首页 | 本学科首页   官方微博 | 高级检索  
     


A simple bacterial transformation method using magnesium- and calcium-aminoclays
Authors:Hyoung-An Choi  Young-Chul Lee  Jin-Young Lee  Hyun-Jae Shin  Hyo-Kyung Han  Geun-Joong Kim
Affiliation:1. Department of Biological Sciences, College of Natural Sciences, Chonnam National University, Gwang-ju 500–757, Republic of Korea;2. Deparment of Biological Engineering, College of Engineering, Inha University, Incheon 402–751, Republic of Korea;3. Department of Chemical and Biochemical Engineering, Chosun University, Gwang-ju 501–759, Republic of Korea;4. College of Pharmacy, Dongguk University, Pil-dong-3-ga, Jung-gu, Seoul 100–715, Republic of Korea
Abstract:An efficient and user-friendly bacterial transformation method by simple spreading cells with aminoclays was demonstrated. Compared to the reported transformation approaches using DNA adsorption or wrapping onto (in)organic fibers, the spontaneously generated clay-coated DNA suprastructures by mixing DNA with aminoclay resulted in transformants in both Gram-negative (Escherichia coli) and Gram-positive cells (Streptococcus mutans). Notably, the wild type S. mutans showed comparable transformation efficiency to that of the E. coli host for recombinant DNA cloning. This is a potentially promising result because other trials such as heat-shock, electroporation, and treatment with sepiolite for introducing DNA into the wild type S. mutans failed. Under defined conditions, the transformation efficiency of E. coli XL1-Blue and S. mutans exhibited ~ 2 × 105 and ~ 6 × 103 CFU/μg of plasmid DNA using magnesium-aminoclay. In contrast, transformation efficiency was higher in S. mutans than that in E. coli XL1-Blue for calcium-aminoclay. It was also confirmed that each plasmid transformed into E. coli and S. mutans was stably maintained and that they expressed the inserted gene encoding the green fluorescent protein during prolonged growth of up to 80 generations.
Keywords:Bacteria   Transformation   Aminoclay   E. coli   S. mutans
本文献已被 ScienceDirect 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号