Simmen U., Obenland D., Boller T., Wiemken A.
Department of Botany, University of Basel, Hebelstrasse 1, CH-4056 Basel, Switzerland.
Plant Physiol. 1993 Feb;101(2):459-468. doi: 10.1104/pp.101.2.459.
Excised leaves of barley (Hordeum vulgare L.) exposed to continuous light accumulate large amounts of soluble carbohydrates. Carbohydrates were analyzed in deionized extracts by high-pressure liquid chromatography on an anion exchange column coupled with pulsed amperometric detection. During the first few hours of illumination, the main sugar to accumulate was sucrose. The levels of glucose and fructans (oligofructosylsucroses) increased later. The trisaccharide 1-kestose (1-kestotriose) predominated initially among the fructans. Later, 6-kestose (6-kestotriose) and tetra- and pentasaccharides accumulated also. Total extracts from barley leaves were chromatographed on a MonoQ column, and each fraction was assayed for enzymes of interest by incubation with 200 mM sucrose for 3 h, followed by carbohydrate analysis. Freshly excised leaves yielded two peaks of invertase, characterized by formation of fructose and glucose, but had almost no trisaccharide-forming activities. In leaves exposed to continuous light, two new enzyme activities appeared that generated fructan-related trisaccharides and glucose from sucrose. One of them was a sucrose-sucrose fructosyl-1-transferase (1-SST), producing 1-kestose exclusively: the peak fractions of this activity contained almost no invertase. The other was a sucrose-sucrose fructosyl-6-transferase (6-SST), producing 6-kestose. It comigrated with one of the constitutive invertases on MonoQ but was separated from it by subsequent chromatography on alkyl Superose. Nevertheless, the preparation retained invertase activity, suggesting that this enzyme may act both as fructosidase and fructosyltransferase. When incubated with 1-kestose in addition to sucrose, this enzyme formed less 6-kestose but instead produced large amounts of the tetrasaccharide bifurcose (1&6-kestotetraose), the main fructan tetrasaccharide accumulating in vivo. These results suggest that two inducible enzymes, 1-SST and 6-SST, act in concert to initiate fructan accumulation in barley leaves.
暴露于持续光照下的大麦(Hordeum vulgare L.)离体叶片积累了大量可溶性碳水化合物。通过在配备脉冲安培检测的阴离子交换柱上进行高压液相色谱分析去离子提取物中的碳水化合物。在光照的最初几个小时内,积累的主要糖类是蔗糖。葡萄糖和果聚糖(低聚果糖基蔗糖)的水平随后升高。三糖1-蔗果三糖(1-kestotriose)最初在果聚糖中占主导地位。后来,6-蔗果三糖(6-kestotriose)以及四糖和五糖也开始积累。将大麦叶片的总提取物在MonoQ柱上进行色谱分析,每个馏分与200 mM蔗糖孵育3小时后,通过碳水化合物分析来检测感兴趣的酶。刚离体的叶片产生了两个转化酶峰,其特征是形成果糖和葡萄糖,但几乎没有形成三糖的活性。在持续光照下的叶片中,出现了两种新的酶活性,它们从蔗糖生成与果聚糖相关的三糖和葡萄糖。其中一种是蔗糖-蔗糖果糖基-1-转移酶(1-SST),仅产生1-蔗果三糖:该活性的峰馏分几乎不含转化酶。另一种是蔗糖-蔗糖果糖基-6-转移酶(6-SST),产生6-蔗果三糖。它在MonoQ上与一种组成型转化酶共迁移,但在随后的烷基Superose色谱上与之分离。然而,该制剂保留了转化酶活性,表明这种酶可能同时作为果糖苷酶和果糖基转移酶起作用。当除了蔗糖之外还与1-蔗果三糖一起孵育时,这种酶形成的6-蔗果三糖较少,而是产生大量的四糖分枝糖(1&6-kestotetraose),这是体内积累的主要果聚糖四糖。这些结果表明,两种诱导酶1-SST和6-SST协同作用,启动大麦叶片中的果聚糖积累。