Talbott L D, Ray P M
Department of Biological Sciences, Stanford University, Stanford, California 94305.
Plant Physiol. 1992 Jan;98(1):357-68. doi: 10.1104/pp.98.1.357.
Relative molecular size distributions of pectic and hemicellulosic polysaccharides of pea (Pisum sativum cv Alaska) third internode primary walls were determined by gel filtration chromatography. Pectic polyuronides have a peak molecular mass of about 1100 kilodaltons, relative to dextran standards. This peak may be partly an aggregate of smaller molecular units, because demonstrable aggregation occurred when samples were concentrated by evaporation. About 86% of the neutral sugars (mostly arabinose and galactose) in the pectin cofractionate with polyuronide in gel filtration chromatography and diethylaminoethyl-cellulose chromatography and appear to be attached covalently to polyuronide chains, probably as constituents of rhamnogalacturonans. However, at least 60% of the wall's arabinan/galactan is not linked covalently to the bulk of its rhamnogalacturonan, either glycosidically or by ester links, but occurs in the hemicellulose fraction, accompanied by negligible uronic acid, and has a peak molecular mass of about 1000 kilodaltons. Xyloglucan, the other principal hemicellulosic polymer, has a peak molecular mass of about 30 kilodaltons (with a secondary, usually minor, peak of approximately 300 kilodaltons) and is mostly not linked glycosidically either to pectic polyuronides or to arabinogalactan. The relatively narrow molecular mass distributions of these polymers suggest mechanisms of co- or postsynthetic control of hemicellulose chain length by the cell. Although the macromolecular features of the mentioned polymers individually agree generally with those shown in the widely disseminated sycamore cell primary wall model, the matrix polymers seem to be associated mostly noncovalently rather than in the covalently interlinked meshwork postulated by that model. Xyloglucan and arabinan/galactan may form tightly and more loosely bound layers, respectively, around the cellulose microfibrils, the outer layer interacting with pectic rhamnogalacturonans that occupy interstices between the hemicellulose-coated microfibrils.
通过凝胶过滤色谱法测定了豌豆(阿拉斯加品种豌豆)第三节间初生壁中果胶和半纤维素多糖的相对分子质量分布。相对于葡聚糖标准品,果胶多聚半乳糖醛酸的峰值分子量约为1100千道尔顿。这个峰值可能部分是较小分子单元的聚集体,因为当样品通过蒸发浓缩时会出现明显的聚集现象。在凝胶过滤色谱法和二乙氨基乙基纤维素色谱法中,果胶共级分中约86%的中性糖(主要是阿拉伯糖和半乳糖)与多聚半乳糖醛酸共分级,并且似乎共价连接到多聚半乳糖醛酸链上,可能作为鼠李糖半乳糖醛酸聚糖的成分。然而,至少60%的细胞壁阿拉伯聚糖/半乳聚糖不是通过糖苷键或酯键与大部分鼠李糖半乳糖醛酸聚糖共价连接,而是存在于半纤维素级分中,伴随的糖醛酸可忽略不计,其峰值分子量约为1000千道尔顿。木葡聚糖是另一种主要的半纤维素聚合物,其峰值分子量约为30千道尔顿(还有一个次要的通常较小的峰值约为300千道尔顿),并且大多不通过糖苷键与果胶多聚半乳糖醛酸或阿拉伯半乳聚糖连接。这些聚合物相对较窄的分子量分布表明细胞对半纤维素链长度进行共合成或合成后控制的机制。尽管上述聚合物的大分子特征总体上与广泛传播的悬铃木细胞初生壁模型中所示的特征一致,但基质聚合物似乎大多通过非共价结合,而不是像该模型所假设的那样以共价交联网络的形式存在。木葡聚糖和阿拉伯聚糖/半乳聚糖可能分别在纤维素微纤丝周围形成紧密和较松散结合的层,外层与占据半纤维素包被微纤丝之间空隙的果胶鼠李糖半乳糖醛酸聚糖相互作用。