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Plant and Cell Physiology Advance Access originally published online on November 21, 2006
Plant and Cell Physiology 2007 48(1):42-53; doi:10.1093/pcp/pcl035
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© The Author 2006. Published by Oxford University Press on behalf of Japanese Society of Plant Physiologists. All rights reserved. For permissions, please email: journals.permissions@oxfordjournals.org

Utilization and Transport of Mannitol in Olea europaea and Implications for Salt Stress Tolerance

Carlos Conde1, Paulo Silva1, Alice Agasse1, Rémi Lemoine2, Serge Delrot2, Rui Tavares1 and Hernâni Gerós1,*

1Departamento de Biologia, Universidade do Minho, Campus de Gualtar, 4710-057 Braga, Portugal
2UMR CNRS 6161, Transport des Assimilats, Laboratoire de Physiologie, Biochimie et Biologie Moléculaires Végétales, Bâtiment Botanique, UFR Sciences, 40 Avenue du Recteur Pineau, 86022 Poitiers Cédex, France

*Corresponding author: E-mail, geros{at}bio.uminho.pt; Fax, + 351-253678980.


   Abstract

Mannitol is one of the primary photosynthetic products and the major phloem-translocated carbohydrate in Olea europaea L., an important crop in the Mediterranean basin. Uptake of mannitol in heterotrophic cell suspensions of O. europaea was shown to be mediated by a 1 : 1 polyol : H+ symport system with a Km of 1.3 mM mannitol and a Vmax of 1.3 nmol min–1 mg–1 DW. Dulcitol, sorbitol and xylitol competed for mannitol uptake, whereas glucose and sucrose did not. Reverse transcription–PCR (RT–PCR) performed on mRNA extracted from cultured cells exhibiting high mannitol transport activity allowed the cloning of a partial O. europaea mannitol carrier OeMaT1. The Vmax of mannitol uptake and the amount of OeMaT1 transcripts increased along with polyol depletion from the medium, suggesting that the mannitol transport system may be regulated by its own substrate. Addition of 100–500 mM NaCl to cultured cells enhanced the capacity of the polyol : H+ symport system and the amount of OeMaT1 transcripts, whereas it strongly repressed mannitol dehydrogenase activity. Measurements of cell viability showed that mannitol-grown cells remained viable 24 h after a 250 and 500 mM NaCl pulse, whereas extensive loss of cell viability was observed in sucrose-grown cells. OeMaT1 transcripts increased throughout maturation of olive fruits, suggesting that an OeMaT is involved in the accumulation of mannitol during ripening of olive. Thus, mannitol transport and compartmentation by OeMaT are important to allocate this source of carbon and energy, as well as for salt tolerance and olive ripening.

Keywords: Mannitol - Olea europaea - Polyol transport - Salt stress

Abbreviations: CCCP, carbonyl cyanide m-chlorophenylhydrazone; FDA, fluorescein diacetate; MTD, mannitol dehydrogenase; mltD, mannitol-1-phosphate dehydrogenase; PI, propidium iodide; TPP+, tetraphenylphosphonium; RT–PCR, reverse transcription–PCR.

(Received September 12, 2006; Accepted November 12, 2006)
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