Difference between revisions of "Team:Montpellier/Toolbox"

This toolbox contains all kind of information that can be useful for working with Lactobacillus jensenii. First, we provide culture conditions that we used and were proven to be working. Second, it contains a transformation protocol that we optimized and found to be the most efficient of all those we tested. Finally, the toolbox contains all DNA sequences (vectors and biobricks parts including L. jensenii specific promoters) that we used in L. jensenii for our project. We hope that this toolbox will facilitate the use of L. jensenii by other iGEM and research teams. We plan to extend the toolbox in the future by providing the community with a physical distribution of well-characterized vectors and regulatory elements.

How to grow Lactobacillus jensenii?

Strain and medium

For our project we used the following strain and culture medium :

Bacteria

Lactobacillus jensenii Gasser et al. (ATCC® 25258™)

Culture

BD Difco™ Lactobacilli MRS Broth

We used this broth for both our liquid and solid culture media. The liquid medium was used to do the solid medium by adding agar to it. We tested different concentrations of Agar to measure which one was the best.

5g/L

7g/L

10g/L

12g/L

15g/L

The plates with 5g/L and 7 g/L of Agar were not showing any colonies. For the three others there were more colonies for 12g/L. From this experiment we decided to use 12g/L of Agar for our experiments.

Cell culture

Growth on solid medium

L. jensenii is a facultative anaerobic bacterium, it does not absolutely need CO₂ to survive but grows way better in anaerobic conditions. For our project we did not have a CO₂ incubator available for growing bacteria. We thus decided to grow our bacteria using an “old school” microbiology method. The goal of the method is to get rid of the Oxygen present in the environment of the bacteria. To do so, we put the plates in a hermetic container and placed a burning candle inside it before closing the lid. The candle consumes all the oxygen and turns it into in CO₂, until all O₂ is consumed and the candle extinguish.

For our culture we used two kinds of plates and thus two kinds of containers.

As L. jensenii grows in small colonies we usually used small plates (60mm diameter) and put them in a jar (Figure 2) as follows:

For transformant selection, we needed more colonies so we used normal culture plates (100mm diameter). We put them in an airtight-closing bowl with three candles (Figure 3).

Growth in liquid medium

The stationary phase is reached at 8 hours of culture (Figure 4).
The culture takes generally 24 hours in liquid and solid media and can take up to 48 hours to see colonies on plates. It is much slower than E. coli and this can pose be a constraint for research on this strain.

How to transform L. jensenii?

To transform L. jensenii, we found several protocols. All of these protocols were specific to Lactobacillus plantarum or Lactobacilli in general, but not to Lactobacillus jensenii.
We selected different protocols that used or not magnesium in the electroporation buffer. Indeed, our electroporation machine could not stand magnesium, as it can causes electric arcs and damage the machine. We had to find another electroporator at the University of Montpellier. These electroporator had advanced settings such as the resistance (Figure 5).

The three protocols that we chose were one from Berthier in 1996, one from Speer in 2012, and the last one from Chatel [1].

We tried to transform our bacteria several times with these three different protocols. Finally, we decided to focus on Berthier 1996 as we had better results. A reason why Speer 2012 did not work well was the addition of glycine to grow bacteria. It weaken the bacterial wall too much, and inhibited the grow. We did not focus on Chatel because the use of magnesium in the electroporation buffer gave us bad time constants, that means that bacteria were not well transformed.

Once we chose the most promising protocol, we had to optimize it. We tried different conditions for the following parameters:

• Amount of DNA per reaction: 10ng, 100ng, 1000ng, 5000ng (of pLEM415) ⇒ did not change anything. We decided to add about 1000ng of plasmid per reaction.
• Voltage: 9kV/cm, 10kV/cm, 12.5kV/cm ⇒ we obtained better time constant (closer to 11ms to 13ms as explained in Berthier 1996) with 12.5kV/cm for the electroporation.
• Resistance (ohm Ω): 300Ω, 500Ω, 600Ω ⇒ to reach a time constant between 11ms and 13ms, we decided to follow the protocol and to use 600Ω.
• Antibiotic concentration for transformant selection: erythromycin 0.5µg/mL, 5µg/mL ⇒ we chose 0.5µg/mL as it was enough to select the transformants. 0.5µg/mL can kill non-resistant L. jensenii.

You can find the exact protocol for transforming L. jensenii on our protocol page: protocol.

L. jensenii plasmid

The choice of the plasmid has been complicated because the strain is little used in synthetic biology. Thus, it has been difficult to find plasmids "free" of intellectual property. Indeed, the only existing plasmids (pOSELp23 and pOSEL144) were created by the company Osel Inc (USA). Unfortunately, we could not obtain the constructs from the company.

We therefore had to find a vector responding to the following specifications:

1. An E. coli specific origin of replication.
2. An antibiotic resistance gene for selection in E. coli ⇒ These parts are required to support cloning and propagation of our vectors into E. coli before transforming them into L. jensenii.
3. A L. jensenii specific origin of replication.
4. An antibiotic resistance gene for selection in L. jensenii ⇒ These parts will allow propagation and maintenance of the plasmids in L. jensenii.

We chose not to create a vector from scratch but to start by trying to reuse different already ones existing. Our choice turned toward specific vector with different origins of replications operating into Lactobacillus species available on the Addgene website. While none of them was previously used for L. jensenii, we hoped that at least one of these vectors could be functional in L. jensenii:

• pTRKH2
• pTRKH3-slpGFP
• pLEM415-ldhL-mRFP1
• pTRK669
• pTRK892

We were able to transform pLEM415. If we had more time, we would have tested all the plasmids in L. jensenii. Some of them might be functional.

Testing and choosing a vector

pLEM415 is the most documented so it the easiest to use for our manipulations. This construct was used to transform Lactobacillus casei, Lactobacillus delbrueckii and Lactobacillus acidophilus [1]. Because of time constraints, we were not able to test the other plasmids.

Shuttle vector pLEM415 was obtained by ligating PstI-digested pLEM5 with PstI-linearized Escherichia coli vector pBII [2]. pLEM5 contain the putative replication protein gene (rep). Moreover, the plasmid contain the minus origin of replication (ori-), the plus origin of replication (ori+) (CTaTCTTtATCTTGATACTTA) from Lactobacillus fermentum.

To compare, all of the OSEL vectors contain the repA and erm genes are from a naturally occurring L. reuteri plasmid pLEM7 [3]. pLEM7 was generated by inserting of multiple cloning site into pLEM5 [2].

To conclude, OSEL vectors and pLEM415 have the same origin vector. While OSEL work with L. jensenii, we could suppose that our vector work as well in our strain.

In recent OSEL research, they create a modular shuttle vector pOSEL175, a modified version of pOSEL144 that can be integrated into the minor capsid gene of L. jensenii through homologous recombination [4].

Antibiotic resistances

Reporter

Promoter studies

We aimed at developing a library of differents promoters that work in L. jensenii. We first retrieved known L. jensenii promoters from the literature. We also generated a bioinformatic tool using MEME to find pre-gene sequences in bacterial genomes. Wwe then chose the most relevant ones to design and clone the constructs for testing their strength. For more information see our modeling page. Moreover, as we wanted to use B. subtilis a surrogate Gram positive chassis, we designed a set of construct operating into this bacterium.

In total, we selected 3 Promoters from Osel papers [1], 10 in silico predicted sequences, and 4 promoters for B. subtilis [5] and we synthesized these promoter sequences. We use the already described RpsU promoter used in our constructs that are supposed to be coding the proteins for our project.

These 17 promoter candidates were placed upstream RFP gene coupled with a strong RBS to quantify their strength by analysing the fluorescence intensity of the cells.

All sequences were cloned into E. coli. Unfortunately their strength couldn’t be analyzed on time.

Putative promoters:

• Primer NC
• Primerprom3
• Primerprom43
• Primerprom43-1SUV
• Primerprom188SUV
• Primerprom241-1SUV
• Primerprom259-1JV
• Primerprom267-1SUV
• Primerprom378-1JV
• Primerprom403JV
• Primerprom500JV

B. subtilis promoters

• PrimerpromBS-Ppgi-R0
• PrimerpromBS-PrelA-R0
• PrimerpromBS-Pveg-R0
• PrimerpromBS-PymdA-R0

L. jensenii promoters

• PrimerpromPWM
• PrimerpromRpsU
• PrimerpromptsH

To get the sequences, click here.

Secretion tags

We quickly encountered a problem in the project. We need to express spermicidal molecules in the supernatant so that they can act directly on the spermatozoa.

In the case of peptides, we have not added an excretion system because proteins already undergo many post-translational rearrangements. We did not want to burden the process with the addition of a secretion system.

In the case of antibodies, we looked for different secretory peptides associated with gram + bacteria:

• The first that we chose is CbsA. This signal peptide (SP) is used for secretion of antibodies in L. jensenii [4][6]. The SP is synthesized on the N-terminus domain. Downstream the CbsA sequence are added 4 amino acids (APVT) at the N-terminus domain of the scFv. These 4 amino acids are similar to a native signal peptidase cleavage site of this protein. The addition of the APVT sequence shown to improve the secretion of a full-length protein in L. jensenii.
• YncM, Epr, YjfA: These SPs are coming from a screening of SPs of Bacillus subtilis. As they can be used to secrete proteins in B. subtilis which is a gram positive bacteria [7], we decided to try to use them to secrete our stuff in L. jensenii that is also a gram positive bacteria. We used the same template for the construction. These SPs are on the N-terminus domain, and followed by the APVT sequence on their N-terminus domain.