Method for degrading polyethylene terephthalate

A technology of construction method and inoculum amount, applied in the field of environmental science, which can solve problems such as poisoning

Active Publication Date: 2019-06-25
TIANJIN UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, the degradation product ethylene glycol (EG) is toxic to the environment and animals, so it is necessa

Method used

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  • Method for degrading polyethylene terephthalate
  • Method for degrading polyethylene terephthalate
  • Method for degrading polyethylene terephthalate

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0029] Embodiment 1: a kind of host bacterium

[0030] Construction of PETase and MHETase plasmids: PETase (GAP38373.1) and MHETase (A0A0K8P8E7.1) genes synthesized by the company and pHP13-43 expression vector were digested with BamHI and EcoRI, purified by agarose gel electrophoresis, and linearized PETase and MHETase after pHP13-43 expression vector and endonuclease digestion. The digested fragment and the vector were ligated with T4 DNA ligase, transformed into Escherichia coli, and after successful verification by colony PCR, enzyme digestion and sequencing, the plasmid was extracted as the vector plasmid for Bacillus subtilis expression.

[0031] Bacillus subtilis transformation method:

[0032] 1) Take glycerol to freeze Bacillus subtilis, streak on LB plate, and culture at 37°C. On the next day, take fresh single bacteria and inoculate them into 4ml GM1 medium test tubes, and culture overnight at 37°C and 200rpm.

[0033] 2) Transfer 400 μl of bacterial liquid into ...

Embodiment 2

[0037] Embodiment 2, mixed bacteria system degrades PET

[0038] Before inoculation, Bacillus subtilis, Pseudomonas putida and Rhodococcus were cultured overnight in LB medium earlier, and 5 milliliters of medium were collected by centrifugation at 4000rmp to collect the thalline, and the thalline was washed with W medium, and then the The OD600 of the bacteria was diluted to 1. The inoculum volume of single bacteria is 100 microliters, and the inoculation volume ratio of mixed bacteria (Bacillus subtilis (BB), Pseudomonas putida and Rhodococcus is 1:10) -5 :10) Inoculate a total volume of 100 microliters into W medium. from figure 1It can be seen that wild-type Bacillus subtilis (BS168), Rhodococcus (RJ) and Pseudomonas putida (PP) cannot degrade PET. Only Bacillus subtilis (BB) carrying PETase and MHETase plasmids could hydrolyze PET, and the quality of PET film decreased by 1.3 mg after seven days of reaction. However, compared with the single bacteria system, the degra...

Embodiment 3

[0040] Embodiment 3, change the impact of the inoculum size of Pseudomonas putida on PET degradation:

[0041] Before inoculation, Bacillus subtilis, Pseudomonas putida and Rhodococcus were cultured overnight in LB medium earlier, and 5 milliliters of medium were collected by centrifugation at 4000rmp to collect the thalline, and the thalline was washed with W medium, and then the The OD600 of the bacteria was diluted to 1. Pseudomonas putida was diluted 1, 10, 100, 1000, 100000, 10000000 times and inoculated into 100 μL. The initial inoculation volume of Rhodococcus was 100 μL, and the inoculum volume of Bacillus subtilis was 100 μL, and inoculated into 20 ml of W medium. After adding the PET film and degrading it at 37°C for 7 days, wash the PET film with 10% SDS, absolute ethanol and water respectively, and weigh the quality change of the PET film after drying. The results are as follows: image 3 .

[0042] Depend on image 3 The results showed that when the inoculum of...

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Abstract

The invention belongs to the field of environmental science, and discloses a construction method of a host bacterium for expressing a PETase enzyme and a MHTEase enzyme, a composite strain composed ofthe host bacterium, pseudomonas putida and rhodococcus and a method for degrading the polyethylene terephthalate (PET). The composite strain is formed by mixing the host bacterium expressing the PETase enzyme and the MHTEase enzyme, the pseudomonas putida and the rhodococcus, and adopted to degrade the PET to solve the problem of the inhibition effect of a PET degradation product TPA and the toxic effects of the degradation product TPA and ethylene glycol (EG) on the environment, thereby achieving green degradation of PET.

Description

technical field [0001] The invention belongs to the field of environmental science, and in particular relates to a method for degrading polyethylene terephthalate. Background technique [0002] Over the past century, plastics have become an essential part of modern society. Widely used in furniture, auto parts, packaging, human implants, aviation and aerospace, it has become one of the most used commodities in everyday life. Among them, polyethylene terephthalate (PET) has good folding resistance, oil resistance, fat resistance, acrylic acid resistance, dilute alkali resistance, most solvent resistance, high transparency, good gloss, non-toxic, tasteless and hygienic. It is safe and can be directly used in many excellent properties such as food packaging and has the ability to be customized, so it can be mass-produced as consumer goods. As a result, a large amount of PET is introduced into the environment through production, resulting in the accumulation of PET in the glob...

Claims

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Application Information

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IPC IPC(8): C12N1/21C12N15/75C12N1/20A62D3/02A62D101/28C12R1/125C12R1/40C12R1/01
Inventor 元英进马渊丁明珠何博李炳志
Owner TIANJIN UNIV
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