Department of Plant Sciences, University of Tennessee, Knoxville, Tennessee 37996.
Graduate School of Genome Science and Technology, University of Tennessee, Knoxville, Tennessee 37996.
Plant Physiol. 2019 Feb;179(2):382-390. doi: 10.1104/pp.18.01413. Epub 2018 Dec 11.
Red algae (Rhodophyta) and land plants belong to the monophyletic clade Archaeplastida, and taxa of both groups are rich producers of terpene secondary metabolites. The terpene carbon skeletons of land plants are made by two types of terpene synthases: typical plant terpene synthases and microbial-type terpene synthases (MTPSLs); however, terpene biosynthesis in red algae is poorly understood. By systematic sequence analysis of seven genomes and 34 transcriptomes of red algae, homologs were identified within one genome and two transcriptomes, whereas no homolog of typical plant terpene synthase genes was found. Phylogenetic analysis showed that red algae MTPSLs group with bacterial terpene synthases. Analysis of the genome assembly and characterization of neighboring genes demonstrated red algal to be bona fide red algal genes and not microbial contaminants. genes from and were characterized via heterologous expression in and demonstrated to have sesquiterpene synthase activities. We detected a number of volatile sesquiterpenes in the headspace of and cultures, most identical to the in vitro products of the respective MTPSLs. Expression of the gene in was found to be induced by methyl jasmonate, suggesting a role for this gene in host defense. In summary, this study indicates that the formation of terpene carbon skeletons in red algae is carried out by MTPSLs that are phylogenetically unrelated to typical plant terpene synthases and most likely originated in Rhodophyta via horizontal gene transfer from bacteria.
红藻(红藻门)和陆地植物属于单系类群古生菌,这两个类群的生物都富含萜类次生代谢产物。陆地植物的萜烯碳骨架由两种类型的萜烯合酶合成:典型的植物萜烯合酶和微生物型萜烯合酶(MTPSLs);然而,红藻中的萜类生物合成仍知之甚少。通过对 7 个红藻基因组和 34 个转录组的系统序列分析,在一个基因组和两个转录组中鉴定到了同源物,而没有发现典型植物萜烯合酶基因的同源物。系统发育分析表明,红藻 MTPSLs 与细菌萜烯合酶聚为一类。对基因组组装和邻近基因的特征分析表明, 是真正的红藻基因,而不是微生物污染物。通过在 和 中异源表达 和 ,并对其进行了特征分析,结果表明它们具有倍半萜合酶活性。我们在 和 培养物的顶空部分检测到了一些挥发性倍半萜,其中大多数与各自 MTPSLs 的体外产物相同。发现 在 中的表达受茉莉酸甲酯诱导,表明该基因在宿主防御中发挥作用。总之,这项研究表明,红藻萜类碳骨架的形成是由 MTPSLs 完成的,这些 MTPSLs 在系统发育上与典型的植物萜烯合酶无关,很可能是通过从细菌的水平基因转移在红藻中起源的。