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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
1985-10-25
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pubmed:abstractText |
A pBR322-derived expression vector, plasmid pKD1, was constructed containing the strong leftward promoter (pL) of bacteriophage lambda, the ribosome-binding site (RBS) of the cII gene of lambda, and a unique downstream NdeI restriction site for construction of an ATG initiation codon. The section of the pol gene of Moloney murine leukemia virus (M-MLV) that codes for reverse transcriptase (RT) was cloned into the NdeI site of this vector generating the plasmid pRT103. Upon thermal induction, enzymatically active RT was expressed in Escherichia coli [pRT103]. The identity of this activity was confirmed by its template specificity and its sensitivity to inhibition by immunoglobulin G (IgG) prepared against authentic murine RT. RT represented 20% of the newly synthesized protein in these cells 20 min after induction.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:issn |
0378-1119
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
35
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
249-58
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pubmed:dateRevised |
2001-11-2
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pubmed:meshHeading |
pubmed-meshheading:2412939-Bacteriophage lambda,
pubmed-meshheading:2412939-Cloning, Molecular,
pubmed-meshheading:2412939-DNA, Recombinant,
pubmed-meshheading:2412939-Escherichia coli,
pubmed-meshheading:2412939-Gene Expression Regulation,
pubmed-meshheading:2412939-Molecular Weight,
pubmed-meshheading:2412939-Moloney murine leukemia virus,
pubmed-meshheading:2412939-Protein Conformation,
pubmed-meshheading:2412939-RNA-Directed DNA Polymerase
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pubmed:year |
1985
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pubmed:articleTitle |
Cloning and overexpression of Moloney murine leukemia virus reverse transcriptase in Escherichia coli.
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pubmed:publicationType |
Journal Article
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