Team:HokkaidoU Japan/Project/PHB Synthesis

Planning

We attempted to make Escherichia coli producing bio-plastic for demonstrating industrial applicability of “Aggregation Module” that makes “bio-capsules” formed by aggregation of E. coli through cell-cell interaction via adhesion molecule, Ag43, located on the surface of outer membrane. Development of a cost-effective method for manufacturing biodegradable plastic is one of important issue for making sustainable future society. Common plastic is made from oil. Oil is limited resource, since it is estimated to be exhausted just in 46.2 years^[1]. Synthetic plastic also cause problem as a stable waste material since it is not bio-degradable. Bio-Plastic will never contribute to the increase of atmospheric carbon dioxide since bacteria utilizes glucose as resource for its biosynthesis.

Background

Poly-3-hydroxy-butyrate P(3HB) is one of bio-plastic made by bacteria and archaea. They store P(3HB) in their cells as energy-storage molecule^[2]. So bio-plastic is bio-degradable. Those bacteria synthesize it from acetyl-CoA, the intermediate product of glycolysis. Monomer of P(3HB) is also used as material for making several other useful plastics (co-polymer) through coupling with other types of component molecules like valeric acid or lactic acid^[3]. Ralstonia eutropha is well-known as hydrogen bacteria that produce P(3HB).

In R. eutropha cells, P(3HB) is made through 3 steps. Two acetyl-CoA molecules made from carbohydrate converted to acetoacetyl-CoA by acetyl-CoA acetyltransferase encoded by PhaA gene. Then acetoacetyl-CoA reductase encoded by PhaB gene catalyzes the reduction of acetoacetyl-CoA to (R)-3-hydroxybutyryl-CoA (3HB-CoA). Finally, P(3HB) synthase encoded by PhaC gene catalyzes polymerization reaction of monomer molecules to polymer P(3HB)^[2].

Experiments

Optimization of P(3HB) production

We tried optimization of P(3HB) production under four each conditions: E. coli host strain, addition of pantothenic acid (PA), Glucose concentration and liquid culture mediun. P(3HB) wad produced by using pGEM(phaCAB) that covers all region for P(3HB) biosynthesis found in R. eutropha genome, which was provided by Taguchi Lab.

Construction of P(3HB) producing module

Genes encoding PhaA and PhaB were obtained by subcloning from pGEM(phaCAB). PhaC has already registered as [http://partsregistry.org/Part:BBa_K342001 BBa_K342001] by INSA-Lyon2010. We appreciate INSA-Lyon 2010 teams effort. We ligated these genes in the order of PhaC, PhaA, PhaB for making BioBrick of “Plastic Producing Module”. TetR repressible promoter (BBa_R0040 ) and RBS (BBa_B0034) are fused to upstream of above gene cluster.

Results

Optimization of P(3HB) production

“Plastic producing module” in JM109 have shown more efficient plastic production than that in DH5α (1.45 fold). In the same condition, concentration of glucose and presence of PA affects the yield of plastic production. For the purpose of optimizing P(3HB) production, we found that TB medium, rich medium, produced 1.64 fold more plastic than LB medium.

Construction of bio-plastic producing module

We did not succeed in producing plastic by culturing JM109/pSB(phaCAB) containing BioBrick part in pSB1C3 yet. Now we are checking several culture condition and promoter species for controlling their gene expression.

Discussion

We succeeded in optimization of plastic production using pGEM(phaCAB), however, pSB(phaCAB) did not work as we expected. E. coli which was transformed with pGEM(phaCAB) produced plenty of PHB, so that our method of culturing and producing PHB works well. As for the reason why PHB was not produced with our phaCAB BioBrick part, we think that an over expression of phaCAB genes caused the resulting enzymes transferred into inclusion bodies. We assure that E. coli which is transformed pGEM produces PHB because pGEM includes phaCAB operon which derived from R. eutropha genome. However, in our experiment, we used PhaC (BBa_K342001, INSA-Lyon2010) which has codon optimization to be fit for translation of E.coli. Furthermore, RBS and promoter which we used is proper for E. coli genes, especially TetR repressible promoter (BBa_R0040 ) is stronger than a promoter on pGEM. In this case, phaCAB genes may be expressed more in E. coli than in the case of pGEM.

To confirm our hypothesis, we should examine whether the intermediates are produced. The data that two intermediates of PHB producing pathway are synthesized but not the final product should mean that the enzymes are put in inclusion bodies. In addition, to make our phaCAB BioBrick part perfect we will replace TetR repressible promoter with pGEM promoter. We guess that due to the pGEM promoter the expression of phaCAB genes will be less than before, and PHB is produced successfully.

We hope many iGEM teams will be able to produce plastic easily with our parts and they will make future iGEM projects more eco-friendly and more attractive.

References

1. H.Ohara. Change from Oil-based to Bio-based. Sen’i gakkaishi 66, 4.129-132 (2010)
2. Pohlmann, A. et al. Genome sequence of the bioplastic-producing “Knallgas” bacterium Ralstonia eutropha H16. Nature biotechnology 24, 1257–62 (2006).
3. 田口精一: バイオプラスチックのつくられ方とつくり方 蛋白質 核酸 酵素，50.3: 262-269 (2005) (in Japanese)