Redgwell R. J., Fry S. C.
Centre for Plant Science, Division of Biological Sciences, Daniel Rutherford Building, The University of Edinburgh, King's Buildings, Mayfield Road, Edinburgh EH9 3JH, United Kingdom.
Plant Physiol. 1993 Dec;103(4):1399-1406. doi: 10.1104/pp.103.4.1399.
The activity of xyloglucan endotransglycosylase (XET) was as-sayed in three tissue zones of kiwifruit (Actinidia deliciosa [A. Chev.] C.F. Liang et A.R. Ferguson var deliciosa cv Hayward) at harvest and at several softening stages following a postharvest ethylene treatment. At harvest, extractable XET activity per unit fresh weight in the inner pericarp (IP) and core tissue was 4.5 and 42 times higher, respectively, than in the outer pericarp (OP). Within 24 h of ethylene treatment there was an increase in the activity and specific activity of XET in all tissues that continued throughout softening. Activity increased most in the OP, where it showed a 12-fold rise 6 d after ethylene treatment compared with 4.5- and 2.5-fold increases in the IP and core tissues, respectively. Visible swelling of the cell wall in each tissue was observed 24 h after the first detectable rise in XET activity and was most pronounced in the OP, which showed the greatest percentage increase in XET activity. Xyloglucan, galactoglucomannan, and cell wall materials isolated and purified from kiwifruit OP were tested as donor substrates for kiwifruit XET. The enzyme showed activity against xyloglucan but was inactive against galactoglucomannan. XET was active against cell wall materials from unripe and ripe fruit, with swollen walls from the latter being the better substrate. The results indicate that XET may have a key role early in fruit ripening, loosening the cell wall in preparation for further modification by other cell wall-associated enzymes.
在猕猴桃(美味猕猴桃[A. Chev.] C.F. Liang和A.R. Ferguson var deliciosa cv Hayward)收获时以及采后乙烯处理后的几个软化阶段,对三个组织区域的木葡聚糖内转糖基酶(XET)活性进行了测定。收获时,内果皮(IP)和核心组织中每单位鲜重的可提取XET活性分别比外果皮(OP)高4.5倍和42倍。乙烯处理24小时内,所有组织中XET的活性和比活性均增加,且在整个软化过程中持续增加。OP中的活性增加最多,乙烯处理6天后,其活性增加了12倍,而IP和核心组织中的活性分别增加了4.5倍和2.5倍。在XET活性首次可检测到升高24小时后,观察到每个组织的细胞壁明显肿胀,OP中最为明显,其XET活性增加的百分比最大。从猕猴桃OP中分离纯化的木葡聚糖、半乳葡甘露聚糖和细胞壁物质被用作猕猴桃XET的供体底物进行测试。该酶对木葡聚糖有活性,但对半乳葡甘露聚糖无活性。XET对未成熟果实和成熟果实的细胞壁物质均有活性,成熟果实肿胀的细胞壁是更好的底物。结果表明,XET可能在果实成熟早期起关键作用,使细胞壁松弛,为其他与细胞壁相关的酶进行进一步修饰做好准备。