Microsomal isoflavone 2′- and 3′-hydroxylases from chickpea (Cicer arietinum L.) cell suspensions induced for pterocarpan phytoalexin formation

التفاصيل البيبلوغرافية
العنوان: Microsomal isoflavone 2′- and 3′-hydroxylases from chickpea (Cicer arietinum L.) cell suspensions induced for pterocarpan phytoalexin formation
المؤلفون: U. Flentje, Wolfgang Barz, Walter Hinderer
المصدر: FEBS Letters. (1):101-106
بيانات النشر: Published by Elsevier B.V.
مصطلحات موضوعية: chemistry.chemical_classification, Isoflavonoid phytoalexin, 2′-Hydroxyisoflavone, Phytoalexin, Daidzein, Biophysics, Pterocarpan, Genistein, Calycosin, Cell Biology, Isoflavone hydroxylase, Pterocarpan synthesis, Isoflavones, Biology, Biochemistry, Biochanin A, chemistry.chemical_compound, chemistry, Structural Biology, Pratensein, Genetics, Formononetin, Medicarpin, Molecular Biology
الوصف: Microsomal fractions derived from suspension-cultured chickpea (Cicer arietinum L.) cells induced for phytoalexin biosynthesis catalyzed the monohydroxylation of 4′-methoxyisoflavones (biochanin A and formononetin) in the 2′- and 3′-positions. The reactions depended on NADPH and molecular oxygen. Post-microsomal supernatants or microsomes from non-induced cells are without detectable activity in the hydroxylase assay. 4′-Hydroxyisoflavones (genistein and daidzein) were not hydroxylated to any significant extent. The occurrence of these hydroxylases proceeds concomitantly with the accumulation of two pterocarpan phytoalexins, medicarpin and maackiain, by induced cell cultures. The results are discussed with regard to the biosynthetic sequences in the conversion of isoflavones to pterocarpans.
اللغة: English
تدمد: 0014-5793
DOI: 10.1016/0014-5793(87)80021-2
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d64be1f9d634823a6b2f8cac3a2fff3eTest
حقوق: OPEN
رقم الانضمام: edsair.doi.dedup.....d64be1f9d634823a6b2f8cac3a2fff3e
قاعدة البيانات: OpenAIRE
الوصف
تدمد:00145793
DOI:10.1016/0014-5793(87)80021-2