Our Parts

<groupparts>iGEM010 SDU-Denmark</groupparts>

Characterization of parts

K343004

The FlhDC operon is the master regulator of flagella synthesis. A more detailed description of the operon can be found here
In our system the purpose of the composite part is to hyper flagellate our cells so that a grater force can be generated in the microtubes. The FlhDC operon is naturally found in the E. coli strain MG1655 genome. We extracted the operon and inserted a silent mutation (T to C) at position 822 in the operon because without the mutation this site is a Pst1 digestion site and it would therefor constitute problems when assembling the composit part.
We have made three FlhDC parts:
K343100 is the coding sequence of the native FlhDC operon with the Pst1 digestion site
K343000 is the coding sequence of the mutated FlhDC operon
K343004 is the composite part containing the TetR repressable promoter (constitutive when no TetR is pressent) + RBS (J13002), the K343000 part and the double terminator (B0015).
The composite part is caracterized firstly by using a motility assay and secondly by measuring plasmid stability and cell growth.

Motility assay

The purpose of this experiment is to test the motility of the transformed cells containing either pSB1C3-K343004 or pSB3K3-K343004. We also want to test if it makes a difference in the motility whether the bacteria contain low-medium- or high-copy plasmids.

For the motility assays we added 5ul of an ON culture to petridishes containing motility agar (LB media with 0.3% agar) instead of regular LA (Luria agar). This semi-solid media lets the bacteria swim more easily.
In the assays three control plates were made: A negative control containing E. coli strain DH5alpha which does not express flagella and therefore movement in the media should be minimal. A positive control containing E. coli strain H10407 which is a hyper flagellated class II pathogen, these bacteria should show high motility. And a wild type E. coli strain MG1655 that has about 4 flagella per cell these cells would be expected to move farther than the DH5alpha but not as far as the positive control.

The plates were incubated at 37 degrees celcius for up to 48 hours.
The assay was carried out three times. All three times pictures were taken after 24 hours and in two of the assays pictures were also taken after 48 hours. In two of the assays 8.5 cm petridishes was used, the purpose of these assays was to se if the motility of our transformants differed from the control strains. In the third assay we used 13.5 cm petridishes to se how far our transformants were able to swim compared to the wild type E. coli strain MG1655 since the motility of the transformed cells seem to surpass the size of the 8.5 cm petri dishes.

All pictures taken after 24 hours are shown in the last part of this section while the pictures taken after 48 hours are shown and described.
WT, negative- and positive-control after 48 hours:




In all three assays we saw that the control plates that contain no antibiotics are contaminated with other bacterial colonies. We also see that the negative control has low motility, but they are not immotile. After 24 hours the negative control has not moved much but after 48 hours the length from center to edge of the colony is 1.5cm. The wild type has moved a bit farther than the negative control after 24 hours, and after 48 hours the difference from center to edge of the wild type is 2.5cm. The positive control moved about as far in 24 hours as the wild type did in 48 which and after 48 hours it had moved to the edges of the petridish (4.25cm).

The E. Coli strain MG1655 cells transformed with pSB1C3-K343004 shows that after 24 hours these bacteria have moved which is farther than the wild type and the negative control. The E. coli strain MG1655/pSB3K3-K343004 have moved farthest of all 5 cultures after 24 hours.
A difference in the way the two transformants move are seen in all three assays. The cells containing the pSB3K3 plasmid show a uniform circle whereas the cells transformed with the pSB1C3 plasmid shows a budding-pattern spreading from the center. After 48 hours the pSB1C3 cells are still not covering the entire plate.

Pictures of plates after 24 hours
Experiment 1.


Experiment 2.

In conclusion
From the pictures above we can definately se that the bacteria containing our part is much more motile than the wild type and the negative control. We assume this is caused by overexpression of the FlhDC master flagella operon which leads to hyperflagellation of the cells.
The pictures taken after 24 hours show that bacteria with pSB1C3-K343004 have not moved as far as the bacteria containing pSB3K3-K343004. pSB1C3 is a high copy plasmid while pSB3K3 is a low-medium copy plasmid. The promoter in K343004 is a constitutive promoter (tetR repressable promoter). Bacteria containing a high copy plasmid with a constitutive promoter are more metabolically challanged than bacteria containing a low- or medium-copy plasmid with a constitutive promoter because of the higher number of plasmids per the cell. Therefore the high copy plasmid bacteria move slower than low- or medium-copy plasmid bacteria. However, after 48 hours there was only little difference in the spread.

Flagella staining

When the E.coli strain MG1655 have a constitutive active transcription of the FlhDC operon more flagella’s is expected. The idea was to get a quantitative measurement of the increased flagella production by comparing the observed number flagellas on the wildtype MG1655 and the hyperflagellated MG1655. We tried to stain the flagella using silver staining and afterwards examined the bacteria under the microscope. We started the staining procedure before we had the mutated FlhDC operon as a composite part because we then had time to optimize the staining protocol and become really good at it. We started with staining of DH5α and H10407; A E.coli strain which do not express flagellas (negative controle) and a hyperflagellated E.coli (positive control), respectively. The bacteria were grown on agar plates ON and stained with this protocol FS1.2.

Unfortunately it was not possible to see a clear and significant difference between the positive and negative control. Though at some placeses it could look like flagellas on the positive control but it was never enough to determine a difference. After repeating the protocol four times, each time with multible samples, we decided to reject this method, and another approach for characterizing our bio brick was employed.

Scanning Electron microscopy

Scanning Electron microscopy

After the failed staning of flagellas we tried to visualize the flagellas with scanning electron microscopy (SEM). The bacteria were grown ON in liquid cultures (5 ml LB-media). The bacteria were diluted to approximately 106 cells pr 10 µl solution. At the time being we did not have our FlhDC as a composite part so therefore we only tried SEM with the negative control strains DH5alpa and MG1655. We did this as a preliminary work so we were ready to do microscopy on the MG1655 containing the composite part when it is ready. Unfortunately the limited resolution and magnitude of the SEM at our disposal made it practically impossible to visualize any flagella in the microscope. Thus if this approach is to be used for characterization, a SEM of higher magnitude and resolution is required.
The pictures below are SEM pictures the negative control strains DH5alpha and MG1655.

Stability assay

To dertermine the stability of our pSB1C3-K343004 plasmid, a stability experiment was carried out according to protocol[SA1.1]. E.coli MG1655/pSB1C3-K343004 was grown in LB media without chloramphenicol, whereby no selection pressure is excerted on the bacteria. Dilutions of the culture was spreaded on LA plates and LA plates with 35ug/mL chloramphenicol, respectively, and the colony forming units (cfu) was determined for each plate. The cfu for the LA plates represents the total amount of bacteria in the culture, and the cfu of LA plates with chloraphenicol corresponds to the amount of plasmid carrying bacteria. The percentage of the total amount of bacteria carrying the plasmid was plotted in a semi-logarithmic graph as a function of number of generation. As seen in the graph, almost all of the bacteria had shedded the plasmid after 20 generations, suggesting that the plasmid is only stable within the cell for a few generations (<20). This is presumably due to the strain brought upon the bacteria by the plasmid. Thereby when the bacteria are carrying a high-copy plasmid like pSB1C3-K343004 it is to expect that the bacteria will quickly shed the plasmid when no longer exposed to a selection pressure. It is likely to believe that pSB3C5-K343007, since being a low-copy plasmid, will not excert as much strain on the bacteria, and might therefore be stable for more genrations than pSB1C3-K343007. Therefore a stability assay of this plasmid might be of interest.

Growth rate assay

The purpose of this assay is to see if our transformants deviate from the wild type in growth rate. In the growth measurement assay we have measured OD at 550 nm every hour for 12 hours and at hour 24. In the experimental setup we used no lag phase was observed in any of the measurments.
The graph below shows the growth of our wild type E. coli strain MG1655, the MG1655 transformed with K343004 in pSB3K3 and in pSB1C3 respectively.




Raw data

From our data we see no significant difference between the plasmid carrying bacteria and the wild type. This can be said to be quite conteradictory to our results obtained from the stability assay. The transitory stability of pSB1C3-K343004 suggests that it is highly unfavorable for the bacteria, wherefore it might be expected that the growth raate of the bacteria containg this plasmid would be affected. Thus, however much a disadvantage the plasmid pose to the bacteria, their growth rates are not significantly influenced by the plasmid.

K343007

The part K343007 (from now on shortly called PS) is a generator for the SopII-HtrII photosensor from Natronomonas Pharaonis coupled to E.Colis chemotaxis pathway via the Salmonella protein Tar. This part's effect on the system is to make E.Coli phototactic, so that it becomes aware of different light conditions. So for characterization of this part we made examination of motility and motility patterns our first priority and plasmid stability and growth of the cells our second.
There is a wide range of motility assays for chemotaxis in bacteria, which meant that we had a broad spectrum of experiments to choose from, which just had to be tweaked for making them suited for the analysis of phototaxis. The two experiments we chose for analysing the effect of this part (PS), were growth of the bacterial cultures in semi-solid agar and computer analysis of swimming motility through video microscopy:

Growth of bacterial culture on semi-solid agar plates

Experiment 1

The bacteria and plates were prepared after our own protocol, which you can find here: PS1.1
Since exposure to blue light should decrease the phototaxic bacterias tumbling frequency, the expected result was that the colony which was placed between the light and dark half of the plate would spread out in the darkness and would not move further when it reached the light. This is counter-intuitive, since decreased tumbling should lead to a longer distance traveled. What happens at the microscopic scale in semisolid agar is that the agar creates a matrix like structure where there are channels through the agar, which the bacteria can swim through. The decrease in tumbling frequency of the bacteria will make it harder for them to find the channels in the agar to swim through, which leads to them being trapped where they were placed. The result is that a colony which shows an increased run time, will look as if it it was non-motile on these plates [1] Our results showed exactly this; the bacterial culture had spread out to on the dark half of the plate and did not get nearly as far on the half exposed to light. This experiment was done with a normal wildtype MG1655 and a non-motile strain of E.coli, DH5alpha, as controls. As expected these cells did not show anything like the behavior described above, which indicates that the effect stems from the modification to our photosensor bacteria.

These results were useable, but not fully conclusive, since there were some non-optimal conditions present in this experiment. We used ambient light instead of pure blue light, and the exposure to light for the multiple samples was not exactly even. Therefore we had to improve our experiment setup and see if we could reproduce these results with a more reliable setup.

Experiment 2

The experiment described above was repeated in a more controlled environment. This means that there were no changes as to how the plates or bacterial cultures were prepared, so we refer again to PS1.1 in regards to how this was done. The difference lies in the setup of the light-controlled environment. What we did this time was that the plates was illuminated from above by a single light source in an otherwise completely dark environment, we prepared a cut-out so that the light would only hit one half of our plates and the other half would remain in the dark. Since the problem with the last experiment was that the light source was just normal white light (which contains a lot of different wavelengths), this time around we used an optical filter so that only light with a wavelength of around 470nm could pass through, which resulted in a blue light shining down on the plates. The light-source itself was a run-of-the-mill flashlight, with a blue light filter installed in front of the lens. To eliminate the effect of temperature gradients inside the incubator, the three samples were placed in a triangle formation in the center of the incubator.

Another deviation from the protocol is that the culture was inoculated at the center of the plate, instead one colony each was inoculated in the center of the light exposed and dark half respectively. This would give us more information on how the bacteria would behave when directly exposed to either the dark or light surroundings, instead of the gradient that was present in the first experiment.
From the results of the first experiment we expected the culture containing K343007 to spread out in the dark and not to spread when exposed to light. The wildtype bacteria should spread out evenly no matter if exposed to light or not and the non-motile strain (DH5alpha) should not move regardless of the light conditions. Our expectations from the first experiment were fulfilled, as the bacteria behaved exactly as expected. This made it possible to conclude that the photosensor has an effect on the bacteria's tumbling frequency, but if it does in fact reduce the tumbling is not possible to say, since both an increased and reduced tumbling frequency will look alike.


After this we could conclude that the part had an impact on the bacterial motility, but we had to find out which. This lead us to our next experiment, which was intended for determining what happened to the tumbling frequency:

Videomicroscopy and computer analysis of bacterial motility

To get an exact idea of what is happening to the bacteria when expressing the photosensor we decided on doing video microscopy of motile bacteria. The bacterial cultures were prepared acording to protocol PS1.1. Wildtype MG1655 and DH5alpha was used as controls. The actual microscopy was done on a Nikon eclipse TE2000-S microscope with an optical magnification of 1000x.
To be able to observe an effect in the modified bacteria we had to expose the cultures to light, which was done through the microscope's integrated light source, which could switch between blue, green and ambient light. To ensure that the blue light was at the correct wavelength the same optical filter that was used for the plate experiments was inserted between the lightsource and the microscopy slide. Since microscopy is impossible without light, we had to use red light as a replacement for darkness, the source of the red light was ambient light from the microscope's light source filtered through a red optical filter (about 580nm). This should not have any effect on the phototactic bacteria according to [2]. The room where the experiment was carried out was kept as dark as possible, as to eliminate the chance of the phototactic bacteria being unwantedly exposed to light. The actual experiment was carried out in the following manner:

1. Expose bacteria to red light for 1 minute, while recording video.
2. Move to another spot on the slide, repeat 1. (repeated until 5 videos were recorded)
3. Expose bacteria to blue light for 1 minute, while recording video.
4. Wait for 30 seconds, for the bacteria to reset themselves.
5. Move the focus to another spot on the slide, repeat 3. (x5)

This was done with all three strains of bacteria.
An example of the results:


When played at real time speed these videos seem slow and not showing any tendency, though when played at 4 times the normal speed, the photosensor will seem to show slightly increased motility when exposed to blue light. Even though the bacteria displayed disappointing motility, we went on and did computer analysis on the videos by the help of the open source software "CellTrack". The paths that were mapped showed a longer traveling distance for the bacteria expressing the photosensor compared to the rest of the samples when exposed to blue light. We picked 10 bacteria from each sample, which amounts to 60 bacteria that were tracked. This is a rather small amount, but because of the time-intensive procedure a more thorough data analysis was not possible.

Samples of the tracked paths (from left to right): Photosensor exposed to blue light, photosensor exposed to red light, wildtype exposed to blue light.

This might indicate a decreased tumbling frequency, but the low motility of the bacteria, the inadequacy of the cell track software and the small amount of data analysed make results of this experiment unreliable and a new protocol had to be devised.

Computerized analysis of the bacterial motility with the THOR prototype by Unisensor A/S and the Unify software

For this experiment we changed our protocol for cultivating swimming bacteria in order to optimize their mobility PS1.2
The machine and software used for the analysis are prototypes and still under heavy development. Because of trade secrets it is impossible for us to explain how the machine works or give a detailed explanation of it's mechanism until the THOR has reached production status. Simplistically said it is a very advanced video microscope, with which it is possible to analyse liquids and the particles inside in both 2D and 3D, while also tracking them over time. 2.5 ul of the bacterial dilution were placed on the center of the microscopy slide and covered by a coverslide. Afterwards the sample was sealed with mineral oil as to prevent a flow in the liquid. The data collection was done exactly as described in the previously experiment, with the exeption that instead of optical filters we used diodes that emitted light at the wanted wavelengths (500nm and 600nm respectively). Moreover we also recorded the bacteria's behaviour when exposed to a blue light gradient and varying intensities of light measured in milliampere. All the measurements were carried out on the modified phototactic bacteria and the wildtype MG1655.
The results look like these:



The bacteria that are not moving in the video are assumed to be sticking to the glass or coverslip.

Stability assay

To dertermine the stability of our pSB1C3-K343007 plasmid, a stability experiment was carried out according to protocol[SA1.1]. E.coli MG1655/pSB1C3-K343007 was grown in LB media without chloramphenicol, whereby no selection pressure is excerted on the bacteria. Dilutions of the culture was spreaded on LA plates and LA plates with 35ug/mL chloramphenicol, respectively, and the colony forming units (cfu) was determined for each plate. The cfu for the LA plates represents the total amount of bacteria in the culture, and the cfu of LA plates with chloraphenicol corresponds to the amount of plasmid carrying bacteria. The percentage of the total amount of bacteria carrying the plasmid was plotted in a semi-logarithmic graph as a function of number of generation. As seen in the graph, almost all of the bacteria had shedded the plasmid after 20 generations, suggesting that the plasmid is only stable within the cell for a few generations (<20). This is presumably due to the strain brought upon the bacteria by the plasmid. Thereby when the bacteria are carrying a high-copy plasmid like pSB1C3-K343007 it is plausible that the bacteria will quickly shed the plasmid when no longer exposed to a selection pressure. It is likely to believe that pSB3C5-K343007, since being a low-copy plasmid, will not excert as much strain on the bacteria, and might therefore be stable for more genrations than pSB1C3-K343007. Therefore a stability assay of this plasmid might be of interest.

Growth assay

The purpose of this assay is to see if our transformants deviate from the wild type in growth rate. In the growth measurement assay we have measured OD at 550 nm every hour for 12 hours and at hour 24. In the experimental setup we used no lag phase was observed in any of the measurments.
The graph below shows the growth of our wild type E. coli strain MG1655, the MG1655 transformed with K343007 in pSB3T5 and in pSB1C3 respectively.


Raw data

From our data we see no significant difference between the plasmid carrying bacteria and the wild type. This can be said to be quite conteradictory to our results obtained from the stability assay. The transitory stability of pSB1C3-K343007 suggests that it is highly unfavorable for the bacteria, wherefore it might be expected that the growth raate of the bacteria containg this plasmid would be affected. Thus, however much a disadvantage the plasmid pose to the bacteria, their growth rates are not significantly influenced by the plasmid.

K343005

UV-Vis determination of beta-carotene and retinal production

In this experiment cells were prepared and harvested according to protocol EX1.1. This experiment was performed with six different strains of E. coli:

Wild type TOP10
Wild type MG1655
TOP10/pSB1A2-K274210
MG1655/pSB1A2-K274210
TOP10/pSB1A2-K274210/pSB1C3-K343005
MG1655/pSB1A2-K274210/pSB1C3-K343005
Both K343005 and K274210 were constitutively expressed.

Since the first experiment showed no or small amounts of product in cells grown to exponensial phase the measurements were performed on cells incubated for 20 hours at 37degrees celcius and 180rpm. The graphs obtained from the experiment are presented below:



In the spectre a sudden drop from 330 to 320 nm occurs, this can be caused when the samples was auto zeroed according to acetone which is the solvent used in the extraction of the beta-carotene and Retinal.
The graph also shows that cell material interferes with the UV-vis measurement where the retinal has the strongest absorption. Therefore, an organic separation is required prior to the measurements.
In order to assess the results, standard dilutions of beta-carotene and retinal were made and measured. The concentrations were 1mM, 100 µM, 50 µM, 25 µM, 10 µM, 5 µM, 1 µM, 100 nM and 10 nM. The standard dilutions were measured on the spectrophotometer. The resulting graphs are presented below:


The spectrum for the Beta-carotene looks normal and reliable, the standards for retinal however doesn’t look reliable. The spectrum for the three lowest concentrations appears to be give distorted and implies that something is interfering with the measurement.
The measurement jumps rapidly from nearly nothing to the maximum absorbance, this might be because the concentration of retinal is to low to be measured as a spectrum, but the concentration of the individual derivates of retinal might be high enough to be measured.
It might also just be that the concentrations are to low and something ells are influencing the measurements.
Because of the error in the UV-vis spectre concerning retinal detection in both the standards and samples the next characterization experiments is preformed on a HPLC.

All data can be seen under Raw data

K343006

HPLC determination of beta-carotene and retinal production

In this experiment cells were prepared and harvested according to protocol EX1.1. This experiment was performed with six different strains of E. coli:

Wild type TOP10
Wild type MG1655
TOP10/pSB1A2-K274210
MG1655/pSB1A2-K274210
TOP10/pSB1A2-K274210/pSB1C3-K343005
MG1655/pSB1A2-K274210/pSB1C3-K343005
Both K343005 and K274210 were constitutively expressed.

The measurements were performed on cells incubated for 20 hours at 37degrees celcius and 180rpm. The graphs obtained from the experiment is presented beneath the text.
In order to assess and quantify the results a standard dilution of beta-carotene and retinal was made and measured: 10 µM, 5 µM, 1 µM, 2 µM, 0,5 µM. The standard dilutions was also measured on the HPLC with the same injection volumen and program as the samples. The resulting graphs is presented beneath the text
When combining the graphs of the samples and the standard dilutions it is possible to….

When doing a HPLC analysis it is possible to quantify the amounts of the chemical compounds in the samples.
This is done by doing a standard curve with known solutions of the chemical and recording the area under the peaks. The peak area correspond to the concentration of the chemical in the sample.
Then plotting the area under the peaks on the y- axis, the know concentrations of the standards on the x-axis and calculating the regression line.
Now it is possible to calculate unknown concentrations from samples using the regression line from the standard curves.
The results for our HPLC analysis can be seen beneath the text.

All data can be seen under Raw data

Stability assay

To dertermine the stability of our pSB1C3-K343006 plasmid, a stability experiment was carried out according to protocol[SA1.1]. E.coli MG1655/pSB1C3-K343006 was grown in LB media without chloramphenicol, whereby no selection pressure is excerted on the bacteria. Dilutions of the culture was spreaded on LA plates and LA plates with 35ug/mL chloramphenicol, respectively, and the colony forming units (cfu) was determined for each plate. The cfu for the LA plates represents the total amount of bacteria in the culture, and the cfu of LA plates with chloraphenicol corresponds to the amount of plasmid carrying bacteria. The percentage of the total amount of bacteria carrying the plasmid was plotted in a semi-logarithmic graph as a function of number of generation. As seen in the graph, almost all of the bacteria had shedded the plasmid after 20 generations, suggesting that the plasmid is only stable within the cell for a few generations (<20). This is presumably due to the strain brought upon the bacteria by the plasmid. Thereby when the bacteria are carrying a high-copy plasmid like pSB1C3-K343006 it is plausible that the bacteria will quickly shed the plasmid when no longer exposed to a selection pressure.

Growth measurement

The purpose of this assay is to see if our transformants deviate from the wild type in growth rate. In the growth measurement assay we have measured OD at 550 nm every hour for 12 hours and at hour 24. In the experimental setup we used no lag phase was observed in any of the measurments.
The graph below shows the growth of our wild type E. coli strain MG1655, the MG1655 transformed with K343006 in pSB1C3.


Raw data

From our data we see no significant difference between the plasmid carrying bacteria and the wild type. This can be said to be quite conteradictory to our results obtained from the stability assay. The transitory stability of pSB1C3-K343006 suggests that it is highly unfavorable for the bacteria, wherefore it might be expected that the growth raate of the bacteria containg this plasmid would be affected. Thus, however much a disadvantage the plasmid pose to the bacteria, their growth rates are not significantly influenced by the plasmid.

Helping another iGEM Team with characterization

2010 Bielefeld brick K389016

We recieved a miniprep with K389016 in pSB1C3 together with a list of experiments and characterization assays the Bielefeld team would like us to carrie out.
We transformed the plasmid into E. coli strain MG1655 and ran a colony PCR of four different colonies the following day. The picture below shows that cells in all four colonies contained K389016 in pSB1C3.

Characterization

Characterizing an exicting biobrick

2009 Cambridge brick K274210

The K274210 brick was cultivated from the 2010 kit plate 3 well N6 in the PSB1A2 plasmid and transformed into E. coli strains TOP10 and MG1655.

Characterization

UV-vis determination of beta-carotene production
In this experiment cells were prepared and harvested according to protocol [1]. This experiment was performed with four different strains of E. coli:

Wild type TOP10
Wild type MG1655
TOP10/pSB1A2-K274210
MG1655/pSB1A2-K274210
TOP10/pSB1A2-K274210/pSB1C3-K343005
MG1655/pSB1A2-K274210/pSB1C3-K343005
K274210 were constitutively expressed.

The measurements were performed on cells both in the exponential and stationary phase. The resulting graphs are presented below:

In order to assess the results, a series of standard dilutions of beta-carotene were made. The concentrations were 1mM, 100 µM, 50 µM, 25 µM, 10 µM, 5 µM, 1 µM, 100 nM and 10 nM. The standard dilutions were also measured on the spectrophotometer. The resulting graphs are presented low:


When combining the graphs of the samples and the standard dilutions, it is clear that the spectres are uniform. This similarity of the spectres indicates that the cells actually do produce beta-carotene. The graphs also give a qualitative indication of the amount of beta-carotene produced by the MG1655 and the Top10 E. coli cells. The resulting graphs are presented below:


The graph shows that the beta-carotene production of TOP10 containing PSB1A2 with constitutively active K274210 produces beta-carotene in a concentration just above 5 µM.
The MG1655 containing PSB1A2 with constitutively active K274210 produces beta-carotene in a concentration just above 10 µM.
All data can be seen under Raw data
The K274210 brick have also been characterized together with the K343005 and K343006 parts the data are represented in the characterization for the K343005 and K343006 parts.

References

[1] Derek L. Englert, Arul Jayaraman, Michael D. Manson,Methods in Molecular Biology, 2009, Volume 571, 1-23.