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pLSE4
pLSE4
規(guī)格:
貨期:
編號(hào):B200708
品牌:Mingzhoubio

標(biāo)準(zhǔn)菌株
定量菌液
DNA
RNA

規(guī)格:
凍干粉
斜面
甘油
平板


產(chǎn)品名稱 pLSE4
商品貨號(hào) B200708
Designations pLSE4
Depositors J Garcia
Biosafety Level 1
Vector Information
Construct size (kb): 6.60
Vector: pLSE4 (plasmid)
Construction: pLSE1, pGL103
Marker(s): eryR,tetR

Features:
insert detection:
lytA
marker(s): tetR, eryR
replicon: rep
Applications
Contains sequence N-acetyl-muramyl-L-alanine amidase (autolysin)
Promoter-cloning vector
Shuttle vector
Comments
The sequence surrounding the polylinker is known so that inserts can be sequenced directly.
pLS1 and its derivatives can replicate in Streptococcus pneumoniae, S. oralis, Bacillus subtilis, and E. coli.
Contains the complete coding sequence for lytA. The 3' HindIII site is approximately 50 bp beyond the termination codon.
The polylinker sites are upstream of the promoter-less lytA gene. There are stop codons in all 3 reading frames between the cloning sites and the initiation codon.
The ScaI and EcoRV sites interrupt the tetracycline resistance gene.
A HindIII fragment containing polylinker sequences from pUC19 and an XbaI/HindIII fragment containing the promoterless gene was cloned into the HindIII site of pLES1. The XbaI site was created 18 bp upstream of the initiation codon.
Media ATCC® Medium 1273: LB medium (ATCC medium 1065) with 20 mcg/ml tetracycline
Growth Conditions
Temperature: 37°C
References

Diaz E, Garcia JL. Construction of a broad-host-range pneumococcal promoter-probe plasmid. Gene 90: 163-167, 1990. PubMed: 1974231

Ronda C, et al. Characterization of genetic transformation in Streptococcus oralis NCTC 11427: expression of the pneumococcal amidase in S. oralis using a new shuttle vector. Mol. Gen. Genet. 215: 53-57, 1988. PubMed: 3241622

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