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参与铝耐受树种赤桉中没食子酸生物合成的脱氢奎宁酸脱水酶/莽草酸脱氢酶。

Dehydroquinate dehydratase/shikimate dehydrogenases involved in gallate biosynthesis of the aluminum-tolerant tree species Eucalyptus camaldulensis.

机构信息

Interdisciplinary Center for Crop Plant Research, Martin-Luther University Halle-Wittenberg, Hoher Weg 8, 06120, Halle, Germany.

Department of Forest Molecular Genetics and Biotechnology, Forestry and Forest Products Research Institute, 1 Matsunosato, Tsukuba, Ibaraki, 305-8687, Japan.

出版信息

Planta. 2020 Dec 21;253(1):3. doi: 10.1007/s00425-020-03516-w.

Abstract

Eucalyptus camaldulensis EcDQD/SDH2 and 3 combine gallate formation, dehydroquinate dehydratase, and shikimate dehydrogenase activities. They are candidates for providing the essential gallate for the biosynthesis of the aluminum-detoxifying metabolite oenothein B. The tree species Eucalyptus camaldulensis shows exceptionally high tolerance against aluminum, a widespread toxic metal in acidic soils. In the roots of E. camaldulensis, aluminum is detoxified via the complexation with oenothein B, a hydrolyzable tannin. In our approach to elucidate the biosynthesis of oenothein B, we here report on the identification of E. camaldulensis enzymes that catalyze the formation of gallate, which is the phenolic constituent of hydrolyzable tannins. By systematical screening of E. camaldulensis dehydroquinate dehydratase/shikimate dehydrogenases (EcDQD/SDHs), we found two enzymes, EcDQD/SDH2 and 3, catalyzing the NADP-dependent oxidation of 3-dehydroshikimate to produce gallate. Based on extensive in vitro assays using recombinant EcDQD/SDH2 and 3 enzymes, we present for the first time a detailed characterization of the enzymatic gallate formation activity, including the cofactor preferences, pH optima, and kinetic constants. Sequence analyses and structure modeling suggest the gallate formation activity of EcDQD/SDHs is based on the reorientation of 3-dehydroshikimate in the catalytic center, which facilitates the proton abstraction from the C5 position. Additionally, EcDQD/SDH2 and 3 maintain DQD and SDH activities, resulting in a 3-dehydroshikimate supply for gallate formation. In E. camaldulensis, EcDQD/SDH2 and 3 are co-expressed with UGT84A25a/b and UGT84A26a/b involved in hydrolyzable tannin biosynthesis. We further identified EcDQD/SDH1 as a "classical" bifunctional plant shikimate pathway enzyme and EcDQD/SDH4a/b as functional quinate dehydrogenases of the NAD/NADH-dependent clade. Our data indicate that in E. camaldulensis the enzymes EcDQD/SDH2 and 3 provide the essential gallate for the biosynthesis of the aluminum-detoxifying metabolite oenothein B.

摘要

赤桉 EcDQD/SDH2 和 3 结合了没食子酸形成、脱氢奎宁酸脱水酶和莽草酸脱氢酶的活性。它们是提供必需没食子酸用于生物合成铝解毒代谢物表棓儿茶精 B 的候选酶。桉树物种赤桉对铝表现出极高的耐受性,铝是酸性土壤中广泛存在的有毒金属。在赤桉的根中,铝通过与表棓儿茶精 B(一种可水解单宁)的络合而解毒。在我们阐明表棓儿茶精 B 生物合成的方法中,我们在此报告鉴定出赤桉催化没食子酸形成的酶,没食子酸是可水解单宁的酚类成分。通过赤桉脱氢奎宁酸脱水酶/莽草酸脱氢酶(EcDQD/SDH)的系统筛选,我们发现两种酶,EcDQD/SDH2 和 3,催化 NADP 依赖性 3-脱氢莽草酸氧化生成没食子酸。基于使用重组 EcDQD/SDH2 和 3 酶的广泛体外测定,我们首次详细描述了酶促没食子酸形成活性的特征,包括辅助因子偏好、pH 最佳值和动力学常数。序列分析和结构建模表明,EcDQD/SDH 的没食子酸形成活性基于催化中心 3-脱氢莽草酸的重新定向,这有利于从 C5 位置提取质子。此外,EcDQD/SDH2 和 3 保持 DQD 和 SDH 活性,从而为没食子酸形成提供 3-脱氢莽草酸供应。在赤桉中,EcDQD/SDH2 和 3 与参与可水解单宁生物合成的 UGT84A25a/b 和 UGT84A26a/b 共表达。我们进一步鉴定 EcDQD/SDH1 为“经典”植物莽草酸途径的双功能酶,EcDQD/SDH4a/b 为 NAD/NADH 依赖性类群的功能奎尼酸脱氢酶。我们的数据表明,在赤桉中,酶 EcDQD/SDH2 和 3 为生物合成铝解毒代谢物表棓儿茶精 B 提供必需的没食子酸。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45cb/7752791/be38cdde793a/425_2020_3516_Fig1_HTML.jpg

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