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本文引用的文献

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2
Cloning of a gene cluster encoding enzymes responsible for the mevalonate pathway from a terpenoid-antibiotic-producing Streptomyces strain.从一株产萜类抗生素的链霉菌菌株中克隆编码甲羟戊酸途径相关酶的基因簇。
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3
An unusual isopentenyl diphosphate isomerase found in the mevalonate pathway gene cluster from Streptomyces sp. strain CL190.在链霉菌属CL190菌株甲羟戊酸途径基因簇中发现的一种不寻常的异戊烯基二磷酸异构酶。
Proc Natl Acad Sci U S A. 2001 Jan 30;98(3):932-7. doi: 10.1073/pnas.98.3.932. Epub 2001 Jan 23.
4
Cloning of the gene encoding 3-hydroxy-3-methylglutaryl coenzyme A reductase from terpenoid antibiotic-producing Streptomyces strains.从产萜类抗生素的链霉菌菌株中克隆编码3-羟基-3-甲基戊二酰辅酶A还原酶的基因。
Mol Gen Genet. 2000 Jan;262(6):957-64. doi: 10.1007/pl00008664.
5
Functional analysis of the two interacting cyclase domains in ent-kaurene synthase from the fungus Phaeosphaeria sp. L487 and a comparison with cyclases from higher plants.来自真菌Phaeosphaeria sp. L487的贝壳杉烯合酶中两个相互作用的环化酶结构域的功能分析以及与高等植物环化酶的比较。
J Biol Chem. 2000 Jan 28;275(4):2276-80. doi: 10.1074/jbc.275.4.2276.
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Diterpene synthesis in Stevia rebaudiana: recruitment and up-regulation of key enzymes from the gibberellin biosynthetic pathway.甜叶菊中的二萜类化合物合成:赤霉素生物合成途径关键酶的招募与上调
Plant J. 1999 Aug;19(4):411-21. doi: 10.1046/j.1365-313x.1999.00531.x.
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The first step of gibberellin biosynthesis in pumpkin is catalyzed by at least two copalyl diphosphate synthases encoded by differentially regulated genes.南瓜中赤霉素生物合成的第一步由至少两种由差异调控基因编码的贝壳杉烯二磷酸合酶催化。
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8
Squalene-hopene cyclase from Methylococcus capsulatus (Bath): a bacterium producing hopanoids and steroids.来自荚膜甲基球菌(巴斯)的鲨烯-藿烯环化酶:一种产生藿烷类化合物和类固醇的细菌。
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Plant terpenoid synthases: molecular biology and phylogenetic analysis.植物萜类合酶:分子生物学与系统发育分析
Proc Natl Acad Sci U S A. 1998 Apr 14;95(8):4126-33. doi: 10.1073/pnas.95.8.4126.
10
The GA2 locus of Arabidopsis thaliana encodes ent-kaurene synthase of gibberellin biosynthesis.拟南芥的GA2基因座编码赤霉素生物合成中的贝壳杉烯合酶。
Plant Physiol. 1998 Apr;116(4):1271-8. doi: 10.1104/pp.116.4.1271.

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.

DOI:10.1128/JB.183.20.6085-6094.2001
PMID:11567009
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC99688/
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。