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†Origin and genetic composition of the strains are indicated.
Hence, the absence of antibacterial activity of the Cry toxins tested may be related to cell wall composition of the strains used.
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These two isolates were not grouped together in this MIRU-VNTR-based tree nor in the minimum spanning tree, although they were in the first tree including the total collection (Fig. 1), linked to a distant relationship rendering their linkage more vulnerable to the composition of the strain sample used.
The genetic composition of the strain we used is: MATα, his3Δ, leu2Δ, LYS2, met15Δ, ura3Δ, ho::HIS5-P GAL1 -YFP.
In fact, virulence genes and serogroup are independent at the genetic level, and an important point of our article is that HUS is determined by the virulence gene composition of the strain rather than the serogroup.
However, there was no information on the clonal composition of these strains.
We inferred the chromosome composition of these strains using lys1, his5, and ade6 alleles and their meiotic phenotypes.
The genomic composition of these strains within lineages and subgroups suggests that both genomic divergence from an ancestral form and the lateral transfer of gene clusters have contributed to their evolution.
The taxonomic composition of the remaining strains was remarkably different in the FSC isolates and APD isolates.
Since the consumption of C6/C5 sugar mixture depends on the composition of the two strains used in the culture, the optimal cell ratio of co-culture can be varied with varying composition of sugars available in different sources of biomass feedstock.
The subtelomeric composition of the progenitor strains was identical; 13 chromosome arms encoded a TLO gene.
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