Biochemistry and Applied Microbiology Laboratory, UNESP-São Paulo State University, Rua Cristóvão Colombo no. 2265, São José do Rio Preto, São Paulo, Brazil.
Appl Biochem Biotechnol. 2011 Jan;163(1):14-24. doi: 10.1007/s12010-010-8963-7. Epub 2010 Apr 23.
Three mutations, Ser54→Pro, Thr314→Ala, and His415→Tyr, were identified in Aspergillus awamori glucoamylase gene expressed by Saccharomyces cerevisiae. The mutant glucoamylase (GA) was substantially more thermostable than a wild-type GA at 70 °C, with a 3.0 KJ mol(-1) increase in the free energy of thermo-inactivation. The effect of starch from different botanical sources on the production of this GA was measured in liquid fermentation using commercial soluble starch, cassava, potato, and corn as the carbon source. The best substrate for GA production was the potato starch showing an enzymatic activity of 6.6 U/mL. The commercial soluble starch was also a good substrate for the enzyme production with 6.3 U/mL, followed by cassava starch and corn starch with 5.9 and 3.0 U/mL, respectively. These results showed a significant difference on GA production related to the carbon source employed. The mutant GA was purified by acarbose-Sepharose affinity chromatography; the estimated molecular mass was 100 kDa. The mutant GA exhibited optimum activity at pH 4.5 and an optimum temperature of 65 °C.
在表达于酿酒酵母的aspergillus awamori 葡糖淀粉酶基因中鉴定出三个突变,即 Ser54→Pro、Thr314→Ala 和 His415→Tyr。与野生型 GA 相比,突变型葡糖淀粉酶(GA)在 70°C 下的热稳定性显著提高,热失活的自由能增加了 3.0KJ/mol。在液体发酵中使用商业可溶性淀粉、木薯、土豆和玉米作为碳源,测量了这种 GA 对不同植物来源淀粉生产的影响。土豆淀粉是 GA 生产的最佳底物,酶活为 6.6U/mL。商业可溶性淀粉也是该酶生产的良好底物,酶活为 6.3U/mL,其次是木薯淀粉和玉米淀粉,分别为 5.9 和 3.0U/mL。这些结果表明,与所使用的碳源相比,GA 的生产存在显著差异。突变型 GA 通过阿卡波糖-琼脂糖亲和层析进行纯化;估计的分子量为 100kDa。突变型 GA 在 pH4.5 时表现出最佳活性,最适温度为 65°C。