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The irrigation methods indicated a highly significant difference in irrigation water use efficiency.
Both methods indicated a lack of significant quantities of viable cells 14 days after transplantation.
The developed tracking methods indicated a high tracking ratio and tracking success ratio of nearly 100% in a wide strain range, which included the assumed strain in a practical experiment.
A fit to equation 5 (METHODS) indicated a binding affinity of ≥100 µM for both luteolin and myricetin.
All three methods indicated a very high overall consistency, with the WT10 and WT14 samples showing the closest profiles, as expected.
However, certain molecular delimitation methods indicated a recent decrease in diversification rate.
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All of the methods indicate a clear abnormal increase in time series of AOD data, 2 days prior to event.
Absolute values of intracellular metabolites extracted with this modified method are comparable to the results of the two previously optimized methods, indicating a good extraction procedure according to the chosen response variables.
Both genotypic methods indicate a low diversity between strains isolated from the same sourdough and a higher diversity between strains isolated from different sourdoughs, suggesting an influence of baker practices and/or environmental conditions on the selection of strains.
Tests on several target proteins for both technologies show high purity and activity at reasonable yields, while initial economic analyses of these methods indicate a potential to dramatically reduce the cost of protein purification.
The comparisons with the state-of-the-art methods indicate a comparable performance for the proposed KLRC-p and KLRC-g.
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