Literature DB >> 11983700

A metal-binding member of the late embryogenesis abundant protein family transports iron in the phloem of Ricinus communis L.

Claudia Kruger1, Oliver Berkowitz, Udo W Stephan, Rudiger Hell.   

Abstract

The transport of metal micronutrients to developing organs in a plant is mediated primarily by the sieve elements. Ligands are thought to form complexes with the free ions in order to prevent cellular damage, but no binding partners have been unequivocally identified from plants so far. This study has used the phloem-mediated transport of micronutrients during the germination of the castor bean seedling to identify an iron transport protein (ITP). It is demonstrated that essentially all (55)Fe fed to seedlings is associated with the protein fraction of phloem exudate. It is shown that ITP carries iron in vivo and binds additional iron in vitro. ITP was purified to homogeneity from minute amounts of phloem exudate using immobilized metal ion affinity chromatography. It preferentially binds to Fe(3+) but not to Fe(2+) and also complexes Cu(2+), Zn(2+), and Mn(2+) in vitro. The corresponding cDNA of ITP was cloned using internal peptide fragments. The deduced protein of 96 amino acids shows high similarity to the stress-related family of late embryogenesis abundant proteins. Its predicted characteristics and its RNA expression pattern are consistent with a function in metal ion binding. The ITP from Ricinus provides the first identified micronutrient binding partner for phloem-mediated long distance transport in plants and is the first member of the late embryogenesis abundant protein family shown to have such a function.

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Year:  2002        PMID: 11983700     DOI: 10.1074/jbc.M201896200

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  60 in total

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2.  Rapid cloning and bioinformatic analysis of spinach Y chromosome-specific EST sequences.

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4.  Identification in pea seed mitochondria of a late-embryogenesis abundant protein able to protect enzymes from drying.

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7.  Barley Dhn13 encodes a KS-type dehydrin with constitutive and stress responsive expression.

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Review 8.  Plant dehydrins and stress tolerance: versatile proteins for complex mechanisms.

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9.  Conformation of a group 2 late embryogenesis abundant protein from soybean. Evidence of poly (L-proline)-type II structure.

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10.  Expression of KS-type dehydrins is primarily regulated by factors related to organ type and leaf developmental stage during vegetative growth.

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