Recycling of pyridoxine (vitamin B6) by PUP1 in Arabidopsis
Plant Exudates
Recombinant Fusion Proteins
info:eu-repo/classification/ddc/580
Arabidopsis
Gene Expression
Genetically Modified
Saccharomyces cerevisiae
Arabidopsis/genetics/metabolism/ultrastructure
Nucleobase Transport Proteins/genetics/metabolism
Plant Roots
Plant Epidermis
12. Responsible consumption
03 medical and health sciences
Gene Expression Regulation, Plant
Nucleobase Transport Proteins
[SDV.BV]Life Sciences [q-bio]/Vegetal Biology
[SDV.BBM]Life Sciences [q-bio]/Biochemistry, Molecular Biology
Plant Roots/genetics/metabolism/ultrastructure
Plant Exudates/analysis
Arabidopsis Proteins/genetics/metabolism
Microscopy
0303 health sciences
Pyridoxine/chemistry/metabolism
Microscopy, Confocal
Arabidopsis Proteins
Cell Membrane/metabolism
Cell Membrane
Genetic Complementation Test
Pyridoxine
Biological Transport
Plant
Plants
Plants, Genetically Modified
Plant Epidermis/genetics/metabolism/ultrastructure
ddc:580
Phenotype
Gene Expression Regulation
Confocal
Multigene Family
Mutation
Saccharomyces cerevisiae/genetics/metabolism
DOI:
10.1111/tpj.12195
Publication Date:
2013-04-01T15:18:39Z
AUTHORS (6)
ABSTRACT
SummaryVitamin B6 is a cofactor for more than 140 essential enzymatic reactions and was recently proposed as a potent antioxidant, playing a role in the photoprotection of plants. De novo biosynthesis of the vitamin has been described relatively recently and is derived from simple sugar precursors as well as glutamine. In addition, the vitamin can be taken up from exogenous sources in a broad range of organisms, including plants. However, specific transporters have been identified only in yeast. Here we assess the ability of the family of Arabidopsis purine permeases (PUPs) to transport vitamin B6. Several members of the family complement the growth phenotype of a Saccharomyces cerevisiae mutant strain impaired in both de novo biosynthesis of vitamin B6 as well as its uptake. The strongest activity was observed with PUP1 and was confirmed by direct measurement of uptake in yeast as well as in planta, defining PUP1 as a high affinity transporter for pyridoxine. At the tissue level the protein is localised to hydathodes and here we use confocal microscopy to illustrate that at the cellular level it is targeted to the plasma membrane. Interestingly, we observe alterations in pyridoxine recycling from the guttation sap upon overexpression of PUP1 and in a pup1 mutant, consistent with the role of the protein in retrieval of pyridoxine. Furthermore, combining the pup1 mutant with a vitamin B6 de novo biosynthesis mutant (pdx1.3) corroborates that PUP1 is involved in the uptake of the vitamin.
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