Scientists
from New York University have now developed a sophisticated assay to track cell
growth at very low nutrient concentrations. The assay uses time-lapse
microscopy to monitor individual yeast cells undergoing a small number of
divisions to form microcolonies. The assay can measure the lag times and growth
rates of as many as 80,000 individual microcolonies in a single 24-hour
experiment, opening up a powerful new high-throughput tool to study the complex
interplay between cell growth, division and metabolism under environmental
conditions that are likely to be ecologically relevant but had previously been
difficult to study in the laboratory.
The
researchers studied growth rates and lag times in both lab strains and wild
yeast by varying the amount of its prime carbon food source, glucose. They
confirmed the prediction made over 60 years ago by Noble-prize-winning
biologist Jacques Monod regarding changes in microbial growth rates with
limited nutrients (the Monod equation). They also found significant differences
among strains in both the average lag response (the amount of time it takes to
transition from cell quiescence to restarting cell growth) and average growth
rates in response to different environmental conditions.
In
addition to average differences between strains and conditions, the powerful
assay revealed metabolic differences among cells of the same strain in the same
environment. Moreover, yeast strains differed in their variances in growth
rate.
For
more details, refer to the following research paper:
Posted by Tim Sandle
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