IP Library › Granted Patent US 12,344,714
Granted Patent B2
US 12,344,714 · App. 17/625,783 · Granted Jul 1, 2025

Esterases and uses thereof

Inventors: Alain Marty (Toulouse, FR); Vincent Tournier (Toulouse, FR)
Assignee: CARBIOS
C08J11/105C11D3/38636C12N9/18C12Y301/01074
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 12,344,714
App. No.
17/625,783
Filed
Jan 10, 2022
Granted
Jul 1, 2025
Kind
B2
Art Unit
1652
USPC
435/135
Abstract

The present invention relates to novel esterases, more particularly to esterase variants having improved activity and/or improved thermostability compared to the esterase of SEQ ID NO: 1 and the uses thereof for degrading polyester containing material, such as plastic products. The esterases of the invention are particularly suited to degrade polyethylene terephthalate, and material containing polyethylene terephthalate.

Claims (35)

1. An esterase which (i) has at least 75% identity to the full length amino acid sequence set forth in SEQ ID NO: 1, (ii) comprises at least the combination of amino acid substitutions selected from the group consisting of L210T/A/R/W/H+V172I and L210T/A/R/W/H+V172, wherein the position is numbered by reference to the amino acid sequence set forth in SEQ ID NO: 1, and (iii) has an increased degrading activity and/or an increased thermostability as compared to the esterase of SEQ ID NO: 1.

2. The esterase according to claim 1 , wherein said esterase further comprises at least one amino acid substitution at a position selected from T12, E13, S14, S15, I16, E17, A18, V19, R20, R32, A35, F38, G62, F63, T64, A65, G66, Q67, E68, S69, I70, A71, W72, P75, R76, D88, T89, R92, L93, D94, Q95, P96, D97, H130, M132, G133, S139, W156, T158, R159, Q175, T178, I179, A180, P181, S184, F189, L204, G206, A207, S208, V211, S212, N213, T214, P215, D216, T217, T218, T219, A220, K221, Y222, Q239, F240, L241, P243, A244, P245, D246, D247, F248, A249, I250, G136 or T169.

3. The esterase according to claim 1 , wherein said esterase comprises at least one combination of substitutions selected from L210T+V172I+Q95G, L210T+V172I+Q95G+S184E, L210T+V172I+N213M and L210T+V172I+Q95G+G136A+T169Q+S184E.

4. The esterase according to claim 1 , wherein said esterase further comprises at least one substitution at position selected from A2, D233, and S255.

5. The esterase according to claim 4 , wherein said esterase further comprises at least one substitution or combination of substitutions selected from A2E, D233N and S255A.

6. The esterase according to claim 1 , wherein said esterase further comprises at least one amino acid residue selected from S131, D177 and H209, or the combination S131+D177+H209 and/or least one amino acid residue selected from C242 and C257, or the combination C242+C257.

7. The esterase according to claim 1 , wherein said esterase comprises at least the combination of substitutions L210T+V172I.

8. The esterase according to claim 7 , wherein said esterase further comprises at least one amino acid substitution at a position selected from T12, E13, S14, S15, I16, E17, A18, V19, R20, R32, A35, F38, G62, F63, T64, A65, G66, Q67, E68, S69, 170, A71, W72, P75, R76, D88, T89, R92, L93, D94, Q95, P96, D97, H130, M132, G133, S139, W156, T158, R159, Q175, T178, I179, A180, P181, S184, F189, L204, G206, A207, S208, V211, S212, N213, T214, P215, D216, T217, T218, T219, A220, K221, Y222, Q239, F240, L241, P243, A244, P245, D246, D247, F248, A249, I250, G136 or T169.

9. The esterase according to claim 7 , wherein said esterase further comprises the combination S131+D177+H209 and/or the combination C242+C257.

10. The esterase according to claim 9 , wherein said esterase has at least 95% identity compared to the full length amino acid sequence set forth in SEQ ID NO: 1.

11. The esterase according to claim 9 , wherein said esterase has at least 90% identity compared to the full length amino acid sequence set forth in SEQ ID NO: 1.

12. The esterase according to claim 7 , wherein said esterase comprises at least one combination of substitutions selected from L210T+V172I+Q95G, L210T+V172I+Q95G+S184E, L210T+V172I+N213M and L210T+V172I+Q95G+G136A+T169Q+S184E.

13. The esterase according to claim 12 , wherein said esterase has at least 90% identity compared to the full length amino acid sequence set forth in SEQ ID NO: 1.

14. The esterase according to claim 12 , wherein said esterase has at least 95% identity compared to the full length amino acid sequence set forth in SEQ ID NO: 1.

15. The esterase according to claim 7 , wherein said esterase further comprises at least one substitution at position selected from A2, D233, and S255.

16. The esterase according to claim 7 , wherein said esterase further comprises at least one substitution or combination of substitutions selected from A2E, D233N and S255A.

17. The esterase according to claim 7 , wherein said esterase has at least 90% identity compared to the full length amino acid sequence set forth in SEQ ID NO: 1.

18. A detergent composition comprising the esterase according to claim 17 or a host cell expressing said esterase.

19. The esterase according to claim 7 , wherein said esterase has at least 95% identity compared to the full length amino acid sequence set forth in SEQ ID NO: 1.

20. A detergent composition comprising the esterase according to claim 19 or a host cell expressing said esterase.

21. A composition comprising an esterase according to claim 7 or a or a host cell expressing said esterase, or an extract of said host cell comprising said esterase.

22. The composition according to claim 21 , wherein said esterase has at least 90% identity compared to the full length amino acid sequence set forth in SEQ ID NO: 1.

23. The composition according to claim 21 , wherein said esterase has at least 95% identity compared to the full length amino acid sequence set forth in SEQ ID NO: 1.

24. A nucleic acid encoding an esterase according to claim 7 .

25. An expression cassette or vector comprising a nucleic acid of claim 24 .

26. A host cell comprising a nucleic acid of claim 24 or an expression cassette or vector comprising said nucleic acid.

27. A polyester containing material comprising an esterase according to claim 7 or a host cell expressing said esterase or a composition comprising said esterase.

28. A detergent composition comprising the esterase according to claim 7 or a host cell expressing said esterase.

29. A method of degrading at least one polyester of a polyester containing material comprising:

(a) contacting the polyester containing material with an esterase according to claim 7 or a host cell expressing said esterase or a composition comprising said esterase; and, optionally

(b) recovering monomers and/or oligomers.

30. The method according to claim 29 , wherein the polyester is selected from polyethylene terephthalate (PET), polytrimethylene terephthalate (PTT), polybutylene terephthalate (PBT), polyethylene isosorbide terephthalate (PEIT), polylactic acid (PLA), polyhydroxy alkanoate (PHA), polybutylene succinate (PBS), polybutylene succinate adipate (PBSA), polybutylene adipate terephthalate (PBAT), polyethylene furanoate (PEF), Polycaprolactone (PCL), poly(ethylene adipate) (PEA), polyethylene naphthalate (PEN) and blends/mixtures of these materials.

31. The method according to claim 29 , wherein the polyester is polyethylene terephthalate.

32. The method according to claim 31 , wherein said esterase has at least 90% identity compared to the full length amino acid sequence set forth in SEQ ID NO: 1.

33. The method according to claim 31 , wherein said esterase has at least 95% identity compared to the full length amino acid sequence set forth in SEQ ID NO: 1.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 1, 2022
From: MARTY, ALAIN; TOURNIER, VINCENT
To: CARBIOS
Reel/Frame 058845/0457 →
Priority Claims (1)
EP 19185789 · Jul 11, 2019 · regional
Continuity (1)
Related Publication 20220251327A1 · Aug 11, 2022
References Cited (69)
US 10124512B2 · Boisart et al. · 2018 [cited by applicant]
US 10287561B2 · Alvarez et al. · 2019 [cited by applicant]
US 10385183B2 · Maille · 2019 [cited by applicant]
US 10508269B2 · Li et al. · 2019 [cited by applicant]
US 10584320B2 · Topham et al. · 2020 [cited by applicant]
US 10590401B2 · Tournier et al. · 2020 [cited by applicant]
US 10626242B2 · Ferreira et al. · 2020 [cited by applicant]
US 10717996B2 · Dusseaux et al. · 2020 [cited by applicant]
US 10723848B2 · Chateau et al. · 2020 [cited by applicant]
US 10767026B2 · Desrousseaux et al. · 2020 [cited by applicant]
US 10829598B2 · Ferreira et al. · 2020 [cited by applicant]
US 10829754B2 · Marty et al. · 2020 [cited by applicant]
US 11072784B2 · Tournier et al. · 2021 [cited by applicant]
US 11198767B2 · Guemard et al. · 2021 [cited by applicant]
US 11345906B2 · Marty et al. · 2022 [cited by applicant]
US 11377533B2 · Desrousseaux et al. · 2022 [cited by applicant]
US 11384218B2 · Guemard et al. · 2022 [cited by applicant]
US 11414651B2 · Topham et al. · 2022 [cited by applicant]
US 11535832B2 · David et al. · 2022 [cited by applicant]
US 11549105B2 · Marty et al. · 2023 [cited by applicant]
US 11692181B2 · Andre et al. · 2023 [cited by applicant]
US 11802185B2 · Chateau et al. · 2023 [cited by applicant]
US 11851689B2 · Duquesne et al. · 2023 [cited by applicant]
US 11926851B2 · David et al. · 2024 [cited by applicant]
US 20220002516A1 · Chateau · 2022 [cited by applicant]
US 20220177697A1 · Guillamot et al. · 2022 [cited by applicant]
US 20220227957A1 · Guemard et al. · 2022 [cited by applicant]
US 20220282232A1 · Tournier · 2022 [cited by applicant]
US 20220282235A1 · Duquesne et al. · 2022 [cited by applicant]
US 20220363861A1 · Marty · 2022 [cited by applicant]
US 20230034354A1 · Chateau · 2023 [cited by applicant]
US 20230048275A1 · Marty · 2023 [cited by applicant]
US 20230049607A1 · Aloui Dalibey et al. · 2023 [cited by applicant]
US 20230135014A1 · Topham et al. · 2023 [cited by applicant]
US 20230392129A1 · Tournier · 2023 [cited by applicant]
US 20230392130A1 · Tournier · 2023 [cited by applicant]
US 20230399628A1 · Tournier · 2023 [cited by applicant]
US 20230399629A1 · Tournier · 2023 [cited by applicant]
US 20240052114A1 · Chateau et al. · 2024 [cited by applicant]
US 20240059859A1 · Bouchiba et al. · 2024 [cited by applicant]
US 20240228731A1 · Marty et al. · 2024 [cited by applicant]
US 20240228732A1 · Marty et al. · 2024 [cited by applicant]
EP 3517608 · 2019 [cited by applicant]
WO WO2012099018 · 2012 [cited by applicant]
WO WO2013033318 · 2013 [cited by applicant]
WO WO2018011281 · 2018 [cited by applicant]
WO WO2021005199 · 2021 [cited by applicant]
WO WO2023088908 · 2023 [cited by applicant]
WO WO2023088909 · 2023 [cited by applicant]
WO WO2023088910 · 2023 [cited by applicant]
GenBank, Accession No. HLT70754.1, 2024, www.ncbi.nlm.nih.gov. (Year: 2024). [cited by examiner]
Toriner et al., An engineered PET depolymerase to break down and recycle plastic bottles, Nature 580, 2020, 216-19. (Year: 2020). [cited by examiner]
Sonnendecker et al., Low Carbon Footprint Recycling of Post-Consumer PET Plastic with a Metagenomic Polyester Hydrolase, ChemSusChem 15, 2022, e202101062. (Year: 2022). [cited by examiner]
French et al., What is a conservative substitution, J. Mol. Evol. 19, 1983, 171-175. (Year: 1983). [cited by examiner]
Database Uniprot [Online] “SubName: Full=Hydrolase 7 {ECO:0000313 | EMBL:SAY37592.1}”, Accession No. A0A165B1I1, Jul. 6, 2016, p. 1, XP002779405. [cited by applicant]
Database Uniprot [Online] “SubName: Full=Hydrolase 3 {ECO:0000313 | EMBL:SAY37583.1}”, Accession No. A0A171DE79, Oct. 5, 2016, p. 1, XP002796546. [cited by applicant]
Database Uniprot [Online] “SubName: Full=Cutinase {ECO:0000313 | EMBL:SCG74671.1}”, Accession No. A0A1C5JWH8, Nov. 2, 2016, p. 1, XP002796547. [cited by applicant]
Database EBI [Online] “Micromonospora aurantiaca ATCC 27029 lipase 2, SEQ ID 33”, Accession No. BAL79660, Apr. 23, 2013, p. 1, XP002796548. [cited by applicant]
Database Uniprot [Online] “SubName: Full=Lipase {ECO:0000313:EMBL:OKI36883.1}”, Accession No. A0A1Q4YQI4, Jun. 5, 2019, p. 1, XP002796549. [cited by applicant]
Database EBI [Online] “Streptomyces exfoliatus lipase, SEQ:10”, Accession No. AZY25627, Sep. 13, 2012, p. 1, XP002796550. [cited by applicant]
Yan, X. et al. “Strain Prioritization and Genome Mining for Enediyne Natural Products” [cited by applicant]
Austin, H. P. et al. “Characterization and engineering of a plastic-degrading aromatic polyesterase” [cited by applicant]
Liu, B. et al. “Protein Crystallography and Site-Direct Mutagenesis Analysis of the Poly(ethylene terephthalate) Hydrolase PETase from [cited by applicant]
Written Opinion in International Application No. PCT/EP2020/069499, Nov. 13, 2020, pp. 1-15. [cited by applicant]
Joo, S. et al. “Structural insight into molecular mechanism of poly (ethylene terephthalate) degradation” [cited by applicant]
Claims as filed in U.S. Appl. No. 18/621,330, filed Mar. 29, 2024, pp. 1-4. [cited by applicant]
Claims pending in U.S. Appl. No. 18/710,658, filed Aug. 1, 2024, pp. 1-13. [cited by applicant]
Claims pending in U.S. Appl. No. 18/710,735, filed Aug. 1, 2024, pp. 1-4. [cited by applicant]
Claims pending in U.S. Appl. No. 18/710,760, filed Aug. 1, 2024, pp. 1-5. [cited by applicant]