Abstract
The pol gene from a biologically active clone of the human T-cell lymphotropic virus type III provirus was inserted into a bacterial expression vector. The resulting gene fusion induced the formation of active reverse transcriptase that could be readily detected in extracts of bacterial cells. The activity exhibited the template and divalent cation requirements of the authentic enzyme. These constructs will be useful for safe and rapid analysis of potential inhibitors of this important enzyme.
MeSH Terms
DNA, Recombinant
Deltaretrovirus/enzymology,genetics
Escherichia coli/enzymology,genetics
Genes, Viral
Magnesium/pharmacology
Manganese/pharmacology
Oligodeoxyribonucleotides/metabolism
Poly A/metabolism
Poly C/metabolism
RNA-Directed DNA Polymerase/biosynthesis,genetics,metabolism
Chemicals
DNA, Recombinant
Oligodeoxyribonucleotides
poly (rC).oligo (dG)
Poly A
Poly C
Manganese
poly(rA).oligo(dT)
RNA-Directed DNA Polymerase
Magnesium
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Tanese N
Sodroski J
Haseltine W A
Goff S P
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