This webpage contains legacy information. The product is either no longer available from the supplier or has been delisted at Labome.
product summary
company name :
Addgene
product type :
cDNA
product name :
pCVD442
catalog :
11074
citations: 4
Reference
Rasheedkhan Regina V, Noorian P, Bo Wen C, Constancias F, Kaliyamoorthy E, Booth S, et al. Loss of the acetate switch in Vibrio vulnificus enhances predation defence against Tetrahymena pyriformis. Appl Environ Microbiol. 2021;:AEM0166521 pubmed publisher
Kochanowsky R, Bradshaw C, Forlastro I, Stock S. Xenorhabdus bovienii strain jolietti uses a type 6 secretion system to kill closely related Xenorhabdus strains. FEMS Microbiol Ecol. 2020;96: pubmed publisher
Gregg K, Harberts E, Gardner F, Pelletier M, Cayatte C, Yu L, et al. Rationally Designed TLR4 Ligands for Vaccine Adjuvant Discovery. MBio. 2017;8: pubmed publisher
Donnenberg M, Kaper J. Construction of an eae deletion mutant of enteropathogenic Escherichia coli by using a positive-selection suicide vector. Infect Immun. 1991;59:4310-7 pubmed
product information
Catalog Number :
11074
Product Name :
pCVD442
article :
doi
id470
pubmed_id1937792
bacterial resistance :
Ampicillin
cloning :
backbonepGP704
backbone_mutation
backbone_origin
backbone_size
promoter
sequencing_primer_3
sequencing_primer_5
vector_types
Bacterial Expression
growth notes :
This suicide vector was created to engineer mutations in host strains via allelic exchange. The important properties of this vector are: 1) a pir dependent origin of replication from plasmid R6K, 2) the bla gene encoding resistance to ampicillin, 3) the mob region allowing efficient transfer by conjugation from strains containing the tra locus, and 4) the sacB gene conferring sensitivity to sucrose in Gram-negative bacteria. Plasmid pCVD442 was created by cloning the sacB gene on a PstI fragment from plasmid pUM24 (Ried and Collmer. Gene 57:239-46, 1987) into plasmid pGP704 (Miller and Mekalanos. J.Bacteriol. 170:2575-83, 1988) that had been partially digested with PstI. Plasmid pCVD442 and its derivatives can only grow in strains that have the pir gene encoding the Pi protein, which is necessary for replication of R6K plasmids. The pir gene is usually supplied by a lambda lysogen. Such strains include DH5alpha-lambdapir, SY327-lambdapir, SM10-lambdapir, and S17-lambdapir. The last two strains supply the tra genes for efficient conjugation. Sucrose sensitivity is far from absolute. The strain carrying the plasmid grows well on sucrose plates. To detect sucrose sensitivity make serial dilutions of the bacteria and plate both on plates containing and lacking 5% sucrose. There should be substantially fewer colonies and the colonies are smaller on the sucrose plates.
growth temp :
Needs pir gene (see comments below)
inserts :
SY327 lambda pir
origin :
37
pi :
alt_names
cloning
clone_methodRestriction Enzyme
cloning_site_3PstI
cloning_site_5PstI
promoter
sequencing_primer_3
sequencing_primer_5na
site_3_destroyed
site_5_destroyed
entrez_gene
aliasesBSU_34450, BSU34450
genesacB
id936413
genbank_ids
mutation
namesacB
shRNA_sequence
size1400
species
Bacillus subtilis
tags
resistance markers :
119
2273
tags :
High Copy
company information
Addgene
490 Arsenal Way, Suite 100
Watertown, MA 02472
info@addgene.org
https://www.addgene.org
617.225.9000
headquarters: USA