Pen J, Molendijk L, Quax W J, Sijmons P C, van Ooyen A J, van den Elzen P J, Rietveld K, Hoekema A
MOGEN N.V., Leiden, The Netherlands.
Biotechnology (N Y). 1992 Mar;10(3):292-6. doi: 10.1038/nbt0392-292.
As a first example of the feasibility of producing industrial bulk enzymes in plants, we have expressed Bacillus licheniformis alpha-amylase in transgenic tobacco, and applied the seeds directly in starch liquification. The enzyme was properly secreted into the intercellular space, and maximum expression levels of about 0.3% of total soluble protein were obtained. No apparent effect of the presence of the enzyme on plant phenotype was observed. The molecular weight of the enzyme produced in tobacco was around 64 kD. The difference, compared to 55.2 kD for the bacterial enzyme, was found to result from complex-type carbohydrate chains attached to the protein. Application studies on the liquefaction of starch were done with transgenic seeds containing the recombinant alpha-amylase. The resulting hydrolysis products were virtually identical with those obtained from degradation with alpha-amylase from Bacillus licheniformis.
作为在植物中生产工业用大量酶可行性的首个实例,我们已在转基因烟草中表达了地衣芽孢杆菌α淀粉酶,并将种子直接应用于淀粉液化。该酶被正确分泌到细胞间隙,获得了约占总可溶性蛋白0.3%的最大表达水平。未观察到该酶的存在对植物表型有明显影响。烟草中产生的酶的分子量约为64 kD。与细菌酶的55.2 kD相比,发现差异源于附着在蛋白质上的复合型碳水化合物链。用含有重组α淀粉酶的转基因种子进行了淀粉液化的应用研究。所得水解产物与用地衣芽孢杆菌α淀粉酶降解得到的产物几乎相同。