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优化用于DNA质粒回收的碱裂解法。

Optimizing alkaline lysis for DNA plasmid recovery.

作者信息

Clemson Michael, Kelly William J

机构信息

Department of Chemical Engineering, Villanova University, Villanova, PA 19085, USA.

出版信息

Biotechnol Appl Biochem. 2003 Jun;37(Pt 3):235-44. doi: 10.1042/BA20030002.

Abstract

Optimization of the alkaline lysis (P2) and neutralization (N3) steps in the recovery of DNA plasmids was pursued. Experiments were conducted at the test-tube and 5-litre scales with 3 kb (pUC18) and 20 kb (pQR150) plasmids. The scale and degree of mixing/shear did not affect the optimum yield of supercoiled plasmid during the P2 step, but did effect the time required for the optimum to be achieved. This optimum time for P2 at the large scale was longer (8-9 min), especially when a low-shear impeller was used. Also, when the yield of supercoiled plasmid reached a maximum during the P2 step, the purity (percentage of plasmids in the supercoiled form) simultaneously reached a minimum. As the duration of the N3 step increased from 1 to 6 min, the yield of the supercoiled plasmids remained fairly constant, provided that a lowshear impeller was used. The neutralized (post-N3) plasmid solution was shear-sensitive; however, mixing with a Rushton turbine in a tank (maximum energy dissipation rate in the mixing tank, epsilon (max), 12 m(2)/s(3); mixing-tank power consumption/volume of mixing tank, 2.0 W/m(3)) for 5-10 min resulted in a slight decrease in supercoiled plasmid and a notable increase in genomic DNA concentrations. The loss of the larger 20 kb plasmid (20%) was more than for the 3 kb plasmid. Finally, preparing the cells for alkaline lysis with lysozyme or low-pressure homogenization did not increase the plasmid yield. Furthermore, the homogenizer broke up the genomic DNA into fragments that followed through the entire Qiagen prep with the plasmids as impurities.

摘要

对碱裂解(P2)和中和(N3)步骤进行了优化,以提高DNA质粒的回收效率。实验分别在试管和5升规模下进行,使用了3 kb(pUC18)和20 kb(pQR150)的质粒。在P2步骤中,混合/剪切的规模和程度不影响超螺旋质粒的最佳产量,但会影响达到最佳产量所需的时间。大规模下P2步骤的最佳时间更长(8 - 9分钟),特别是使用低剪切叶轮时。此外,当P2步骤中超螺旋质粒的产量达到最大值时,纯度(超螺旋形式质粒的百分比)同时达到最小值。随着N3步骤的持续时间从1分钟增加到6分钟,只要使用低剪切叶轮,超螺旋质粒的产量保持相当稳定。中和后的(N3之后)质粒溶液对剪切敏感;然而,在罐中使用Rushton涡轮进行混合(混合罐中的最大能量耗散率,ε(max),12 m²/s³;混合罐功耗/混合罐体积,2.0 W/m³)5 - 10分钟会导致超螺旋质粒略有减少,基因组DNA浓度显著增加。较大的20 kb质粒的损失(20%)比3 kb质粒更多。最后,用溶菌酶或低压匀浆法使细胞进行碱裂解并不能提高质粒产量。此外,匀浆器将基因组DNA破碎成片段,这些片段会作为杂质随着质粒一起贯穿整个Qiagen制备过程。

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