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丝状真菌病原体的脂肪酸双加氧酶-细胞色素 P450 融合酶。

Fatty acid dioxygenase-cytochrome P450 fusion enzymes of filamentous fungal pathogens.

机构信息

Division of Biochemical Pharmacology, Department of Pharmaceutical Biosciences, Uppsala University, Box 591, SE-751 24 Uppsala, Sweden.

出版信息

Fungal Genet Biol. 2021 Dec;157:103623. doi: 10.1016/j.fgb.2021.103623. Epub 2021 Sep 11.

Abstract

Oxylipins designate oxygenated unsaturated C fatty acids. Many filamentous fungi pathogens contain dioxygenases (DOX) in oxylipin biosynthesis with homology to human cyclooxygenases. They contain a DOX domain, which is often fused to a functional cytochrome P450 at the C-terminal end. A Tyr radical in the DOX domain initiates dioxygenation of linoleic acid by hydrogen abstraction with formation of 8-, 9-, or 10-hydroperoxy metabolites. The P450 domains can catalyze heterolytic cleavage of 8- and 10-hydroperoxides with oxidation of the heme thiolate iron for hydroxylation at C-5, C-7, C-9, or C-11 and for epoxidation of the 12Z double bond; thus displaying linoleate diol synthase (LDS) and epoxy alcohol synthase (EAS) activities. LSD activities are present in the rice blast pathogen Magnaporthe oryzae, Botrytis cinerea causing grey mold and the black scurf pathogen Rhizoctonia solani. 10R-DOX-EAS has been found in M. oryzae and Fusarium oxysporum. The P450 domains may also catalyze homolytic cleavage of 8- and 9-hydroperoxy fatty acids and dehydration to produce epoxides with an adjacent double bond, i.e., allene oxides, thus displaying 8- and 9-DOX-allene oxide synthases (AOS). F. oxysporum, F. graminearum, and R. solani express 9S-DOX-AOS and Zymoseptoria tritici 8S-and 9R-DOX-AOS. Homologues are present in endemic human-pathogenic fungi with extensive studies in Aspergillus fumigatus, A. flavus (also a plant pathogen) as well as the genetic model A. nidulans. 8R-and 10R-DOX appear to bind fatty acids "headfirst" in the active site, whereas 9S-DOX binds them "tail first" in analogy with cyclooxygenases. The biological relevance of 8R-DOX-5,8-LDS (also designated PpoA) was first discovered in relation to sporulation of A. nidulans and recently for development and programmed hyphal branching of A. fumigatus. Gene deletion DOX-AOS homologues in F. verticillioides, A. flavus, and A. nidulans alters, inter alia, mycotoxin production, sporulation, and gene expression.

摘要

氧化脂类指定含氧不饱和 C 脂肪酸。许多丝状真菌病原体在氧化脂生物合成中含有与人类环氧化酶同源的双加氧酶 (DOX)。它们包含一个 DOX 结构域,该结构域通常在 C 末端融合到功能性细胞色素 P450。DOX 结构域中的 Tyr 自由基通过氢提取引发亚麻酸的双加氧作用,形成 8-、9-或 10-过氧化物代谢物。P450 结构域可以催化 8-和 10-过氧化物的异裂裂解,氧化血红素硫醇铁进行 C-5、C-7、C-9 或 C-11 羟基化和 12Z 双键环氧化;因此表现出亚麻酸二醇合酶 (LDS) 和环氧化醇合酶 (EAS) 活性。LSD 活性存在于稻瘟病菌 Magnaporthe oryzae、引起灰霉病的 Botrytis cinerea 和黑色痂病菌 Rhizoctonia solani 中。在 M. oryzae 和 Fusarium oxysporum 中发现了 10R-DOX-EAS。P450 结构域还可以催化 8-和 9-过氧脂肪酸的均裂裂解和脱水,以产生具有相邻双键的环氧化物,即丙二烯氧化物,从而表现出 8-和 9-DOX-丙二烯氧化物合酶 (AOS)。F. oxysporum、F. graminearum 和 R. solani 表达 9S-DOX-AOS 和 Zymoseptoria tritici 8S-和 9R-DOX-AOS。在地方性人类致病真菌中存在同源物,在 Aspergillus fumigatus、A. flavus(也是一种植物病原体)以及遗传模型 A. nidulans 中进行了广泛研究。8R-和 10R-DOX 似乎在活性位点中“先头”结合脂肪酸,而 9S-DOX 则类似于环氧化酶“先尾”结合它们。8R-DOX-5,8-LDS(也称为 PpoA)的生物学相关性首先在 A. nidulans 的孢子形成中发现,最近在 A. fumigatus 的发育和程序性菌丝分枝中发现。F. verticillioides、A. flavus 和 A. nidulans 中的基因缺失 DOX-AOS 同源物改变了产真菌毒素、孢子形成和基因表达等。

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