Mouille G., Maddelein M. L., Libessart N., Talaga P., Decq A., Delrue B., Ball S.
Laboratoire de Chimie Biologique, Unite Mixte de Recherche du Centre National de la Recherche Scientifique No. 111, Universite des Sciences et Technologie de Lille, 59655 Villeneuve d'Ascq Cedex, France.
Plant Cell. 1996 Aug;8(8):1353-1366. doi: 10.1105/tpc.8.8.1353.
It has been generally assumed that the [alpha]-(1->4)-linked and [alpha]-(1->6)-branched glucans of starch are generated by the coordinated action of elongation (starch synthases) and branching enzymes. We have identified a novel Chlamydomonas locus (STA7) that when defective leads to a wipeout of starch and its replacement by a small amount of glycogen-like material. Our efforts to understand the enzymological basis of this phenotype have led us to determine the selective disappearance of an 88-kD starch hydrolytic activity. We further demonstrate that this enzyme is a debranching enzyme. Cleavage of the [alpha]-(1->6) linkage in a branched precursor of amylopectin (preamylopectin) has provided us with the ground rules for understanding starch biosynthesis in plants. Therefore, we propose that amylopectin clusters are synthesized by a discontinuous mechanism involving a highly specific glucan trimming mechanism.
人们普遍认为,淀粉中α-(1→4)连接和α-(1→6)分支的葡聚糖是由延伸酶(淀粉合酶)和分支酶的协同作用产生的。我们鉴定出了衣藻中的一个新基因座(STA7),该基因座缺陷时会导致淀粉消失,并被少量类糖原物质取代。我们为了解这种表型的酶学基础所做的努力,使我们确定了一种88-kD淀粉水解活性的选择性消失。我们进一步证明,这种酶是一种脱支酶。支链淀粉前体(前支链淀粉)中α-(1→6)键的切割,为我们理解植物淀粉生物合成提供了基本规则。因此,我们提出支链淀粉簇是通过一种涉及高度特异性葡聚糖修剪机制的不连续机制合成的。