Depolymerization of a polyhydroxyalkanoate and recycling of hydroxyalkonoate monomer obtained thereby via a metabolic process

Patent metadata

Field	Value
Publication number	US-12297328-B2
Application number	US-202118686912-A
Country	US
Kind code	B2
Filing date	Sep 30, 2021
Priority date	Sep 30, 2021
Publication date	May 13, 2025
Grant date	May 13, 2025

Abstract

A process is disclosed for production of a polyhydroxyalkanoate that includes depolymerization of a post-consumer polyhydroxyalkanoate and utilization of the hydroxyalkanoate monomer thus produced as a carbon source for a microorganism capable of production of a polyhydroxyalkanoate. Methods can be utilized for true cyclic use of polyhydroxyalkanoates including polyhydroxybutyrates. Various aspects are described including simultaneous depolymerization and polymer production, utilization of purified depolymerase enzymes and/or microorganisms that express a depolymerase in conjunction with a microorganism that produces polymer, utilization of microorganisms that produce both a depolymerase and a new polymer, and utilization of genetically modified organisms to produce natural or modified depolymerase enzymes.

First claim

What is claimed:

1. A method for treatment of a post-consumer product, comprising:
contacting a post-consumer product with a polyhydroxyalkanoate depolymerase (PHADase), the post-consumer product comprising a first polyhydroxyalkanoate, the PHADase catalyzing depolymerization of the first polyhydroxyalkanoate and releasing a hydroxyalkanoate monomer from the first polyhydroxyalkanoate;
culturing a first microorganism in the presence of the hydroxyalkanoate monomer, the first microorganism being capable of metabolizing the hydroxyalkanoate monomer as a metabolic carbon source, the first microorganism being capable of producing a second polyhydroxyalkanoate, wherein the culturing is carried out under a condition that encourages production of the second polyhydroxyalkanoate by the first microorganism, wherein the first microorganism is selected from the genus Lysobacter.

2. The method of claim 1 , wherein the first polyhydroxyalkanoate is a first polyhydroxybutyrate.

3. The method of claim 1 , wherein the PHADase is a purified enzyme.

4. The method of claim 3 , wherein the PHADase is expressed by the first microorganism or is a modified enzyme that includes one or more amino acid modifications as compared to a PHADase expressed by the first microorganism, or wherein the PHADase is expressed by a second microorganism.

5. The method of any of claim 1 , wherein the PHADase is expressed by a second microorganism, the method including culturing the second microorganism in the presence of the post-consumer product and thereby contacting the post-consumer product with the PHADase.

6. The method of claim 5 , wherein the first microorganism and the second microorganism are the same.

7. The method of claim 5 , wherein the second microorganism is a genetically modified microorganism.

8. The method of claim 1 , wherein the first microorganism is contacted with the hydroxyalkanoate monomer following completion of the depolymerization of the first polyhydroxyalkanoate.

9. The method of claim 1 , wherein the first microorganism is contacted with the hydroxyalkanoate monomer in conjunction with the depolymerization of the first polyhydroxyalkanoate.

10. The method of claim 1 , wherein at least one of the contacting step and the culturing step takes place at an extreme condition, wherein the polyhydroxyalkanoate depolymerase comprises an extremozyme.

11. The method of claim 10 , the extreme condition comprising one or more of a salt concentration of about 0.5 M or greater, a temperature of about 40° C. or greater or a temperature of about 10° C. or less, a pressure of about 0.5 MPa or greater, a pH of from about 1 to about 5.5 or a pH of about 7.5 to about 11.5, in the presence of ionizing radiation of about 1000 Gy or greater, or any combination thereof.

12. The method of claim 1 , wherein the condition that encourages production of the second polyhydroxyalkanoate by the first microorganism comprises one or more of the following:
metabolic carbon source other than the hydroxyalkanoate monomer present at a concentration of about 2 millimolar or less;
deprivation of nitrogen-containing nutrients;
deprivation of phosphate-containing nutrients;
an environmental condition at or near a limit of the environmental condition at which the microorganism survives.

13. The method of claim 1 , wherein the condition that encourages production of the second polyhydroxyalkanoate by the first microorganism comprises providing the hydroxyalkanoate monomer as the only metabolic carbon source in the culture.

14. The method of claim 1 , wherein the condition that encourages production of the second polyhydroxyalkanoate by the first microorganism comprises metabolic carbon source other than the hydroxyalkanoate monomer present at a concentration of about 2 millimolar or less.

15. The method of claim 1 , wherein the first microorganism is selected from Lysobacter aestuarii, Lysobacter antibioticus, Lysobacter bugurensis, Lysobacter capsica, Lysobacter lacus, Lysobacter lycopersici, Lysobacter maris, Lysobacter niastensis, Lysobacter profundi, Lysobacter sp. A03 , Lysobacter sp. cf310 , Lysobacter sp. H21R20 , Lysobacter sp. H21R4 , Lysobacter sp. H23M41 , Lysobacter sp. R19 , Lysobacter sp. Root604 , Lysobacter sp. Root690 , Lysobacter sp. Root916 , Lysobacter sp. Root983 , Lysobacter sp. TY2-98 , Lysobacter spongiae, Lysobacter spongiicola, Lysobacter alkalisoli, Lysobacter arseniciresistens, Lysobacter daejeonensis, Lysobacter dokdonensis, Lysobacter gilvus, Lysobacter gummosus, Lysobacter maris, Lysobacter oculi, Lysobacter panacisoli, Lysobacter penaei, Lysobacter prati, Lysobacter psychrotolerans, Lysobacter pythonis, Lysobacter ruishenii, Lysobacter segetis, Lysobacter silvestris, Lysobacter silvisoli, Lysobacter soli, Lysobacter sp. 17J7-1 , Lysobacter sp. Alg18-2.2 , Lysobacter sp. Cm-3-T8 , Lysobacter sp. H23M47 , Lysobacter sp. HDW10 , Lysobacter sp. II4 , Lysobacter sp. N42 , Lysobacter sp. OAE881 , Lysobacter sp. Root494 , Lysobacter sp. URHA0019 , Lysobacter sp. WF-2 , Lysobacter sp. yr284 , Lysobacter tabacisoli, Lysobacter telluris, Lysobacter tolerans, Lysobacter xinjiangensis.

16. A system for carrying out the method of claim 1 , wherein the system includes a single vessel within which the step of contacting and the step of culturing both take place or wherein the system includes a first vessel within which the step of contacting takes place and includes a second vessel within which the step of culturing takes place.

17. The method of claim 4 , wherein the second microorganism is a genetically modified microorganism.

18. The method of claim 1 , wherein the first microorganism comprises a Lysobacter enzymogene.

Assignees

• Kimberly Clark Co

Inventors

• Quirk Stephen
• Dulcamara Peter B

Classifications

• C12P7/625

  Polyesters of hydroxy carboxylic acids · CPC title

• C12N1/20

  Bacteria; Culture media therefor · CPC title

• C08J2367/04

  Polyesters derived from hydroxy carboxylic acids, e.g. lactones (C08J2367/06 takes precedence) · CPC title

• C12R2001/63

  Vibrio · CPC title

• C12R2001/64

  Xanthomonas · CPC title