Minimal pBAD + I13500 GFP
This part contains pBAD promoter and a GFP reporter which is activated by AraC in presence of L-arabinose. pBAD promoter is derived from the L-arabinose operon from Escherichia coli. This version of pBAD retains all binding sites for the regulatory protein AraC, but lacks the full araC coding region. Potential "araC" start codon has been mutated from ATG to AGT.
This promoter gives 2000x fold induction when on pSB1C3 backbone, or x300 fold induction when on low copy number plasmid pSB3k3 when used with BioBrick BBa_K2442104 in a strain lacking AraC.
This part belongs to a collection of parts made by Team Glasgow 2017:
- BBa_K2442101: minimal pBAD promoter
- BBa_K2442102: reporter plasmid - minimal pBAD promoter + GFP
- BBa_K2442103: araC coding sequence
- BBa_K2442104: regulatory plasmid - araC coding sequence under control of LacI-regulated promoter
Usage and Biology
The L-arabinose operon is naturally found in Escherichia coli. The regulatory protein, AraC, acts as a dimer. The operon contains two regulatory cis elements: the PC promoter for the synthesis of AraC, and the pBAD promoter for synthesis of enzymes required for catabolism of L-arabinose. pBAD promoter contains 3 half sites that each bind to one subunit of AraC - O2, I1, I2. The O1 site is composed of O1L and O1R half sites, which bind both subunits. The O2 half site is within the araC coding region.
To improve BBa_I0500, we split the araC and pBAD into two separate parts. We isolated the minimal DNA sequence from the native pBAD that is sufficient to retain its function. The promoter retains all the operator sites O1, O2, I1 and I2 required for binding of AraC (Fig. 1). As some of these sites lie within the PC promoter and overlap with AraC coding sequence, the minimal pBAD has the araC start codon ATG mutated to AGT to prevent the protein from being made.
In absence of L-arabinose the AraC dimer binds to operator half-sites O2 and I1. This causes DNA looping upstream of the pBAD promoter which represses transcription by excluding RNA polymerase from binding to pBAD or PC. Binding of L-arabinose causes a conformational change in the protein such that the DNA-binding domains of the dimer bind to adjacent I1 and I2 half-sites, giving access for RNA polymerase and cyclic AMP receptor protein (CRP) to bind pBAD. In this case, this results in production of GFP.
The aim of our project was to mutagenize 4 residues within the AraC ligand-binding pocket to generate mutants with altered effector specificity. To allow mutant screening we transformed araC-negative E. coli strain, DH5α, with regulatory plasmid carrying the araC mutant library and reporter plasmid BBa_K2442102. Mutants were tested for responsiveness to xylose, decanal, arabinose and no inducer based on fluorescence.
pBAD promoter can be placed upstream of any gene of choice to construct arabinose -inducible systems. Moreover, our protocol for AraC mutagenesis can be followed to generate biosensors responsive to any other small molecule of interest, with BBa_K2442102 serving the role of reporter in mutant screens and detection systems. We generated 4 mutants which deviate in behaviour from wild-type araC: BBa_K2442105, BBa_K2442106, BBa_K2442107 and BBa_K2442108. Visit our wiki for details.
First of all, to test for the functionality of pBAD promoter we transformed BBa_K2442102 into E. coli strain DH5α. DH5α possesses a functional copy of arac on its chromosome. Transformants were restreaked onto LB agar with 0.2% arabinose, and 0.5% glucose as control (Fig. 2). 13 out of 14 picked transformants exhibited fluorescence under +arabinose conditions, and none of the colonies showed fluorescence under +glucose conditions. We therefore concluded that minimal pBAD is fully functional and is only induced in the presence of L-arabinose. Chromosomal copy of ‘’araC’’ showed to be sufficient to induce expression of GFP.
We then tested the part in presence of arabinose, xylose, decanal and no inducer (Fig. 3), as these were the compounds we used in mutant screening. Empty DH5α cells served as control for basal level of fluorescence. Supporting result obtained in previous experiment (Fig. 2), DH5α cells carrying BBa_K2442102 showed 2000x fold increase in fluorescence in presence of arabinose, but no significant increase in fluorescence on other sugars.
DH5α cells carrying minimal pBAD and I13500 on a low copy number plasmid pSB3K3 instead of pSB1C3 also showed expression of GFP only under arabinose conditions. However, levels of fluorescence were much lower, suggesting that the level of GFP production is dependent on the plasmid copy number and must be taken into account in further experiments.
We then transformed BBa_K2442102 into E. coli strain DS941, which does not possess a functional copy of araC on its chromosome. Empty DS941 cells served as control for basal level of fluorescence. Transformed cells showed no increase in fluorescence. This showed that AraC is necessary for activation of pBAD.
Next, we transformed DS941 cells with minimal pBAD+GFP in pSB3k3 and our regulatory plasmid encoding for AraC - BBa_K2442104 (pSB1C3). Increase in fluorescence was comparable to DH5α carrying minimal pBAD+GFP in pSB3k3 only. This shows that AraC expressed from BBa_K2442104 plasmid is sufficient to activate pBAD. Expressing AraC from a high copy number plasmid (pSB1C3) versus from a single chromosomal copy does not increase GFP expression.
Overall, we conclude that both L-arabinose and AraC are necessary to activate pBAD. pBAD promoter shows no leakage. 2000x fold increase in fluorescence of DH5α cells carrying BBa_K2442102 on arabinose shows high efficiency of pBAD and proves improvement over BBa_I0500
Sequence and Features
- 10COMPATIBLE WITH RFC
- 12COMPATIBLE WITH RFC
- 21Illegal BamHI site found at 241
- 23COMPATIBLE WITH RFC
- 25Illegal AgeI site found at 76
- 1000Illegal BsaI.rc site found at 973