Department of Plant Sciences, University of Tennessee, Knoxville, TN, USA.
Center for Agricultural Synthetic Biology, University of Tennessee, Knoxville, TN, USA.
Plant Cell Rep. 2024 Jun 5;43(6):162. doi: 10.1007/s00299-024-03245-4.
A robust agroinfiltration-mediated transient gene expression method for soybean leaves was developed. Plant genotype, developmental stage and leaf age, surfactant, and Agrobacterium culture conditions are important for successful agroinfiltration. Agroinfiltration of Nicotiana benthamiana has emerged as a workhorse transient assay for plant biotechnology and synthetic biology to test the performance of gene constructs in dicot leaves. While effective, it is nonetheless often desirable to assay transgene constructs directly in crop species. To that end, we innovated a substantially robust agroinfiltration method for Glycine max (soybean), the most widely grown dicot crop plant in the world. Several factors were found to be relevant to successful soybean leaf agroinfiltration, including genotype, surfactant, developmental stage, and Agrobacterium strain and culture medium. Our optimized protocol involved a multi-step Agrobacterium culturing process with appropriate expression vectors, Silwet L-77 as the surfactant, selection of fully expanded leaves in the VC or V1 stage of growth, and 5 min of vacuum at - 85 kPa followed by a dark incubation period before plants were returned to normal growth conditions. Using this method, young soybean leaves of two lines-V17-0799DT, and TN16-5004-were high expressors for GUS, two co-expressed fluorescent protein genes, and the RUBY reporter product, betalain. This work not only represents a new research tool for soybean biotechnology, but also indicates critical parameters for guiding agroinfiltration optimization for other crop species. We speculate that leaf developmental stage might be the most critical factor for successful agroinfiltration.
我们开发了一种稳健的农杆菌介导的大豆叶片瞬时基因表达方法。植物基因型、发育阶段和叶片年龄、表面活性剂和农杆菌培养条件对于成功的农杆菌浸润都是重要的。农杆菌浸润 Nicotiana benthamiana 已成为植物生物技术和合成生物学的一种常用瞬时分析方法,用于测试基因构建体在双子叶叶片中的性能。虽然有效,但在作物物种中直接检测转基因构建体仍然是理想的。为此,我们创新了一种用于 Glycine max(大豆)的稳健的农杆菌浸润方法,Glycine max 是世界上种植最广泛的双子叶作物植物。发现几个因素与大豆叶片农杆菌浸润的成功相关,包括基因型、表面活性剂、发育阶段以及农杆菌菌株和培养基。我们优化的方案涉及一个多步骤的农杆菌培养过程,使用适当的表达载体、Silwet L-77 作为表面活性剂、选择生长的 VC 或 V1 阶段的完全展开的叶片,以及在 -85kPa 下进行 5 分钟的真空处理,然后在将植物恢复到正常生长条件之前进行黑暗孵育。使用这种方法,两个品系-V17-0799DT 和 TN16-5004-的幼大豆叶片对 GUS、两个共表达荧光蛋白基因和 RUBY 报告产物甜菜红素的表达较高。这项工作不仅代表了大豆生物技术的新研究工具,还为指导其他作物物种的农杆菌浸润优化提供了关键参数。我们推测叶片发育阶段可能是农杆菌浸润成功的最关键因素。