Regulation of pisatin biosynthesis in pea leaves by elicitor and suppressor produced by Mycosphaerella pinodes.

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  • HIRAMATSU Motohiro
    College of Agriculture, Okayama University Central Research Laboratories, Hokko Chemical Industry, Co., Ltd Institute for Microbial Disease, Osaka University Faculty of Agriculture, Kinki University
  • ICHINOSE Yuki
    College of Agriculture, Okayama University Central Research Laboratories, Hokko Chemical Industry, Co., Ltd Institute for Microbial Disease, Osaka University Faculty of Agriculture, Kinki University
  • SHIRAISHI Tomonori
    College of Agriculture, Okayama University Central Research Laboratories, Hokko Chemical Industry, Co., Ltd Institute for Microbial Disease, Osaka University Faculty of Agriculture, Kinki University
  • OKU Hachiro
    College of Agriculture, Okayama University Central Research Laboratories, Hokko Chemical Industry, Co., Ltd Institute for Microbial Disease, Osaka University Faculty of Agriculture, Kinki University
  • OUCHI Seiji
    College of Agriculture, Okayama University Central Research Laboratories, Hokko Chemical Industry, Co., Ltd Institute for Microbial Disease, Osaka University Faculty of Agriculture, Kinki University

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Other Title
  • エンドウ褐紋病菌の生産するエリシターおよびサプレッサーによるピサチン生合成の制御について
  • エンドウ褐紋病菌の生産するエリシターおよびサプレッサーによるピサチン生合成の制御について〔英文〕
  • エンドウ カツモンビョウキン ノ セイサンスル エリシター オヨビ サプレッサ

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Abstract

Regulation of pisatin biosynthesis in naked mesophyll tissue of pea leaves by suppressor (F5) and elicitor isolated from Mycosphaerella pinodes was studied using a radioactive precursor of pisatin synthesis, 14C-phenylalanine. Incorporation of radioactivity became detectable 4.5-6 hr after elicitor treatment and increased thereafter. Concomitant presence of F5 inhibited the pisatin inducing activity of the elicitor completely. Treatment of pea leaves with F5 after elicitor-activation caused a reduction of pisatin synthesis and an increased accumulation of cinnamic acid, an intermediate of pisatin synthesis. F5 was found to inhibit in vitro the activity of phenylalanine ammonia-lyase and cinnamate 4-hydroxylase. The suppressing ability of F5 on pisatin synthesis seemed to be reversible.

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