Difference between revisions of "Part:BBa K3779018:Experience"

(→‎Applications of BBa_K3779018)
(→‎Applications of BBa_K3779018)
 
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Within a certain range, the expression level of target protein increased with the increase of copy number, but when it reached a certain value, the expression level of target protein decreased with the increase of copy number. We screened for high copies by increasing the resistance concentration, and the copy number was determined by fluorescence quantification.
 
Within a certain range, the expression level of target protein increased with the increase of copy number, but when it reached a certain value, the expression level of target protein decreased with the increase of copy number. We screened for high copies by increasing the resistance concentration, and the copy number was determined by fluorescence quantification.
  
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https://2021.igem.org/wiki/images/0/0a/T--NWU-CHINA-B--_pPICZ%CE%B1A-SS-bgly_.png
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https://2021.igem.org/wiki/images/d/d3/T--NWU-CHINA-B--_Z_A_.png
  
 
Using the previously extracted and preserved plasmid pPIC9K-SS-bgly as the template, the SS bgly gene fragment containing cleavage sites KpnⅠand NotⅠwas amplified by primers, with a size of about 1500 BP. The electrophoresis results showed that it was successfully amplified.
 
Using the previously extracted and preserved plasmid pPIC9K-SS-bgly as the template, the SS bgly gene fragment containing cleavage sites KpnⅠand NotⅠwas amplified by primers, with a size of about 1500 BP. The electrophoresis results showed that it was successfully amplified.

Latest revision as of 06:19, 13 October 2021


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Applications of BBa_K3779018

Gene copy number

Within a certain range, the expression level of target protein increased with the increase of copy number, but when it reached a certain value, the expression level of target protein decreased with the increase of copy number. We screened for high copies by increasing the resistance concentration, and the copy number was determined by fluorescence quantification.

T--NWU-CHINA-B--_Z_A_.png

Using the previously extracted and preserved plasmid pPIC9K-SS-bgly as the template, the SS bgly gene fragment containing cleavage sites KpnⅠand NotⅠwas amplified by primers, with a size of about 1500 BP. The electrophoresis results showed that it was successfully amplified.

The following is a gel electrophoresis map of SS-bgly gene amplification.

T--NWU-CHINA-B--_SS-bgly_electrophoresis_figure_bgly_gene_amplification_.png

The two ends of the gene SS-bgly amplified by PCR were introduced into the enzyme digestion sites Kpn Ⅰ and Not Ⅰ, and the expression vector pPICZαA double enzyme digestion was performed to confirm plasmid pPICZαA-SS-bgly built successfully.

T--NWU-CHINA-B--_Colony_PCR_was_used_to_verify_positive_inverters_.png T--NWU-CHINA-B--_Identification_of_recombinant_plasmid_pPICZaA-SS-bgly_by_enzyme_digestion_.png

We compared the enzyme activities of the strains.

T--NWU-CHINA-B--_Enzyme_activity.png

The copy number of genes was determined by fluorescence quantitative PCR. Using plasmid pPIC9KSS-bgly as single copy, the copy numbers of SS-bgly gene in GS115/9K-SS-bgly 6# and GS115/9K-ZαA-SS-bgly 4# were 1.89 and 4.03, respectively, and were round 2 and 4.

T--NWU-CHINA-B--_Gene_copy_number_calculation.png

Note 2: GAP was the internal reference gene and was represented by Ref; Plasmid PPIC9K-SS-BGLY was used as reference sample and was represented by Cal. Ss-bgly stands for Target gene and is represented by Target. Strains GS115/9K-bgly 6# and GS115/9K-ZαA-bgly 4# were used as Test samples.

The expression of plasmid was optimized.

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