Littlejohn George R, Mansfield Jessica C, Parker David, Lind Rob, Perfect Sarah, Seymour Mark, Smirnoff Nicholas, Love John, Moger Julian
School of Biosciences, College of Life and Environmental Sciences (G.R.L., N.S., J.L.), and Department of Physics and Astronomy, College of Engineering, Mathematics, and Physical Sciences (J.C.M., J.M.), University of Exeter, Exeter, Devon EX4 4QD, United Kingdom;Biodomain Technology Group, Shell International Exploration and Production, Inc., Westhollow Technology Center, Houston, Texas 77082 (D.P.); andSyngenta, Jealott's Hill International Research Centre, Bracknell, Berkshire RG42 6EY, United Kingdom (R.L., S.P., M.S.).
School of Biosciences, College of Life and Environmental Sciences (G.R.L., N.S., J.L.), and Department of Physics and Astronomy, College of Engineering, Mathematics, and Physical Sciences (J.C.M., J.M.), University of Exeter, Exeter, Devon EX4 4QD, United Kingdom;Biodomain Technology Group, Shell International Exploration and Production, Inc., Westhollow Technology Center, Houston, Texas 77082 (D.P.); andSyngenta, Jealott's Hill International Research Centre, Bracknell, Berkshire RG42 6EY, United Kingdom (R.L., S.P., M.S.)
Plant Physiol. 2015 May;168(1):18-28. doi: 10.1104/pp.15.00119. Epub 2015 Mar 17.
The cuticle is a ubiquitous, predominantly waxy layer on the aerial parts of higher plants that fulfils a number of essential physiological roles, including regulating evapotranspiration, light reflection, and heat tolerance, control of development, and providing an essential barrier between the organism and environmental agents such as chemicals or some pathogens. The structure and composition of the cuticle are closely associated but are typically investigated separately using a combination of structural imaging and biochemical analysis of extracted waxes. Recently, techniques that combine stain-free imaging and biochemical analysis, including Fourier transform infrared spectroscopy microscopy and coherent anti-Stokes Raman spectroscopy microscopy, have been used to investigate the cuticle, but the detection sensitivity is severely limited by the background signals from plant pigments. We present a new method for label-free, in vivo structural and biochemical analysis of plant cuticles based on stimulated Raman scattering (SRS) microscopy. As a proof of principle, we used SRS microscopy to analyze the cuticles from a variety of plants at different times in development. We demonstrate that the SRS virtually eliminates the background interference compared with coherent anti-Stokes Raman spectroscopy imaging and results in label-free, chemically specific confocal images of cuticle architecture with simultaneous characterization of cuticle composition. This innovative use of the SRS spectroscopy may find applications in agrochemical research and development or in studies of wax deposition during leaf development and, as such, represents an important step in the study of higher plant cuticles.
角质层是高等植物地上部分普遍存在的、主要由蜡质构成的一层结构,它发挥着许多重要的生理作用,包括调节蒸散作用、光反射和耐热性、控制发育,以及在生物体与化学物质或某些病原体等环境因子之间提供重要屏障。角质层的结构和组成密切相关,但通常使用结构成像和提取蜡质的生化分析相结合的方法分别进行研究。最近,结合无染色成像和生化分析的技术,包括傅里叶变换红外光谱显微镜和相干反斯托克斯拉曼光谱显微镜,已被用于研究角质层,但检测灵敏度受到植物色素背景信号的严重限制。我们提出了一种基于受激拉曼散射(SRS)显微镜的植物角质层无标记、体内结构和生化分析的新方法。作为原理验证,我们使用SRS显微镜在不同发育阶段分析了多种植物的角质层。我们证明,与相干反斯托克斯拉曼光谱成像相比,SRS几乎消除了背景干扰,并产生了角质层结构的无标记、化学特异性共聚焦图像,同时对角质层组成进行了表征。SRS光谱的这种创新应用可能在农用化学品研发或叶片发育过程中蜡质沉积的研究中找到应用,因此代表了高等植物角质层研究的重要一步。