Difference between revisions of "Part:BBa K592009"

Revision as of 17:00, 21 October 2019

amilCP, blue chromoprotein

This chromoprotein from the coral Acropora millepora, amilCP, naturally exhibits strong color when expressed. The protein has an absorbance maximum at 588 nm giving it a blue/purple color visible to the naked eye, thereby requiring no instruments to observe. The strong color is readily observed in both LB or agar culture, in less than 24 hours of incubation.

This part has been adaptated to B. subtilis with a LVA tail. by the UPMC-Paris Team in 2016. (see part BBa K2180019)

Usage and Biology

This part is useful as a reporter. In the pictures below it's built into BBa_K592015.

iGEM11_Uppsala-Sweden: Expression of chromoproteins. The images above show E coli constitutively expressing amilCP BBa_K592009 (blue), amilGFP BBa_K592010 (yellow) and RFP BBa_E1010 (red). Also see the green chromoprotein cjBlue BBa_K592011.

iGEM12_Uppsala_University: The Uppsala chromoprotein collection and RFP. The image shows pellets of E coli expressing chromoproteins eforRed BBa_K592012, RFP BBa_E1010, cjBlue BBa_K592011, aeBlue BBa_K864401, amilGFP BBa_K592010 and amilCP BBa_K592009.

References

[http://www.ncbi.nlm.nih.gov/pubmed/18648549] Alieva, N. O., et al. 2008. Diversity and evolution of coral fluorescent proteins. PLoS One 3:e2680.

[1] Levy, Appelbaum, Leggat, Gothlif, Hayward, Miller, & Hoegh-Guldberg. (2007). Light-responsive cryptochromes from a simple multicellular animal, the coral Acropora millepora. Science (New York, N.Y.), 318(5849), 467-70. GenBank: AY646075.1

Sequence and Features

CONTRIBUTION: Uppsala 2018

Authors iGEM Uppsala 2018, Matilda Brink, Elin Ramstrom.

The original native AmilCP sequence (Part:BBa_K592009) was codon optimized for E.coli K12 with a codon optimization tool provided by Integrated DNA Technologies (IDT). The codon optimized basic AmilCP part is attached to a constitutive promotor, RBS and a double terminator; Part:BBa_K2669003.

Purpose
The Uppsala 2018 team have performed a codon optimization on the original native AmilCP basic part in order to get a blue protein expression that can be maintained for a longer period of time through several generations of growth, hence making the expression of the blue chromoprotein more stable.

Method
In order to conduct a stability assay through liquid experiment, the codon optimized basic part and the original native AmilCP part was attached to a constitutive promotor, RBS and a double terminator separately. The two Biobrick parts were ordered as customized genes from IDT inserted in pUCIDT (Amp).

Both vectors were transformed into DH5-aplha E.coli cells through single tube transformation and yielded phenotypically blue colonies for cells containing plasmid with original part and plasmid containing codon optimized part. Stability assay through liquid experiemt was performed according to protocol [2].

Results

Figure 3: Results after 10 generations of growth. The upper row represents 10 different culture pellets of the cells with the plasmid containing the codon optimized sequence of AmilCP. The lower row represents 10 different culture pellets with the original native AmilCP (part:BBa_K592009) sequence incorporated in the plasmid.

Already after 10 generations of growth it was clearly visible that the color intensity was better distributed in the cells containing the plasmid with the codon optimized AmilCP sequence. The result confirms that the plasmid containing codon optimized part generates better maintenance of protein expression than the plasmid containing the original native part. The improved stability of expression makes this Biobrick part a good candidate as a reliable reporter or biosensor.

IMPROVEMENT REFERENCE: IONIS_PARIS 2017

The part used to improve BBa_K592009 (Group: iGEM11_Uppsala-Sweden) is : BBa_K2282006 (Group: iGEM17_IONIS-PARIS). https://parts.igem.org/Part:BBa_K2282006

IMPROVEMENT REFERENCE: Austin_UTexas 2017

The original blue chromoprotein part (BBa_K592009) was codon-optimized in order to increase its overall stability as a color reporter. The modified blue chromoprotein part is: BBa_K2253002 (Group: iGEM17_Austin_UTexas). Designed by Surta Dave.

IMPROVEMENT REFERENCE: DTU-Denmark 2017

A 6x his-tag was added to this part, to the C-terminal end of the expressed amilCP. The new part was submitted as BBa_K2355002 (Group: iGEM17_DTU-Denmark), Designed by:Philip Sørensen.

IMPROVEMENT REFERENCE: BNU-China 2017

The part was added to the end of a silk protein from honeybee. The new part is : BBa_K2220028(Group: iGEM17_BNU-China), Designed by: Jiawei Xing.

IMPROVEMENT REFERENCE: IISER Pune India 2017

The part was assembled with B0034 RBS and B0015 double terminator. The new part is : BBa_K2258003(Group: iGEM17_IISER Pune India), Designed by: Jyothish S.

IMPROVEMENT REFERENCE: Peshawar 2017

One of the most used chromoprotein used in iGEM is AmilCP blue, BBa_K592009. Because our modelling team was doing homology models for other proteins and AmilCP doesn't have a homology model on it's page, we decided to do one for AmilCP blue.

Click <a href="http://2017.igem.org/Team:Peshawar/Model" target="_blank"> here</a>to check out our modeling page!

Contribution: Valencia UPV iGEM 2018

Authors: Carolina Ropero, Adrián Requena Gutiérrez Part BBa_K2656018 is the amil Chromoprotein coding sequence BBa_K592009 compatible with both BioBricks and [http://2018.igem.org/Team:Valencia_UPV/GB3 Golden Braid 3.0] assembly methods.

In order to carry out a correct characterization of the protein and to be able to use it to make measurements of the different transcriptional units that we have assembled with it, we obtained the absorbance spectrum in the conditions of our equipment. To do so, we assembled composite part BBa_K2656113. By using this [http://2018.igem.org/Team:Valencia_UPV/Modeling#spectra protocol] with the parameters of Table 1, Figure 1 was obtained.

Figure 1. amilCP absorbance spectrum

IMPROVEMENT REFERENCE: NWU-China 2019

The N-terminus of this protein was added with a secreted peptide (Kp-Sp,BBa_K2981006). The new part is : BBa_K2981007(Group: iGEM19_NWU-China), Designed by: Junjie Zhu.

Contribution: Duesseldorf 2019

iGEM Duesseldorf characterized this protein in its capacity to be a biosensor molecule for fatty acids. It was assembled into the composite part BBa_K2924020 and tested with several fatty acids, at several concentrations.

Fig.1: LB-Agar plate of Escherichia coli Top10F with the pBbB6c + amilCP plasmid. The amilCP makes the colonies blue.

Fig. 2: Regulation of fatty acid metabolism by the transcriptional factor FadR. FadR recognizes its cognate binding site (white), thereby repressing transcription. Upon binding of an Acyl-CoA to FadR, the promoter region is freed, enabling gene expression.

This year the iGEM team from Düsseldorf 2019 was working on the characterization of amilCP, a blue chromoprotein from the Acropora millepora (BBa_K592009) for the use as a reporter gene for a biosensor. For the characterization the synthetic P_AR from a previous publication ¹ was used and so the biosensor is sensitive for long chain fatty acids (LCFA). The plan was to implement a chromoprotein as a reporter gene, thus enabling to every laboratory to measure a biosensor without fluorescence applications - in contrast, most laboratories have access to a photometer. The chromoprotein amilCP can be observed with the naked eye, in addition to the measurement method by absorption at the wavelength 588 nm for example with a plate reader. Therefore, this option is available for everyone.

Chromoproteins are a good alternative to fluorescent proteins like red fluorescent protein (RFP). The amilCP protein has an absorption maximum at 588 nm and the blue color can be seen with naked eye. Chromoproteins have the benefit that they can measured by absorption and thus can be used in every laboratory.

The production of long-chain fatty acids (LCFA) is regulated by the transcription factor FadR. This transcription factor can bind to Acyl-CoA which leads to the release of FadR from its cognate operator sequence, thereby increasing gene expression (as shown in Fig. 2). </html>

The constructs were cloned into a variant of the pBbB6c ² medium copy number backbone which lacked the lac-promoter, with the restriction sites EcoRI and XhoI. This backbone has the antibiotic resistance chloramphenicol and the origin of replication (ori) pBBR1. The Escherichia coli strain Top10F was transformed with this biosensor plasmid, as seen in Figure 3.

The transformation of the organism was validated by colony PCR. In some cases, successful transformation could quickly be detected by the different colors of the colonies on the plate and as a cell pellet.

Fig.3: Promoter AR with reporter gene amilCP in a pBb backbone. The backbone has a chloramphenicol resistance and a medium copy ori p15A. EcoRI and XbaI were used as restriction enzymes.

The positive clones were used for experiments and were grown in LB-medium over night. The fatty acid stocks for the experiments were prepared. All of the fatty acids were dissolved in ethanol with the exception of butyric acid, which was dissolved in water. The stock solutions of the fatty acids are shown in Tab.1. Tab.1: Stock solutions for different fatty acids

The absorption of the overnight cultures were measured and the cultures were used to inoculate fresh LB medium to an OD₆₀₀ of 0.05. The cultures were induced with different concentrations of fatty acids. First preliminary tests were carried out with palmitic acid at final concentrations of 0.4 mM, 1 mM and a control without fatty acid. For a better dissolving of the hydrophobic fatty acids in LB-medium, Tergitol which was 0.5% of the whole volume, was added to the medium. The induced samples were transferred on a 24 well plate and the plate was incubated overnight in a 37°C incubator, which shaked the cultures with 250 rpm. After nearly 16 hours, the samples were taken out of the incubator and distributed on a 96 well plate in 200 µL aliquots. To account for biological heterogeneity and technical errors three biological replicates were measured in three technical replicates each. An empty vector control (EVC) was also supplemented with fatty acids at different concentrations and measured. All experimental details are listed in Tab. 2. Tab. 2: List of all part improvement experiments

Fig.2: Response of P_AR+amilCP (blue) to different chain lengths of fatty acids compared to an empty vector control (gray). Plot A presents the response for lauric acid, plot B for myristic acid, plot C for palmitic acid and plot D for stearic acid.

The experiments with the blue chromoprotein amilCP ((BBa_K592009) ¹ showed that the production of the chromoprotein is increased by a higher concentration of fatty acids in the medium. The best result was achieved with the fatty acid stearic acid. The biosensor also worked for the chain lengths from C14:0 and C16:0. Here, the EVC is lower than the samples with amilCP. By adding lauric acid (C12:0) to the culture medium, the production of amilCP increased, but the EVC also increased in a similar manner close to amilCP, so it is not certain if this result can be used for distinct conclusion.

To summarise the experiments, the created biosensors works for the fatty acids myristic acid (C14:0), palmitic acid (C16:0) and stearic acid (C18:0) with every reporter gene. When using lauric acid (C12:0), the results become more inaccurate. A dose response can still be observed, but it is not as strong or linear as with the other fatty acids.

References

1: Fuzhong Zhang, James M Carothers, Jay D Keasling. “Design of a dynamic sensor-regulator system for production of chemicals and fuels derived from fatty acids” Nature Biotechnology volume 30, pages 354–359 (2012)

iGEM19_SCU-China:

We expected amilCP to be expressed efficiently in S. cerevisiae, so we chose amilCP to be improved. We processed codon optimization on original amilCP sequence and added a consensus sequence (AAAAAA) for S. cerevisiae expression. And the new sequence was named yamilCP.

Figure. 1 The map of plasmid pYES2-amilCP                      Figure. 2 The map of plasmid pYES2-yamilCP

We respectively cloned the amilCP and yamilCP on the vector of pYES2-NTA.There are the maps of pYES2-amilCP and pYES2-yamilCP (Figure.1 and Figure.2). And we verified the construction of them by double restriction enzyme digestion(Figure.3) and sequencing.

Figure. 3 The double restriction enzyme digestion verification result. lane 1: pYES2-amilCP plasmid, lane 2: pYES2-amilCP plasmid digestion, lane 3: pYES2-yamilCP plasmid, lane4: pYES2-amilCP plasmid digestion, Marker：Trans 2K plus Ⅱ Marker.

Then we transformed pYES2-amilCP and pYES2-yamilCP into S. cerevisiae respectively. Later on, We observed the expression of blue chromoprotein with the induction of galactose (Figure.4).

Figure. 4 The colony transformed pYES2-amilCP and pYES2-yamilCP expressed blue chromoprotein.

To test the expression effciency of pYES2-amilCP and pYES2-yamilCP in S. cerevisiae, we transformed them into BY4741 and used galactose to induce blue chromoprotein expression. After 10 days, we observed blue colonies on the pYES2-yamilCP plate at first and there was no blue colony on the pYES2-amilCP plate, which confirmed that yamilCP expressed more quickly than amilCP (Figure.5). As Figure. 5, there is no blue clony (0/356) on the amilCP plate while 8 colonies (8/575) on the yamilCP plate. It shows that our improvement is successful.

As the result, the improved yamilCP was successfully expressed, and the expression of yamilCP is more quickly than that of amilCP in S. cerevisiae.

Figure. 5 The transformation results of pYES2-amilCP and pYES2-yamilCP into S. cerevisiae BY4741 with galactose induction after 10 days.

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