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. 2019 Jun 25;12(5):1003–1013. doi: 10.1111/1751-7915.13455

Figure 1.

Figure 1

A. Genetic origins of PRox promoters. Top panel: PRox132 is part of the upstream genetic region of ddcA (light grey). It starts with the RoxR recognition element (Rox RE), the regulatory regions (−35 and −10) and a ribosome binding site (RBS), which is located in the 5′ untranslated region (white). Bottom panel: PRox306 consists of the whole intergenic region between P. putida KT2440 genes PP_3332 and PP_3331.

B. DNA sequences of PRox132, PRox306 and PRox3061. The −35 and −10 regions predicted by BPROM (Solovyev and Salamov, 2011) are depicted in bold. Experimentally determined transcriptional start sites are marked with + 1. In PRox3061, the −10 region was mutated to the consensus sequence of the major σ‐factor of the σ70 family, TATAAT. The initiation codon of the regulated gene is underlined. The sequence of the Rox RE is shaded, the putative RBS sequence depicted in italics.