Involvement of H+-ATPase and carbonic anhydrase in inorganic carbon uptake for endosymbiont photosynthesis

Symbiotic cnidarians absorb inorganic carbon from seawater to supply intracellular dinoflagellates with CO2 for their photosynthesis. To determine the mechanism of inorganic carbon transport by animal cells, we used plasma membrane vesicles prepared from ectodermal cells isolated from tentacles of t...

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Main Authors: P. Furla, D. Allemand, M.N. Orsenigo
Format: Article in Journal/Newspaper
Language:English
Published: American physiological society 2000
Subjects:
Online Access:http://hdl.handle.net/2434/39736
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spelling ftunivmilanoair:oai:air.unimi.it:2434/39736 2024-02-11T10:02:52+01:00 Involvement of H+-ATPase and carbonic anhydrase in inorganic carbon uptake for endosymbiont photosynthesis P. Furla D. Allemand M.N. Orsenigo P. Furla D. Allemand M.N. Orsenigo 2000 http://hdl.handle.net/2434/39736 eng eng American physiological society info:eu-repo/semantics/altIdentifier/pmid/10749774 volume:278 issue:4 firstpage:R870 lastpage:R881 journal:AMERICAN JOURNAL OF PHYSIOLOGY. REGULATORY, INTEGRATIVE AND COMPARATIVE PHYSIOLOGY http://hdl.handle.net/2434/39736 info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-0033995429 Anthozoan Carbon-concentrating mechanism HCO3/- transport Sea anemone Symbiosis Settore BIO/09 - Fisiologia info:eu-repo/semantics/article 2000 ftunivmilanoair 2024-01-23T23:17:01Z Symbiotic cnidarians absorb inorganic carbon from seawater to supply intracellular dinoflagellates with CO2 for their photosynthesis. To determine the mechanism of inorganic carbon transport by animal cells, we used plasma membrane vesicles prepared from ectodermal cells isolated from tentacles of the sea anemone, Anemonia viridis. H14CO3/- uptake in the presence of an outward NaCl gradient or inward H+ gradient, showed no evidence for a Cl- or H+- driven HCO3/- transport. H14CO3/- and 36Cl- uptakes were stimulated by a positive inside-membrane diffusion potential, suggesting the presence of HCO3/- and Cl- conductances. A carbonic anhydrase (CA) activity was measured on plasma membrane (4%) and in the cytoplasm of the ectodermal cells (96%) and was sensitive to acetazolamide (IC50 = 20 nM) and ethoxyzolamide (IC50 = 2.5 nM). A strong DIDS-sensitive H+ATPase activity was observed (IC50 = 14 μM). This activity was also highly sensitive to vanadate and allyl isothiocyanate, two inhibitors of P-type H+-ATPases. Present data suggest that HCO3/- absorption by ectodermal cells is carried out by H+ secretion by H+-ATPase, resulting in the formation of carbonic acid in the surrounding seawater, which is quickly dehydrated into CO2 by a membrane-bound CA. CO2 then diffuses passively into the cell where it is hydrated in HCO3/- by a cytosolic CA. Article in Journal/Newspaper Carbonic acid The University of Milan: Archivio Istituzionale della Ricerca (AIR)
institution Open Polar
collection The University of Milan: Archivio Istituzionale della Ricerca (AIR)
op_collection_id ftunivmilanoair
language English
topic Anthozoan
Carbon-concentrating mechanism
HCO3/- transport
Sea anemone
Symbiosis
Settore BIO/09 - Fisiologia
spellingShingle Anthozoan
Carbon-concentrating mechanism
HCO3/- transport
Sea anemone
Symbiosis
Settore BIO/09 - Fisiologia
P. Furla
D. Allemand
M.N. Orsenigo
Involvement of H+-ATPase and carbonic anhydrase in inorganic carbon uptake for endosymbiont photosynthesis
topic_facet Anthozoan
Carbon-concentrating mechanism
HCO3/- transport
Sea anemone
Symbiosis
Settore BIO/09 - Fisiologia
description Symbiotic cnidarians absorb inorganic carbon from seawater to supply intracellular dinoflagellates with CO2 for their photosynthesis. To determine the mechanism of inorganic carbon transport by animal cells, we used plasma membrane vesicles prepared from ectodermal cells isolated from tentacles of the sea anemone, Anemonia viridis. H14CO3/- uptake in the presence of an outward NaCl gradient or inward H+ gradient, showed no evidence for a Cl- or H+- driven HCO3/- transport. H14CO3/- and 36Cl- uptakes were stimulated by a positive inside-membrane diffusion potential, suggesting the presence of HCO3/- and Cl- conductances. A carbonic anhydrase (CA) activity was measured on plasma membrane (4%) and in the cytoplasm of the ectodermal cells (96%) and was sensitive to acetazolamide (IC50 = 20 nM) and ethoxyzolamide (IC50 = 2.5 nM). A strong DIDS-sensitive H+ATPase activity was observed (IC50 = 14 μM). This activity was also highly sensitive to vanadate and allyl isothiocyanate, two inhibitors of P-type H+-ATPases. Present data suggest that HCO3/- absorption by ectodermal cells is carried out by H+ secretion by H+-ATPase, resulting in the formation of carbonic acid in the surrounding seawater, which is quickly dehydrated into CO2 by a membrane-bound CA. CO2 then diffuses passively into the cell where it is hydrated in HCO3/- by a cytosolic CA.
author2 P. Furla
D. Allemand
M.N. Orsenigo
format Article in Journal/Newspaper
author P. Furla
D. Allemand
M.N. Orsenigo
author_facet P. Furla
D. Allemand
M.N. Orsenigo
author_sort P. Furla
title Involvement of H+-ATPase and carbonic anhydrase in inorganic carbon uptake for endosymbiont photosynthesis
title_short Involvement of H+-ATPase and carbonic anhydrase in inorganic carbon uptake for endosymbiont photosynthesis
title_full Involvement of H+-ATPase and carbonic anhydrase in inorganic carbon uptake for endosymbiont photosynthesis
title_fullStr Involvement of H+-ATPase and carbonic anhydrase in inorganic carbon uptake for endosymbiont photosynthesis
title_full_unstemmed Involvement of H+-ATPase and carbonic anhydrase in inorganic carbon uptake for endosymbiont photosynthesis
title_sort involvement of h+-atpase and carbonic anhydrase in inorganic carbon uptake for endosymbiont photosynthesis
publisher American physiological society
publishDate 2000
url http://hdl.handle.net/2434/39736
genre Carbonic acid
genre_facet Carbonic acid
op_relation info:eu-repo/semantics/altIdentifier/pmid/10749774
volume:278
issue:4
firstpage:R870
lastpage:R881
journal:AMERICAN JOURNAL OF PHYSIOLOGY. REGULATORY, INTEGRATIVE AND COMPARATIVE PHYSIOLOGY
http://hdl.handle.net/2434/39736
info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-0033995429
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