Unité de Glycobiologie Structurale et Fonctionnelle, UMR8576 CNRS-Université Lille 1, sciences et technologies, F-59655 Villeneuve d'Ascq, France.
J Exp Bot. 2011 Aug;62(13):4547-59. doi: 10.1093/jxb/err172. Epub 2011 May 30.
This study assessed the impact on starch metabolism in Arabidopsis leaves of simultaneously eliminating multiple soluble starch synthases (SS) from among SS1, SS2, and SS3. Double mutant ss1- ss2- or ss1- ss3- lines were generated using confirmed null mutations. These were compared to the wild type, each single mutant, and ss1- ss2- ss3- triple mutant lines grown in standardized environments. Double mutant plants developed similarly to the wild type, although they accumulated less leaf starch in both short-day and long-day diurnal cycles. Despite the reduced levels in the double mutants, lines containing only SS2 and SS4, or SS3 and SS4, are able to produce substantial amounts of starch granules. In both double mutants the residual starch was structurally modified including higher ratios of amylose:amylopectin, altered glucan chain length distribution within amylopectin, abnormal granule morphology, and altered placement of α(1→6) branch linkages relative to the reducing end of each linear chain. The data demonstrate that SS activity affects not only chain elongation but also the net result of branch placement accomplished by the balanced activities of starch branching enzymes and starch debranching enzymes. SS3 was shown partially to overlap in function with SS1 for the generation of short glucan chains within amylopectin. Compensatory functions that, in some instances, allow continued residual starch production in the absence of specific SS classes were identified, probaby accomplished by the granule bound starch synthase GBSS1.
本研究评估了同时消除 SS1、SS2 和 SS3 中的多个可溶性淀粉合酶 (SS) 对拟南芥叶片中淀粉代谢的影响。使用确认的无效突变生成了 ss1-ss2- 或 ss1-ss3- 的双突变体系。将这些与野生型、每个单突变体以及 ss1-ss2-ss3- 三重突变体系在标准化环境中进行了比较。尽管双突变体植物的发育与野生型相似,但它们在短日和长日昼夜周期中积累的叶片淀粉较少。尽管双突变体中的含量降低,但仅含有 SS2 和 SS4 或 SS3 和 SS4 的系仍能够产生大量的淀粉颗粒。在这两种双突变体中,残留的淀粉的结构都发生了修饰,包括直链淀粉与支链淀粉的比例增加、支链淀粉内葡聚糖链长分布改变、颗粒形态异常以及相对于每个线性链的还原端α(1→6)分支键的位置改变。这些数据表明,SS 活性不仅影响链的延伸,还影响通过淀粉分支酶和淀粉脱支酶的平衡活性完成的分支放置的净结果。SS3 部分与 SS1 重叠,用于生成支链淀粉中的短葡聚糖链。鉴定了在某些情况下允许在缺乏特定 SS 类的情况下继续残留淀粉生产的补偿功能,可能是通过颗粒结合淀粉合酶 GBSS1 完成的。