Sadler Christina, Schroll Bettina, Zeisler Viktoria, Waßmann Friedrich, Franke Rochus, Schreiber Lukas
Institute of Cellular and Molecular Botany, Department of Ecophysiology, University of Bonn, Kirschallee 1, D-53115 Bonn, Germany.
Institute of Cellular and Molecular Botany, Department of Ecophysiology, University of Bonn, Kirschallee 1, D-53115 Bonn, Germany.
Biochim Biophys Acta. 2016 Sep;1861(9 Pt B):1336-1344. doi: 10.1016/j.bbalip.2016.03.002. Epub 2016 Mar 7.
Using (14)C-labeled epoxiconazole as a tracer, cuticular permeability of Arabidopsis thaliana leaves was quantitatively measured in order to compare different wax and cutin mutants (wax2, cut1, cer5, att1, bdg, shn3 and shn1) to the corresponding wild types (Col-0 and Ws). Mutants were characterized by decreases or increases in wax and/or cutin amounts. Permeances [ms(-1)] of Arabidopsis cuticles either increased in the mutants compared to wild type or were not affected. Thus, genetic changes in wax and cutin biosynthesis in some of the investigated Arabidopsis mutants obviously impaired the coordinated cutin and wax deposition at the outer leaf epidermal cell wall. As a consequence, barrier properties of cuticles were significantly decreased. However, increasing cutin and wax amounts by genetic modifications, did not automatically lead to improved cuticular barrier properties. As an alternative approach to the radioactive transport assay, changes in chlorophyll fluorescence were monitored after foliar application of metribuzine, an herbicide inhibiting electron transport in chloroplasts. Since both, half-times of photosynthesis inhibition as well as times of complete inhibition, in fact correlated with (14)C-epoxiconazole permeances, different rates of decline of photosynthetic yield between mutants and wild type must be a function of foliar uptake of the herbicide across the cuticle. Thus, monitoring changes in chlorophyll fluorescence, instead of conducting radioactive transport assays, represents an easy-to-handle and fast alternative evaluating cuticular barrier properties of different genotypes. This article is part of a Special Issue entitled: Plant Lipid Biology edited by Kent D. Chapman and Ivo Feussner.
以(14)C标记的环氧菌唑作为示踪剂,对拟南芥叶片的角质层通透性进行了定量测量,以便将不同的蜡质和角质突变体(wax2、cut1、cer5、att1、bdg、shn3和shn1)与其相应的野生型(Col-0和Ws)进行比较。突变体的特征是蜡质和/或角质含量减少或增加。与野生型相比,拟南芥角质层的通透率[ms(-1)]在突变体中要么增加,要么不受影响。因此,在一些被研究的拟南芥突变体中,蜡质和角质生物合成的基因变化明显损害了叶片外表皮细胞壁上角质和蜡质的协同沉积。结果,角质层的屏障特性显著降低。然而,通过基因改造增加角质和蜡质的含量并不会自动导致角质层屏障特性的改善。作为放射性运输测定的替代方法,在叶面施用抑制叶绿体电子运输的除草剂嗪草酮后,监测叶绿素荧光的变化。由于光合作用抑制的半衰期以及完全抑制的时间实际上都与(14)C-环氧菌唑的通透率相关,突变体和野生型之间光合产量下降的不同速率必定是除草剂通过角质层叶面吸收的一个函数。因此,监测叶绿素荧光的变化,而不是进行放射性运输测定,是一种易于操作且快速评估不同基因型角质层屏障特性的替代方法。本文是名为:《植物脂质生物学》的特刊的一部分,由肯特·D·查普曼和伊沃·费斯纳编辑。