Department of Biological Chemistry, Institute of Life Sciences, The Hebrew University of Jerusalem, 91904 Jerusalem, Israel.
Plant Physiol. 1988 Apr;86(4):1104-7. doi: 10.1104/pp.86.4.1104.
n-Alkyl (C(6)-C(12)) beta-d-monoglucopyranosides have been found to be highly potent activators of mung bean beta-glucan synthase in vitro, increasing the V(max) of the enzyme as much as 60-fold and with K(a) values as low as 10 micromolar. Activation is highly specific for the beta-linked terminal glucose residue; other alkyl glycosides such as, octyl-alpha-glucoside, dodecyl beta-maltoside, 6-lauryl sucrose, 6-lauryl glucose, which lack this structure, are ineffective as activators. Based on the similarities in their structure and effects on beta-glucan synthesis under a variety of conditions, it is proposed that the alkyl beta-glucosides are structural analogs of the native glucolipid activator of beta-glucan synthase isolated from mung bean extracts.
已发现正烷基(C(6)-C(12))β-D-吡喃葡萄糖苷在体外对绿豆β-葡聚糖合酶有很强的激活作用,使酶的 V(max)提高多达 60 倍,K(a)值低至 10 微摩尔。激活作用高度特异于β-连接的末端葡萄糖残基;其他烷基糖苷,如辛基-α-葡糖苷、十二烷基-β-麦芽糖苷、6-月桂基蔗糖、6-月桂基葡萄糖,缺乏这种结构,作为激活剂无效。根据它们在各种条件下的结构相似性及其对β-葡聚糖合成的影响,建议烷基β-葡萄糖苷是从绿豆提取物中分离出的β-葡聚糖合酶天然糖脂激活剂的结构类似物。