Tags

Type your tag names separated by a space and hit enter

Growth kinetics of algal populations exsymbiotic from Paramecium bursaria by flow cytometry measurements.
Cytometry. 2001 Jul 01; 44(3):257-63.C

Abstract

BACKGROUND

The ciliate Paramecium bursaria normally exists as a green paramecium system because each animal cell carries several hundred, unicellular, green, algal cells in its cytoplasm. One of the remarkable and poorly understood pecularities of this system is the steady state in the number of algae per protozoan cell. A major point in the study of mechanisms governing the persistence of symbiont numbers is adequate understanding of the algal life cycle.

METHODS

Asynchronously growing cell populations of several algal strains (SA-1, SA-3, and SA-9) exsymbiotic from P. bursaria were characterized by flow cytometry. Algal endogenous chlorophyll and DNA contents were monitored to analyze cell growth kinetics at logarithmic and stationary culture phases. Cell sorting visualized the morphology of algae corresponding to the hyperhaploid (2C and 4C) DNA peaks.

RESULTS

Cell-division cycle-dependent changes in chlorophyll and DNA content distributions were most dramatic in logarithmically growing algal populations (an increase in the number of S-phase cells and cells with more chlorophyll), which are thought to be associated with accelerated DNA and chlorophyll metabolism in log-phase algal cultures. Upon reaching the stationary phase of growth, algal populations distinctly showed, in addition to one haploid (1C) DNA peak, two hyperhaploid peaks (2C and 4C) corresponding mainly to cells with two and four nuclei, respectively.

CONCLUSIONS

Growth characteristics of algae exsymbiotic from P. bursaria monitored by flow cytometry provide valuable information for the analysis of the algal life cycle, which is important for understanding the regulation mechanisms of symbiont numbers.

Authors+Show Affiliations

Department of Biological Science, Graduate School of Science, Hiroshima University, Higashi-Hiroshima, Japan.No affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article
Research Support, Non-U.S. Gov't

Language

eng

PubMed ID

11429776

Citation

Gerashchenko, B I., et al. "Growth Kinetics of Algal Populations Exsymbiotic From Paramecium Bursaria By Flow Cytometry Measurements." Cytometry, vol. 44, no. 3, 2001, pp. 257-63.
Gerashchenko BI, Kosaka T, Hosoya H. Growth kinetics of algal populations exsymbiotic from Paramecium bursaria by flow cytometry measurements. Cytometry. 2001;44(3):257-63.
Gerashchenko, B. I., Kosaka, T., & Hosoya, H. (2001). Growth kinetics of algal populations exsymbiotic from Paramecium bursaria by flow cytometry measurements. Cytometry, 44(3), 257-63.
Gerashchenko BI, Kosaka T, Hosoya H. Growth Kinetics of Algal Populations Exsymbiotic From Paramecium Bursaria By Flow Cytometry Measurements. Cytometry. 2001 Jul 1;44(3):257-63. PubMed PMID: 11429776.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Growth kinetics of algal populations exsymbiotic from Paramecium bursaria by flow cytometry measurements. AU - Gerashchenko,B I, AU - Kosaka,T, AU - Hosoya,H, PY - 2001/6/29/pubmed PY - 2001/9/21/medline PY - 2001/6/29/entrez SP - 257 EP - 63 JF - Cytometry JO - Cytometry VL - 44 IS - 3 N2 - BACKGROUND: The ciliate Paramecium bursaria normally exists as a green paramecium system because each animal cell carries several hundred, unicellular, green, algal cells in its cytoplasm. One of the remarkable and poorly understood pecularities of this system is the steady state in the number of algae per protozoan cell. A major point in the study of mechanisms governing the persistence of symbiont numbers is adequate understanding of the algal life cycle. METHODS: Asynchronously growing cell populations of several algal strains (SA-1, SA-3, and SA-9) exsymbiotic from P. bursaria were characterized by flow cytometry. Algal endogenous chlorophyll and DNA contents were monitored to analyze cell growth kinetics at logarithmic and stationary culture phases. Cell sorting visualized the morphology of algae corresponding to the hyperhaploid (2C and 4C) DNA peaks. RESULTS: Cell-division cycle-dependent changes in chlorophyll and DNA content distributions were most dramatic in logarithmically growing algal populations (an increase in the number of S-phase cells and cells with more chlorophyll), which are thought to be associated with accelerated DNA and chlorophyll metabolism in log-phase algal cultures. Upon reaching the stationary phase of growth, algal populations distinctly showed, in addition to one haploid (1C) DNA peak, two hyperhaploid peaks (2C and 4C) corresponding mainly to cells with two and four nuclei, respectively. CONCLUSIONS: Growth characteristics of algae exsymbiotic from P. bursaria monitored by flow cytometry provide valuable information for the analysis of the algal life cycle, which is important for understanding the regulation mechanisms of symbiont numbers. SN - 0196-4763 UR - https://www.unboundmedicine.com/medline/citation/11429776/Growth_kinetics_of_algal_populations_exsymbiotic_from_Paramecium_bursaria_by_flow_cytometry_measurements_ L2 - https://doi.org/10.1002/1097-0320(20010701)44:3<257::aid-cyto1118>3.0.co;2-v DB - PRIME DP - Unbound Medicine ER -