Mugineic acid
Chemical compound
From Wikipedia, the free encyclopedia
Mugineic acid is the organic compound consisting of a azetidine group and three carboxylates. A colorless solid, it is a siderophore. More specifically, it is a phytosiderophore, i.e. a plant-produced siderophore. It functions as an iron accumulating agent for barley and other plants. Related phytosiderophores include nicotianamine and avenic acid.[1]

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| Properties | |
| C12H20N2O8 | |
| Molar mass | 320.298 g·mol−1 |
| Appearance | white solid |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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It is biosynthesized from S-methylmethionine. The compound binds metal ions as a hexadentate ligand.[4]
Biosynthesis
Mugineic acid is a derivative of the nicotianamine, a metal-chelating molecule ubiquitous in higher plants that is produced from three molecules of S-adenosyl methionine by the enzyme nicotianamine synthase.[5][6]
The immediate precursor is 2'-deoxymugineic acid which is produced from nicotianamine by two reactions, catalysed by nicotianamine aminotransferase[7] and 3''-deamino-3''-oxonicotianamine reductase.[8]
This is followed by insertion of another hydroxyl group, catalysed by the alpha-ketoglutarate-dependent hydroxylase, 2'-deoxymugineic-acid 2'-dioxygenase:[9]
Mugineic acid is also used as a precursor for the synthesis of other phytosiderophores which play a key role in iron uptake from the soil in graminaceous plants.[10]
