Literature DB >> 4795859

Biochemical changes during growth and encystment of the cellular slime mold Polysphondylium pallidum.

S Githens, M L Karnovsky.   

Abstract

The growth of the cellular slime mold, Polysphondylium pallidum, was studied on a semidefined medium in shaken suspension. When the medium contained large quantities of particulate material, growth was more rapid and the cellular size and protein content were smaller than when growth occurred on a medium containing less particulate material. The cellular levels of DNA, RNA, and protein; of lysosomal enzymes (acid phosphatase, acid proteinase); and of peroxisomal enzymes (catalase) were assayed during growth and the subsequent stationary phase that led eventually to encystment. Only DNA remained at a constant cellular level. Encystment of exponentially growing cells could also be initiated by washing them and introducing them into a soluble peptone medium. The rate of encystment was proportional to the osmolarity of this medium. The encystment process was followed with respect to the cellular levels of DNA, RNA, protein, carbohydrates, acid phosphatase, acid beta-N-Ac-glucosaminidase, and catalase. The most dramatic change occurred in the cellular cellulose content, which increased by at least an order of magnitude by the time encystment was morphologically complete. It was concluded that the encystment of this slime mold in suspension exhibits a number of biochemical similarities to the development of this and other cellular slime molds on a surface.

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Year:  1973        PMID: 4795859      PMCID: PMC2109073          DOI: 10.1083/jcb.58.3.522

Source DB:  PubMed          Journal:  J Cell Biol        ISSN: 0021-9525            Impact factor:   10.539


  26 in total

1.  Tissue fractionation studies. 17. Intracellular distribution of monoamine oxidase, aspartate aminotransferase, alanine aminotransferase, D-amino acid oxidase and catalase in rat-liver tissue.

Authors:  P Baudhuin; H Beaufay; Y Rahman-Li; O Z Sellinger; R Wattiaux; P Jacques; C De Duve
Journal:  Biochem J       Date:  1964-07       Impact factor: 3.857

2.  [Species specific polysaccharide-rich cell membrane antigens of Dictyostelium discoideum].

Authors:  G Gerisch; H Wilhelms; O Lüderitz
Journal:  Eur J Biochem       Date:  1969-06

3.  Microcysts of the cellular slime mold Polysphondylium pallidum. II. Chemistry of the microcyst walls.

Authors:  M A Toama; K B Raper
Journal:  J Bacteriol       Date:  1967-10       Impact factor: 3.490

4.  RNA metabolism during cytodifferentiation in the cellular slime mold Polysphondelium pallidum.

Authors:  R R Sussman
Journal:  Biochim Biophys Acta       Date:  1967-12-19

5.  Particulate material as a prerequisite for rapid cell multiplication in Tetrahymena cultures.

Authors:  L Rasmussen; T A Kludt
Journal:  Exp Cell Res       Date:  1970-03       Impact factor: 3.905

Review 6.  Functions of lysosomes.

Authors:  C De Duve; R Wattiaux
Journal:  Annu Rev Physiol       Date:  1966       Impact factor: 19.318

Review 7.  Peroxisomes (microbodies and related particles).

Authors:  C De Duve; P Baudhuin
Journal:  Physiol Rev       Date:  1966-04       Impact factor: 37.312

8.  The isolation and characterization of lysosomal particles from myxamoebae of the cellular slime mould Dictyostelium discoideum.

Authors:  E Wiener; J M Ashworth
Journal:  Biochem J       Date:  1970-07       Impact factor: 3.857

9.  Acetylglucosaminidase, an early enzyme in the development of Dictyostelium discoideum.

Authors:  W F Loomis
Journal:  J Bacteriol       Date:  1969-03       Impact factor: 3.490

10.  Microcysts of the cellular slime mold Polysphondylium pallidum. I. Factors influencing microcyst formation.

Authors:  M A Toama; K B Raper
Journal:  J Bacteriol       Date:  1967-10       Impact factor: 3.490

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  1 in total

1.  Phagocytosis by the cellular slime mold Polysphondylium pallidum during growth and development.

Authors:  S Githens; M L Karnovsky
Journal:  J Cell Biol       Date:  1973-09       Impact factor: 10.539

  1 in total

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