Cloning of an E. coli ribosomal RNA gene and its promoter region from $\text{λrif}{}^{\mathrm{<mtext>d</mtext>}}\text{18}$

Abstract

The DNA of the specialized transducing phage $\text{λrif}{}^{\mathrm{<mtext>d</mtext>}}\text{18}$, which carries a bacterial rRNA transcription unit, was digested with restriction enzymes EcoRI and/or BamHI. Attempts were made to clone fragments containing the presumed rRNA promoter region or the entire rRNA gene in RSF2124 or pBR313 plasmid vectors with the following results:

• (1) We failed to clone an EcoRI fragment with the rRNA promoter region in plasmid RSF2124.

• (2) A smaller EcoRI-BamHI fragment with the rRNA promoter was also unclonable by itself, but one recombinant was found containing this fragment together with another large (7 Mdaltons) fragment, derived from phage λ. The presence of this large fragment proved to be essential. The identity of these DNA fragments in the recombinant clone was confirmed by redigestion with several restriction enzymes, hybridization with rRNA, and in vitro transcription experiments, which showed preferential rRNA transcription.

• (3) A BamHI fragment encompassing the entire rRNA gene was easily cloned. Such stable clones carried a doubled number of rRNA genes. In vitro transcription using the recombinant plasmid resulted in 70% rRNA transcription.

These recombinant clones allow the easy purification of the relevant DNA fragments for further investigation including sequencing.