Plant and Animal Biotechnology Laboratory, Department of Agronomy, University of Illinois at Urbana-Champaign, 1201 West Gregory, 61801, Urbana, IL, USA.
Plant Cell Rep. 1991 Jun;10(2):106-10. doi: 10.1007/BF00236468.
Electroporation was used to evaluate parameters affecting transient gene expression in Glycine max protoplasts. Protoplast viability and reporter enzyme activity for chloramphenicol acetyl transferase (CAT) and ß-glucuronidase (GUS) depended on the field strength employed. Maximum CAT and GUS activity was obtained when a field strength of 500 V/cm at 1000 μF and a protoplast concentration of 1-3 × 10(6)/ml was used. Transformation efficiencies up to approximately 1.6% GUS positive protoplasts were obtained. Transient gene expression increased with increasing plasmid DNA concentration and with the time after electroporation, reaching a maximum after 48 hr. Addition of polyethylene glycol at 5.6% and heat shock (5 rain at 45 °C) given to the protoplasts before adding DNA further enhanced the transformation efficiency. Under the optimized experimental conditions, CAT and GUS activity increased simultaneously, thereby indicating that the increased expression is caused by DNA uptake by more cells rather than greater DNA uptake by the same cells. Our results demonstrate that both GUS and CAT can be used as efficient screenable markers for transformation studies in soybean.
电穿孔法被用来评估影响大豆原生质体瞬时基因表达的参数。原生质体的活力和氯霉素乙酰转移酶(CAT)和β-葡萄糖醛酸酶(GUS)的报告酶活性取决于所使用的场强。当使用 500 V/cm 的场强、1000 μF 的电容和 1-3×10(6)/ml 的原生质体浓度时,可获得最大的 CAT 和 GUS 活性。获得了高达约 1.6% GUS 阳性原生质体的转化效率。瞬时基因表达随着质粒 DNA 浓度的增加和电穿孔后时间的增加而增加,在 48 小时后达到最大值。在添加 DNA 之前,向原生质体中添加 5.6%的聚乙二醇和热休克(45°C 下 5 分钟)可进一步提高转化效率。在优化的实验条件下,CAT 和 GUS 活性同时增加,表明表达的增加是由于更多的细胞摄取 DNA 所致,而不是同一细胞摄取更多的 DNA。我们的结果表明,CAT 和 GUS 都可以用作大豆转化研究中的有效筛选标记。