Center for Lignocellulose Structure and Formation, Penn State University, University Park, PA, 16802, USA.
Department of Biology, Penn State University, University Park, PA, 16802, USA.
Plant J. 2018 Jan;93(2):211-226. doi: 10.1111/tpj.13778. Epub 2017 Dec 22.
Xyloglucan has been hypothesized to bind extensively to cellulose microfibril surfaces and to tether microfibrils into a load-bearing network, thereby playing a central role in wall mechanics and growth, but this view is challenged by newer results. Here we combined high-resolution imaging by field emission scanning electron microscopy (FESEM) with nanogold affinity tags and selective endoglucanase treatments to assess the spatial location and conformation of xyloglucan in onion cell walls. FESEM imaging of xyloglucanase-digested cell walls revealed an altered microfibril organization but did not yield clear evidence of xyloglucan conformations. Backscattered electron detection provided excellent detection of nanogold affinity tags in the context of wall fibrillar organization. Labelling with xyloglucan-specific CBM76 conjugated with nanogold showed that xyloglucans were associated with fibril surfaces in both extended and coiled conformations, but tethered configurations were not observed. Labelling with nanogold-conjugated CBM3, which binds the hydrophobic surface of crystalline cellulose, was infrequent until the wall was predigested with xyloglucanase, whereupon microfibril labelling was extensive. When tamarind xyloglucan was allowed to bind to xyloglucan-depleted onion walls, CBM76 labelling gave positive evidence for xyloglucans in both extended and coiled conformations, yet xyloglucan chains were not directly visible by FESEM. These results indicate that an appreciable, but still small, surface of cellulose microfibrils in the onion wall is tightly bound with extended xyloglucan chains and that some of the xyloglucan has a coiled conformation.
木葡聚糖被假设广泛结合到纤维素微纤维表面,并将微纤维束缚成一个承重网络,从而在细胞壁力学和生长中发挥核心作用,但这一观点受到了更新结果的挑战。在这里,我们结合场发射扫描电子显微镜(FESEM)的高分辨率成像、纳米金亲和标签和选择性内切葡聚糖酶处理,评估了洋葱细胞壁中木葡聚糖的空间位置和构象。用木葡聚糖酶消化细胞壁的 FESEM 成像显示微纤维组织发生了改变,但没有清楚地证明木葡聚糖的构象。背散射电子检测在细胞壁纤维组织的背景下提供了对纳米金亲和标签的出色检测。用与纳米金偶联的木葡聚糖特异性 CBM76 进行标记表明,木葡聚糖与伸展和卷曲构象的纤维表面相关,但没有观察到束缚构象。用与纳米金偶联的结合结晶纤维素疏水面的 CBM3 进行标记直到细胞壁用木葡聚糖酶预先消化时才变得频繁,此时微纤维标记非常广泛。当罗望子木葡聚糖被允许与木葡聚糖耗尽的洋葱壁结合时,CBM76 标记为伸展和卷曲构象的木葡聚糖提供了阳性证据,但 FESEM 无法直接观察到木葡聚糖链。这些结果表明,洋葱壁中纤维素微纤维的相当大但仍然很小的表面与伸展的木葡聚糖链紧密结合,并且一些木葡聚糖具有卷曲构象。