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In order to analyze the spatiotemporal dynamics of heterocyst formation at the single filament level, here we developed a culture system to monitor simultaneously bacterial development, gene expression, and phycobilisome fluorescence.
The first is to contact the coal with nutrients to support native bacterial development.
It appeared that the presence of salt induced a delay in both bacterial development and CO2 production.
Impaired mucus clearance and a decrease in the partial pressure of oxygen are optimal conditions for bacterial development and infections, thus creating as a vicious circle of pathological processes [1, 2].
These results further confirmed the requirement of a functional Rab14 for bacterial development and replication.
Streptomycetes are an important model system for the study of bacterial development, and undergo multiple synchronous cell division during the sporulation stage.
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We used a porcine Pseudomonas aeruginosa VAP model with ventilatory and inflammatory pre-exposures before inoculation to evaluate bacterial growth, development of lung damage, total NO production and inflammatory cytokine response.
Recent studies elucidating their cellular functions have established their roles in bacterial growth and development.
On the other hand, overexpression of WRKY4 greatly reduced susceptibility to the bacterial pathogen based on strong enhancement in both bacterial growth and development of disease symptoms.
Such studies of static specimens can never give a complete picture of the dynamic processes of bacterial growth and development within host cells or animals.
Recent studies have also suggested their role in the regulation of bacterial growth and development through novel response regulators [ 52] by turnover of cyclic diguanosine monophosphate.
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