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Literature summary for 2.5.1.36 extracted from

  • Zaehringer, U.; Schaller, E.; Grisebach, H.
    Induction of phytoalexin synthesis in soybean. Structure and reactions of naturally occuring and enzymatically prepared prenylated pterocarpans from elicitor-treated cotyledons and cell cultures of soybean (1981), Z. Naturforsch. C, 36, 234-241.
No PubMed abstract available

Natural Substrates/ Products (Substrates)

Natural Substrates Organism Comment (Nat. Sub.) Natural Products Comment (Nat. Pro.) Rev. Reac.
2 dimethylallyl diphosphate + 2 (6aS,11aS)-3,6a,9-trihydroxypterocarpan Glycine max introduction of the dimethylallyl substituent into trihydroxypterocarpan increases fungitoxicity against Cladosporium cucumerinum 2 diphosphate + (6aS,11aS)-2-dimethylallyl-3,6a,9-trihydroxypterocarpan + (6aS,11aS)-4-dimethylallyl-3,6a,9-trihydroxypterocarpan
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?

Organism

Organism UniProt Comment Textmining
Glycine max
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elicitor-treated
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Source Tissue

Source Tissue Comment Organism Textmining
cell culture
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Glycine max
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cotyledon
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Glycine max
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Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
2 dimethylallyl diphosphate + 2 (6aS,11aS)-3,6a,9-trihydroxypterocarpan
-
Glycine max 2 diphosphate + (6aS,11aS)-2-dimethylallyl-3,6a,9-trihydroxypterocarpan + (6aS,11aS)-4-dimethylallyl-3,6a,9-trihydroxypterocarpan
-
?
2 dimethylallyl diphosphate + 2 (6aS,11aS)-3,6a,9-trihydroxypterocarpan introduction of the dimethylallyl substituent into trihydroxypterocarpan increases fungitoxicity against Cladosporium cucumerinum Glycine max 2 diphosphate + (6aS,11aS)-2-dimethylallyl-3,6a,9-trihydroxypterocarpan + (6aS,11aS)-4-dimethylallyl-3,6a,9-trihydroxypterocarpan
-
?