Revision as of 19:40, 29 August 2015

Phosphate Sensor

Introduction

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Phosphate sensor Design

phoBRp promoter is cross-regulated by phoB and phoR. phoR behaves as an activator as well as an inactivator for phoB. When phosphate is limited, phoR will phosphorylate phoB and the phosphorylated phoB will directly activate the expression of phoBRp promoter. In contrast, when there is phosphate, phoR will repress phoB phosphorylation which in turns inactivates phoBRp promoter. For the constructs design, we have ligated GFP generator to the phoBRp promoter. As a result, under high phosphate concentration, the green fluorescence intensity will be repressed, while under low phosphate concentration, the situation will be vice versa.

Experiment that we did

We have done a characterization on pSB1C3-phoBRp-BBa_I13504 using Luria Broth (LB) medium. Quantitative characterization on the promoter was done by measuring the fluorescence signal intensity using an EnVision multilabel reader.

E. coli strain DH10B was used, and the concentration of the characterization of phoBRp promoter was from 0 to 300 µM phosphate, with an intervals of 50µM.

Preparing test medium with different concentration of phosphate

We have prepared a solution of M9 minimal medium (J. Sambrook & D.W. Russell, 2001) and a solution of M9 minimal medium with Tris replacing phosphate. Test medium with different concentration of phosphate (0, 10, 30, 50, 100, 150, 200, 250, 300 µM) were made by mixing the 2 solution in the following ratio.

Final Phosphate concentration (μM)	M9 minimal medium added (μl)	M9 minimal medium without phosphate (replaced by Tris) added (ml)	150 ng/μl Chloramphenicol Antibiotics added (μl)
0	0.00	60	60
10	8.58	60	60
30	25.73	60	60
50	42.85	60	60
100	85.71	60	60
150	130.43	60	60
200	171.42	60	60
250	216.26	60	60
300	260.87	60	60

phoBRp promoter Characterization

pSB1C3-phoBRp-BBa_I13504, positive control and negative control were first grown overnight in 5 ml Luria Broth (LB) medium containing chloramphenicol at 37^oC. The bacteria were then washed twice with 3 ml M9 minimal medium without phosphate (replaced by Tris), containing Ampicillin. Then, the cells were resuspended in 5ml M9 minimal medium without phosphate(replaced by Tris) to obtain a final OD₆₀₀ of 4.50 μl of the prepared cell suspension were then added into 950μl of test medium with different concentrations of phosphate (containing Chloramphenicol) in the 96-well deep well plate and further incubate at 37^oC until the OD₆₀₀ of the cells reaches the mid-log phase. The fluorescence output were then measured using EnVision multilabel reader.

This result was obtained by combining 3 characterization trials.

Result obtained

Lorem ipsum dolor sit amet, pro aeque temporibus eu, eum qualisque assueverit te. Ad est admodum epicuri suscipit, te alterum aliquando adversarium usu, pro ex omnesque luptatum comprehensam. In vix alia percipit gloriatur, no ferri lorem aliquando cum. Fugit concludaturque sed ne, ea sumo dico adolescens eos, quo eu pertinax expetendis. An his omnes instructior, vide possim eam id. Te cum enim sale offendit, vocent copiosae luptatum ut per. Eam in alienum accusamus, et probo reque vix. Vivendum necessitatibus qui ad, no vis enim veniam perpetua. Eu pri habemus senserit, dicit tation expetenda usu et. Sea eu dolor deserunt dissentias, sed an oportere moderatius assueverit. Usu te tation gloriatur, vidit tollit utinam mea id.