Part:BBa_K808032

Arabinose regulated RBS-PhoA-His6tag-pNBEst13-Myctag-EstA

This is a composite of 2 different BioBricks formed by a standard assembly, forming a scar in between. It contains the following units: AraC-AraO2-AraO1-AraPromo(PBAD-RBS-PhoA-His6tag-pNBEst13-Myctag-EstA which is similiar to BBa_K808000 & BBa_K808030 It is an operon, being induced by adding 0.02% to 0.5% of L-Arabinose. It is made for regulating the cell surface expression of our PET cleaving enzyme pNB-Est13, which is anchored C-terminal to EstA.

Usage and Biology

This site is about the expression rate of BBa_K808032 and its activity in three different E.coli strains:

[http://ecoliwiki.net/colipedia/index.php/TOP10 Top10]
[http://ecoliwiki.net/colipedia/index.php/DH5_alpha DH5alpha]
[http://ecoliwiki.net/colipedia/index.php/MG1655 Mg1655]

To get a more information about our composite part BBa_K808030 please take a look at its own registry page.

Our part BBa_K808032 regulates the expression of a chimeric protein (BBa_K808030) consisting of the following parts:

PhoA signal sequence (BBa_K808028), which leads to periplasmatic expression.
pNB-Est13 (BBa_K808026) is an enzyme that is able to hydrolyse PET
EstA (BBa_K808027) is used as a C-terminal membrane anchor, being able to express even large enzymes on the bacterial surface

Functionality

The functionality of BBa_K808032 is shown by the following methods:

SDS PAGE
Western blot
flow cytometry (after antibody staining)
screening for hydrolysis by bacterial colonies using Tributyrin agar plates
pNP-Assay with living cells using para-Nitrophenylbutyrate

SDS PAGE

Of course the first step for showing any kind of functionality is to perform a [http://2012.igem.org/Team:TU_Darmstadt/Protocols/SDS-Page SDS PAGE](Figure 1). E.coli Top10 is transformed with BBa-K808032 and induced at an OD₆₀₀=0.5 with the arabinose concentrations of 0.02%, 0.2%, 0.5% and no arabinose at all (serving as a negative control). Incubation occured at 30°C over night. Afterwards the expressed chimeric protein gets [http://2012.igem.org/Team:TU_Darmstadt/Protocols/Proteinpurification purified]. The resulting supernatant is loaded but the cell debris pellet is treated with an special detergent (n-Dodecyl β-D-maltoside) ,in order to solve our membrane bound protein, and is loaded as well. We were able to express our protein and to spot it on our SDS PAGE (Figure 1), where as our neagtive control showed no expression.

Figure 1: Expression level of BBa_K808032 in relation to the level of induction. Arabinose concentration (used for induction) decreases from left to right, starting with 0.5% and ending with no arabinose at all. Lane 3, 5 ,7 (pellet treated with detergent) show that our protein gets expressed whereas our negative control in lane 9 remains unexpressed

Western blot

To be sure that our protein is expressed we performed a [http://2012.igem.org/Team:TU_Darmstadt/Protocols/Western_Blot Western blot] (Figure 2). Our construct contains a myc epitope, downstream of pNB-Est13. This myc tag is used for detecting whether our surface expression is successful or not. The expression host is E.coli DH5 alpha, transformed with BBa_K808032, and induced at a OD₆₀₀=0.6 after being incubated for 20 min on ice with arabinose concentrations of 1.5%, 1% and 0.5%. The incubation on ice and the higher arabinose concentrations are crucial for using other expression hosts than Top10, due to their ability to metabolize L-arabinose. The SDS PAGE was performed with supernatant and pellet being treated with a detergent (similiar to Figure 1).

Figure 2: Westernblot of BBa_K808032 expression. Induction level decreases from left to right, starting with 0.4& arabinose in lane 2 and ending with 0.1% arabinose in lane 6. Lane 3, 4 and slightly lane 6 show good results. The lanes showing positive resulst contain pellet treated with detergents. This proofs that our chimeric protein used to be integrated into the membrane. Our construct contains a myctag, which we were able to detect on our blot. Lane 3, 4 and slightly lane 6. Lane 8 is a myc positive probe and worked, too.

Flow Cytometry

Flow cytometry is good for quantifiying the rate of cell surface expression. Our construct contains a myc tag, allowing us to perform an [http://2012.igem.org/Team:TU_Darmstadt/Protocols/Antibody_staining antibody staining]. The second antibody is biotinylated and can be conjugated to streptavidin, being labeld with a fluorescent marker. We used Streptavidin, R-phycoerythrin conjugate (SAPE). Once the fluorescent labeled antibody has bound to the cell surface the relative absorbance can be measured and the marked cells can be detected by our flow cytometer (Accuri C6 flow cytometer). We transformed E.coli Top10 with BBa_K808032 and induced at an OD₆₀₀=0.5 with an arabinose concentration of 0.02%, 0.2%, 0.5% and no arabinose at all, serving as a negative control. The antibody staining was performed after 3 h of incubation at 30°C. The stained and marked cells were counted by our flow cytometer (Figure 3), showing us wether our expression worked (showing charactersic absorbance, so the antibody was able to bind to the surface expressed myctag) or not (negative probe shows different absorbance compared to induced cells).

Figure 3: E.coli Top10 carrying BBa_K808032 and induced at an OD₆₀₀=0.5 with an arabinose concentration of 0.02%, 0.2%, 0.5% and no arabinose at all. The relative absorbance of 50000 cells was meassured and is shown in this plot. The induced cells show a significant difference in their absorbance due to the binding of a fluorescent labeled antibody. Fot this [http://2012.igem.org/Team:TU_Darmstadt/Protocols/Antibody_staining antibody staining] we used an anti-myc antibody.

Tributyrin agar plates

[http://2012.igem.org/Team:TU_Darmstadt/Materials/LB_Tributyrin#About Tributyrin agar plates] are a common way to detect bacteria secreting hydrolases. Hydrolyis results in significant lysis areas around the respective colony.

We transfromed the E.coli strains [http://ecoliwiki.net/colipedia/index.php/TOP10 Top10], [http://ecoliwiki.net/colipedia/index.php/DH5_alpha DH5alpha] and [http://ecoliwiki.net/colipedia/index.php/MG1655 Mg1655] with BBa_K808032 and [http://2012.igem.org/Team:TU_Darmstadt/Protocols/Activity_assay inoculated] Tributyrin agar plates. The concentration of arabinose used for induction was around 0.5%. Incubation occured at 30°C over night.

Of course a longer incubation results in bigger lysis areas, the plate beneath was incubated one night at 30°C and 2 days at room temperature. It contains DH5 alpha, carrying BBa_K808032. Colony 6 only carries BBa_K808030. An arabinose concentration of around 0.2% was used for induction.

pNP-Assay

Using Tributyrin agar plates gave us a good qualitative proof of hydrolytic acivity, but an assay was needed to quantify the enzymatic activity of our induced cells. For this reason we performed a [http://2012.igem.org/Team:TU_Darmstadt/Protocols/pNP_Assay#pNP-Assay pNP-Assay] using our cells (Top10) with an OD₆₀₀=0.1-0.025 (suspended in PBS-buffer) as catalysts and para-Nitrophenylbutyrate as a substrate. We were able to quantify the relation of substrate degradation and induction. Please take a look at the graphs. For more information about our activity tests please take a look at our [http://2012.igem.org/Team:TU_Darmstadt/Labjournal/Degradation#Activity_tests_of_BBa_K808032 labjournal].

Sequence and Features

Assembly Compatibility:

10
COMPATIBLE WITH RFC[10]
12
COMPATIBLE WITH RFC[12]
21
INCOMPATIBLE WITH RFC[21]
Illegal BglII site found at 2392
Illegal BamHI site found at 1144
23
COMPATIBLE WITH RFC[23]
25
INCOMPATIBLE WITH RFC[25]
Illegal NgoMIV site found at 2918
Illegal NgoMIV site found at 3056
Illegal NgoMIV site found at 3596
Illegal NgoMIV site found at 3965
Illegal AgeI site found at 979
Illegal AgeI site found at 2463
1000
INCOMPATIBLE WITH RFC[1000]
Illegal SapI site found at 961