Literature DB >> 2840358

Plasmid pIJ699, a multi-copy positive-selection vector for Streptomyces.

T Kieser1, R E Melton.   

Abstract

A plasmid vector, pIJ699, which provides positive selection for cloned DNA, was constructed using the replication functions of the Streptomyces wide-host-range multi-copy plasmid pIJ101. The selection for inserts is based on the principle that plasmids with long uninterrupted perfect palindromes (inverted repeats) are 'not viable' in bacteria. For cloning, pIJ699 is digested with BglII. This produces two fragments, one of which is the linearized vector, with two arms of the palindrome at its ends, and the other is a 'spacer' which is needed to keep the inverted repeat sequences apart. The vector fragment is separated from the 'spacer' fragment and ligated with the DNA to be cloned. Plasmids with a fragment of cloned DNA, but not the circularized vector, give rise to thiostrepton-resistant transformants in Streptomyces lividans. The inverted repeat sequences contain a strong transcription terminator which reduces transcriptional read-through both in and out of the cloned fragment. This improves the stability of many hybrid plasmids and facilitates the study of the regulation of cloned genes.

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Year:  1988        PMID: 2840358     DOI: 10.1016/0378-1119(88)90419-2

Source DB:  PubMed          Journal:  Gene        ISSN: 0378-1119            Impact factor:   3.688


  46 in total

1.  Amy as a reporter gene for promoter activity in Nocardia lactamdurans: comparison of promoters of the cephamycin cluster.

Authors:  V K Chary; J L de la Fuente; P Liras; J F Martin
Journal:  Appl Environ Microbiol       Date:  1997-08       Impact factor: 4.792

2.  Establishment of a foreign antigen secretion system in mycobacteria.

Authors:  K Matsuo; R Yamaguchi; A Yamazaki; H Tasaka; K Terasaka; M Totsuka; K Kobayashi; H Yukitake; T Yamada
Journal:  Infect Immun       Date:  1990-12       Impact factor: 3.441

3.  Determination of the packaging capacity of bacteriophage VWB.

Authors:  J Anné; L Van Mellaert; H Eyssen
Journal:  J Bacteriol       Date:  1990-02       Impact factor: 3.490

4.  Conserved gene arrangement in the origin region of the Streptomyces coelicolor chromosome.

Authors:  M J Calcutt; F J Schmidt
Journal:  J Bacteriol       Date:  1992-05       Impact factor: 3.490

5.  Efficient Transformation of the Cephamycin C Producer Nocardia lactamdurans and Development of Shuttle and Promoter-Probe Cloning Vectors.

Authors:  C V Kumar; J J Coque; J F Martín
Journal:  Appl Environ Microbiol       Date:  1994-11       Impact factor: 4.792

6.  The SbcCD nuclease of Escherichia coli is a structural maintenance of chromosomes (SMC) family protein that cleaves hairpin DNA.

Authors:  J C Connelly; L A Kirkham; D R Leach
Journal:  Proc Natl Acad Sci U S A       Date:  1998-07-07       Impact factor: 11.205

7.  Denaturation of circular or linear DNA facilitates targeted integrative transformation of Streptomyces coelicolor A3(2): possible relevance to other organisms.

Authors:  S H Oh; K F Chater
Journal:  J Bacteriol       Date:  1997-01       Impact factor: 3.490

8.  Novel post-replicative DNA modification in Streptomyces: analysis of the preferred modification site of plasmid pIJ101.

Authors:  P Dyson; M Evans
Journal:  Nucleic Acids Res       Date:  1998-03-01       Impact factor: 16.971

9.  The sapA promoter from Streptomyces coelicolor requires activation sites and initiator-like sequences but No -10 or -35 sequences.

Authors:  H Im
Journal:  J Bacteriol       Date:  1995-08       Impact factor: 3.490

10.  Cloning and analysis of DNA sequences from Streptomyces hygroscopicus encoding geldanamycin biosynthesis.

Authors:  I W Allen; D A Ritchie
Journal:  Mol Gen Genet       Date:  1994-06-03
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