Chemical disease-resistance mechanism during seedling stage
Chemical disease-resistance mechanism during seedling stage
批准号:
12660104
负责人:
SUZUKI Yoshikatsu
金额:
$2.18万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (C)
财政年份:
2000
资助国家:
日本
项目状态:
已结题
起止时间:
2000 至 2002
中文摘要
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英文摘要
The main aim of this science program is to understand the production and metabolisms as well as disease-resistant mechanism of 5-alkylresorcinols as phytoanticipins during rice seedling stage.1. Disease-resistance effects of ARs : In vitro conidia-germination and mycelia-growth tests using rice-blight disease fungus (Magnaporthe grisea) and an in vivo infection test suggested that ARs play a some role on disease-resistant mechanism as a phytoanticipin.2. ARs metabolisms : New two metabolites (AR-A8 and AR-A10) of ARs were isolated from etiolated rice-seedlings that were irradiated for 2 days, and their structures determined based on GC-MS and ^1H-NMR spectra. These metabolites seemed to be produced via oxidative double-bond cleavage of unsaturated carbon-chains in ARs (AR15 : 1 , AR17 : 1 s, AR17 : 2). From the finding of AR-A10 metabolite, a new homolog of AR17 : 1 , 5-(10'-heptadecenyl) resorcinol was identified.3. Classification of rice varieties based on AR-homolog composition : AR-homo log composition and their amounts were examined for 13 varieties of Japonica-type rices. The homolog compositions had a close relationship to disease- resistant-gene types. Especially, the composition of 3 varieties that produce a trace amount of ARs largely different from those with the other domestic- and indica-type genes.4. ARs biosynthesis : In efficient 5-alkylresorcinol-producing, etiolated rice seedlings, feedings of odd-number fatty acid ester substrates increased only the homologs expected from the predicted ARs biosynthetic pathway. In addition, the dodecyl homolog that was biosynthesized from [^<13>C]-labeled substrate obviously showed that fatty acid unit acted as a direct precursor and formed the side-chain moiety of 5-alkylresorcinol via the predicted biosynthesis pathway.
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Y. Esumi, Y. Suzuki, Y. Itoh , M. Uramoto, K. Kimura, M. Yoshihama, T. Ichikawa: "Propeptin, a new inhibitor of prolyl endopeptidase produced by Microbispora II. Determination of chemical structure"J. Antibiotic. 55 (3). 296-300 (2002)
Y. Esumi,Y. Suzuki,Y. Itoh,M. Uramoto,K. Kimura,M. Yoshihama,T. Ichikawa:“Propeptin,小双孢菌 II 产生的脯氨酰内肽酶的新型抑制剂。化学结构的测定”J。
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Y.Esumi, Y.Suzuki, T.Ichikawa, Y.Ikeda, K.Kimura: "SNF-4794: New enzyme inhibitors produced by Chaetomella sp"J.Anitbiotic. 56・2. 169-172 (2003)
Y.Esumi、Y.Suzuki、T.Ichikawa、Y.Ikeda、K.Kimura:“SNF-4794:由毛壳菌产生的新酶抑制剂”J.Anitbiotic 56·2(2003)。
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R. Zarnowski, Y. Suzuki, Y. Esumi, and S. J. Pietr: "5-n-Alkylresorcinols from the green microalga Apatococcus constipatus"Phytochemistry. 55. 975-977 (2000)
R. Zarnowski、Y. Suzuki、Y. Esumi 和 S. J. Pietr:“来自绿色微藻 Apatococcus constipatus 的 5-n-烷基间苯二酚”植物化学。
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R.Zarnowski, Y.Suzuki, I.Yamaguchi, S.J.Pietr: "Alkylresorcinols in barley (Hordeum vulgare L. distichon)grains"Z.Naturforsch. 57C. 57-62 (2002)
R.Zarnowski、Y.Suzuki、I.Yamaguchi、S.J.Pietr:“大麦 (Hordeum vulgare L. distichon) 谷物中的烷基间苯二酚”Z.Naturforsch。
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Y.Esumi, Y.Suzuki, Y.Itoh, M.Uramoto, K.Kiumra, M.Yoshihama, T.Ichikawa: "Propeptin, a new inhibitor of polyl endopeptidase produced by Microbispora II. Determination of chemical structure"J.Antibiotic.. 55・3. 296-300 (2002)
Y.Esumi、Y.Suzuki、Y.Itoh、M.Uramoto、K.Kiumra、M.Yoshihama、T.Ichikawa:“Propeptin,一种由小双孢菌 II 产生的新型多聚内肽酶抑制剂。结构化学的测定”J.Antibiotic .. 55・3. 296-300 (2002)
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共 16 条
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