Raymond Y, Fincher G B, Maclachlan G A
Department of Biology, McGill University, 1205 McGregor Avenue, Montreal, Quebec, Canada H3A 1B1.
Plant Physiol. 1978 Jun;61(6):938-42. doi: 10.1104/pp.61.6.938.
beta-Glucan synthetase activity in growing regions of pea (Pisum sativum L.) epicotyls was assayed by supplying UDP-glucose to particulate fractions of tissue homogenates or to thin tissue slices. Particulate fractions are less active in forming alkali-insoluble glucan than slices from the same tissue, although many kinetic characteristics (pH and Mg(2+) optimum, apparent K(m)) are similar for the two systems. Synthesis by tissue slices progresses linearly without lag period for at least an hour and is proportional to cut surface area. It is much more rapid from UDP-glucose than from glucose, glucose-1-P, or sucrose. Tests with plasmolyzing agents and trypsin support the conclusion that synthesis from UDP-glucose by slices occurs at accessible surfaces of cut cells. Analyses of glucan products by GLC of partially methylated and acetylated derivatives and by hydrolysis with various beta-glucanases all show that both beta-1,3 and beta-1,4 linkages are formed by particulate fractions and slices at substrate concentrations ranging from micro- to millimolar. beta-1,4 Linkages predominate at low substrate (5 mum) concentration. Kinetic data indicate that the capacity to synthesize beta-1,3-glucan is substrate-activated, and this product predominates in preparations supplied with high (5 mm) substrate.
通过向组织匀浆的颗粒部分或薄组织切片提供UDP-葡萄糖,测定豌豆(Pisum sativum L.)上胚轴生长区域中的β-葡聚糖合成酶活性。颗粒部分在形成碱不溶性葡聚糖方面的活性低于相同组织的切片,尽管这两个系统的许多动力学特征(最适pH和Mg(2+)、表观K(m))相似。组织切片的合成至少一小时内呈线性进行且无延迟期,并且与切割表面积成正比。从UDP-葡萄糖合成比从葡萄糖、葡萄糖-1-P或蔗糖合成要快得多。用质壁分离剂和胰蛋白酶进行的测试支持这样的结论,即切片从UDP-葡萄糖的合成发生在切割细胞的可及表面。通过对部分甲基化和乙酰化衍生物进行气相色谱分析以及用各种β-葡聚糖酶水解来分析葡聚糖产物,结果均表明,在底物浓度从微摩尔到毫摩尔的范围内,颗粒部分和切片都能形成β-1,3和β-1,4键。在低底物(5 μM)浓度下,β-1,4键占主导。动力学数据表明,合成β-1,3-葡聚糖的能力是底物激活的,并且在提供高(5 mM)底物的制剂中该产物占主导。