Team:LMU-Munich/Germination Stop

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GerminationSTOP

The goal of this project is to remove the germination capability of our spores, while keeping their necessary structural functions intact.

There are two approaches to achieve this:

• Knock out genes that are involved in germination.

• Suicideswitch: Toxin production by vegetative cells if germination knockout fails and spores manage to germinate.

Gene Knockouts

Based on the work of [http://www.ncbi.nlm.nih.gov/pubmed/19554258 J. Kim and W. Schumann (2009)] and [http://www.ncbi.nlm.nih.gov/pubmed/11466293 B. Setlow et al (2001)], we decided to knock out genes cwlJ, sleB, cwlB, gerD, and cwlD. The genes cwlJ and sleB code for lytic enzymes which are active in the process of germination. In the work of [http://www.ncbi.nlm.nih.gov/pubmed/11466293 B. Setlow et al (2001)], when cwlJ and sleB were knocked out together, germination frequency was reduced by 5 orders of magnitude. [http://www.ncbi.nlm.nih.gov/pubmed/19554258 J. Kim and W. Schumann (2009)] report a similar reduction in germination when gerD and cwlB are knocked out together, and a reduction in germination ability when the gene cwlD is knocked out. When all five of these genes are knocked out, we hope to yield a B. subtilis strain which produces spores completely incapable of germination.

Two methods are being employed to knock out germination: resistance cassette (RC) knockouts and clean deletions. Single RC knockouts were created first; then they were combined to create multiple knockouts.

Fig. 1: The four germination genes being knocked out, and their resistance cassette replacements, as shown on the Bacillus chromosome.

Fig. 2: The technique employed for resistance cassette knockouts: Long-flanking-homology PCR. This example shows the gene cwlD being replaced with the resistance cassette kanamycin.

This will be checked with germination assays.

Further, we will investigate the possibility of using a redundant toxin system to immediately kill off any spores which somehow germinate in the Suicideswitch system.

How do the Gene Knockouts of GerminationSTOP actually work?

To understand how our germination knockouts actually prevent germination, it is crucial to understand how the Bacillus germination process occurs.

Bacillus cells form spores in a process called sporulation in response to starvation of nutrients (including carbon, nitrogen, or phosphorus) or in response to peptides secreted by other cells which signal too high of population densities to cells.

The “mother” cell forms the endospore within its own cell membrane. The spore contains its DNA in the spore core, which is protected by several layers of coats. The spore is very dry, and contains a substance called dipicolinic acid (DPA), which is replaced with water when the spore germinates. Until the spore is hydrated (and swells), it is resistant to a wide variety of environmental stressors, including UV radiation, toxic chemicals, freezing, high heat, dessication, and pH extremes.

Fig. 3: Taken from [http://www.ncbi.nlm.nih.gov/pubmed/19554258 Kim, J. & Schumann W (2009)].
A: Vegetative cell in the phase 0.
B: Cell at stage II where the asymmetric septum has been formed.
C: Cell at stage III where the cytoplasmic membrane has engulfed the forespore.
D: Cell at stage IV where formation of the coat has already started; the spore is about to be released from the lysed mother cell.

The spore has germinant receptors on its inner spore membrane, and is suspected to have semipermeable or porous outer layers that permit the passage of germinants to the receptors. When germinants such as amino acids and sugars reach germinant receptors, the spore begins a biochemical process of germination. It takes up water, shifts its pH, and swells. It breaks out of its coat and begins the outgrowth process.

Fig. 4: From [http://www.photonics.com/Article.aspx?AID=29892 Photonics. com (2007)] Emergence of vegetative cells: 60- to 70-nm-deep apertures in the rodlet later that gradually enlarged (C and D), and subsequently eroded the entire spore coat (E). Germ cells emerged from these apertures. (Photo courtesy Lawrence Livermore National Laboratory)

We were concerned that because the beginning stage of germination is a strictly biochemical one, that maybe our spores would lose the ability to fully germinate, but would nonetheless become deformed by the initial steps of germination. This would be problematic because the spores should be vectors to carry proteins; deformed spores could be ineffective as delivery vectors. The investigative work of [http://www.ncbi.nlm.nih.gov/pubmed/17535925 Plomp et al (2007)] on Bacillus cells seems to support that the lytic enzyme knockouts we chose could help to maintain the spore shape. They state:

“A significant fraction (≈30%) of spores did not proceed to outgrowth in the timeframe of the observation and did not exhibit degradation of the rodlet layer. However, after drying, >90% of these spores showed a structural collapse, indicating prior replacement of the dipicolinic acid in the spore core with water, i.e. they did proceed through the germination stage, but not the outgrowth stage.” […] “Etch pits were the initiation sites for early germination-induced spore coat fissure formation.” […] “Disassembly of the higher-order rodlet structure initiates at micro-etch pits, and proceeds by the expansion of the pits to form fissures perpendicular to the rodlet direction.” […] “We suggest by analogy that rodlet structure degradation is caused by specific hydrolytic enzyme(s), located within the spore integument and activated during the early stages of germination.”

What we read from this is that spores can be cued to germinate, and the etch pits that lead to the destruction of the spore coat can be formed, but without the activity of lytic enzymes, further steps of germination do not occur. Therefore, it is possible for our spores to be presented with germinants, and still to maintain their structural shape, despite possibly undergoing the first biochemical stage of germination.

Thus, by knocking out the genes coding for lytic enzymes, our goal is to prevent both outgrowth, and the disassembly of the spore coat. This will leave our SporoBeads intact to be delivery vectors for proteins.

Suicideswitch

As a backup plan to make our Sporobeads even safer, we developed the Suicideswitch. In case the spores do germinate, due to degradation or destruction of their outer coats, e.g. by high pressure, the Suicideswitch will be turned on.

It is composed by an alternative sigma factor [http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3426412/ ecf41], which derives from B. lincheniformes and we chose to work with the short version constitutively on. It is synthetically linked to a sigma G regulated promotor responding quite late to sigma G ([http://www.ncbi.nlm.nih.gov/pubmed/15699190 PspoIVB] responding strongly or [http://www.ncbi.nlm.nih.gov/pubmed/15699190 PsspK] responding weakly) which is the last sigma factor activated in the forespore. Through this ecf41 is produced quite late in the forespore. Ecf41 then activates the [http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3426412/ PydfG] promotor, which is the naturally responding promoter to ecf41, which then activates the transcription of [http://jcs.biologists.org/content/118/19/4327.abstract MazF], a bacterial toxin from E.coli degrading mRNA.

The idea behind this is to pack the Sporobeads full with ecf41 when they sporulate, which will in turn kill them upon germination due to the MazF.

Through the system with the alternative sigma factor the forespore gains hopefully enough time to fully mature before MazF starts to be produced.

We chose MazF, as we think it will not be able to harm our Sporobead even if it is made too early, as the spore does not rely on translation to be preserved.

We are planning to model this system.

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