Optimizing alkaline lysis for DNA plasmid recovery

被引:20
作者
Clemson, M [1 ]
Kelly, WJ [1 ]
机构
[1] Villanova Univ, Dept Chem Engn, Villanova, PA 19085 USA
关键词
Escherichia coli; lysis; mixing; plasmid; shear; supercoiled;
D O I
10.1042/BA20030002
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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 (pQR 150) plasmids. The scale and degree of mixing/shear did not affect the optimum yield of super-coiled 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 I to 6 min, the yield of the supercoiled plasmids remained fairly constant, provided that a low-shear 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 homo-genizer broke up the genomic DNA into fragments that followed through the entire Qiagen prep with the plasmids as impurities.
引用
收藏
页码:235 / 244
页数:10
相关论文
共 11 条
[1]   MECHANICAL DISRUPTION OF ESCHERICHIA-COLI FOR PLASMID RECOVERY [J].
CARLSON, A ;
SIGNS, M ;
LIERMANN, L ;
BOOR, R ;
JEM, KJ .
BIOTECHNOLOGY AND BIOENGINEERING, 1995, 48 (04) :303-315
[2]  
Ciccolini LAS, 1998, BIOTECHNOL BIOENG, V60, P768, DOI 10.1002/(SICI)1097-0290(19981220)60:6<768::AID-BIT13>3.0.CO
[3]  
2-D
[4]   A mass balance study to assess the extent of contaminant removal achieved in the operations for the primary recovery of plasmid DNA from Escherichia coli cells [J].
Ciccolini, LAS ;
Shamlou, PA ;
Titchener-Hooker, N .
BIOTECHNOLOGY AND BIOENGINEERING, 2002, 77 (07) :796-805
[5]  
EKAMBARAM A, 2001, P 8 INT C COMP APPL, P257
[6]   The effects of material properties and fluid flow intensity on plasmid DNA recovery during cell lysis [J].
Levy, MS ;
Ciccolini, LAS ;
Yim, SSS ;
Tsai, JT ;
Titchener-Hooker, N ;
Shamlou, PA ;
Dunnill, P .
CHEMICAL ENGINEERING SCIENCE, 1999, 54 (15-16) :3171-3178
[7]   Effect of shear on plasmid DNA in solution [J].
Levy, MS ;
Collins, IJ ;
Yim, SS ;
Ward, JM ;
Titchener-Hooker, N ;
Shamlou, PA ;
Dunnill, P .
BIOPROCESS ENGINEERING, 1999, 20 (01) :7-13
[8]  
LIEPE F, 1971, CHEM TECH-LEIPZIG, V23, P231
[9]  
MARQUET M, 1996, PHARM TECHNOL APR, P28
[10]  
Oldshue J.Y., 1983, Fluid Mixing Technology