Tudzynski Bettina, Rojas María Cecilia, Gaskin Paul, Hedden Peter
Westfälische Wilhelms-Universität Münster, Institut für Botanik, Schlobetagarten 3, D-48149 Münster, Germany.
J Biol Chem. 2002 Jun 14;277(24):21246-53. doi: 10.1074/jbc.M201651200. Epub 2002 Apr 9.
The genes for gibberellin (GA) biosynthesis are clustered in the fungus Gibberella fujikuroi. In addition to genes encoding a GA-specific geranylgeranyl diphosphate synthase and a bifunctional ent-copalyl diphosphate/ent-kaurene synthase, the cluster contains four cytochrome P450 monooxygenase genes (P450-1, -2, -3, -4). Recently it was shown that P450-4 and P450-1 encode multifunctional enzymes catalyzing the three oxidation steps from ent-kaurene to ent-kaurenoic acid and the four oxidation steps from ent-kaurenoic acid to GA14, respectively. Here we describe the functional analysis of the P450-2 gene by gene disruption and by expressing the gene in a mutant that lacks the entire GA biosynthesis gene cluster. Mutants in which P450-2 is inactivated by the insertion of a large piece of DNA accumulated GA14 and lacked biosynthetically more advanced metabolites, indicating that the gene encodes a 20-oxidase. This was confirmed by incubating lines containing P450-2 in the absence of the other GA biosynthesis genes with isotopically labeled substrates. The P450-2 gene product oxidized the 3beta-hydroxylated intermediate, GA14, and its non-hydroxylated analogue GA12 to GA4 and GA9, respectively. Expression of P450-2 is repressed by high amounts of nitrogen in the culture medium but is not affected by the presence of biosynthetically advanced GAs, i.e. there is no evidence for feedback regulation. The fact that the GA 20-oxidase is a cytochrome P450 monooxygenase in G. fujikuroi and not a 2-oxoglutarate-dependent dioxygenase as in plants, together with the significant differences in regulation of gene expression, are further evidence for independent evolution of the GA biosynthetic pathways in plants and fungi.
赤霉素(GA)生物合成相关基因在藤仓赤霉菌中呈簇状分布。除了编码GA特异性香叶基香叶基二磷酸合酶和双功能内根-贝壳杉烯二磷酸/内根-贝壳杉烯合酶的基因外,该基因簇还包含四个细胞色素P450单加氧酶基因(P450-1、-2、-3、-4)。最近研究表明,P450-4和P450-1分别编码多功能酶,催化从内根-贝壳杉烯到内根-贝壳杉烯酸的三个氧化步骤以及从内根-贝壳杉烯酸到GA14的四个氧化步骤。在此,我们通过基因敲除以及在缺乏整个GA生物合成基因簇的突变体中表达该基因,对P450-2基因进行了功能分析。因大片段DNA插入而使P450-2失活的突变体积累了GA14,且缺乏生物合成上更高级的代谢产物,这表明该基因编码一种20-氧化酶。在不存在其他GA生物合成基因的情况下,用同位素标记的底物培养含有P450-2的菌株,证实了这一点。P450-2基因产物分别将3β-羟基化中间体GA14及其非羟基化类似物GA12氧化为GA4和GA9。培养基中高浓度的氮会抑制P450-2的表达,但不受生物合成上更高级GA的影响,即没有反馈调节的证据。GA 20-氧化酶在藤仓赤霉菌中是细胞色素P450单加氧酶,而不像在植物中是依赖2-氧代戊二酸的双加氧酶,以及基因表达调控方面的显著差异,进一步证明了植物和真菌中GA生物合成途径的独立进化。