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真细菌二萜环化酶基因对于类异戊二烯抗生素特戊菌素的生产至关重要。

Eubacterial diterpene cyclase genes essential for production of the isoprenoid antibiotic terpentecin.

作者信息

Dairi T, Hamano Y, Kuzuyama T, Itoh N, Furihata K, Seto H

机构信息

Biotechnology Research Center, Toyama Prefectural University, Toyama, Japan.

出版信息

J Bacteriol. 2001 Oct;183(20):6085-94. doi: 10.1128/JB.183.20.6085-6094.2001.

Abstract

A gene cluster containing the mevalonate pathway genes (open reading frame 2 [ORF2] to ORF7) for the formation of isopentenyl diphosphate and a geranylgeranyl diphosphate (GGDP) synthase gene (ORF1) had previously been cloned from Streptomyces griseolosporeus strain MF730-N6, a diterpenoid antibiotic, terpentecin (TP) producer (Y. Hamano, T. Dairi, M. Yamamoto, T. Kawasaki, K Kaneda, T. Kuzuyama, N. Itoh, and H. Seto, Biosci. Biotech. Biochem. 65:1627-1635, 2001). Sequence analysis in the upstream region of the cluster revealed seven new ORFs, ORF8 to ORF14, which were suggested to encode TP biosynthetic genes. We constructed two mutants, in which ORF11 and ORF12, which encode a protein showing similarities to eukaryotic diterpene cyclases (DCs) and a eubacterial pentalenene synthase, respectively, were inactivated by gene disruptions. The mutants produced no TP, confirming that these cyclase genes are essential for the production of TP. The two cyclase genes were also expressed in Streptomyces lividans together with the GGDP synthase gene under the control of the ermE* constitutive promoter. The transformant produced a novel cyclic diterpenoid, ent-clerod-3,13(16),14-triene (terpentetriene), which has the same basic skeleton as TP. The two enzymes, each of which was overproduced in Escherichia coli and purified to homogeneity, converted GGDP into terpentetriene. To the best of our knowledge, this is the first report of a eubacterial DC.

摘要

之前已从二萜类抗生素特戊菌素(TP)产生菌灰色链霉菌菌株MF730 - N6中克隆出一个基因簇,该基因簇包含用于形成异戊烯基二磷酸的甲羟戊酸途径基因(开放阅读框2 [ORF2]至ORF7)和一个牻牛儿基牻牛儿基二磷酸(GGDP)合酶基因(ORF1)(Y. 滨野、T. 大入、M. 山本、T. 川崎、K. 金田、T. 葛山、N. 伊藤和H. 濑户,《生物科学、生物技术与生物化学》65:1627 - 1635,2001年)。对该基因簇上游区域的序列分析揭示了7个新的开放阅读框,即ORF8至ORF14,推测它们编码TP生物合成基因。我们构建了两个突变体,其中分别编码与真核二萜环化酶(DCs)相似的蛋白质的ORF11和编码真细菌戊烯霉素合酶的ORF12,通过基因破坏使其失活。这些突变体不产生TP,证实这些环化酶基因对于TP的产生至关重要。这两个环化酶基因也在组成型启动子ermE* 的控制下与GGDP合酶基因一起在变铅青链霉菌中表达。该转化体产生了一种新型环状二萜,对映 - 克罗烷 - 3,13(16),14 - 三烯(特戊三烯),其具有与TP相同 的基本骨架。这两种酶分别在大肠杆菌中过量表达并纯化至同质,它们将GGDP转化为特戊三烯。据我们所知,这是关于真细菌DC的首次报道。

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