Implementation of Fluorescent-Protein-Based Quantification Analysis in L-Form Bacteria.

Bioengineering (Basel)

Laboratory of Biology and Information Science, School of Life Sciences, East China Normal University, Shanghai 200062, China.

Published: January 2024

AI Article Synopsis

  • Cell-wall-less (L-form) bacteria show complex shapes, making it hard to analyze them quantitatively under different conditions.
  • We tested various fluorescent proteins (FPs) in the L-form strain LR2 using confocal microscopy and imaging flow cytometry to identify the best options for labeling.
  • The results indicated that certain promoters worked well to produce FPs, allowing us to visualize and quantify the unique structures of L-form bacteria, which can aid in research on these cell models.

Article Abstract

Cell-wall-less (L-form) bacteria exhibit morphological complexity and heterogeneity, complicating quantitative analysis of them under internal and external stimuli. Stable and efficient labeling is needed for the fluorescence-based quantitative cell analysis of L-forms during growth and proliferation. Here, we evaluated the expression of multiple fluorescent proteins (FPs) under different promoters in the L-form strain LR2 using confocal microscopy and imaging flow cytometry. Among others, P-derived showed a superior performance for inducing several FPs including EGFP and mKO2 in both the wild-type and L-form strains. Moreover, was also active in and its L-form strain NC-7. Employing these established FP-labeled strains, we demonstrated distinct morphologies in the L-form bacteria in a quantitative manner. Given cell-wall-deficient bacteria are considered protocell and synthetic cell models, the generated cell lines in our work could be valuable for L-form-based research.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10813599PMC
http://dx.doi.org/10.3390/bioengineering11010081DOI Listing

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