Difference between revisions of "PMAD"

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'''General comments'''
 
'''General comments'''
  
A [[plasmid]] for the generating of gene inactivation mutants in
+
This site is under construction
naturally nontransformable gram-positive bacteria. This vector allows, on X-Gal (5-bromo-4-chloro-3-indolyl-
+
 
beta-D-galactopyranoside) plates, a quick colorimetric blue-white discrimination of bacteria which have lost the
+
A [[plasmid]] for generating gene inactivation mutants in naturally nontransformable gram-positive bacteria.  
plasmid, facilitating clone identification during mutagenesis. The plasmid is can be used in Staphylococcus
+
This vector allows, on X-Gal (5-bromo-4-chloro-3-indolyl-beta-D-galactopyranoside) plates, a quick colorimetric blue-white discrimination of bacteria which have lost the plasmid, facilitating clone identification during mutagenesis.  
aureus, Listeria monocytogenes, and Bacillus spp. to efficiently construct mutants with or without an associated
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The plasmid is can be used in Staphylococcus aureus, Listeria monocytogenes, and Bacillus spp. to efficiently construct mutants with or without an associated
 
antibiotic resistance gene.
 
antibiotic resistance gene.
  
 
* ''E.coli'': multicopy plasmid, select for ampicillin
 
* ''E.coli'': multicopy plasmid, select for ampicillin
* ''B. subtilis'': temperature sensitive ori, select for erythromycin/ lincomycin
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* ''B. subtilis'': temperature-sensitive ori, select for erythromycin/ lincomycin
  
 
'''Hints for the usage'''
 
'''Hints for the usage'''

Revision as of 08:25, 28 August 2012

pMAD: click to enlarge

General comments

This site is under construction

A plasmid for generating gene inactivation mutants in naturally nontransformable gram-positive bacteria. This vector allows, on X-Gal (5-bromo-4-chloro-3-indolyl-beta-D-galactopyranoside) plates, a quick colorimetric blue-white discrimination of bacteria which have lost the plasmid, facilitating clone identification during mutagenesis. The plasmid is can be used in Staphylococcus aureus, Listeria monocytogenes, and Bacillus spp. to efficiently construct mutants with or without an associated antibiotic resistance gene.

  • E.coli: multicopy plasmid, select for ampicillin
  • B. subtilis: temperature-sensitive ori, select for erythromycin/ lincomycin

Hints for the usage

  • for a markerless deletion of a gene amplify 1000 bp up- and downstream of the gene and clone them into the MCS of the plasmid

The reference

Maryvonne Arnaud, Arnaud Chastanet, Michel Débarbouillé
New vector for efficient allelic replacement in naturally nontransformable, low-GC-content, gram-positive bacteria.
Appl. Environ. Microbiol.: 2004, 70(11);6887-91
[PubMed:15528558] [WorldCat.org] [DOI] (P p)