Part:BBa_K658005

a bacteria population-control device with RBS0.07 driven by lacl+pL

It is designed to build a programmed bacterial death circuit, which is based on the quorum sensing system of Vibrio fischeri. iGEM-Team XMU-China has designed a series of bacteria population-control devices using RBSs of different strength in the killer protein producer. This device has the ability to maintain cell density of the bacteria population at a relatively low value compared with bacteria without this circuit and extends the steady state. RBS0.07 (BBa_B0031) was used to regulate the expression of killer protein ccdB.

Figure 1. Animation of proposed reaction mechanism of iccdB0.07.

Description

This device is made up of three subparts: a LuxI producer, a LuxR producer and a killer protein producer. The LuxI protein synthesizes a small, diffusible acyl-homoserinelactone (AHL) signaling molecule. The AHL accumulates as the cell density increases. At sufficiently high concentrations, it binds the LuxR, which induces the expression of the killer gene ccdB under the control of a promoter lux pR. Sufficiently high levels of CcdB which is a bacterial toxin that targets DNA gyrase cause cell death. Low cell density doesn’t have the ability to produce sufficient LuxR/AHL complex to activate the promoter lux pR. The programmed death circuit ends and the cell density increases. When the cells reach a certain concentration, the death circuit is restarted. Back and forth, the programmed death is achieved in the dynamic process of growth and death. In that way, the bacteria population is programmed to maintain one certain cell density.

Performance

In order to test the performance of the bacteria population-control device iccdB0.07, this device was first cloned into plasmid pSB1A2, followed by transformation into E.coli strain BL21.

The cell growth curves in Figure 2 showed the bacteria population-control device successfully maintained the cell density at a lower value at the steady state compared with BL21’s cells without this circuit. Besides, circuit-regulated cell growth (black dot) has a relatively longer steady state than cells without this circuit (red dot).

For iccdB0.07 regulated cell growth, the viable cell density first start to decline around 8h and then reached a steady state after two minor oscillations. Compared with bacterium without this circuit, the iccdB0.07 regulated bacterium has a lower media-consuming rate due to its lower cell density.

The iccdB0.07 regulated cell growth might be explained by “ON-OFF” mechanism based on the quorum sensing system.

Figure 2 Experimentally measured growth curves of BL21’ cells without iccdB0.07 (red dot) and with iccdB0.07 ON (black dot).

Figure 3 Experimentally measured densities of BL21’s cells without population-control circuit and BL21’s cells with four population-control circuits respectively at steady state.

Figure 4 Average of experimentally measured cell densities of BL21’s cells with four population-control circuit at steady state.

Table 1 Data of the steady-state cell density.

iGEM Team XMU-China has also tested the performance of three other bacteria population-control device iccdB1.0 (BBa_K658001), iccdB0.6 (BBa_K658003) and iccdB0.3 (BBa_K658004). Figure 3, figure 4 and table 1 illustrate that by using RBS of different strength in the population-control device, we were able to control the steady-state cell density of a bacteria population at different levels. And a population-control device with RBS of high strength results in a low steady-state cell density. It might be explained by the mechanism that for circuit-regulated growth, the cell death rate is regarded proportional to the intracellular concentration of the killer protein. The expression of the killer gene is regulated by the strength of its upstream RBS. Therefore, a RBS with higher strength promises more killer protein in vivo, which leads to a higher death rate of the bacteria population.

Model

Different RBS sequences leads to different levels of expression of the killer protein CcdB which is directly linked to the effects of our programmed cell-death circuit. So we constructed a series of circuits with different RBS sequences so as to detect how RBS of different efficiency can affect the viable cell density at steady state. We build a model to search for a theory to predict growth rule of bacteria with the programmed cell-death circuit. We assume that：(1) without the circuit，changes in viable cell density（N,/ml）follow logistic kinetics;(2)for population-circuit growth, the cell death rate is proportional to the intracellular concentration of the kill protein(E, nM) ;(3)the production rate of E is proportional to AHL concentration(A, nM) ; (4)AHL production rate is proportional to N;(5)degradation of the kill protein and AHL follows first-order kinetics.

are the rate constants(/h).

is the carrying capacity in the Limited medium without the cell-death circuit.

At steady state, we can get the following equations:

Where subscript ‘s’ represents steady state. There are two steady-state solutions:

We can get the following equation (9) from equation (8) .

With time limited, we only conducted the experiment on the viable cell density at steady-state with the population-control device with RBS0.07 ,RBS0.3, RBS0.6 and RBS1.0.

And we define that:

Computed from our experimental data, we can get the data listed in Table 1.

From the model and Table 1, we can conclude that: the efficiency of RBS (a) may have close relationship with kE . Based on the device of RBS1.0, the viable cell density at steady-state (NS ) of other devices with different efficiency of RBS can be shown as equation(10).

C is -4.96322E-09 in our experiment.

Method

1.Isolation of Plasmid

Using the Procedure for GenEluteTM Plasmid Miniprep Kit

•Collect 1-5 mL bacterium fluid in 1.5 mL centrifuge tube，and centrifuge fluid at 12000 r/min

•Resuspend cells. Discard the supernatant and completely resuspend the bacterial pellet with 250 µl of the Resuspension Solution

•Lyse cells. Lyse the resuspended cells by adding 250 µl of the Lysis Solution

•Neutralize. Precipitate the cell debris by adding 350 µl of the Neutralization/Binding Solution, and centrifuge fluid at 12000r/min

•Load cleared lysate. Transfer the supernatant from step 4 to the spin column. Centrifuge at 12000r/min for 1 minute, and then discard the filtrate

•Optional wash. Add 500 µl of the Optional Wash Solution to the column. Centrifuge at 12000 r/min for 1 minute. Discard the filtrate

•Wash column. Add 500 µl of the diluted Wash Solution to the column. Centrifuge at 12000r/min for 1 minute.

•Elute DNA. Transfer the column to a new collection tube. Add 50~100 µl of Eluent Solution to the column. Centrifuge at 12000 r/min for 1 minute. The DNA is now present in the filtrate and is ready for immediate use or storage at -20℃

2.Reaction system of restriction endonuclease

System1、2、3 and 4 are used for Standard BioBrick Assembly .System 5 and 6 are used for Restriction analysis. Digestion of sample: at least 500 ng DNA / 10 µL volume. Digest for 4 h at 37 °C, afterwards inactivated by adding 10x loading buffer and standing for 10 min at room temperature.

3. Standard BioBrick Assembly

•Digestion of insert: 2 μg~5 μg DNA / 100 µL volume, 10x H buffer, EcoRI, SpeI. Digestion and inactivation. Clean up the insert via gel electrophoresis. When cutting the insert out of the gel, try to avoid staining or exposure to ultraviolet light of the insert.

•Digestion of vector: 2 μg~5 μg DNA / 100 µL volume, 10 x M buffer, EcoRI, XbaI. Digestion and inactivation. Clean up the insert via gel electrophoresis. When cutting the insert out of the gel, try to avoid staining or exposure to ultraviolet light of the insert.

4. Suffix Insertion

•Digestion of insert: 2 μg~5 μg DNA / 100 µL volume, 10x M buffer, XbaI, PstI. Digestion and inactivation. Clean up the insert.

•Digestion of vector : 2 μg~5 μg DNA / 100 µL volume, 10x H buffer, SpeI, PstI. Digestion and inactivation. Clean up the vector.

5. Ligation

•After digestion and clean-up, the next step is ligation. Overnight ligation at 16°C. Table 2 is the system of ligation.

6. Transformation

•Preparation of competent E.coli cells

•Add 10 µL plasmid to 100 µl competent cells in centrifuge tube

•Store tube on ice for 20-30 minutes

•Water bath for 90s at 42℃

•Put the tube on ice for 1-2min

•Add 790 µL LB，and cultivation for 1h at 37 ℃，then plate on selective LB-Medium.

7. Restriction analysis

•Pick one colony with a sterile tip and cultivation in 20ml LB for overnight at 37 ℃

•Isolation of Plasmid

•Digest BioBrick，the system of Restriction analysis refer to table1

•Gel electrophoresis：add 2 µL loading buffer to digestion mixture. An agarose concentration is 1 %.

8. Determining fluorescence intensity

•Add IPTG when A600 0.6~0.8.

•Cool the culture 10 minutes on ice.

•Centrifuge at 6000rpm. Wash it with pre-cooled PBS buffer.

•Use fluorescence spectrophotometer tomeasure the fluorescenceof GFP:

•Before measuring, dilute the bacteria with PBS buffer so that it can be within the measuring #range. Set excitation wavelength 491 nm, emission wavelength 511 nm.

•Transfer the measured bacteria in a new centrifuge tube and measure the OD of the bacteria.

9. Cell growth

•100µL suspension was inoculated from a Glycerin tube into 20ml fresh LB and incubated overnight at 37℃ and 250 r.p.m.

•100µL suspension was inoculated again from step1 into 50ml fresh LB and incubated at 37℃ and 250r.p.m

•IPTG was added when A600≈0.6-0.8

•1 ml suspension was taken on every sample taken time. 3 samples were taken in each time.

•Diluted each sample to 10-6(Sometimes 10-5),and then plate on selective LB-Medium.

•After 12h, count the number of CFU on the plate on different time point and then draw the cell growth curve.

10. Site Directed Mutagenesis

•Digest the template plasmid by adding 1 µL of DpnI and incubate for 1-2 h

•Transform 10 µL of t PCR product into competent E. coli cells

•Screen the transformants using restiction digest and sequencing

Reference

[1] You L, Cox RS, Weiss R, Arnold FH. Programmed population control by cell-cell communication and regulated killing[J]. Nature, 2004, 428(6985): 868-871.

[2] Miki T,Yoshioka K,Horiuchi T. Control of cell division by sex factor F in Escherichia coli. I. The 42.84-43.6 F segment couples cell division of the host bacteria with replication of plasmid DNA. Molecular Biology,1984,177(4):605-625.

[3] http://en.wikipedia.org/wiki/N-Acyl_homoserine_lactone

[4] Hanzelka BL, Greenberg E. Quorum sensing in Vibrio fischeri: evidence that S-adenosyl methionine is the amino acid substrate for autoinducer synthesis[J]. Journal of Bacteriology, 1996, 178(17): 5291-5294.

[5] Urbanowski M, Lostroh C, Greenberg E. Reversible acyl-homoserine lactone binding to purified Vibrio fischeri LuxR protein[J]. Journal of Bacteriology, 2004, 186(3): 631-637.

[6] Hansen LH, Knudsen S, Sorensen SJ . The effect of the lacY gene on the induction of IPTG inducible promoters, studied in Escherichia coli and Pseudomonas fluorescens. Curr microbiol，1998， 36 (6): 341–345.

[7]Bernard P，Couturier M. Cell killing by the F plasmid CcdB protein involves poisoning of DNA-topoisomerase II complexes. Molecular Biology,1992,226:735-745.

[8]Semit M.H,Duin J. Secondary structure of the ribosome binding site determines translational efficiency: a quantitative analysis. Molecular Biology,1990,87(19):7668-7672.

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 718
  
• 23
  COMPATIBLE WITH RFC[23]
• 25
  COMPATIBLE WITH RFC[25]
• 1000
  INCOMPATIBLE WITH RFC[1000]

  Illegal BsaI.rc site found at 1874
  Illegal BsaI.rc site found at 2601