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Synechocystis PCC6803 strain for producing alkaline pectate lyase and construction method of synechocystis PCC6803 strain

A PCC6803, pectin lyase technology, applied in microorganism-based methods, lyases, carbon-oxygen lyases, etc., can solve the problems of energy conversion and unreasonable economics, limiting the efficiency and feasibility of bioenergy conversion, etc.

Pending Publication Date: 2020-12-22
TIANJIN UNIVERSITY OF SCIENCE AND TECHNOLOGY
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  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, these heterotrophic microorganisms use organic carbon sources such as bran, corn stalks, and rice straw as raw materials for production, and consume a large amount of organic carbon sources in the enzyme production process. Efficiency and feasibility of utilizing biomass for bioenergy conversion

Method used

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  • Synechocystis PCC6803 strain for producing alkaline pectate lyase and construction method of synechocystis PCC6803 strain
  • Synechocystis PCC6803 strain for producing alkaline pectate lyase and construction method of synechocystis PCC6803 strain
  • Synechocystis PCC6803 strain for producing alkaline pectate lyase and construction method of synechocystis PCC6803 strain

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Experimental program
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Effect test

Embodiment 1

[0026]Construction of p5st1t2npt plasmid

[0027]Using SEQ ID NO: 4 and SEQ ID NO: 5 in the sequence list as the upstream and downstream primers, and using the E. coli with GenBank accession number U02439.1 as the template, the E. coli terminator T1T2 gene fragment was obtained by PCR amplification technology. The sequence is shown in SEQ ID NO: 6 in the sequence listing. The amplification program is: 94°C, 3min; 98°C, 10s, 55°C, 15s, 72°C, 40s, 30 cycles; 72°C, 5min, 4°C, 10min. After the PCR reaction, the gel is cut and recovered by electrophoresis. The obtained E. coli terminator T1T2 gene fragment was subjected to double digestion with PStI and BamHI, ligated with the pBluescript SK plasmid after the same double digestion with T4 ligase, transformed into E. coli DH5α, positive clones were screened and sequenced to obtain plasmid pBluescript SKT1T2. The digestion system is: DNA 3μL, endonuclease 1μL, 10×Buffer 1μL, ddH2O 4μL, digestion temperature is 30℃, digestion time is 2h. Using...

Embodiment 2

[0030]Construction of recombinant expression vector PSTY1

[0031]Using SEQ ID NO: 10 and SEQ ID NO: 11 in the sequence list as the upstream and downstream primers, and the corresponding gene sequence of Klebsiella sp. Y1 in the GenBank database as the template, the basicity was obtained by PCR amplification technology The sequence of the pectin lyase gene fragment pety1 is shown in SEQ ID NO: 12 in the sequence table. The amplification program is: 94°C, 3min; 98°C, 10s, 55°C, 15s, 72°C, 2min, 30 cycles; 72°C, 5min, 4°C, 10min. The plasmid p5st1t2npt was cut with restriction enzyme HpaI to obtain the p5st1t2npt vector fragment. After phosphorylation, the vector fragment was subjected to homologous recombination with the pety1 gene fragment under the action of recombinase, transformed into E. coli DH5α, and positive clones were screened and sequenced , The recombinant expression vector PSTY1 was obtained. The digestion system is: DNA 3μL, endonuclease 2μL, 10×Buffer 1μL, ddH2O 4μL, dige...

Embodiment 3

[0033]Obtaining and expanding culture of Synechocystis PCC6803 genetically engineered strain PSTY1

[0034]The recombinant expression vector PSTY1 was recombined into the Synechocystis PCC6803 genome by the natural transformation method, and the engineered strain PSTY1 was obtained after antibiotic screening. The specific steps are: take the logarithmic culture period (OD730=0.6) Synechocystis PCC680 350ml centrifuged at 5000r / min for 10min at room temperature, discard the supernatant, add fresh BG-11 liquid medium and wash once, add fresh BG-11 liquid medium to the final concentration OD730= 4.8, and immediately used for conversion. Divide the collected algae liquid into 1.5ml EP tubes (400ul per tube), add 10ug PSTY1 plasmid to each tube, and incubate under low light conditions with light for 6 hours, shaking once during the period. The mixture was applied to a BG11 plate medium containing kanamycin resistance (50 μg / mL), and transformants were visible in about 10 days. The grown alg...

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Abstract

The invention discloses a synechocystis PCC6803 strain for producing alkaline pectate lyase and a construction method of the synechocystis PCC6803 strain, and belongs to the field of industrial microorganisms. An alkaline pectate lyase gene petyl derived from Klebsiella sp.Y1 is recombined into a synechocystis PCC6803 genome through a homologous recombination method, and a synechocystis PCC6803 genetic engineering strain PSY1 for producing the alkaline pectate lyase petyl is constructed, so that a method for producing pectinase by utilizing photosynthetic organisms is realized, a new way for producing the pectinase by using inorganic salt and carbon dioxide is obtained, and the consumption of energy (mainly carbon source) in a biomass conversion process is reduced.

Description

Technical field[0001]The invention relates to a Synechocystis PCC6803 strain for producing alkaline pectin lyase and a construction method thereof, and belongs to the field of industrial microorganisms.Background technique[0002]With the gradual increase in global population density, energy shortages and environmental problems are becoming more and more severe. As a mild and effective catalyst, pectin lyase has huge potential in the degradation of biomass. It has great potential in industrial production. The application is also more and more extensive. Plant cell walls are mainly composed of polysaccharides and proteins, some of which contain lignin. Cell wall polysaccharides are mainly divided into cellulose, hemicellulose and pectin. Cellulose is located in the matrix formed by hemicellulose and pectin. Pectin is widely present in higher plants. It is an important component of plant intercellular substance and primary cell wall, and it plays a binding role in plant cells. Pectin is...

Claims

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Application Information

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IPC IPC(8): C12N1/13C12N15/79C12N9/88C12N15/60C12R1/89
CPCC12N9/88C12Y402/02002C12N15/79
Inventor 戴玉杰孟庆营贺傲赵潇潇孟旋陈高贾士儒张语婕李浩湖
Owner TIANJIN UNIVERSITY OF SCIENCE AND TECHNOLOGY
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