Literature DB >> 2859369

Processing of digestive vacuoles in Tetrahymena and the effects of dichloroisoproterenol.

A K Fok, B U Shockley.   

Abstract

The digestive-lysosomal system in Tetrahymena has been extensively studied; however, the various vacuole stages and the existence of a required processing period prior to defecation have not been clearly defined. In this study the presence of such a required processing period and the rate of DV defecation in Tetrahymena thermophila were determined. Like the cycle in Paramecium, a digestive cycle in Tetrahymena consisted of two periods: the processing period was 45 min and the defecation period was approximately 2 h, making the complete cycle approximately 3 h. During the defecation period vacuole egestion followed the kinetics of a first-order rate reaction and had a rate constant of 0.0187/min and a t1/2 of 37 min (82 min into the cycle). Using the naphthol AS-TR phosphate-hexazotized rosanilin method to visualize acid phosphatase activity at the light microscopic level, DVs became positive beginning at 10 min. The number of positive DVs increased to a maximum of 13% when DVs were 20-min old and declined to 5-7% beyond 30 min. Although dichloroisoproterenol (DCI) has been reported by others to stimulate vacuole defecation, we found it inhibited the defecation rate. The extent of inhibition depended on the age of the DVs when exposed to DCI. Vacuole formation was completely blocked in cells preexposed to 40 microM DCI for only 10 min; however, upon further exposure, cells could recover from this inhibition. The time required for complete recovery increased with increasing DCI concentrations. If DCI was given to cells simultaneously with latex beads, it was found to exert a dose-dependent inhibitory effect on DV formation.(ABSTRACT TRUNCATED AT 250 WORDS)

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Year:  1985        PMID: 2859369     DOI: 10.1111/j.1550-7408.1985.tb03004.x

Source DB:  PubMed          Journal:  J Protozool        ISSN: 0022-3921


  5 in total

1.  Interception of small particles by flocculent structures, sessile ciliates, and the basic layer of a wastewater biofilm.

Authors:  H Eisenmann; I Letsiou; A Feuchtinger; W Beisker; E Mannweiler; P Hutzler; P Arnz
Journal:  Appl Environ Microbiol       Date:  2001-09       Impact factor: 4.792

2.  Rates of digestion of bacteria by marine phagotrophic protozoa: temperature dependence.

Authors:  B F Sherr; E B Sherr; F Rassoulzadegan
Journal:  Appl Environ Microbiol       Date:  1988-05       Impact factor: 4.792

3.  Size-selective grazing of coastal bacterioplankton by natural assemblages of pigmented flagellates, colorless flagellates, and ciliates.

Authors:  S S Epstein; M P Shiaris
Journal:  Microb Ecol       Date:  1992-05       Impact factor: 4.552

4.  Grazing of Tetrahymena sp. on adhered bacteria in percolated columns monitored by in situ hybridization with fluorescent oligonucleotide probes.

Authors:  H Eisenmann; H Harms; R Meckenstock; E I Meyer; A J Zehnder
Journal:  Appl Environ Microbiol       Date:  1998-04       Impact factor: 4.792

5.  A simple microscopy assay to teach the processes of phagocytosis and exocytosis.

Authors:  Ross Gray; Andrew Gray; Jessica L Fite; Renée Jordan; Sarah Stark; Kari Naylor
Journal:  CBE Life Sci Educ       Date:  2012       Impact factor: 3.325

  5 in total

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