Team:LMU-Munich/Bacillus BioBricks

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Revision as of 17:07, 21 September 2012

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Bacillus BioBricks

We will create a toolbox of Bacillus BioBricks to contribute to the registry.

This BacillusBioBrickBox contains Bacillus specific:

Vectors	Promoters	Reporters	Affinity tags
pSBBs1C pSBBs4S pSBBs2E pSBBs1C-lacZ pSBBs3C-luxABCDE pSBBs4S-PXyl pSBBs0K-Pspac	Pveg PliaI PlepA Anderson	mkate2 luc lacZ	Flag His cMyc Strep HA

Bacillus Vectors

Here is a list of all the vectors we cloned and used. Please note that pMAD is not in a BioBrick standard, but it is a useful tool to knock out genes in Bacillus subtilis.

For the use of our vectors, please see our Protocols page. A general introduction to Bacillus subtilis and its integrative vectors can be found here. All vectors have ampicillin as E. coli resistance and RFP in the multiple cloning site as selection marker.

Here you can find the respective vector maps:

The number in the vector's name codes for the insertion locus and the following letter for the Bacillus subtilis resistance gene according to the following table:

The concentrations of the antibiotics and the insertion tests can be found in our Protocol section.

Bacillus Promoters

To get a set of promoters with different strength we characterized several promoters in B. subtilis. They can be divided in three different groups: the constitutive promoters from the Anderson collection from the Partsregistry, the constitutive promoters P_liaG, P_veg and P_lepA from B. subtilis, and the inducible promoters P_liaI and P_xyl-XylR from B. subtilis. For the characterization of the different promoters we used the two reporter vectors pSB_Bs3C-luxABCDE and pSB_Bs1C-lacZ as well as the reporters lacZ, luc and mKate2 in BioBrick standard.

Anderson promoters

The first group of promoters evaluated are the promoters of the Anderson collection which we call Anderson promoters. They have already been measured in Escherichia coli where they all showed a constitutive behavior with a different strength. In this project, eleven Anderson promoters were characterized in B. subtilis. Therefore we used the reporter vector pSB_Bs3C-luxABCDE from the BioBrickBox were they showed quiet a low activity in B. subtilis (see Data). To confirm this result some Anderson promoters were also evaluated in the reporter vector pSB_Bs1C-lacZ(see Data).

• J23100 (BioBrick:BBa_K823004)
• J23101 (BioBrick:BBa_K823005)
• J23102 (BioBrick:BBa_K823006)
• J23103 (BioBrick:BBa_K823007)
• J23106 (BioBrick:BBa_K823008)
• J23107 (BioBrick:BBa_K823009)
• J23113 (BioBrick:BBa_K823010)
• J23114 (BioBrick:BBa_K823011)
• J23115 (BioBrick:BBa_K823012)
• J23117 (BioBrick:BBa_K823013)
• J23118 (BioBrick:BBa_K823014)

Constitutive promoters from B. subtilis

The second group of promoters charaterized are constitutive promoters from B. subtilis. We evaluated the promoters P_liaG, P_veg and P_lepA. Therefore we used the reporter vectors pSB_Bs3C-luxABCDE and pSB_Bs1C-lacZ as well as the BioBrick reporters lacZ, luc and mKate2.

• P_liaG (BioBrick:BBa_K823000)

P_liaG is a weak, constitutive promoter from B. subtilis. It is responsible for the transcription of the last four genes of the liaIHGFSR locus and therefore for the production of the components of the LiaRS system, which is important for the detection of cell wall antibiotics (Jordan et al., 2006). P_liaG was evaluated with the reporter vectors pSB_Bs3C-luxABCDE and pSB_Bs1C-lacZ as well as the reporter BioBrick lacZ. This promoter showed a much higher activity than the Anderson promoters which was still weak in comparison to the other evaluated Bacillus promoters (see Data).

• P_veg (BioBrick:BBa_K823003)

P_veg is known to show a strong constitutive activity during the vegetative growth phase and sporulation phase. This promoter is important for the transcription of the veg gene, which plays an important role during sporulation (Fukushima et al., 2003). P_veg was measured by using the reporter vector pSB_Bs1C-lacZ as well as the reporter BioBrick lacZ. This promoter was the strongest of our evaluated promoters (see Data).

• P_lepA (BioBrick:BBa_K823002)

P_lepA is constitutive promoter which is important for the transcription of a bicistronic operon. One of the expressed proteins is the protein PlepA (Homuth et al., 1996). This protein plays an important role during the translation as it can move the mRNA-tRNA complex one step back in the ribosome which is expected to improve the fidelity of translation (Qin et al., 2006). This promoter was evaluated with the reporter vector pSB_Bs3C-luxABCDE as well as the reporter BioBricks luc and mKate2. The activity of this promoter is between the activity of the strongest promoter P_veg and the weak Bacillus promoter P_liaG (see Data).

Inducible promoters from B. subtilis

The last group of promoters consists of two inducible promoters of B. subtilis , P_liaI and P_xyl-XylR. They are useful to decide when to turn on gene expression because these promoters need an inducer to start transcription. They are evaluated with the reporter vectors pSB_Bs3C-luxABCDE and pSB_Bs1C-lacZ and the BioBrick reporters lacZ, luc and mKate2.

• P_liaI (BioBrick:BBa_K823001)

P_liaI is an inducible promoter from B. subtilis which is induced by antibiotics that interact with the lipidII cycle, e.g. bacitracin. If the cell senses stress there is a phosphorylation of the two proteins LiaS and LiaR. LiaR binds to the operator of the promoter and induces the transcription. When the promoter is turned on the two proteins LiaI and LiaH are expressed which play an important role in the stress response (Jordan et al., 2006). This promoter is evaluated with the reporter vectors pSB_Bs3C-luxABCDE and pSB_Bs1C-lacZ as well as the reporter genes lacZ, luc and mKate2. The induction was measured with different concentrations of bacitracin (see Data).

• P_Xyl-XylR (BioBrick:BBa_K823015)

P_Xyl-XylR is a inducible promoter from B. subtilis which is induced by xylose. XylR is constitutively expressed, and is the repressor of P_Xyl in absence of the sugar Xylose. In presence of Xylose, XylR leaves the operator and the P_Xyl is active [see e.g. Kreuzer et al.. This promoter was evaluated with the BioBrick reporter lacZ (see Data).

Bacillus Reporters

We designed some reporters that are commonly used in B. subtilis or are codon optimized versions of popular reporter genes. All reporters have a modified iGEM Freiburg standard (RCF 25) pre- and suffix for assembly of in-frame fusion proteins. Our prefix also includes the B. subitlis optimized RBS.

prefix: GAATTCCGCGGCCGCTTCTAGATAAGGAGGAACTACTATGGCCGGC

suffix: ACCGGTTAATACTAGTAGCGGCCGCTGCAGT

• GFP (BioBrick:BBa_K823039)

We took a gfp derivate of the Bacillus subtilis plasmids pGFPamy and added the BioBrick compatiple pre- and suffix of the Freiburg standard (Assembly 25).

• mKate (BioBrick:BBa_K823029)

We synthesized this rfp derivate with a codon-optimized version for the use in B. subtilis with pre- and suffix of the Freiburg standard

• LacZ (BioBrick:BBa_K823019)

lacZ under the control of Pspac in pSB_Bs0K-P_spac. Plate induced with IPTG

This lacZ gene is derived from the Bacillus reporter vector pAC6. It is constructed in the Freiburg Standard (Assembly 25) for in-frame fusion proteins. It also includes a Shine-Dalgarno Sequence optimized for Bacillus subtilis translation.

• luc (BioBrick:BBa_K823028)

We synthesized this luciferase for luminescence assays with luciferin as substrate.

Affinity Tags

• 3x Flag - tag (BioBrick:BBa_K823034)

• HA - tag (BioBrick:BBa_K823035)

• cMyc - tag (BioBrick:BBa_K823036)

• His - tag (BioBrick:BBa_K823037)

• Strep - tag (BioBrick:BBa_K823038)

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