Induction of encystment of Polysphondylium pallidum amoeba

1977 ◽  
Vol 23 (5) ◽  
pp. 518-521 ◽  
Author(s):  
Joseph Lonski ◽  
Nicholas Pesut

The induction of microcyst formation could be triggered in washed amoebae of the cellular slime mold Polysphondylium pallidum (strain-2) by the addition of 2 mM ethionine. Methionine at a ratio of 2:1 with ethionine would inhibit microcyst induction by ethionine. The involvement of polyamines in morphogenesis was also shown. Putrescine (0.02 to 0.1 M) induced the formation of microcysts, whereas spermidine (2 to 4 mM) was capable of causing a fourfold reduction in 0.05 M putrescine-induced microcysts but incapable of inhibiting microcyst induction by 0.08 M putrescine. Glycerol (0.5 M or 0.4 M) was also found to be an effective inducer of microcysts.

1988 ◽  
Vol 38 (2) ◽  
pp. 73-81 ◽  
Author(s):  
Edward C. Cox ◽  
Fred W. Spiegel ◽  
Gerard Byrne ◽  
James W. McNally ◽  
Leslie Eisenbud

1990 ◽  
Vol 153 (5) ◽  
pp. 413-416 ◽  
Author(s):  
Akiko Mizutani ◽  
Hiromitsu Hagiwara ◽  
Kaichiro Yanagisawa

1973 ◽  
Vol 51 (2) ◽  
pp. 301-310 ◽  
Author(s):  
Danton H. O'Day ◽  
David W. Francis

The enzyme alkaline phosphatase (EC 3.1.3.1) was studied during axenic growth, microcyst differentiation and fruiting body formation in the cellular slime mold Polysphondylium pallidum. The enzyme activity decreases during growth and microcyst differentiation but increases during fruiting body formation where it is localized in prestalk cells. Two major isozymes exist for the enzyme and these change qualitatively and quantitatively during multicellular development. Beryllium was found to be a potent inhibitor of the slime mold phosphatase. When beryllium was added to growing cells or cells undergoing fruiting body formation markedly reduced alkaline phosphatase activity was detectable in the cells but growth and development were unaffected. The results are discussed in relation to other work on the cellular slime molds.


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