Oming G W, Darbinian N S, Mochulski A V, Piruzian E S
Department of Plant Molecular Genetics, Russian Academy of Sciences.
Mol Gen Mikrobiol Virusol. 1997(1):30-4.
A gene which codes for a thermostable endo beta-1,3-glucanase (EC 3.2.1.39) from a Gram positive anaerobic thermophilic bacteria Clostridium thermocellum F7, was fused to 35S promoter and polyadenylation signal of Cauliflower Mosaic Virus (CaMV) strain Cabb B-D. This chimaeric gene fusion was introduced into Nicotiana plumbaguinifolia protoplasts using PEG-mediated DNA transfer method of transformation. Transient expression of the thermostable endo beta-1,3-glucanase was carried out in the protoplasts and was assayed at 70 degrees C pH 8.0, suggesting that the chimaeric gene fusion: (i) is correctly transcribed and translated in plant cells; (ii) the product of translation (the thermostable endo beta-1,3-glucanase protein) is easy to assay since most of the plants' enzymes have their optimal reaction temperature at 40-60 degrees C and at neutral or weak-acidic condition which is a characteristic of plant cells; (iii) can be used as a model for studying and understanding some of the mechanisms of plant defence systems at the enzyme protein level, in case of stress conditions.
一个编码来自革兰氏阳性厌氧嗜热细菌热纤梭菌F7的耐热内切β-1,3-葡聚糖酶(EC 3.2.1.39)的基因,与花椰菜花叶病毒(CaMV)Cabb B-D株的35S启动子和聚腺苷酸化信号融合。使用聚乙二醇(PEG)介导的DNA转化方法将这种嵌合基因融合体导入烟草叶肉原生质体。在原生质体中进行耐热内切β-1,3-葡聚糖酶的瞬时表达,并在70℃、pH 8.0条件下进行测定,这表明该嵌合基因融合体:(i)在植物细胞中能正确转录和翻译;(ii)翻译产物(耐热内切β-1,3-葡聚糖酶蛋白)易于检测,因为大多数植物酶在40-60℃以及中性或弱酸性条件下具有最佳反应温度,这是植物细胞的一个特征;(iii)在应激条件下,可作为在酶蛋白水平研究和理解植物防御系统某些机制的模型。