Carl R. Woese Institute for Genomic Biology, University of Illinois at Urbana-Champaign; Department of Plant Biology, Morrill Hall, University of Illinois at Urbana-Champaign.
Carl R. Woese Institute for Genomic Biology, University of Illinois at Urbana-Champaign.
J Vis Exp. 2022 Jul 6(185). doi: 10.3791/63485.
Photosynthesis is not optimized in modern crop varieties, and therefore provides an opportunity for improvement. Speeding up the relaxation of non-photochemical quenching (NPQ) has proven to be an effective strategy to increase photosynthetic performance. However, the potential to breed for improved NPQ and a complete understanding of the genetic basis of NPQ relaxation is lacking due to limitations of oversampling and data collection from field-grown crop plants. Building on previous reports, we present a high-throughput assay for analysis of NPQ relaxation rates in Glycine max (soybean) using pulse amplitude modulated (PAM) chlorophyll fluorometry. Leaf disks are sampled from field-grown soybeans before transportation to a laboratory where NPQ relaxation is measured in a closed PAM-fluorometer. NPQ relaxation parameters are calculated by fitting a bi-exponential function to the measured NPQ values following a transition from high to low light. Using this method, it is possible to test hundreds of genotypes within a day. The procedure has the potential to screen mutant and diversity panels for variation in NPQ relaxation, and can therefore be applied to both fundamental and applied research questions.
光合作用在现代作物品种中没有得到优化,因此提供了改进的机会。事实证明,加快非光化学猝灭(NPQ)的弛豫是提高光合作用性能的有效策略。然而,由于田间生长作物过度采样和数据收集的限制,缺乏用于培育改良 NPQ 和完全理解 NPQ 弛豫遗传基础的潜力。在之前报告的基础上,我们提出了一种使用脉冲幅度调制(PAM)叶绿素荧光计分析大豆(大豆)NPQ 弛豫率的高通量测定法。在将叶片圆盘从田间生长的大豆中取出运送到实验室进行 NPQ 弛豫测量之前,将其从田间生长的大豆中取出。NPQ 弛豫参数通过在从高光到低光的过渡后拟合双指数函数来计算测量的 NPQ 值。使用这种方法,一天内可以测试数百种基因型。该程序有可能筛选突变体和多样性面板中的 NPQ 弛豫变化,因此可应用于基础研究和应用研究问题。