nisin A, the red line nisin H, and the blue line nisin H F 1 I. As a control we added buffer shown as green line.
Article Snippet: All bacteria used for minimum inhibitory concentration (MIC) determination of
Techniques: Incubation, Fluorescence, Control
Journal: Frontiers in Microbiology
Article Title: Insights in the Antimicrobial Potential of the Natural Nisin Variant Nisin H
doi: 10.3389/fmicb.2020.573614
Figure Lengend Snippet: MIC values for nisin A, nisin H, and nisin H F 1 I against different pathogenic strains.
Article Snippet: All bacteria used for minimum inhibitory concentration (MIC) determination of
Techniques: