Biosynthesis of Phytosiderophores
Author(s) -
Shinsuke Shojima,
NaokoKishi Nishizawa,
Shinji Fushiya,
Shigeo Nozoe,
Tomohiro Irifune,
Satoshi Mori
Publication year - 1990
Publication title -
plant physiology
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 3.554
H-Index - 312
eISSN - 1532-2548
pISSN - 0032-0889
DOI - 10.1104/pp.93.4.1497
Subject(s) - methionine , biosynthesis , biochemistry , siderophore , chemistry , enzyme , hordeum vulgare , amino acid , in vitro , stereochemistry , biology , gene , botany , poaceae
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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