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通过电提取蓝细菌回收质粒和染色体DNA。

Plasmid and chromosomal DNA recovery by electroextraction of cyanobacteria.

作者信息

Moser D, Zarka D, Hedman C, Kallas T

机构信息

Department of Biology and Microbiology, University of Wisconsin-Oshkosh, USA.

出版信息

FEMS Microbiol Lett. 1995 May 15;128(3):307-13. doi: 10.1111/j.1574-6968.1995.tb07541.x.

Abstract

High voltage electroporation has been investigated as a method for rapid recovery of plasmid and chromosomal DNA from the cyanobacteria Nostoc PCC 7121, Synechococcus PCC 7002, and Anabaena PCC 7120. Pulses of 18 kV/cm and higher applied to concentrated Nostoc cells carrying a shuttle plasmid (pRL25) resulted in copious release of nucleic acids and phycobiliproteins into the suspending medium. Small portions of these supernatants, when electroporated with Escherichia coli, gave rise to hundreds of E. coli transformants which contained pRL25. Electroporation of Synechococcus carrying plasmid pAQE19 did not cause detectable release of macromolecules but did reveal a low-level, voltage independent 'leakage' of pAQE19 into the medium. Electroextraction of Nostoc or Anabaena followed by addition of E. coli and delivery of a second high-voltage pulse permitted direct, one-cuvette transfer of shuttle plasmids from these cyanobacteria into E. coli. Electroextraction of single cyanobacterial colonies, as shown for Nostoc, also released sufficient chromosomal DNA for amplification of specific sequences by the polymerase chain reaction.

摘要

高压电穿孔已被作为一种从蓝细菌集胞藻PCC 7121、聚球藻PCC 7002和鱼腥藻PCC 7120中快速回收质粒和染色体DNA的方法进行了研究。对携带穿梭质粒(pRL25)的集胞藻浓缩细胞施加18 kV/cm及更高的脉冲,导致大量核酸和藻胆蛋白释放到悬浮培养基中。这些上清液的小部分在用大肠杆菌进行电穿孔时,产生了数百个含有pRL25的大肠杆菌转化体。携带质粒pAQE19的聚球藻进行电穿孔不会导致可检测到的大分子释放,但确实显示出pAQE19有低水平的、与电压无关的“泄漏”到培养基中。对集胞藻或鱼腥藻进行电提取,然后加入大肠杆菌并施加第二个高压脉冲,可使穿梭质粒从这些蓝细菌直接一次性转移到大肠杆菌中。如对集胞藻所示,单个蓝细菌菌落的电提取也释放了足够的染色体DNA,用于通过聚合酶链反应扩增特定序列。

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