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Poly(3-hydroxybutyrate-4-hydroxybutyrate-5-hydroxyvaleric acid) terpolymer and construction of its microbial production strain

A technology of hydroxybutyric acid and hydroxyvaleric acid, which is applied in the field of biotechnology and biomaterials, and can solve the problems of insufficient variety of PHA and limited fields

Active Publication Date: 2022-04-08
TSINGHUA UNIV +1
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, compared with petroleum-based plastics, the types of PHA are still not rich enough, and the fields of application are still quite limited.

Method used

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  • Poly(3-hydroxybutyrate-4-hydroxybutyrate-5-hydroxyvaleric acid) terpolymer and construction of its microbial production strain
  • Poly(3-hydroxybutyrate-4-hydroxybutyrate-5-hydroxyvaleric acid) terpolymer and construction of its microbial production strain
  • Poly(3-hydroxybutyrate-4-hydroxybutyrate-5-hydroxyvaleric acid) terpolymer and construction of its microbial production strain

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0206] transform Halomonas bluephagenesis TD01 CGMCC. No. 4353 for the production of poly(3-hydroxybutyrate-4-hydroxybutyrate-5-hydroxyvaleric acid)

[0207] 1. Plasmid and production strain construction

[0208] 1. Construction of plasmid pY01-pY07

[0209] The backbone of the pY01-pY07 plasmid is pSEVA321 (see Martínez-García E, Aparicio T, Goñi-Moreno A, et al. SEVA 2.0: an update of the Standard European Vector Architecture for de- / re-construction of bacterial functionalities[J] . Nucleicacids research, 2015, 43(D1): D1183-D1189.)

[0210] Preparation of plasmid pY01, the schematic diagram of the structure of plasmid pY01 is shown in Figure 2a As shown, it is a circular plasmid, and its sequence is shown in SEQ ID NO:5.

[0211] Among them, nucleotides 44-261 are porin promoter (GenBank Accession CP007757.1) and its RBS, nucleotides 310-1494 are dhaT gene (GenBank Accession AE015451.2), and nucleotides 1501-3021 The nucleotide is the aldD gene (GenBank Accession AE01...

Embodiment 2

[0287] engineered Halomonas Halomonas campaniensis LS21 CGMCC No.6593 Controlled Production P34HB5HV

[0288] one. Construct production bacteria

[0289] Transform any of the plasmids pY01-pY07 and the pQ08 plasmid (plasmid construction is the same as in Example 1) into Halomonas by conjugative transformation Halomonas campaniensis In LS21 CGMCC No.6593, the obtained Halomonas were named as H. LS21(pY01), H. LS21(pY02), H. LS21(pY03), H. LS21(pY04), H. LS21(pY05), H. LS21(pY06), H. LS21(pY07).

[0290] two. characterize

[0291] 1. Prepare the seed solution.

[0292] 2. Take 2.5mL of the Halomonas seed solution obtained in step 1, inoculate it into a 500mL shake flask containing 47.5mL of shake flask culture medium, and incubate with shaking at 37°C and 200rpm for 48 hours.

[0293] After the shake flask culture was completed, the dry weight of cells, the content of PHA and the content of monomers were measured. Three repeated experiments were carried ou...

Embodiment 3

[0324] After applying the modified Halomonas aydingkolgenesis M1 CGMCC NO.19880 Controlled Production P34HB5HV

[0325] one. Construct production bacteria

[0326] Transform any of the plasmids pY01-pY07 and the pQ08 plasmid (plasmid construction is the same as in Example 1) into Halomonas by conjugative transformation Halomonas aydingkolgenesis In M1 CGMCC NO.19880, the obtained Halomonas were named as H. aydingkolgenesis M1(pY01), H. aydingkolgenesis M1(pY02), H. Aydingkolgenesis M1(pY03), H. aydingkolgenesis M1(pY04), H. aydingkolgenesis M1(pY05), H. aydingkolgenesis M1(pY06), H. aydingkolgenesis M1(pY07).

[0327] two. characterize

[0328] 1. Prepare the seed solution.

[0329] 2. Fermentation

[0330] Take 2.5 mL of the seed liquid obtained in step 1, inoculate it into a 500 mL shake flask containing 47.5 mL of shake flask culture medium, and culture it with shaking at 37°C and 200 rpm for 48 hours.

[0331] After the shake flask culture ...

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Abstract

The present invention provides a novel polyhydroxyalkanoate (PHA) trimer poly(3-hydroxybutyric acid-4-hydroxybutyric acid-5-hydroxyvaleric acid), and the construction of recombinant bacteria for its production, specifically related to The microorganism may be any bacterium, especially Halomonas. By constructing Halomonas bacteria producing the above-mentioned trimer, selecting a specific substrate, and fermenting and producing the degradable PHA trimer.

Description

technical field [0001] The invention relates to the fields of biotechnology and biomaterials, in particular to poly(3-hydroxybutyrate-4-hydroxybutyrate-5-hydroxyvaleric acid), a novel trimer of polyhydroxy fatty acid PHA, and its microbial synthesis Construction methods of metabolic pathways. Background technique [0002] PHA is a biological polyester synthesized by microorganisms, and its monomers are hydroxy fatty acids. Studies have found that this kind of biopolyester has similar material properties to petroleum-based plastics, and is a substitute for petroleum-based plastics, with good biocompatibility and degradability (Wang Y, Yin J, Chen G Q. Polyhydroxyalkanoates, challenges and opportunities[J]. Current opinion in biotechnology, 2014, 30: 59-65.). In recent years, with the gradual strengthening of environmental protection awareness, the emergence of plastic bans and the gradual depletion of resources, the development of new degradable, renewable and bio-based mat...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C12N1/21C12N15/53C12N15/54C12N15/74C12P7/625C12R1/01
CPCC12N9/0006C12N9/0008C12N9/13C12N9/1029C12N15/74C12P7/625C12Y101/01C12Y102/01C12Y208/03C12Y102/01016C12Y101/01061C12Y203/01041
Inventor 陈国强闫煦吴赴清兰宇轩
Owner TSINGHUA UNIV
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