Scion, Rotorua 3010, New Zealand.
Plant Physiol. 2012 Feb;158(2):642-53. doi: 10.1104/pp.111.184036. Epub 2011 Dec 5.
The distribution of noncellulosic polysaccharides in cell walls of tracheids and xylem parenchyma cells in normal and compression wood of Pinus radiata, was examined to determine the relationships with lignification and cellulose microfibril orientation. Using fluorescence microscopy combined with immunocytochemistry, monoclonal antibodies were used to detect xyloglucan (LM15), β(1,4)-galactan (LM5), heteroxylan (LM10 and LM11), and galactoglucomannan (LM21 and LM22). Lignin and crystalline cellulose were localized on the same sections used for immunocytochemistry by autofluorescence and polarized light microscopy, respectively. Changes in the distribution of noncellulosic polysaccharides between normal and compression wood were associated with changes in lignin distribution. Increased lignification of compression wood secondary walls was associated with novel deposition of β(1,4)-galactan and with reduced amounts of xylan and mannan in the outer S2 (S2L) region of tracheids. Xylan and mannan were detected in all lignified xylem cell types (tracheids, ray tracheids, and thick-walled ray parenchyma) but were not detected in unlignified cell types (thin-walled ray parenchyma and resin canal parenchyma). Mannan was absent from the highly lignified compound middle lamella, but xylan occurred throughout the cell walls of tracheids. Using colocalization measurements, we confirmed that polysaccharides containing galactose, mannose, and xylose have consistent correlations with lignification. Low or unsubstituted xylans were localized in cell wall layers characterized by transverse cellulose microfibril orientation in both normal and compression wood tracheids. Our results support the theory that the assembly of wood cell walls, including lignification and microfibril orientation, may be mediated by changes in the amount and distribution of noncellulosic polysaccharides.
辐射松正常木和压缩木管胞和木质部薄壁细胞细胞壁中非纤维素多糖的分布,以确定与木质化和纤维素微纤丝取向的关系。使用荧光显微镜结合免疫细胞化学,使用单克隆抗体检测木葡聚糖(LM15)、β(1,4)-半乳糖醛酸聚糖(LM5)、杂木聚糖(LM10 和 LM11)和半乳甘露聚糖(LM21 和 LM22)。木质素和结晶纤维素分别通过自发荧光和偏光显微镜定位在用于免疫细胞化学的相同切片上。正常木和压缩木中非纤维素多糖分布的变化与木质素分布的变化有关。压缩木次生壁木质化程度的增加与β(1,4)-半乳糖醛酸聚糖的新沉积以及 S2(S2L)区域木聚糖和甘露聚糖含量的减少有关。木聚糖和甘露聚糖存在于所有木质化的木质部细胞类型(管胞、射线管胞和厚壁射线薄壁组织)中,但不存在于未木质化的细胞类型(薄壁射线薄壁组织和树脂道薄壁组织)中。甘露聚糖不存在于高度木质化的复合中层,但木聚糖存在于管胞的细胞壁中。通过共定位测量,我们证实含有半乳糖、甘露糖和木糖的多糖与木质化具有一致的相关性。在正常木和压缩木管胞中,低取代或未取代的木聚糖定位于具有横向纤维素微纤丝取向的细胞壁层中。我们的结果支持这样一种理论,即木质部细胞壁的组装,包括木质化和微纤丝取向,可能是通过非纤维素多糖的数量和分布的变化来介导的。