Literature DB >> 6948998

Excision of chromosomal DNA sequences from Streptomyces coelicolor forms a novel family of plasmids detectable in Streptomyces lividans.

M J Bibb, J M Ward, T Kieser, S N Cohen, D A Hopwood.   

Abstract

When strains of Streptomyces coelicolor A3(2) lacking the previously identified autonomous plasmids SCP1 and SCP2 are crossed with Streptomyces lividans 66, some of the S. lividans progeny are able to elicit zones of growth inhibition (lethal zygosis), previously associated with the transfer of conjugative Streptomyces plasmids, when grown in contact with S. lividans 66. Some such progeny yield covalently closed circular (CCC) plasmid DNA, the size and restriction endonuclease cleavage pattern of which is constant for a particular isolate, but varies among isolates. These plasmids, which have been named SLP1.1, SLP1.2, etc., all confer resistance to lethal zygosis elicited by the others. Genetic and molecular characterization of the plasmids reveals that they are derived from the strA region of the chromosome of S. coelicolor. It is proposed that, before or during mating with S. lividans, the SLP1 sequences are excised from the chromosome, bringing varying regions of the surrounding chromosome with them, and can circularize to yield the SLP1 family of plasmids. Autonomous SLP1 plasmids can also be generate by cleaving total DNA of S. coelicolor with certain restriction enzymes, ligating it, and transforming the DNA into S. lividans. The autonomous SLP1 plasmids exist within S. lividans in a few copies per chromosome, and act as fertility factors. They provide suitable vectors for DNA cloning since the segments of chromosomal DNA carried by the larger members of the family are dispensable.

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Year:  1981        PMID: 6948998     DOI: 10.1007/bf00272910

Source DB:  PubMed          Journal:  Mol Gen Genet        ISSN: 0026-8925


  24 in total

1.  Isolation of covalently closed circular deoxyribonucleic acid from Streptomyces coelicolor A3(2).

Authors:  H Schrempf; H Bujard; D A Hopwood; W Goebel
Journal:  J Bacteriol       Date:  1975-02       Impact factor: 3.490

2.  Plasmid-determined antibiotic synthesis and resistance in Streptomyces coelicolor.

Authors:  R Kirby; L F Wright; D A Hopwood
Journal:  Nature       Date:  1975-03-20       Impact factor: 49.962

Review 3.  Extrachromosomally determined antibiotic production.

Authors:  D A Hopwood
Journal:  Annu Rev Microbiol       Date:  1978       Impact factor: 15.500

Review 4.  Genetics of antibiotic production by actinomycetes.

Authors:  D A Hopwood
Journal:  J Nat Prod       Date:  1979 Nov-Dec       Impact factor: 4.050

5.  Isolation and characterization of plasmids from Streptomyces.

Authors:  T Hayakawa; N Otake; H Yonehara; T Tanaka; K Sakaguchi
Journal:  J Antibiot (Tokyo)       Date:  1979-12       Impact factor: 2.649

6.  DNA cloning in Streptomyces: resistance genes from antibiotic-producing species.

Authors:  C J Thompson; J M Ward; D A Hopwood
Journal:  Nature       Date:  1980-07-31       Impact factor: 49.962

7.  Transformation of plasmid DNA into Streptomyces at high frequency.

Authors:  M J Bibb; J M Ward; D A Hopwood
Journal:  Nature       Date:  1978-07-27       Impact factor: 49.962

8.  A DNA cloning system for interspecies gene transfer in antibiotic-producing Streptomyces.

Authors:  M Bibb; J L Schottel; S N Cohen
Journal:  Nature       Date:  1980-04-10       Impact factor: 49.962

9.  TYROSINASE INHERITANCE IN STREPTOMYCES SCABIES. I. GENETIC RECOMBINATION.

Authors:  K F GREGORY; J C HUANG
Journal:  J Bacteriol       Date:  1964-06       Impact factor: 3.490

10.  TYROSINASE INHERITANCE IN STREPTOMYCES SCABIES. II. INDUCTION OF TYROSINASE DEFICIENCY BY ACRIDINE DYES.

Authors:  K F GREGORY; J C HUANG
Journal:  J Bacteriol       Date:  1964-06       Impact factor: 3.490

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  45 in total

Review 1.  Conjugative plasmid transfer in gram-positive bacteria.

Authors:  Elisabeth Grohmann; Günther Muth; Manuel Espinosa
Journal:  Microbiol Mol Biol Rev       Date:  2003-06       Impact factor: 11.056

2.  Genetic instability in Streptomyces niveus plasmid pSN2: in vivo formation of deletion derivatives.

Authors:  H A Hussain; J I Mitchell; D A Ritchie
Journal:  Arch Microbiol       Date:  1990       Impact factor: 2.552

3.  Site-specific integration and excision of pMEA100 in Nocardia mediterranei.

Authors:  J Madon; P Moretti; R Hütter
Journal:  Mol Gen Genet       Date:  1987-09

4.  Characterization of the replication, transfer, and plasmid/lytic phage cycle of the Streptomyces plasmid-phage pZL12.

Authors:  Li Zhong; Qiuxiang Cheng; Xinli Tian; Liqian Zhao; Zhongjun Qin
Journal:  J Bacteriol       Date:  2010-05-14       Impact factor: 3.490

5.  Characterization of an 8.7-kilobase thiostrepton resistance-encoding plasmid (pGIF3) of Streptomyces incarnatus.

Authors:  H Malina; M Robert-Gero
Journal:  Appl Environ Microbiol       Date:  1992-03       Impact factor: 4.792

6.  Characterization of replication and conjugation of Streptomyces circular plasmids pFP1 and pFP11 and their ability to propagate in linear mode with artificially attached telomeres.

Authors:  Ran Zhang; Ana Zeng; Ping Fang; Zhongjun Qin
Journal:  Appl Environ Microbiol       Date:  2008-04-04       Impact factor: 4.792

7.  Identification and functional analysis of the transfer region of plasmid pMEA300 of the methylotrophic actinomycete Amycolatopsis methanolica.

Authors:  J W Vrijbloed; N M van der Put; L Dijkhuizen
Journal:  J Bacteriol       Date:  1995-11       Impact factor: 3.490

Review 8.  Streptomyces cloning: useful recombinant DNA systems and a summation of cloned genes.

Authors:  P K Tomich
Journal:  Antimicrob Agents Chemother       Date:  1988-10       Impact factor: 5.191

9.  Mercury resistance is encoded by transferable giant linear plasmids in two chesapeake bay Streptomyces strains.

Authors:  J Ravel; H Schrempf; R T Hill
Journal:  Appl Environ Microbiol       Date:  1998-09       Impact factor: 4.792

10.  The very large amplifiable element AUD2 from Streptomyces lividans 66 has insertion sequence-like repeats at its ends.

Authors:  C Eichenseer; J Altenbuchner
Journal:  J Bacteriol       Date:  1994-11       Impact factor: 3.490

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