Difference between revisions of "Part:BBa K5366022"
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| − | <img class="bild" src="https://static.igem.wiki/teams/5366/part/mapping-of-pet-28a-ajc7-plasmid.png"> | + | <img class="bild" src="https://static.igem.wiki/teams/5366/part/mapping-of-pet-28a-ajc7-plasmid.png"><br> |
| + | <i><b> Fig. 1 Mapping of pET-28a(+)-AJC7 plasmid<br><br></b></I> | ||
<div class="unterschrift"><bFig. 1 Construction of pMTL-Pfba-Bs2 recombinant plasmid</b> | <div class="unterschrift"><bFig. 1 Construction of pMTL-Pfba-Bs2 recombinant plasmid</b> | ||
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<h1>Indicator</h1> | <h1>Indicator</h1> | ||
The pET-28a(+)-AJC7 construct was transformed into <i>E. coli</i> BL21 (DE3) and incubated in an inverted culture at a constant temperature of 37°C for 14 hours. Individual colonies were selected from the transformed growth, and colony PCR was performed. Single colonies with the correct bacterial plasmid were then transferred to LB medium containing kanamycin (LB Kan) for activation and amplification culturing, followed by protein purification as outlined in [Experiment]. The final concentration of fructose in the reaction system was set at 10 g/L, supplemented with 10 µL of Ni<sup>2+</sup> as a catalyst. The volume of pure enzyme solution required was determined based on the protein concentration, as indicated in [Experimental]. The reaction was conducted at 70℃ for 5 hours, and the products were analyzed using high-performance liquid chromatography (HPLC) (Figure 2). | The pET-28a(+)-AJC7 construct was transformed into <i>E. coli</i> BL21 (DE3) and incubated in an inverted culture at a constant temperature of 37°C for 14 hours. Individual colonies were selected from the transformed growth, and colony PCR was performed. Single colonies with the correct bacterial plasmid were then transferred to LB medium containing kanamycin (LB Kan) for activation and amplification culturing, followed by protein purification as outlined in [Experiment]. The final concentration of fructose in the reaction system was set at 10 g/L, supplemented with 10 µL of Ni<sup>2+</sup> as a catalyst. The volume of pure enzyme solution required was determined based on the protein concentration, as indicated in [Experimental]. The reaction was conducted at 70℃ for 5 hours, and the products were analyzed using high-performance liquid chromatography (HPLC) (Figure 2). | ||
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| − | <img class="bild" src="https://static.igem.wiki/teams/5366/part/wt-concentration-of-product-tagatose.png"> | + | <img class="bild" src="https://static.igem.wiki/teams/5366/part/wt-concentration-of-product-tagatose.png"><br> |
| + | <i><b> Fig. 2 Concentration of tagatose produced by AJC7 and UxaE under identical reaction conditions.<br><br></b></I> | ||
<div class="unterschrift"><bFig. 1 Construction of pMTL-Pfba-Bs2 recombinant plasmid</b> | <div class="unterschrift"><bFig. 1 Construction of pMTL-Pfba-Bs2 recombinant plasmid</b> | ||
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| − | + | <h1>Result</h1> | |
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From the results obtained in the liquid phase, it is evident that the concentration of tagatose produced by AJC7 is approximately four times higher than that produced by UxaE under the same reaction conditions. This indicates that AJC7 demonstrates significantly greater potential activity as a tagatose-4-epimerase, leading to its selection for subsequent studies. | From the results obtained in the liquid phase, it is evident that the concentration of tagatose produced by AJC7 is approximately four times higher than that produced by UxaE under the same reaction conditions. This indicates that AJC7 demonstrates significantly greater potential activity as a tagatose-4-epimerase, leading to its selection for subsequent studies. | ||
Latest revision as of 16:05, 30 September 2024
T7 promoter-RBS-AJC7-6xHis -T7 termonator
AJC7 structural gene expression plasmid
Construction
The screened sequence AJC7, which has potential tagatose-4-epimerase activity, was sent to a company for synthesis, and the sequence was subsequently ligated into the pET-28a(+) vector. (Figure 1).
Fig. 1 Mapping of pET-28a(+)-AJC7 plasmid
Indicator
The pET-28a(+)-AJC7 construct was transformed into E. coli BL21 (DE3) and incubated in an inverted culture at a constant temperature of 37°C for 14 hours. Individual colonies were selected from the transformed growth, and colony PCR was performed. Single colonies with the correct bacterial plasmid were then transferred to LB medium containing kanamycin (LB Kan) for activation and amplification culturing, followed by protein purification as outlined in [Experiment]. The final concentration of fructose in the reaction system was set at 10 g/L, supplemented with 10 µL of Ni2+ as a catalyst. The volume of pure enzyme solution required was determined based on the protein concentration, as indicated in [Experimental]. The reaction was conducted at 70℃ for 5 hours, and the products were analyzed using high-performance liquid chromatography (HPLC) (Figure 2).
Fig. 2 Concentration of tagatose produced by AJC7 and UxaE under identical reaction conditions.
Result
From the results obtained in the liquid phase, it is evident that the concentration of tagatose produced by AJC7 is approximately four times higher than that produced by UxaE under the same reaction conditions. This indicates that AJC7 demonstrates significantly greater potential activity as a tagatose-4-epimerase, leading to its selection for subsequent studies.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 1534
- 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 540
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal AgeI site found at 1042
- 1000COMPATIBLE WITH RFC[1000]