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在鱼腥藻属PCC 7120菌株中使用条件致死基因来筛选双重组体并捕获插入序列。

Use of a conditionally lethal gene in Anabaena sp. strain PCC 7120 to select for double recombinants and to entrap insertion sequences.

作者信息

Cai Y P, Wolk C P

机构信息

MSU-DOE Plant Research Laboratory, Michigan State University, East Lansing 48824-1312.

出版信息

J Bacteriol. 1990 Jun;172(6):3138-45. doi: 10.1128/jb.172.6.3138-3145.1990.

DOI:10.1128/jb.172.6.3138-3145.1990
PMID:2160938
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC209118/
Abstract

Use of the sacB gene (J. L. Ried and A. Collmer, Gene 57:239-246, 1987) provides a simple, effective, positive selection for double recombinants in Anabaena sp. strain PCC 7120, a filamentous cyanobacterium. This gene, which encodes the secretory levansucrase of Bacillus subtilis, was inserted into the vector portion of a suicide plasmid bearing a mutant version of a chromosomal gene. Cells of colonies in which such a plasmid had integrated into the Anabaena chromosome through single recombination were plated on solid medium containing 5% sucrose. Under this condition, the presence of the sacB gene is lethal. A small fraction of the cells from initially sucrose-sensitive colonies became sucrose resistant; the majority of these sucrose-resistant derivatives had undergone a second recombinational event in which the sacB-containing vector had been lost and the wild-type form of the chromosomal gene had been replaced by the mutant form. By the use of this technique, we mutated two selected genes in the chromosome of Anabaena sp. strain PCC 7120. The conditionally lethal nature of the sacB gene was also used to detect insertion sequences from this Anabaena strain. Sucrose-resistant colonies derived from cells bearing a sacB-containing autonomously replicating plasmid were analyzed. Five different, presumed insertion sequences were found to have inserted into the sacB gene of the plasmids in these colonies. One of them, denoted IS892, was characterized by physical mapping. It is 1.7 kilobases in size and is present in at least five copies in the genome of Anabaena sp. strain PCC 7120.

摘要

使用sacB基因(J. L. 里德和A. 科尔默,《基因》57:239 - 246,1987年)为丝状蓝细菌鱼腥藻属菌株PCC 7120中的双重组体提供了一种简单、有效的正向选择。该基因编码枯草芽孢杆菌的分泌型果聚糖蔗糖酶,被插入到携带染色体基因突变体版本的自杀质粒的载体部分。通过单重组将这种质粒整合到鱼腥藻染色体中的菌落细胞,被接种在含有5%蔗糖的固体培养基上。在这种条件下,sacB基因的存在是致命的。最初对蔗糖敏感的菌落中有一小部分细胞变得对蔗糖具有抗性;这些对蔗糖具有抗性的衍生物中的大多数经历了第二次重组事件,其中含有sacB的载体丢失,染色体基因的野生型形式被突变型所取代。通过使用这种技术,我们对鱼腥藻属菌株PCC 7120染色体中的两个选定基因进行了突变。sacB基因的条件致死性质也被用于检测来自该鱼腥藻菌株的插入序列。对携带含sacB自主复制质粒的细胞所产生的蔗糖抗性菌落进行了分析。发现有五个不同的、推测的插入序列插入到了这些菌落中质粒的sacB基因中。其中一个被命名为IS892,通过物理图谱进行了表征。它的大小为1.7千碱基,在鱼腥藻属菌株PCC 7120的基因组中至少有五个拷贝。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3ff/209118/429ed5de6573/jbacter00160-0336-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3ff/209118/f0548c20af4a/jbacter00160-0335-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3ff/209118/bd6f70373045/jbacter00160-0336-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3ff/209118/429ed5de6573/jbacter00160-0336-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3ff/209118/f0548c20af4a/jbacter00160-0335-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3ff/209118/bd6f70373045/jbacter00160-0336-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3ff/209118/429ed5de6573/jbacter00160-0336-b.jpg

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