Overview

In order to inhibit Fusarium oxysporum cubense growth, several anti-fungal substances will be produced when fusaric acid is sensed. Those being 2,4-DAPG, chitinase, DMDS,DMTS and pyoverdine. 2,4-DAPG or 2,4-Diacetylphloroglucinol is an antibiotic against plant pathogens[1]. Chitinase is a lytic enzyme that breaks down fungal cell walls. Dimethyldisulfide (DMDS) and dimethyltrisulfide (DMTS) are sulfur by-products produced by Pseudomonas putida and have shown to stimulate plant growth and inhibit F.oxyposrum respectively[2,3]. And lastly, pyoverdines are iron-chelating compounds that are produced when iron is limited in order to scavenge for iron to induce iron competition. With these anti-fungal substances our engineered P. putida will be able to better inhibit F. oxysporum.

2,4-Diacetylphloroglucinol(2,4-DAPG)

2,4-DAPG, full name 2,4-diacetylphloroglucinol, is an antibiotic that is widely used in the agricultural industry against pathogens. It’s a broad spectrum antibiotic has been shown to play a key role in the biological control of various plant pathogens including F. oxysporum[4]. In addition to that, it has also shown to induce systematic resistance in plants[5]. Since P. putida does not produce DAPG by itself, a gene cluster obtained from Pseudomonas flourescens was introduced into P. putida. The phl gene cluster contains eight genes, from phlA to phlH. Gene cluster phlABCDE was be used for this project as literature has shown that phlABCD are the DAPG synthesis genes(see figure 1) and phlE codes for an efflux pump[6,7]. phlABCD has been expressed before in P. putida and has shown to produce 2,4-DAPG[8].

Dimethyldisulfide (DMDS) and dimethyltrisulfide (DMTS)

When breaking down methionine for ammonium, methanethiol gets formed as a by-product. Then methanethiol gets oxidized into dimethyldisulphide (DMDS) and dimethyltrisulphide (DMTS) (see figure 2). DMTS was shown to have an inhibitory effect against F. oxysporum with an inhibition at the start of 78, but then slowly declined to 26%[3]. DMDS is used as plant growth promoter and at the same time also shown a slight inhibition to foc of 10%[2]. Both DMTS and DMDS are naturally produced in P. putida but a higher production is desired. One thing that causes low yield of DMDS is the low affinity of methionine-γ-lyase to methionine, which means less conversion of methanethiol, which then leads to low DMTS and DMDS production. So, we decided to overexpress an enzyme that has a higher affinity towards methionine and will therefore increase DMDS and DMTS production, this enyzme is a methionine-γ-lyase from Brevibacterium linens, which has shown to increase DMDS production in Lactocossus lactis[9]. This gene was codon-optimized and synthetsized by IDT for P. putida.

Pyoverdine

Pyoverdines are siderophores produced by P. putida[10,11]. Siderophores are small green/yellow fluorescent compounds that have high affinity to iron(III), which by scavenging free iron can inhe end can lead to iron limitation. Due to iron starvation, the growth of pathogenic fungi and bacteria in the rhizosphere will be restricted[12]. It was shown that there was a direct correlation of siderophore production and their inhibition to germination of chlamydospores of F. oxysporum[13]. In addition to that, siderophores have also been shown to induce resistance in radish plants[14]. However the effects of siderophore decreases when the disease incidence increases above 74%[15]. P. putida WCS358 is able to produce a siderophore, pseudobactin 358 (PBS358), which has been shown to be involved in inhibition of Fusarium[16]. Pyoverdine production is iron dependent as it is regulated by a ferric uptake regulator protein (Fur)[17], see figure 4. PfrI is a transcription activator that is needed for activation of genes involved in pyoverdine synthesis[18]. So an overexpression was be done of pfrI, which is expected to result in pyoverdine production, even when in an iron abundant environment.

Chitinase

Chitinase is a hydrolytic enzyme that breaks down hydrolytic bonds in chitin and is produced in both bacteria and plants. Chitinase has shown to be useful in biological control against fungi[21,22]. In bacteria their function is to attack shellfish animals or fungi, and degrade their chitin cell walls. In plants they are known as pathogen related proteins that are involved in the induced systematic resistance of plants in order to defend themselves against pathogens. P. putida KT2440 has a lytic enzyme PP3066 that is predicted to have chitinase activity, so this gene was overexpressed to increase chitinase activity.

Results

2,4-Diacetylphloroglucinol(2,4-DAPG)

PhlABCDE was successfully cloned and put into plasmid pSEVA254[23]. This plasmid was used instead of the iGEM plasmid because it has shown to work before in P. putida, it contains LacI coupled with an IPTG inducible promoter and it has terminators behind the gene insert. Both E. coli and P. putida KT2440 were transformed with a SEVA plasmid containing the phlABCDE gene cluster. Succesfull Transformants were verified via colony PCR (see journal). During colony PCR of P. putida, we were not able to get an expected 5.4kbp band. However, when using a primer pair that forms a 1kbp product, we could then see possible transformants. The method used in High-performance liquid chromatography (HPLC) was correct (see protocol). Standards were detected and a standard curve was made. However, verifying production of 2,4-DAPG via HPLC turned out to be difficult due to a lot of background noise of the samples, even after an extraction step.

In order to test 2,4-DAPG against F. oxysporum, an in vitro assay was done on Komada agar plates. In this assay different concentrations of pure 2,4-DAPG were plated and then inoculated with a 5mm Fusarium plug. Plates were then incubated at 25°C for several days.

From figure 6 it can be seen that with an increase of 2,4-DAPG there is a decrease in F. oxysporum growth. However when it reached to 100ug/ml results were not reproducible with one plate having more growth that the other. Afterwards, another in vitro experiment was set up to test 2,4-DAPG concentration from 100-400ug/ml. However here spores (3.87E+07 spores/ml) were used as an inoculum, instead of a F. oxysporum plug, due to unavailability of a fresh F. oxysporum plug on agar plate. Plates were then incubated in 25°C for several days.

When comparing figure 6 and 7 it can be seen that when inoculated with spores even in 5 days there is absolutely no growth of F. oxysporum at a concentration of 100ug/ml 2,4-DAPG, whereas when for the F. oxysporum plug there is growth after 6 days with mixed results at the same concentration of 100ug/ml 2,4-DAPG. After in vitro assay, an in vivo assay was also done using our P. putida tranformants, containing the phl gene cluster for 2,4-DAPG production. An overnight P. putida liquid culture was spread on a LB agar plate, grown overnight at 30°C and then inoculated with a 5mm F. oxysporum plug.

In figure 8, plates were modified with a red circle to better visualize the fungal disc. It can be seen that the wild type P. putida KT24400 already inhibits F. oxysporum very well. Our transformant (DAPG) seems to show a slightly small F. oxysporum disc when comparing it with the wild type. It is very hard to see a big difference between the wildtype and our transformants, as the wildtype has shown to already inhibit F. oxysporum greatly when comparing wildtype and foc control. Please note that phlABCDE was not yet made into the Biobrick standard, due to too many illegal sites and insufficient time to remove them.

Dimethyldisulfide (DMDS) and dimethyltrisulfide (DMTS)

Methionine-γ-lyase was successfully made into a Biobrick standard format (Bba_K1493300). It was then put into plasmid pSEVA254 plasmid, which was transformed in both E. coli and P. putida KT2440. Succesfull Transformants were verified via colony PCR for E. coli and P. putida. P. putida were grown, induced and harvested after 3 hours. Cell free extracts were obtained via sonification and were then used for an assay. DMDS and DMTS were supposed to be measured via Gas Chromatography (GC)(see protocol) .But it was in the end not possible due to unexpected problems with the GC. However an in vivo assay was done co-inoculating our transformed P. putida with F. oxysporum.

In figure 9 it can be seen when comparing our transformant containing Methionine-γ-lyase with the wildtype P. putida there is a much small fungal disc, probably meaning a higher inhibition of our transformant.

Pyoverdine

The pfri gene was successfully made into a Biobrick standard format (Bba_K1493200), validated and characterized. pfrI was cloned and put into plasmid pSEVA254. Transformed in both E. coli and P. putida KT2440. Succesfull transformants were verified via colony PCR. Afterwards growth experiments were done in minimal M9 medium supplemented with iron and pyoverdine was measured using spectrophotomery. When grown overnight it was possible to see that Pfri transformants were slightly greener when compared to the control. Control used here was a P. putida containing an empty pSEVA254 plasmid.

In figure 10 it can be seen that the peak (400nm) of Pfri transforamant is higher than the peak from a P. putida containing an empty plasmid.

When looking only at the aborbance at 400nm (figure 11), it can be seen that there is a 4-fold increase of pyoverdine production when pfri is overexpressed in P. putida. In addition to this experiment, an in vivo experiment was also done with pfri tranformants co-inoculated with a 5mm F. oxysporum plug.

In figure 12 it can be seen that pfri transformant has a smaller F. oxysporum disk when compared to the wildtype. Meaning it's inhibition is increased but only ever so slightly.

Chitinase

Chitinase was succesfully cloned into broad host range plasmid (pSEVA254) and transformed into P. putida. Succesfull tranformants were verified via colony PCR. Transformants were grown, induced and harvest 3 hours after induction. Cell free extracted were obtained via sonification of cells (see protocols). Transformants containing overexpression of chitinase were also co-inoculated with Fusarium in an in vivo assay, results in figure 13.

In figure 13, it can be seen that the tranformants with an overexpression of chitinase seems to have a smaller fungal disc as when compared to the wild type.

All transformants together

In addition to testing just one tranformant with F. oxysporum TR4, two cocktail mixes were made.

1. Chitinase, Methionine-γ-lyase and Pfri.
2. phlABCDE, Chitinase, Methionine-γ-lyase and Pfri

These two cocktail mix were then spread on agar plates using overnight liquid culture, grown overnight in 30°C and co-inoculated with F. oxysporum the following day.

In figure 14, chit+MGL+Pfri seems to have a better inhibitory effect when compared to the wildtype as it can be seen that the fungal disc is smaller than the one of the wildtype. For the cocktail mix that contains all four, mix(all 4) the fungal disc is only slightly smaller when compared to the wildtype.

Conclusion

Over the past few months we tried to engineer P. putida with four different genes in order to increase its inhibitory effects against F. oxysporum. All four different transformants were obtained and have been tested on. Methionine-γ-lyase and pfri were both made into biobricks, Bba_K1493300 and Bba_K1493200 respectively. With both biobricks validated, and for Pfri characterized. Pfri has shown to give a four fold increase of pyoverdine production in the pressence of iron in the medium.

It was also shown that 2,4-DAPG is indeed a good anti-fungal against F. oxysporum TR4. With decrease growth of F. oxysporum when there is an increase of 2,4-DAPG (figure. Even P. putida transformants containing phlABCDE gene cluster had a bit higher inhibition when compared to the wildtype(figure 6 and 7). Even though production of 2,4-DAPG was never confirmed via HPLC but method detecting 2,4-DAPG was correct with a standard curve made(figure 5).

However it was hard to distinguish the increase inhibition effect of our transformants against F. oxysporum. With some we could say that there is a increase of inhibition (figure 9) and with others we can only say that there is a indication of a slight increase in inhibition (figure 8, 12 and 13). This is because the chassis we have chosen is already very good at controlling F. oxysporum inhibiting it already very wel in these assay that in end makes it hard to see a difference with our transformants.

Future work

For future work, it would be nice if all the anti-fungal genes are coupled together behind the fusaric acid promoter in order to test production rate that is induced by fusaric acid. Also testing in the green house with a co-inoculation of F. oxysporum in order to see if production of the anti-fungals can reach high enough levels that it causes inhibition affect to F. oxysporum. This really depends on the amount of fusaric acid present in the soil when F. oxysporum is present. Other works would be to try other anti-fungal genes to increase inhibition by using other anti-fungal compounds such as phenazine-1-carboxylic acid which was shown to also have anti-fungal effects

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