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木葡聚糖内转糖基酶,一种来自植物的新型细胞壁松弛酶活性。

Xyloglucan endotransglycosylase, a new wall-loosening enzyme activity from plants.

作者信息

Fry S C, Smith R C, Renwick K F, Martin D J, Hodge S K, Matthews K J

机构信息

Division of Biological Sciences, University of Edinburgh, U.K.

出版信息

Biochem J. 1992 Mar 15;282 ( Pt 3)(Pt 3):821-8. doi: 10.1042/bj2820821.

Abstract
  1. Cell-free extracts of all plants tested contained a novel enzyme activity (xyloglucan endotransglycosylase, XET) able to transfer a high-Mr portion from a donor xyloglucan to a suitable acceptor such as a xyloglucan-derived nonasaccharide (Glc4Xyl3GalFuc; XG9). 2. A simple assay for the enzyme, using [3H]XG9 and based on the ability of the [3H]polysaccharide product to bind to filter paper, is described. 3. The enzyme was highly specific for xyloglucan as the glycosyl donor, and showed negligible transglycosylation of other polysaccharides, including CM-cellulose. 4. The Km for XG9 was 50 microM; certain other 3H-labelled xyloglucan oligosaccharides also acted as acceptors, and certain non-radioactive xyloglucan oligosaccharides competed with [3H]XG9 as acceptor; the minimum acceptor structure was deduced to be: [formula: see text] 5. The pH optimum was approx. 5.5 and the enzyme was less than half as active at pH 7.0. The enzyme was slightly activated by Ca2+, Mg2+, Mn2+, spermidine, ascorbate and 2-mercaptoethanol, and inhibited by Ag+, Hg2+, Zn2+ and La3+. 6. XET activity was essentially completely extracted by aqueous solutions of low ionic strength; Triton X-100, Ca2+, La3+, and Li+ did not enhance extraction. Negligible activity was left in the unextractable (cell-wall-rich) residue. 7. The enzyme differed from the major cellulases (EC 3.2.1.4) of pea in: (a) susceptibility to inhibition by cello-oligosaccharides, (b) polysaccharide substrate specificity, (c) inducibility by auxin, (d) requirement for salt in the extraction buffer and (e) activation by 2-mercaptoethanol. XET is therefore concluded to be a new enzyme activity (xyloglucan: xyloglucan xyloglucanotransferase; EC 2.4.1.-). 8. XET was detected in extracts of the growing portions of dicotyledons, monocotyledons (graminaceous and liliaceous) and bryophytes. 9. The activity was positively correlated with growth rate in different zones of the pea stem. 10. We propose that XET is responsible for cutting and rejoining intermicrofibrillar xyloglucan chains and that it thus causes the wall-loosening required for plant cell expansion.
摘要
  1. 所有测试植物的无细胞提取物都含有一种新型酶活性(木葡聚糖内转糖基酶,XET),它能够将高相对分子质量部分从供体木葡聚糖转移到合适的受体上,如木葡聚糖衍生的九糖(Glc4Xyl3GalFuc;XG9)。2. 描述了一种基于[3H]XG9并利用[3H]多糖产物与滤纸结合能力的该酶的简单测定方法。3. 该酶对木葡聚糖作为糖基供体具有高度特异性,对其他多糖(包括羧甲基纤维素)的转糖基化作用可忽略不计。4. XG9的米氏常数为50微摩尔;某些其他3H标记的木葡聚糖寡糖也可作为受体,某些非放射性木葡聚糖寡糖可作为受体与[3H]XG9竞争;推断最小受体结构为:[分子式:见正文] 5. 最适pH约为5.5,该酶在pH 7.0时的活性不到其一半。Ca2+、Mg2+、Mn2+、亚精胺、抗坏血酸和2-巯基乙醇可轻微激活该酶,而Ag+、Hg2+、Zn2+和La3+则抑制该酶。6. 低离子强度的水溶液可基本完全提取XET活性;Triton X-100、Ca2+、La3+和Li+不能增强提取效果。不可提取的(富含细胞壁的)残渣中残留的活性可忽略不计。7. 该酶与豌豆的主要纤维素酶(EC 3.2.1.4)在以下方面不同:(a)对纤维寡糖抑制的敏感性,(b)多糖底物特异性,(c)生长素诱导性,(d)提取缓冲液中对盐的需求,以及(e)2-巯基乙醇的激活作用。因此得出结论,XET是一种新的酶活性(木葡聚糖:木葡聚糖木葡聚糖转糖基酶;EC 2.4.1.-)。8. 在双子叶植物、单子叶植物(禾本科和百合科)以及苔藓植物生长部位的提取物中检测到了XET。9. 豌豆茎不同区域的活性与生长速率呈正相关。10. 我们认为XET负责切割和重新连接微纤丝间的木葡聚糖链,从而导致植物细胞扩张所需的细胞壁松弛。

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