Larsen J, Joergensen L
DB Lab, Dansk Bioprotein A/S, Odense M, Denmark.
Appl Microbiol Biotechnol. 1996 Mar;45(1-2):137-40. doi: 10.1007/s002530050661.
A method for reducing RNA and DNA in the bacterium Methylococcus capsulatus (Bath) has been developed. Endogenous RNase and DNase were activated by a 10 s heat shock at 90 degrees C. Cells were then incubated at 60 degrees C for 20 min to allow degradation of the nucleic acids. The optimum pH for the process was 7.0. The protein loss was less than 10% and occurred during the initial heat shock. No protein loss was found during incubation. The total dry-weight loss in connection with an 80% reduction of the nucleic acid content was 20%-25%, giving a final product with a raw protein content of approximately 75%. Reduction of both RNA and DNA was inhibited by CuSO4 and ZnSO4. DNA reduction was stimulated by other minerals. Optimal stimulation was found at 1 mM FeSO4. Reduction of RNA was not increased by any of the minerals tested.
已开发出一种降低荚膜甲基球菌(巴斯德种)中RNA和DNA的方法。通过在90℃下热激10秒激活内源性核糖核酸酶和脱氧核糖核酸酶。然后将细胞在60℃下孵育20分钟以使核酸降解。该过程的最适pH为7.0。蛋白质损失小于10%,且发生在初始热激期间。孵育期间未发现蛋白质损失。与核酸含量降低80%相关的总干重损失为20%-25%,得到的最终产品粗蛋白含量约为75%。硫酸铜和硫酸锌抑制RNA和DNA的降低。其他矿物质刺激DNA的降低。在1 mM硫酸亚铁时发现最佳刺激效果。所测试的任何矿物质均未增加RNA的降低。