Hesse H, Willmitzer L
Institut für Genbiologische Forschung Berlin, Germany.
Plant Mol Biol. 1996 Mar;30(5):863-72. doi: 10.1007/BF00020799.
To investigate the expression pattern of sucrose synthase, a cDNA from tap roots of sugar beet (Beta vulgaris L.) was isolated using a heterologous sucrose synthase cDNA from potato. The 2762 bp long cDNA clone designated SBSS 1 encodes for a 822 amino acid polypeptide of a predicted molecular mass of 93.7 kDa. The deduced amino acid sequence of sugar beet sucrose synthase has homologies of 65-70% when compared to predicted amino acid sequences of sucrose synthases from other species. RNA blot analysis shows that SBSS1 is expressed most predominant in tap root under normal growth conditions. Cold treatment and anaerobiosis lead to an increase in the steady-state levels of SBSS 1 mRNA in leaf and root tissue. In tap root slices, sugars in various concentrations had no influence on the SBSS 1 transcript level. On the other hand, wounding resulted in a decreased transcript level.
为了研究蔗糖合酶的表达模式,利用来自马铃薯的异源蔗糖合酶cDNA从甜菜(Beta vulgaris L.)的主根中分离出一个cDNA。命名为SBSS 1的2762 bp长的cDNA克隆编码一个预测分子量为93.7 kDa的822个氨基酸的多肽。与其他物种蔗糖合酶的预测氨基酸序列相比,甜菜蔗糖合酶的推导氨基酸序列具有65 - 70%的同源性。RNA印迹分析表明,在正常生长条件下,SBSS1在主根中表达最为显著。冷处理和无氧处理导致叶片和根组织中SBSS 1 mRNA的稳态水平增加。在主根切片中,不同浓度的糖对SBSS 1转录水平没有影响。另一方面,创伤导致转录水平降低。