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Physiological stabilization of Euglena gracilis cells by high extracellular calcium (100 mM)

  • Applied Genetics and Regulation
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Summary

Experiments were performed to test whether or not high concentrations of CaCl2 (100 mM) are able to arrest and stabilize internal structures and associated functions in Euglena gracilis Z cells stored in darkness at 4° C. Storage of photoheterotrophically grown green cells in high Ca2+ media (2–100 mM) retards pheophytinization of the chlorophylls, preserves photosynthetic activities and stabilizes the structural organization of the associated light-harvesting complexes of the photosystem II units. Alterations of photosynthesis and respiration by chlorpromazine or by temperature are strongly reduced in cells stored under such conditions. More precisely, a chlorpromazine inhibition site is evidenced in the mitochondrial electron pathway and its location in the chloroplastic electron pathway is clarified. Adaptation of Euglena cells from 2 mM to 100 mM Ca2+ medium is accompanied by an increase both in the externally bound and total internal calcium concentration. A mechanism involving a Ca2+ deposit on internal membranes is proposed. Such interpretation is extended to the storage of cells immobilized in Ca2+-alginate gel.

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Abbreviations

(Ca2+)ex:

external calcium concentration

Chl:

chlorophylls

(Cl)ex:

external chloride concentration

CPZ:

chlorpromazine or 2-chloro-10-(3-dimethylaminopropyl)-phenothiazine

DCMU:

diuron or (3,4-dichorophenyl)-1,1-dimethylurea

EGTA:

ethylene glycol-bis(β-aminoethylether) N,N,N′ ,N′-tetraacetic acid

Fc:

initial level of chlorophyll fluorescence with DCMU

Fmax:

maximal level of chlorophyll fluorescence with DCMU

Fo:

level of chlorophyll fluorescence after transients

Ft:

level of chlorophyll fluorescence with DCMU

Pheo:

pheophytins

PS I and PS II:

photosystems I and II

SMi:

storage medium

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Tamponnet, C., Barbotin, JN. & Calvayrac, R. Physiological stabilization of Euglena gracilis cells by high extracellular calcium (100 mM). Appl Microbiol Biotechnol 32, 211–217 (1989). https://doi.org/10.1007/BF00165890

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  • DOI: https://doi.org/10.1007/BF00165890

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