Method and element for screening different-intensity ribosome binding sites and promoters

Inactive Publication Date: 2019-06-07
HUBEI UNIV
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Problems solved by technology

[0005] (1) At present, the mining of a large amount of accumulated systems biology data is not enough, so there are few biological components of Z. mobilis that have been identified;
[0006] (2) With the development of metabolic engineering and synthetic biology, the demand for avail...

Method used

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  • Method and element for screening different-intensity ribosome binding sites and promoters
  • Method and element for screening different-intensity ribosome binding sites and promoters
  • Method and element for screening different-intensity ribosome binding sites and promoters

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Embodiment

[0089] The different-strength ribosome binding sites and promoter screening methods of Zymomonas mobilis provided by the embodiments of the present invention include:

[0090] 1) Firstly, genes with strong downstream expression are screened out according to different omics data, and Venn analysis is performed to screen out genes shared by all omics data. In different omics data, each gene is ranked according to the average value under all conditions, and the promoters ranked above 90% are defined as strong promoters, those ranked 40-60% are moderately strong promoters, and ranked 10 Below % are weak promoters. 19 strong promoters, 9 medium-strength promoters and 10 weak promoters were screened.

[0091] like figure 2 As shown, the Venn analysis provided in the embodiment of the present invention screens promoters with different strengths.

[0092] 2) Prediction of ribosome binding site sequences (RBS) with different strengths: Prediction is performed using RBS Calculator V...

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Abstract

The invention belongs to the technical field of zymomonas mobilis, and discloses a method and an element for screening different-intensity ribosome binding sites and promoters. The method comprises the following steps: firstly, screening genes with strong downstream expression according to different genomics data, carrying out Wayne analysis, and screening common gene of the genomics data; predicting the binding site sequence of ribosome with different intensities; acquiring an RBS sequence promoter with specific intensity; acquiring a double-fluorescence reporter gene system framework; acquiring recombinant plasmid; acquiring a strain of the double-fluorescence reporter gene system plasmid containing the promoter with specific RBS intensity; and performing intensity verification. The method can integrate existing systematic biological data, and quickly and efficiently screen promoters with specific intensity. The intensities of the RBS and the promoter which are predicted and screenedby the method have good correlation with experimental data (respectively is R2)0.9 and R2)0.7).

Description

technical field [0001] The invention belongs to the technical field of monocysts, and in particular relates to a method and elements for screening ribosome binding sites and promoters with different strengths. Background technique [0002] At present, the existing technologies commonly used in the industry are as follows: [0003] Zymomonas mobilis is a Gram-negative, facultative anaerobic bacterium with perinatal flagella and a size of 1.4-2.0*4.0-5.0μm; the suitable growth temperature is 30°C, and the pH range it can tolerate Between 3.5 and 9, it can efficiently utilize glucose, fructose and sucrose to produce ethanol through the Enter-Doudoroff pathway (ED pathway). Z.mobilis has many advantages such as high ethanol yield and tolerance, high osmotic pressure tolerance, low biomass, and no need to add oxygen during fermentation, so it has become one of the main production strains of bioethanol. In order to increase the range of its available substrates, improve ethanol ...

Claims

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Application Information

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IPC IPC(8): C12N15/74C12Q1/6806
Inventor 杨世辉杨永富沈威黄钜马立新
Owner HUBEI UNIV
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