» Articles » PMID: 12788764

Density-dependent Sorting of Physiologically Different Cells of Vibrio Parahaemolyticus

Overview
Date 2003 Jun 6
PMID 12788764
Citations 4
Authors
Affiliations
Soon will be listed here.
Abstract

A pure bacterial culture is composed of clonal cells in different physiological states. Separation of those subpopulations is critical for further characterization and for understanding various processes in the cultured cells. We used density-dependent cell sorting with Percoll to separate subpopulations from cultures of a marine bacterium, Vibrio parahaemolyticus. Cells from cultures in the exponential and stationary phases were fractionated according to their buoyant density, and their culturability and ability to maintain culturability under low-temperature and low-nutrient stress (stress resistance) were determined. The buoyant density of the major portion of the cells decreased with culture age. The culturability of stationary-phase cells increased with increasing buoyant density, but that of exponential-phase cells did not. Stress resistance decreased with increasing buoyant density regardless of the growth phase. The results indicate that density-dependent cell sorting is useful for separating subpopulations of different culturabilities and stress resistances. We expect that this method will be a powerful tool for analyzing cells in various physiological states, such as the viable but nonculturable state.

Citing Articles

The Conjugation Window in an Escherichia coli K-12 Strain with an IncFII Plasmid.

Headd B, Bradford S Appl Environ Microbiol. 2020; 86(17).

PMID: 32591383 PMC: 7440788. DOI: 10.1128/AEM.00948-20.


Separation of viable lactic acid bacteria from fermented milk.

Nishino T, Matsuda Y, Yamazaki Y Heliyon. 2018; 4(4):e00597.

PMID: 29862359 PMC: 5968145. DOI: 10.1016/j.heliyon.2018.e00597.


Bacteria-surface interactions.

Tuson H, Weibel D Soft Matter. 2013; 9(18):4368-4380.

PMID: 23930134 PMC: 3733390. DOI: 10.1039/C3SM27705D.


Separation of marine bacteria according to buoyant density by use of the density-dependent cell sorting method.

Inoue K, Nishimura M, Nayak B, Kogure K Appl Environ Microbiol. 2006; 73(4):1049-53.

PMID: 17158617 PMC: 1828684. DOI: 10.1128/AEM.01158-06.

References
1.
Baldwin W, Myer R, Powell N, Anderson E, Koch A . Buoyant density of Escherichia coli is determined solely by the osmolarity of the culture medium. Arch Microbiol. 1995; 164(2):155-7. DOI: 10.1007/s002030050248. View

2.
Dicker D, Higgins M . Cell cycle changes in the buoyant density of exponential-phase cells of Streptococcus faecium. J Bacteriol. 1987; 169(3):1200-4. PMC: 211919. DOI: 10.1128/jb.169.3.1200-1204.1987. View

3.
Poole R . Fluctuations in buoyant density during the cell cycle of Escherichia coli K12: significance for the preparation of synchronous cultures by age selection. J Gen Microbiol. 1977; 98(1):177-86. DOI: 10.1099/00221287-98-1-177. View

4.
Baldwin W, KUBITSCHEK H . Evidence for osmoregulation of cell growth and buoyant density in Escherichia coli. J Bacteriol. 1984; 159(1):393-4. PMC: 215645. DOI: 10.1128/jb.159.1.393-394.1984. View

5.
Higgins M, HAINES M, Whalen M, Glaser D, Bylund J . Relationship between changes in buoyant density and formation of new sites of cell wall growth in cultures of streptococci (Enterococcus hirae ATCC 9790) undergoing a nutritional shift-up. J Bacteriol. 1990; 172(8):4415-9. PMC: 213269. DOI: 10.1128/jb.172.8.4415-4419.1990. View