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T7-LacO Promoter

Introduction

T7 Promoters are promoters that work with T7 RNA Polymerase. T7 RNA Polymerase is commonly used in biotechnology, as evidenced by the large number of parts found in the iGEM registry. T7 Polymerase has high affinity for its associated promoters and was identified as a useful tool for producing high amounts of RNA back in the 1980’s [1]. T7 Polymerase is also non-natively expressed in E. coli. Our team aimed to take advantage of this fact to decrease leaky expression, as explained in the figure below. If T7 polymerase is expressed inducibly under the control of a LacI promoter, and the protein of interest is transcribed under the control of an inducible T7 promoter, you are unlikely to get high amounts of “leaky” production of your protein of interest. This is because it would require two simultaneous “leaks” at two inducible promoters, rather than just one leak. Clearly, T7 Polymerase is a useful promoter to add to the synthetic biologist’s repertoire. Therefore, we were surprised to see there were no inducible T7 Promoters that were well-documented and verified to function in the registry. BBa_R0184,BBa_R0185,BBa_R0186, and BBa_R0187 were all supposed to be inducible T7 promoters, yet they had no functional verification. We sought to improve these parts by developing our own T7 promoter that could be induced.

Schematic showing how T7 RNA polymerase can be utilised to create a two-tiered induction system

Results

We designed our T7 promoter so that it could be induced by IPTG. Therefore, we simply ligated the Lac Operator sequence to the popular BBa_I712074 constitutive T7 promoter. Sequencing results (accessible by download and linked on this page) showed that we had successfully attached the T7-LacO promoter to our recombinase protein expression units, creating inducible expression generators (BBa_K2406080, BBa_K2406081, BBa_K2406082, BBa_K2406083, BBa_K2406084). We assayed the inducible activity of each recombinase generator. The image below shows the activity of Dre Recombinase protein. Focus on bars indicating Rox-Rox constructs (BBa_K2406051 part has more information on how this assay works), which were tested with and without IPTG. Essentially, RFP would be expressed and give off fluorescence when Dre recombinase expression was induced. Clearly, there is a significant difference between induced and non-induced control, demonstrating that our T7-LacO promoter works as would be desired.

Results of using Dre recombinase under control of our T7-LacO promoter

Discussion

There was some leakiness observed by the T7-LacO promoter. Comparing un-induced Rox-Rox construct to other controls that did not give RFP output with or without Dre recombinase, there is clearly significantly more RFP fluorescence in the un-induced Rox-Rox construct. This indicates some Dre recombinase being produced despite no induction occurring. As explained in the introduction, this could be minimised by using a strain of E. coli that does not constitutively express T7 RNA Polymerase, like we did, but instead by using a strain that requires an inducer to produce T7 RNA Polymerase. Furthermore, other teams could attempt to alter the sequence of our promoter, perhaps by decreasing affinity for T7 RNA polymerase, in an attempt to decrease the intrinsic leakiness of this promoter. However, we have clearly produced an inducible T7 promoter that functions, therefore improving parts BBa_R0184, BBa_R0185, BBa_R0186, and BBa_R0187, all of which had slightly different sequences and no evidence of functioning.

References

Milligan, J.F., Groebe, D.R., Witherell, G.W., and Uhlenbeck, O.C. 1987. “Oligoribonucleotide synthesis using T7 RNA polymerase and synthetic DNA templates”. Nucleic Acids Research 15 (21): 8783-8798

Sequences

Media:File:Sequencing Results Edinburgh UG.zip

Sequence and Features