Literature DB >> 34235658

Electroporation of Mycobacteria.

Tanya Parish1.   

Abstract

The introduction of DNA into bacterial cells is one of the foundational methods of bacterial genetics. Transformation of mycobacterial species is complicated due to the structure of the cell wall, which has a complex outer layer with low permeability. Electroporation has become a routine procedure in genetic studies. In this process, cells are subjected to a brief high-voltage electrical impulse which allows the entry of DNA. It can be used to introduce plasmid DNA, phage DNA, or oligonucleotides. This chapter presents methods for introducing DNA into a representative slow-growing species, M. tuberculosis, and a representative fast-growing species, M. smegmatis. Other mycobacteria can be transformed using variations of these methods, although the efficiency of transformation will vary.

Entities:  

Keywords:  Bacterial Genetics; DNA delivery; Electroporation; Mycobacteria; Plasmids

Year:  2021        PMID: 34235658     DOI: 10.1007/978-1-0716-1460-0_12

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  23 in total

Review 1.  Genetic systems for mycobacteria.

Authors:  W R Jacobs; G V Kalpana; J D Cirillo; L Pascopella; S B Snapper; R A Udani; W Jones; R G Barletta; B R Bloom
Journal:  Methods Enzymol       Date:  1991       Impact factor: 1.600

2.  Electroporation at elevated temperatures substantially improves transformation efficiency of slow-growing mycobacteria.

Authors:  B J Wards; D M Collins
Journal:  FEMS Microbiol Lett       Date:  1996-11-15       Impact factor: 2.742

3.  Transformation and transposition of the genome of Mycobacterium marinum.

Authors:  A M Talaat; M Trucksis
Journal:  Am J Vet Res       Date:  2000-02       Impact factor: 1.156

4.  Insertional mutagenesis and illegitimate recombination in mycobacteria.

Authors:  G V Kalpana; B R Bloom; W R Jacobs
Journal:  Proc Natl Acad Sci U S A       Date:  1991-06-15       Impact factor: 11.205

5.  Apramycin resistance as a selective marker for gene transfer in mycobacteria.

Authors:  E Paget; J Davies
Journal:  J Bacteriol       Date:  1996-11       Impact factor: 3.490

6.  Transformation of Mycobacterium aurum and Mycobacterium smegmatis with the broad host-range gram-negative cosmid vector pJRD215.

Authors:  J Hermans; C Martin; G N Huijberts; T Goosen; J A de Bont
Journal:  Mol Microbiol       Date:  1991-06       Impact factor: 3.501

7.  Transformation of mycobacterial species using hygromycin resistance as selectable marker.

Authors:  T R Garbe; J Barathi; S Barnini; Y Zhang; C Abou-Zeid; D Tang; R Mukherjee; D B Young
Journal:  Microbiology       Date:  1994-01       Impact factor: 2.777

8.  Construction and use of integrative vectors to express foreign genes in mycobacteria.

Authors:  O A Dellagostin; S Wall; E Norman; T O'Shaughnessy; J W Dale; J McFadden
Journal:  Mol Microbiol       Date:  1993-12       Impact factor: 3.501

9.  Analysis of the replication region of a mycobacterial plasmid, pMSC262.

Authors:  M Qin; H Taniguchi; Y Mizuguchi
Journal:  J Bacteriol       Date:  1994-01       Impact factor: 3.490

10.  Isolation and sequencing of the replication region of Mycobacterium avium plasmid pLR7.

Authors:  M L Beggs; J T Crawford; K D Eisenach
Journal:  J Bacteriol       Date:  1995-09       Impact factor: 3.490

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