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真菌中脱落酸的生物合成:鉴定出 Botrytis cinerea 中的一种倍半萜环化酶为关键酶。

Biosynthesis of abscisic acid in fungi: identification of a sesquiterpene cyclase as the key enzyme in Botrytis cinerea.

机构信息

Departamento de Química Orgánica, Facultad de Ciencias, Universidad de Cádiz, Cádiz, 11510 Puerto Real, Spain.

Departamento de Biomedicina, Biotecnología y Salud Pública, Laboratorio de Microbiología, Facultad de Ciencias de Mar y Ambientales, Universidad de Cádiz, Puerto Real, Cádiz 11510, Spain.

出版信息

Environ Microbiol. 2018 Jul;20(7):2469-2482. doi: 10.1111/1462-2920.14258. Epub 2018 Jul 26.

DOI:10.1111/1462-2920.14258
PMID:29708647
Abstract

While abscisic acid (ABA) is known as a hormone produced by plants through the carotenoid pathway, a small number of phytopathogenic fungi are also able to produce this sesquiterpene but they use a distinct pathway that starts with the cyclization of farnesyl diphosphate (FPP) into 2Z,4E-α-ionylideneethane which is then subjected to several oxidation steps. To identify the sesquiterpene cyclase (STC) responsible for the biosynthesis of ABA in fungi, we conducted a genomic approach in Botrytis cinerea. The genome of the ABA-overproducing strain ATCC58025 was fully sequenced and five STC-coding genes were identified. Among them, Bcstc5 exhibits an expression profile concomitant with ABA production. Gene inactivation, complementation and chemical analysis demonstrated that BcStc5/BcAba5 is the key enzyme responsible for the key step of ABA biosynthesis in fungi. Unlike what is observed for most of the fungal secondary metabolism genes, the key enzyme-coding gene Bcstc5/Bcaba5 is not clustered with the other biosynthetic genes, i.e., Bcaba1 to Bcaba4 that are responsible for the oxidative transformation of 2Z,4E-α-ionylideneethane. Finally, our study revealed that the presence of the Bcaba genes among Botrytis species is rare and that the majority of them do not possess the ability to produce ABA.

摘要

虽然脱落酸(ABA)被认为是植物通过类胡萝卜素途径产生的一种激素,但少数植物病原真菌也能够产生这种倍半萜,但它们使用的是一种独特的途径,从法呢基二磷酸(FPP)环化为 2Z,4E-α-异亚丙基乙烷开始,然后经过几个氧化步骤。为了鉴定真菌中 ABA 生物合成的倍半萜环化酶(STC),我们在 Botrytis cinerea 中进行了基因组研究。ABA 过量产生菌株 ATCC58025 的基因组被完全测序,鉴定出了 5 个 STC 编码基因。其中,Bcstc5 的表达谱与 ABA 的产生相一致。基因失活、互补和化学分析表明,BcStc5/BcAba5 是真菌中 ABA 生物合成关键步骤的关键酶。与大多数真菌次生代谢基因不同,关键酶编码基因 Bcstc5/Bcaba5 没有与其他生物合成基因簇在一起,即 Bcaba1 到 Bcaba4,它们负责 2Z,4E-α-异亚丙基乙烷的氧化转化。最后,我们的研究表明,Bcaba 基因在 Botrytis 属中很少见,而且它们大多数都不具备产生 ABA 的能力。

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