Abstract
Two DNA fragments prepared from the transducing bacteriophage strains ø80psuIII+ and ø80hpsuIII+,- by digestion with restriction enzymes contain one tyrosine tRNA gene (suIII+) and two tyrosine tRNA genes (suIII+, su-) in tandem, respectively, a single promoter in both cases, and some additional DNA regions at the two ends of both. Using these fragments, we have studied characteristics of the promoter-dependent transcription of the tyrosine tRNA genes. The promoter-dependent transcripts were shown to correspond to the expected tRNA precursors. Exposure of the transcript from the single gene fragment to an S100 extract from Escherichia coli gave, via intermediates, 4S material which was active in enzymatically accepting tyrosine and contained some modified bases.
MeSH Terms
Adenosine Triphosphate/pharmacology
Base Sequence
Cytosine Nucleotides/pharmacology
DNA Restriction Enzymes/metabolism
DNA, Bacterial/metabolism
Endonucleases/metabolism
Escherichia coli/metabolism
Genes
Guanosine Triphosphate/pharmacology
Heparin/pharmacology
Oligonucleotides/pharmacology
RNA Nucleotidyltransferases/metabolism
RNA, Transfer/metabolism
Rifampin/pharmacology
Transcription, Genetic/drug effects
Tyrosine
Chemicals
Cytosine Nucleotides
DNA, Bacterial
Oligonucleotides
Tyrosine
Guanosine Triphosphate
Adenosine Triphosphate
Heparin
RNA, Transfer
RNA Nucleotidyltransferases
Endonucleases
DNA Restriction Enzymes
Rifampin
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Küpper H
Contreras R
Landy A
Khorana H G
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