Dingermann, Theodor Sharp, Stephen Appel, Bernd DeFranco, Donald Mount, Stephen Heiermann, Reinhard Pongs, Olaf Söll, Dieter
We describe the preparation of a cell-free extract from Drosophila Kc cells which allows transcription of a variety of cloned eukaryotic RNA polymerase III genes. The extract has low RNA-processing nuclease activity and thus the major products obtained are primary transcripts.
The nucleotide sequence of the promoter region and the first five genes of the atp (or unc) operon of Escherichia coli has been determined. The first proposed gene in the operon contains four AUA codons and may be poorly expressed; it encodes a basic but yet hydrophobic protein which could function as a pilot protein for assembly of ATP-synthase. T...
The nucleotide sequence of the promoter region and the first five genes of the atp (or unc) operon of Escherichia coli has been determined. The first proposed gene in the operon contains four AUA codons and may be poorly expressed; it encodes a basic but yet hydrophobic protein which could function as a pilot protein for assembly of ATP-synthase. T...
Gay, Nicholas J. Walker, John E.
The nucleotide sequence of the promoter region and the first five genes of the atp (or unc) operon of Escherichia coli has been determined. The first proposed gene in the operon contains four AUA codons and may be poorly expressed; it encodes a basic but yet hydrophobic protein which could function as a pilot protein for assembly of ATP-synthase. T...
Nicholas J. Gay John E. Walker
The nucleotide sequence of the promoter region and the first five genes of the atp (or unc) operon of Escherichia coli has been determined. The first proposed gene in the operon contains four AUA codons and may be poorly expressed; it encodes a basic but yet hydrophobic protein which could function as a pilot protein for assembly of ATP-synthase. T...
Theodor Dingermann Stephen Sharp Bernd Appel Donald DeFranco Stephen Mount Reinhard Heiermann Olaf Pongs Dieter Söll
We describe the preparation of a cell-free extract from Drosophila Kc cells which allows transcription of a variety of cloned eukaryotic RNA polymerase III genes. The extract has low RNA-processing nuclease activity and thus the major products obtained are primary transcripts.
Theodor Dingermann Stephen Sharp Bernd Appel Donald DeFranco Stephen Mount Reinhard Heiermann Olaf Pongs Dieter Söll
We describe the preparation of a cell-free extract from Drosophila Kc cells which allows transcription of a variety of cloned eukaryotic RNA polymerase III genes. The extract has low RNA-processing nuclease activity and thus the major products obtained are primary transcripts.
Theodor Dingermann Stephen Sharp Bernd Appel Donald DeFranco Stephen Mount Reinhard Heiermann Olaf Pongs Dieter Söll
We describe the preparation of a cell-free extract from Drosophila Kc cells which allows transcription of a variety of cloned eukaryotic RNA polymerase III genes. The extract has low RNA-processing nuclease activity and thus the major products obtained are primary transcripts.
Christiane Branlant Alain Krol Mohamed Ali Machatt Jean Pouyet Jean-Pierre Ebel Kaylene Edwards Hans Kössel
We determined 90% of the primary structure of E.coli MRE 600 23S rRNA by applying the sequencing gel technique to products of T1, S1, A and Naja oxiana nuclease digestion. Eight cistron heterogeneities were detected, as well as 16 differences with the published sequence of a 23S rRNA gene of an E.coli K12 strain. The positions of 13 post-transcript...
Christiane Branlant Alain Krol Mohamed Ali Machatt Jean Pouyet Jean-Pierre Ebel Kaylene Edwards Hans Kössel
We determined 90% of the primary structure of E.coli MRE 600 23S rRNA by applying the sequencing gel technique to products of T1, S1, A and Naja oxiana nuclease digestion. Eight cistron heterogeneities were detected, as well as 16 differences with the published sequence of a 23S rRNA gene of an E.coli K12 strain. The positions of 13 post-transcript...