Characterization of intracellular accumulation of poly‐β‐hydroxybutyrate (PHB) in individual cells of Alcaligenes eutrophus H16 by flow cytometry

Poly‐β‐hydroxybutyrate (PHB) accumulates in individual cells of Alcaligenes eutrophus in the form of refractile bodies which alter the light‐scattering properties of individual cells. Flow cytometry has been applied to measure the distributions of single‐cell light‐scattering intensity in Alc. eutrophus populations during batch cultivation of the organism. These measurements clearly identify heterogeneities in the inoculum which influence the lag interval prior to beginning of exponential growth. Light‐scattering distributions show greater homogeneity and are extremely similar during balanced, exponential growth. After exhaustion of the nitrogen source and with carbon source still available, significant PHB accumulations occur and the flow cytometry measurements reveal extreme heterogeneity in single‐cell light‐scattering properties. These measurements clearly demonstrate the potential advantages of single‐cell light‐scattering measurements by flow cytometry for analysis and control of certain fermentation processes. Single‐cell light‐scat light‐scattering measurements in conjunction with flow sorting instrumentation have been applied to demonstrate enrichment of PHB‐producing cells, initially present in a number concentration of 0.01%by a factor of 300 in a single pass. Flow cytometry–cell sorting technology should find significant application in strain improvement and mutant selection.

[1]  J G Holt,et al.  Nile blue A as a fluorescent stain for poly-beta-hydroxybutyrate , 1982, Applied and environmental microbiology.

[2]  J. Bailey,et al.  Characterization of bacterial growth by means of flow microfluorometry. , 1977, Science.

[3]  B. J. Price,et al.  Multiangle light scattering flow photometry of cultured human fibroblasts: comparison of normal cells with a mutant line containing cytoplasmic inclusions. , 1979, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

[4]  E. Dawes,et al.  The role and regulation of energy reserve polymers in micro-organisms. , 1973, Advances in microbial physiology.

[5]  Flow microfluorometry study of diauxic batch growth of Saccharomyces cerevisiae , 1978, Applied and environmental microbiology.

[6]  T. Jovin,et al.  Computer‐controlled cell (particle) analyzer and separator. Use of light scattering , 1974, FEBS letters.

[7]  W. Donachie,et al.  Changes in cell size and shape in thymine-requiring Escherichia coli associated with growth in low concentrations of thymine , 1978, Journal of bacteriology.

[8]  J E Bailey,et al.  Flow cytometric analysis of plasmid heterogeneity in Escherichia coli populations , 1983, Biotechnology and bioengineering.

[9]  G. Gottschalk,et al.  Formation and Utilization of Poly-β-Hydroxybutyric Acid by Knallgas Bacteria (Hydrogenomonas) , 1961, Nature.

[10]  A. Paau,et al.  Flow-microfluorometric analysis of Escherichia coli, Rhizobium meliloti, and Rhizobium japonicum at different stages of the growth cycle. , 1977, Canadian journal of microbiology.

[11]  H. Steen,et al.  Applications of flow cytometry on bacteria: cell cycle kinetics, drug effects, and quantitation of antibody binding. , 2005, Cytometry.

[12]  J. Hodkinson,et al.  Computations of Light-Scattering and Extinction by Spheres According to Diffraction and Geometrical Optics, and Some Comparisons with the Mie Theory , 1963 .

[13]  J. H. Law,et al.  A Rapid Spectrophotometric Assay of Alpha, Beta-Unsaturated Acids and Beta-Hydroxy Acids , 1960 .

[14]  J. Bailey,et al.  Continuous cultivation of fission yeast: Classical and flow microfluorometry observations , 1981 .

[15]  H. Steen,et al.  Bacterial growth studied by flow cytometry. , 1980, Cytometry.

[16]  C. Forsberg,et al.  Effect of Phosphate Limitation on the Morphology and Wall Composition of Bacillus licheniformis and Its Phosphoglucomutase-Deficient Mutants , 1973, Journal of bacteriology.

[17]  A. Pardee,et al.  Inhibition of an early event in the cell division cycle of Escherichia coli by FL1060, an amidinopenicillanic acid , 1975, Journal of bacteriology.