4.7 Article

Transmembrane topology of FRO2, a ferric chelate reductase from Arabidopsis thaliana

Journal

PLANT MOLECULAR BIOLOGY
Volume 62, Issue 1-2, Pages 215-221

Publisher

SPRINGER
DOI: 10.1007/s11103-006-9015-0

Keywords

FRO2; gp91phox; ferric-chelate reductases; superoxide generating NADPH oxidases; alkaline phosphatase; iron transport

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Iron uptake in Arabidopsis thaliana is mediated by ferric chelate reductase FRO2, a transmembrane protein belonging to the flavocytochrome b family. There is no high resolution structural information available for any member of this family. We have determined the transmembrane topology of FRO2 experimentally using the alkaline phosphatase fusion method. The resulting topology is different from that obtained by theoretical predictions and contains 8 transmembrane helices, 4 of which build up the highly conserved core of the protein. This core is present in the entire flavocytochrome b family. The large water soluble domain of FRO2, which contains NADPH, FAD and oxidoreductase sequence motifs, was located on the inside of the membrane.

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