Rubén Mateos-Fernández, Elena Moreno-Giménez, S. Gianoglio, Alfredo Quijano-Rubio, Jose Gavaldá-García, Lucía Estellés, A. Rubert, J. Rambla, M. Vazquez-Vilar, E. Huet, Asun Fernández-del-Carmen, A. Espinosa-Ruiz, Mojca Juteršek, S. Vacas, I. Navarro, V. Navarro‑Llopis, J. Primo-Millo, D. Orzáez
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The constructs comprised the Amyelois transitella AtrΔ11 desaturase gene, the Helicoverpa armigera farnesyl reductase HarFAR gene, and the Euonymus alatus diacylglycerol acetyltransferase EaDAct gene in different configurations. All the pheromone-producing plants showed dwarf phenotypes, whose severity correlated with pheromone levels. All but one of the recovered lines produced high levels of Z11-16OH but very low levels of Z11-16OAc, probably as a result of recurrent truncations at the level of the EaDAct gene. Only one plant line (SxPv1.2) was recovered harbouring an intact pheromone pathway and producing moderate levels of Z11-16OAc (11.8 µg g-1 FW), next to high levels of Z11-16OH (111.4 µg g-1). Z11-16OAc production was accompanied in SxPv1.2 by a partial recovery of the dwarf phenotype. SxPv1.2 was used to estimate the rates of volatile pheromone release, which resulted in 8.48 ng g-1 FW per day for Z11-16OH and 9.44 ng g-1 FW per day for Z11-16OAc. 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引用次数: 12
摘要
以植物为基础的昆虫性信息素生物生产已被提出作为一种创新策略,以提高农业害虫防治的可持续性。本文描述了生产鳞翅目性信息素混合物中两种主要挥发性成分(Z)-11-十六烯-1-醇(Z11-16OH)和(Z)-11-十六烯乙酸酯(Z11-16OAc)的转基因植物工程。我们组装了编码信息素生物合成途径的多基因DNA构建体,并在烟叶中稳定转化。构建了不同结构的transitella Amyelois AtrΔ11去饱和酶基因、Helicoverpa armigera farnesyl还原酶HarFAR基因和Euonymus alatus二酰基甘油乙酰转移酶EaDAct基因。所有产生信息素的植株均呈现矮化表型,矮化程度与信息素水平相关。除一条外,所有恢复的系都产生高水平的Z11-16OH,但极低水平的Z11-16OAc,可能是EaDAct基因水平反复截断的结果。只有一个植物品系(SxPv1.2)具有完整的信息素通路,并产生中等水平的Z11-16OAc(11.8µg -1 FW),其次是高水平的Z11-16OH(111.4µg -1)。Z11-16OAc的产生伴随着矮化表型的部分恢复。利用SxPv1.2估算挥发性信息素的释放速率,Z11-16OH和Z11-16OAc的挥发性信息素释放速率分别为8.48 ng g-1 FW / d和9.44 ng g-1 FW / d。我们的研究结果表明,信息素释放是信息素生物分配策略的限制因素,并为生物技术改进建立了路线图。
Production of Volatile Moth Sex Pheromones in Transgenic Nicotiana benthamiana Plants
Plant-based bio-production of insect sex pheromones has been proposed as an innovative strategy to increase the sustainability of pest control in agriculture. Here we describe the engineering of transgenic plants producing (Z)-11-hexadecen-1-ol (Z11-16OH) and (Z)-11-hexadecenyl acetate (Z11-16OAc), two main volatile components in many Lepidoptera sex pheromone blends. We assembled multigene DNA constructs encoding the pheromone biosynthetic pathway and stably transformed them in Nicotiana benthamiana plants. The constructs comprised the Amyelois transitella AtrΔ11 desaturase gene, the Helicoverpa armigera farnesyl reductase HarFAR gene, and the Euonymus alatus diacylglycerol acetyltransferase EaDAct gene in different configurations. All the pheromone-producing plants showed dwarf phenotypes, whose severity correlated with pheromone levels. All but one of the recovered lines produced high levels of Z11-16OH but very low levels of Z11-16OAc, probably as a result of recurrent truncations at the level of the EaDAct gene. Only one plant line (SxPv1.2) was recovered harbouring an intact pheromone pathway and producing moderate levels of Z11-16OAc (11.8 µg g-1 FW), next to high levels of Z11-16OH (111.4 µg g-1). Z11-16OAc production was accompanied in SxPv1.2 by a partial recovery of the dwarf phenotype. SxPv1.2 was used to estimate the rates of volatile pheromone release, which resulted in 8.48 ng g-1 FW per day for Z11-16OH and 9.44 ng g-1 FW per day for Z11-16OAc. Our results suggest that pheromone release acts as a limiting factor in pheromone bio-dispenser strategies and establish a roadmap for biotechnological improvements.