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We effectively transformed our raw behavioral metrics into a set of six principal components that defined the behavior of the strains in response to the thermal pulses.
Growth parameters (lag and generation times calculated with Gompertz equation) were used to compare the behavior of the strains with respect to the conditions of culture.
We examined the tame behavior of the strains at 6 weeks of age.
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Nevertheless, this model does not directly explain the asymptotic behavior of the strain as the LPL thickness increases.
In the case of the control specimens, the behavior of the strain gauges installed on the lateral surface was affected by the unpredictability of the crack-growing path, whereas, in the presence of FRCM, data collected from strengthened specimens showed less variability.
The behavior of the strain was consistent with the expectations of the design of the camphor system.
We were interested in determining if any of these phenotypes show correlations with each other and to what extent each additional assay is providing new information about the behavior of the strain.
The consomic strains for Chr 5, Chr 7C and Chr 10 did not breed well, and the behavior of these strains could not be characterized.
To further investigate this pathway in telomerase-deficient cells, we examined the behavior of these strains in both our high-throughput and low-throughput screens.
To characterize the behavior of these strains when treated with antibiotics with known mechanisms of action, we observed these reporter strains via time-lapse microscopy with antibiotics known to inhibit DNA replication, transcription, or translation (ciprofloxacin, rifampin, and chloramphenicol, respectively).
Thus, the different types of lipopeptide produced by the different Collimonas strains may partly explain the variability in the fungal inhibition behavior of these strains.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com