Bohlmann J, Steele C L, Croteau R
Institute of Biological Chemistry, and Department of Biochemistry and Biophysics, Washington State University, Pullman, Washington 99164-6340, USA.
J Biol Chem. 1997 Aug 29;272(35):21784-92. doi: 10.1074/jbc.272.35.21784.
Grand fir (Abies grandis) has been developed as a model system for studying defensive oleoresin formation in conifers in response to insect attack or other injury. The turpentine fraction of the oleoresin is a complex mixture of monoterpene (C10) olefins in which (-)-limonene and (-)-alpha- and (-)-beta-pinene are prominent components; (-)-limonene and (-)-pinene synthase activities are also induced upon stem wounding. A similarity based cloning strategy yielded three new cDNA species from a wounded stem cDNA library that appeared to encode three distinct monoterpene synthases. After expression in Escherichia coli and enzyme assay with geranyl diphosphate as substrate, subsequent analysis of the terpene products by chiral phase gas chromatography and mass spectrometry showed that these sequences encoded a (-)-limonene synthase, a myrcene synthase, and a (-)-pinene synthase that produces both alpha-pinene and beta-pinene. In properties and reaction stereochemistry, the recombinant enzymes resemble the corresponding native monoterpene synthases of wound-induced grand fir stem. The deduced amino acid sequences indicated the limonene synthase to be 637 residues in length (73.5 kDa), the myrcene synthase to be 627 residues in length (72.5 kDa), and the pinene synthase to be 628 residues in length (71.5 kDa); all of these monoterpene synthases appear to be translated as preproteins bearing an amino-terminal plastid targeting sequence. Sequence comparison revealed that these monoterpene synthases from grand fir resemble sesquiterpene (C15) synthases and diterpene (C20) synthases from conifers more closely than other monoterpene synthases from angiosperm species. This similarity between extant monoterpene, sesquiterpene, and diterpene synthases of gymnosperms is surprising since functional diversification of this enzyme class is assumed to have occurred over 300 million years ago. Wound-induced accumulation of transcripts for monoterpene synthases was demonstrated by RNA blot hybridization using probes derived from the three monoterpene synthase cDNAs. The availability of cDNA species encoding these monoterpene synthases will allow an understanding of the regulation of oleoresin formation in conifers and will ultimately permit the transgenic manipulation of this defensive secretion to enhance resistance to insects. These cDNAs also furnish tools for defining structure-function relationships in this group of catalysts that generate acyclic, monocyclic, and bicyclic olefin products.
巨冷杉(Abies grandis)已被开发成为一个模型系统,用于研究针叶树在受到昆虫攻击或其他伤害时防御性树脂道形成的机制。树脂道的松节油部分是单萜(C10)烯烃的复杂混合物,其中(-)-柠檬烯和(-)-α-蒎烯以及(-)-β-蒎烯是主要成分;茎干受伤后,(-)-柠檬烯和(-)-蒎烯合酶的活性也会被诱导。基于相似性的克隆策略从受伤茎干的cDNA文库中获得了三个新的cDNA种类,它们似乎编码三种不同的单萜合酶。在大肠杆菌中表达并以香叶基二磷酸为底物进行酶活性测定后,随后通过手性相气相色谱和质谱对萜类产物进行分析,结果表明这些序列分别编码一种(-)-柠檬烯合酶、一种月桂烯合酶和一种能产生α-蒎烯和β-蒎烯的(-)-蒎烯合酶。在性质和反应立体化学方面,重组酶类似于受伤诱导的巨冷杉茎干中相应的天然单萜合酶。推导的氨基酸序列表明,柠檬烯合酶长度为637个残基(73.5 kDa),月桂烯合酶长度为627个残基(72.5 kDa),蒎烯合酶长度为628个残基(71.5 kDa);所有这些单萜合酶似乎都被翻译为带有氨基端质体靶向序列的前体蛋白。序列比较显示,巨冷杉的这些单萜合酶与针叶树的倍半萜(C15)合酶和二萜(C20)合酶的相似性,比与被子植物物种的其他单萜合酶的相似性更高。裸子植物现存的单萜、倍半萜和二萜合酶之间的这种相似性令人惊讶,因为据推测这类酶的功能多样化发生在3亿多年前。使用源自三种单萜合酶cDNA的探针,通过RNA印迹杂交证明了受伤诱导的单萜合酶转录本的积累。编码这些单萜合酶的cDNA种类的获得,将有助于了解针叶树中树脂道形成的调控机制,并最终允许对这种防御性分泌物进行转基因操作,以增强对昆虫的抗性。这些cDNA还为确定这组能生成无环、单环和双环烯烃产物的催化剂的结构-功能关系提供了工具。