DNA extraction of bacterial cells using a semi-automated filtration system

被引:0
|
作者
Hoorzook, K. B. [1 ]
Barnard, T. G. [1 ]
机构
[1] Univ Johannesburg, Johannesburg, South Africa
基金
新加坡国家研究基金会;
关键词
Celite; Environmental water; Escherichia coli; Genomic and plasmid extraction; Guanidium thiocyanate; Membrane filtration; Semi-automated filtration system; ESCHERICHIA-COLI; PURIFICATION; RECOVERY;
D O I
10.1016/j.mex.2022.101785
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The COVID-19 pandemic lockdown created problems with importing of commercial kits resulting in extended turnaround times for consumable deliveries. One way to circumvent this was to use an inexpensive optimized in-house method for DNA extraction from water. The DNA extraction methods were optimized on a 96-well plate using a semi-automated filtration system to increase the number of samples from 24 to 96 at a time in 2 h. The DNA extraction method optimizations included: (a) Guanidium thiocyanate method plus dilution series of celite to determine DNA binding capacity; (b) QIamp 96 Qiacube HT kit (Qiagen (R)); (c) Guanidium thiocyanate with the celite replaced with a binding buffer. The in-house DNA extraction methods and adapted in-house DNA extraction method were compared to QIamp 96 Qiacube HT kit (Qiagen (R)), which is used on a 96-well semi-automated filtration system. The results showed maximum capacity of the 96-well filter plates was 400 mu l broth (OD600 = 0.45 = 3.6 x 10(8) cells/ml) before the 96-well filters blocked. When the methods were compared, there was no significant difference between the in-house DNA extraction method with 1:420 celite dilution (P-value = 0.126) and the adapted in-house method with binding buffer (P-value = 0.298) DNA yield or amplification of PCR products. (C) 2022 The Authors. Published by Elsevier B.V.
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页数:11
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