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海洋天然产物对C4酸循环酶丙酮酸磷酸二激酶的体外抑制作用向体内C4植物组织死亡的转化。

Translation of in vitro inhibition by marine natural products of the C4 acid cycle enzyme pyruvate P(i) dikinase to in vivo C4 plant tissue death.

作者信息

Haines Dianne S, Burnell James N, Doyle Jason R, Llewellyn Lyndon E, Motti Cherie A, Tapiolas Dianne M

机构信息

Department of Biochemistry and Molecular Biology, James Cook University, Townsville, Queensland 4811, Australia.

出版信息

J Agric Food Chem. 2005 May 18;53(10):3856-62. doi: 10.1021/jf048010x.

Abstract

Marine organism derived extracts, previously identified as containing compounds that inhibited the C4 acid cycle enzyme pyruvate P(i) dikinase (PPDK), were assessed for their ability to exhibit an effect on the C4 plants Digitaria ciliaris and Echinochloa crus-galli. Oxygen electrode studies revealed that over half of these extracts inhibited C4 acid driven photosynthesis in leaf slices. Seventeen extracts had a deleterious effect on C4 plants in vivo within 24 h, whereas 36 caused an observable phytotoxic response in one or both of the C4 plants used for in vivo testing. None of the extracts inhibited PPDK metabolism of pyruvate via a directly competitive mechanism, instead hindering the enzyme by either mixed or uncompetitive means. This screening strategy, using a suite of assays, led to the isolation and identification of the herbicidal marine natural product ilimaquinone.

摘要

先前已鉴定出含有抑制C4酸循环酶丙酮酸磷酸双激酶(PPDK)的化合物的海洋生物提取物,对其影响C4植物纤毛马唐和稗草的能力进行了评估。氧电极研究表明,这些提取物中有超过一半抑制了叶片切片中由C4酸驱动的光合作用。17种提取物在24小时内对C4植物产生了体内有害影响,而36种提取物在用于体内测试的一种或两种C4植物中引起了可观察到的植物毒性反应。没有一种提取物通过直接竞争机制抑制丙酮酸的PPDK代谢,而是通过混合或非竞争性方式阻碍该酶。这种使用一系列测定方法的筛选策略导致了除草海洋天然产物伊立喹酮的分离和鉴定。

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