Revision as of 21:21, 21 October 2019

PETase T88A_S121E_D186H_R280A

Usage and Biology

The enzymes PETase and MHETase were first discovered in Ideonella sakaiensis in 2016 by a group of researchers in Japan. These enzymes were found to degrade polyethylene terephthalate (PET) into its monomers, terephthalic acid (TPA) and ethylene glycol (EG). PETase degrades PET into Mono-(2-hydroxyethyl)terephthalic acid (MHET), Bis(2-Hydroxyethyl) terephthalate (BHET) and TPA, the main product being MHET. MHET is further degraded by MHETase into TPA and EG. We are aiming to use mutants of these enzymes to degrade the microfibres that are coming off clothing during washing cycles. The enzymes would be secreted into a filter that captures the microfibres. Different mutations that have been reported in past papers to increase the activity of PETase have been combined into a novel mutant, in order to test if this would result in an overly active mutant. This sequence is the Escherichia coli K12 (E. coli K12) codon optimized DNA of the novel mutant of PETase, with an attached His tag. The His tag was attached in order to more easily identify the enzymes.

The native predicted signal peptide (Met1-Ala33) was removed from the WT PETase sequence (Seo et al 2019) and replaced with a start codon (Met), however all mutations are numbered according to the full-length WT sequence. The amino acid sequence was submitted to Twist Bioscience who codon optimised the sequence for E. coli, ensuring that there were no forbidden restriction sites, BsaI or SapI, to allow for potential TypeIIS assembly. The resulting CDS was synthesised and cloned, by Twist, into pET28. This added a 63 AA His-tag and thrombin cleavage site to the N-terminal of the protein, a T7 promoter and T7 terminator.

Characterisation

In order to characterise our part and determine the rate of its activity and prove its functionality we have run a series of experiments. After transforming the Arctic Express, Rosetta Gami and BL21 DE3 strains of E. coli with our plasmid we induced the expression of the enzymes using IPTG. In order to confirm that the enzyme expression has been successful we ran a western blot which showed the presence of the enzyme in the soluble fractions of the sonicated cells. Afterwards the enzyme was purified and used in assays to show its functionality and determine the rate of its activity.

Western blot of the soluble fraction of Arctic Express strain showing expression of all mutants. The PageRuler Plus prestained protein ladder was used and labeled with the corresponding sizes. The negative control is labeled with 1. This part (PETase T88A_S121E_D186H_R280A) is labeled with 2. A clear band is visible with a size of about 30 kDa which is the size of PETase with the His tag attached to it.

Western blot of the soluble fraction of Rosetta Gami strain showing expression of all mutants. The PageRuler Plus prestained protein ladder was used and labeled with the corresponding sizes. The negative control is labeled with 1. This part (PETase T88A_S121E_D186H_R280A) is labeled with 2. A clear band is visible with a size of about 30 kDa which is the size of PETase with the His tag attached to it.

Expression in E.coli

Nickel Affinity Chromatography

Nickel affinity column trace taken during initial purification of the enzyme. The light blue line shows the change in imidazole concentration with increasing volume run through the column and the purple line shows the corresponding change in A280 of eluent from the column. The peak at 50 ml shows protein elution

Size Exclusion Chromatography (Superdex-200)

Further purification of the enzyme by size exclusion chromatography using a calibrated Superdex-200 column. The large peak at an elution volume of ~90 ml shows the monomeric form of the protein. There is a smaller peak at ~65 ml which could be a higher oligomeric state. This will be investigated further in the future as sometimes larger oligomeric states have been found to be more thermal stable.

Esterase Activity

The esterase activity assay shows the production of p-nitrophenol (A405nm) at different substrate concentrations

The specific activity of the enzyme at differing substrate concentrations

Thermal Stability Graphs

Thermal Stability

The thermal stability assay shows the production of p-nitrophenol (A405nm) after the pre-incubation of the enzyme at increasing temperatures before the esterase assay was carried out.

The SP1 enzyme shows activity between 20 and 50

Thermal Stability of BBa_K3039001 (SP1) Vs. Wild Type PETase

Fibre Assay Graphs

The breakdown of PET fibres harvested from our filter into its constitutive parts with a change in enzyme concentration over a 76 hour period.

BHET Assay

The breakdown of PET fibres harvested from our filter into BHET with a change in enzyme concentration over a 76 hour period.

MHET Assay

The breakdown of PET fibres harvested from our filter into MHET with a change in enzyme concentration over a 76 hour period.

TPA Assay

The breakdown of PET fibres harvested from our filter into TPA with a change in enzyme concentration over a 76 hour period.

Conclusion

Enter conclusion

References

[1] Hyeoncheol Francis Son, In Jin Cho, Seongjoon Joo, Hogyun Seo, Hye-Young Sagong, So Young Choi, Sang Yup Lee, Kyung-Jin Kim; Rational Protein Engineering of Thermo-Stable PETase from Ideonella sakaiensis for Highly Efficient PET Degradation (2019) ACS Catal. 9(4), 3519-3526

Sequences and Features