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We described a dynamic flux balance model strategy based on a genome-scale metabolic model of Y. lipolytica and SCO fermentation kinetics that applied for rational design of optimized fed-batch process with high single cell oil accumulation.
In this study, to systematically investigate the metabolism of Y. lipolytica and gain novel insight into TAG biosynthesis of this strain, a new genome-scale metabolic model of Y. lipolytica, named iYL_2.0, was reconstructed.
The distribution of spacers and their arrays in Y. pestis strains is strongly region and focus-specific, allowing the construction of a hypothetic evolutionary model of Y. pestis.
We found that various spacers/spacers arrays had obvious connection with geographic source, and an evolutionary model of Y. pestis was proposed.
We proposed an evolutionary model of Y. pestis based on polymorphism of CRISPR loci, and our model suggested a main transmission route of Y. pestis.
The fundamental question is whether it is possible to infer in tephritid flies a model of Y evolution applicable to a male-determining factor-carrying chromosome.
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Moreover, the secondary atomization model was modified on the basis of previous random atomization model of Y-jet nozzle.
The predicted results agreed well with the experimental ones, and the improved atomization model of Y-jet nozzle was well validated to design the nozzle geometry and to predict the droplet size distributions for single-hole Y-jet nozzle with high liquid mass flow rate.
Figure 4 Growth model of Y-shaped CNFs.
According to our experimental results, the growth mechanism of Y-shaped carbon nanofibers has been discussed and a possible growth model of Y-shaped carbon nanofibers has been proposed.
Contributions of non-essential genes to growth in glucose and glycerol carbon sources were assessed and used to evaluate two recent genome-scale models of Y. lipolytica metabolism.
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