Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
2050886 | FEBS Letters | 2006 | 5 Pages |
Abstract
Isoflavans and pterocarpans are the major biosynthetically connected phytoalexins in legumes. A search of the expressed sequence tag library of a model legume Lotus japonicus, which produces an (−)-isoflavan, for homologs of phenylcoumaran benzylic ether reductase catalyzing the reductive cleavage of dihydrofurans, yielded seven full-length cDNAs, and the encoded proteins were analyzed in vitro. Four of them cleaved the dihydrofuran of a pterocarpan medicarpin to yield an isoflavan (−)-vestitol and were designated pterocarpan reductase (PTR). Two PTRs displayed enantiospecificity to (−)-medicarpin, representing genuine L. japonicus PTRs, while the other two lacked enantiospecificity and were presumed to be evolutionarily primitive types.
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Authors
Tomoyoshi Akashi, Shoko Koshimizu, Toshio Aoki, Shin-ichi Ayabe,