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Isolation and characterization of salt-associated protein in Citrus

Identifieur interne : 003788 ( Main/Curation ); précédent : 003787; suivant : 003789

Isolation and characterization of salt-associated protein in Citrus

Auteurs : Gozal Ben-Hayyim [Israël] ; Zehava Faltin [Israël] ; Shimon Gepstein [Israël] ; Luc Camoin [France] ; A. Donny Strosberg [France] ; Yuval Eshdat [Israël]

Source :

RBID : ISTEX:E62C7DE9F4E5580E2F6E39FFB07AD689D1394870

Descripteurs français

English descriptors

Abstract

A significant increase in the amount of a protein, whose migration in two-dimensional gel electrophoresis corresponds to an apparent olecular weight of 23–25 kDa and pI=6.1, was observed in adapted salt-tolerant cultured cells derived from Shamuti orange (Citrus sinesis L. Osbeck) ovular callus cells. An increase was also determined when these cells were grown in the presence of abscisic acid (ABA) or polyethylene glycol (PEG) instead of NaCl, similarly to what was previously observed for osmotin, the tobacco salt-associated protein. However, no similarity has been so far observed between these proteins in their biochemical and immunochemical properties. Pulse labeling of the salt-tolerant cells suggests a low turnover of the accumulated protein. Its salt-induced accumulation in the cells was also relatively slow and gradually increased during a period of several days following exposure of the cells to NaCl. Cell fractionation experiments suggest that the protein is allocated in the soluble fraction and is not an integral membrane protein. Examination of the presence of the protein in citrus plants, such as Etrog citron (C. medicaL.) and Cleopatra mandarin (C. reticulata) cultivars, revealed an increase in its concentration in all organs examined, following irrigation of the plants with saline water. Thus, this protein is associated with stress conditions employed on growing plants as well and is not a unique phenomenon restricted to cultured cells only.

Url:
DOI: 10.1016/0168-9452(93)90084-D

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ISTEX:E62C7DE9F4E5580E2F6E39FFB07AD689D1394870

Le document en format XML

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<wicri:regionArea>Laboratoire d'Immuno-Pharmacologie Moléculaire, CNRS, Université Paris VII and Institut Cochin de Génetique Moléculaire, 22 rue Méchain, 75014 Paris</wicri:regionArea>
<placeName>
<region type="region" nuts="2">Île-de-France</region>
<settlement type="city">Paris</settlement>
</placeName>
</affiliation>
</author>
<author>
<name sortKey="Eshdat, Yuval" sort="Eshdat, Yuval" uniqKey="Eshdat Y" first="Yuval" last="Eshdat">Yuval Eshdat</name>
<affiliation wicri:level="1">
<country xml:lang="fr">Israël</country>
<wicri:regionArea>Department of Friut Tree Breeding and Genetics, Agricultural Research Organization, The Volcani Center, 50250 Bet Dagan</wicri:regionArea>
<wicri:noRegion>50250 Bet Dagan</wicri:noRegion>
</affiliation>
</author>
</analytic>
<monogr></monogr>
<series>
<title level="j">Plant Science</title>
<title level="j" type="abbrev">PSL</title>
<idno type="ISSN">0168-9452</idno>
<imprint>
<publisher>ELSEVIER</publisher>
<date type="published" when="1993">1993</date>
<biblScope unit="volume">88</biblScope>
<biblScope unit="issue">2</biblScope>
<biblScope unit="page" from="129">129</biblScope>
<biblScope unit="page" to="140">140</biblScope>
</imprint>
<idno type="ISSN">0168-9452</idno>
</series>
<idno type="istex">E62C7DE9F4E5580E2F6E39FFB07AD689D1394870</idno>
<idno type="DOI">10.1016/0168-9452(93)90084-D</idno>
<idno type="PII">0168-9452(93)90084-D</idno>
</biblStruct>
</sourceDesc>
<seriesStmt>
<idno type="ISSN">0168-9452</idno>
</seriesStmt>
</fileDesc>
<profileDesc>
<textClass></textClass>
<langUsage>
<language ident="en">en</language>
</langUsage>
</profileDesc>
</teiHeader>
<front>
<div type="abstract" xml:lang="en">A significant increase in the amount of a protein, whose migration in two-dimensional gel electrophoresis corresponds to an apparent olecular weight of 23–25 kDa and pI=6.1, was observed in adapted salt-tolerant cultured cells derived from Shamuti orange (Citrus sinesis L. Osbeck) ovular callus cells. An increase was also determined when these cells were grown in the presence of abscisic acid (ABA) or polyethylene glycol (PEG) instead of NaCl, similarly to what was previously observed for osmotin, the tobacco salt-associated protein. However, no similarity has been so far observed between these proteins in their biochemical and immunochemical properties. Pulse labeling of the salt-tolerant cells suggests a low turnover of the accumulated protein. Its salt-induced accumulation in the cells was also relatively slow and gradually increased during a period of several days following exposure of the cells to NaCl. Cell fractionation experiments suggest that the protein is allocated in the soluble fraction and is not an integral membrane protein. Examination of the presence of the protein in citrus plants, such as Etrog citron (C. medicaL.) and Cleopatra mandarin (C. reticulata) cultivars, revealed an increase in its concentration in all organs examined, following irrigation of the plants with saline water. Thus, this protein is associated with stress conditions employed on growing plants as well and is not a unique phenomenon restricted to cultured cells only.</div>
</front>
</TEI>
</ISTEX>
</double>
</record>

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