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. 1990 Aug;93(4):1497–1503. doi: 10.1104/pp.93.4.1497

Biosynthesis of Phytosiderophores 1

In Vitro Biosynthesis of 2′-Deoxymugineic Acid from l-Methionine and Nicotianamine

Shinsuke Shojima 1,2, Naoko-Kishi Nishizawa 1,2, Shinji Fushiya 1,2, Shigeo Nozoe 1,2, Tomohiro Irifune 1,2, Satoshi Mori 1,2
PMCID: PMC1062701  PMID: 16667646

Abstract

2′ -Deoxymugineic acid (DMA), one of mugineic acid-family phytosiderophores (MAs), was synthesized in vitro both from l-methionine and from nicotianamine (NA) with a cell-free system derived from root tips of iron-deficient barley (Hordeum vulgare L.). The reactions producing DMA from NA needed an amino group acceptor (i.e. 2-oxoglutarate, pyruvate, or oxalacetic acid) and a reductant (i.e. NADH or NADPH). The activity of the enzymes to produce NA from l-methionine was the highest at about pH 9. This biosynthetic activity was markedly induced by iron-deficiency stress. The synthesis of NA from S-adenosyl-l-methionine was more efficient than from l-methionine. From the results with the cell-free system reported here, we propose a revised biosynthetic pathway of MAs.

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  1. Römheld V., Marschner H. Evidence for a specific uptake system for iron phytosiderophores in roots of grasses. Plant Physiol. 1986 Jan;80(1):175–180. doi: 10.1104/pp.80.1.175. [DOI] [PMC free article] [PubMed] [Google Scholar]

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