Röber M, Geider K, Müller-Röber B, Willmitzer L
Institut für Genbiologische Forschung Berlin GmbH, Germany.
Planta. 1996;199(4):528-36. doi: 10.1007/BF00195183.
Inhibition of starch biosynthesis in transgenic potato (Solanum tuberosum L. cv. Désirée) plants (by virtue of antisense inhibition of ADP-glucose pyrophosphorylase) has recently been reported to influence tuber formation and drastically reduce dry matter content of tubers, indicating a reduction in sink strength (Müller-Röber et al. 1992, EMBO J 11: 1229-1238). Transgenic tubers produced low levels of starch, but instead accumulated high levels of soluble sugars. We wanted to know whether these changes in tuber development/sink strength could be reversed by the production of a new high-molecular-weight polymer, i.e. fructan, that incorporates sucrose and thereby should reduce the level of osmotically active compounds. To this end the enzyme levan sucrase from the gram-negative bacterium Erwinia amylovora was expressed in tubers of transgenic potato plants inhibited for starch biosynthesis. Levan sucrase was targeted to different subcellular compartments (apoplasm, vacuole and cytosol). Only in the case of apoplastic and vacuolar targeting was significant accumulation of fructan observed, leading to fructan representing between 12% and 19% of the tuber dry weight. Gel filtration and 13C-nuclear magnetic resonance spectroscopy showed that the molecular weight and structure of the fructan produced in transgenic plants is identical to levan isolated from E. amylovora. Whereas apoplastic expression of levansucrase had deleterious effects on tuber development, tubers containing the levansucrase in the vacuole did not differ in phenotype from tubers of the starch-deficient plants used as starting material for transformation with the levansucrase. When tuber yield was analysed, no increase but rather a further decrease relative to ADP-glucose pyro-phosphorylase antisense plants was observed.
最近有报道称,在转基因马铃薯(Solanum tuberosum L. cv. Désirée)植株中抑制淀粉生物合成(通过反义抑制ADP-葡萄糖焦磷酸化酶)会影响块茎形成,并大幅降低块茎的干物质含量,这表明库强降低(Müller-Röber等人,1992年,《欧洲分子生物学组织杂志》11: 1229 - 1238)。转基因块茎产生的淀粉水平较低,反而积累了高水平的可溶性糖。我们想知道,通过产生一种新的高分子量聚合物,即果聚糖,是否可以逆转块茎发育/库强的这些变化,果聚糖能结合蔗糖,从而应该会降低渗透活性化合物的水平。为此,将来自革兰氏阴性细菌梨火疫病菌的果聚糖蔗糖酶在淀粉生物合成受抑制的转基因马铃薯植株的块茎中进行表达。果聚糖蔗糖酶被靶向到不同的亚细胞区室(质外体、液泡和细胞质)。只有在质外体和液泡靶向的情况下,才观察到果聚糖的显著积累,导致果聚糖占块茎干重的12%至19%。凝胶过滤和13C-核磁共振光谱表明,转基因植物中产生的果聚糖的分子量和结构与从梨火疫病菌中分离的果聚糖相同。虽然果聚糖蔗糖酶的质外体表达对块茎发育有有害影响,但液泡中含有果聚糖蔗糖酶的块茎在表型上与用作果聚糖蔗糖酶转化起始材料的淀粉缺陷型植物的块茎没有差异。当分析块茎产量时,相对于ADP-葡萄糖焦磷酸化酶反义植株,没有增加,反而进一步下降。