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pEMBL:一类新型单链质粒。

pEMBL: a new family of single stranded plasmids.

作者信息

Dente L, Cesareni G, Cortese R

出版信息

Nucleic Acids Res. 1983 Mar 25;11(6):1645-55. doi: 10.1093/nar/11.6.1645.

DOI:10.1093/nar/11.6.1645
PMID:6300771
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC325826/
Abstract

We have constructed a series of plasmids, the pEMBL family, characterized by the presence of 1) the bla gene as selectable marker, 2) a short segment coding for the alpha-peptide of beta-galactosidase and containing a multiple cloning sites polylinker, 3) the intragenic region of phage F1. pEMBL plasmids have the property of being encapsidated as single stranded DNA, upon superinfection with phage F1. These vectors have been used successfully for DNA sequencing with the dideoxy-method, and can be used for any other purpose for which M13 derivatives are used. However, the pEMBL plasmids have the advantage of being smaller than M13 vectors, and the purification of the DNA is simpler. In addition, and most importantly, long inserts have a higher stability in pEMBL plasmids than M13 vectors.

摘要

我们构建了一系列质粒,即pEMBL家族,其特征在于存在:1)作为选择标记的bla基因;2)一段编码β-半乳糖苷酶α-肽并包含多克隆位点多接头的短片段;3)噬菌体F1的基因内区域。pEMBL质粒具有在被噬菌体F1超感染时被包装成单链DNA的特性。这些载体已成功用于双脱氧法DNA测序,并且可用于任何其他使用M13衍生物的目的。然而,pEMBL质粒具有比M13载体更小的优势,并且DNA的纯化更简单。此外,最重要的是,长插入片段在pEMBL质粒中比在M13载体中具有更高的稳定性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c58a/325826/f724e70f6fd6/nar00351-0027-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c58a/325826/3346c1d2528b/nar00351-0026-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c58a/325826/f724e70f6fd6/nar00351-0027-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c58a/325826/3346c1d2528b/nar00351-0026-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c58a/325826/f724e70f6fd6/nar00351-0027-a.jpg

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1
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2
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Virology. 1981 Oct 30;114(2):463-73. doi: 10.1016/0042-6822(81)90226-9.
3
Replication of a plasmid containing two origins of bacteriophage.含有两个噬菌体复制起点的质粒的复制
鉴定 IncA/C 质粒骨架中的 oriT 和重组热点。
Sci Rep. 2017 Sep 6;7(1):10595. doi: 10.1038/s41598-017-11097-0.
4
Genes encoding ferredoxins from Anabaena sp. PCC 7937 and Synechococcus sp. PCC 7942: structure and regulation.来自鱼腥藻 PCC 7937 和聚球藻 PCC 7942 的铁氧还蛋白基因的编码:结构和调控。
Photosynth Res. 1988 Oct;18(1-2):179-204. doi: 10.1007/BF00042984.
5
Activity expressed from cloned Anacystis nidulans large and small subunit ribulose bisphosphate carboxylase genes.从克隆的鱼腥藻大、小亚基核酮糖二磷酸羧化酶基因表达的活性。
Plant Mol Biol. 1985 Jul;5(4):257-63. doi: 10.1007/BF00020643.
6
Silene cDNA clones for a divergent chlorophyll-a/b-binding protein and a small subunit of ribulosebisphosphate carboxylase.拟南芥 cDNA 克隆的一个叶绿素 a/b 结合蛋白和一个核酮糖二磷酸羧化酶小亚基的差异。
Plant Mol Biol. 1986 Nov;7(6):433-40. doi: 10.1007/BF00020327.
7
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Plant Mol Biol. 1988 Jul;10(4):339-47. doi: 10.1007/BF00029884.
8
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Theor Appl Genet. 1986 Mar;72(2):207-10. doi: 10.1007/BF00266993.
J Mol Biol. 1981 Nov 25;153(1):169-76. doi: 10.1016/0022-2836(81)90532-5.
4
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