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Biosynthesis and cell-wall deposition of a pectin–xyloglucan complex in pea

机译:豌豆中果胶-木葡聚糖复合物的生物合成和细胞壁沉积

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Golgi-enriched enzyme preparations prepared from etiolated pea epicotyls incorporated [U−14C]galactose from UDP-[U−14C]galactose into the 1,4-β-galactan sidechains of a pectin–xyloglucan complex. This complex could bind to paper and was degraded both by pectin-degrading enzymes and by a xyloglucan-specific endoglucanase. Gel permeation chromatography was used to assess the molecular size of the complex and of enzymically-degraded, galactan-containing fragments of it. Etiolated pea stems were labelled with [U−14C]sucrose for 1 h, and the newly-synthesised cell wall polysaccharides were extracted with EDTA or NaOH and fractionated by ion-exchange chromatography. The NaOH-extracted, acidic radioactive polysaccharides obtained in this way were also degraded both by pectin-degrading enzymes and by xyloglucan-specific endoglucanase. Analysis of the radioactive sugar composition indicated that neutral sugars characteristic of both pectin and xyloglucan were present. Analysis of the total non-radioactive, neutral sugar composition of the NaOH-extracted, acidic cell-wall polysaccharides indicated that pectin–xyloglucan complexes were a general feature of the cell wall in this tissue
机译:由黄化的豌豆上胚轴制备的高尔基酶富含酶,将UDP- [U-14 C]半乳糖中的[U-14 C]半乳糖掺入到果胶的1,4-β-半乳聚糖侧链中,木葡聚糖复合物。该复合物可与纸结合,并被果胶降解酶和木葡聚糖特异性内切葡聚糖酶降解。凝胶渗透色谱法用于评估复合物及其酶降解的含半乳聚糖片段的分子大小。用[U-14 C]蔗糖标记黄化的豌豆茎1 h,然后用EDTA或NaOH提取新合成的细胞壁多糖,并通过离子交换色谱分离。用果胶降解酶和木葡聚糖特异性内切葡聚糖酶也降解了以这种方式获得的经NaOH萃取的酸性放射性多糖。放射性糖组成的分析表明,果胶和木葡聚糖均具有中性糖特征。对NaOH提取的酸性细胞壁多糖的总非放射性,中性糖成分的分析表明,果胶-木葡聚糖复合物是该组织中细胞壁的一般特征

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