Research and Innovation Department, Luxembourg Institute of Science and Technology, 5 Avenue des Hauts-Fourneaux, 4362, Esch/Alzette, Luxembourg.
Department of Life Sciences, University of Siena, via P.A. Mattioli 4, 53100, Siena, Italy.
Planta. 2019 Nov;250(5):1539-1556. doi: 10.1007/s00425-019-03245-9. Epub 2019 Jul 27.
The immuno-ultrastructural investigation localized cell-wall polysaccharides of bast fibers during hemp hypocotyl growth. Moreover, for the first time, the localization of a peroxidase and laccase is provided in textile hemp. In the hypocotyl of textile hemp, elongation and girth increase are separated in time. This organ is therefore ideal for time-course analyses. Here, we follow the ultrastructural rearrangement of cell-wall components during the development of the hemp hypocotyl. An expression analysis of genes involved in the biosynthesis of cellulose, the chief polysaccharide of bast fiber cell walls and xylan, the main hemicellulose of secondary cell walls, is also provided. The analysis shows a higher expression of cellulose and xylan-related genes at 15 and 20 days after sowing, as compared to 9 days. In the young hypocotyl, the cell walls of bast fibers show cellulose microfibrils that are not yet compacted to form a mature G-layer. Crystalline cellulose is detected abundantly in the S1-layer, together with unsubstituted/low-substituted xylan and, to a lesser extent, in the G-layer. The LM5 galactan epitope is confined to the walls of parenchymatic cells. LM6-specific arabinans are detected at the interface between the cytoplasm and the gelatinous cell wall of bast fibers. The class III peroxidase antibody shows localization in the G-layer only at older developmental stages. The laccase antibody shows a distinctive labelling of the G-layer region closest to the S1-layer; the signal becomes more homogeneous as the hypocotyl matures. The data provide important insights on the cell wall distribution of polysaccharide and protein components in bast fibers during the hypocotyl growth of textile hemp.
免疫超微结构研究定位大麻下胚轴生长过程中纤维细胞壁多糖。此外,本文首次提供了在纺织大麻中过氧化物酶和漆酶的定位信息。在纺织大麻的下胚轴中,伸长和周长增加是时间分离的。因此,该器官非常适合进行时间进程分析。在这里,我们跟踪大麻下胚轴发育过程中细胞壁成分的超微结构重排。还提供了与纤维素生物合成相关基因的表达分析,纤维素是韧皮纤维细胞壁的主要多糖,木聚糖是次生细胞壁的主要半纤维素。分析表明,与播种后 9 天相比,播种后 15 天和 20 天纤维素和木聚糖相关基因的表达更高。在幼嫩的下胚轴中,韧皮纤维细胞壁显示出尚未压缩形成成熟 G 层的纤维素微纤维。结晶纤维素在 S1 层中大量存在,与未取代/低取代木聚糖一起存在,在 G 层中含量较少。LM5 半乳糖抗原表位局限于薄壁细胞的壁上。LM6 特异性阿拉伯聚糖存在于韧皮纤维细胞质和胶状细胞壁之间的界面处。类 III 过氧化物酶抗体仅在较老的发育阶段定位于 G 层。漆酶抗体对最接近 S1 层的 G 层区域进行了独特的标记;随着下胚轴的成熟,信号变得更加均匀。该数据提供了关于纺织大麻下胚轴生长过程中韧皮纤维中多糖和蛋白质成分细胞壁分布的重要见解。