Difference between revisions of "Part:BBa K4255014:Experience"

 
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===Applications of BBa_K4255014===
 
===Applications of BBa_K4255014===
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This year our project is focused on the synthesis of anthocyanin, which has a lot of research and reporting on this canonical pathway. But due to anthocyanins are ubiquitous in plants, therefore, each enzyme can find multiple homologous proteins. To get the better yeild, we first compared enzymes in different species and selected the most suitable sequence for E.coli expression, we constructed several new parts, which has been submitted this year.
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[[Image:SHSBNU.1.gif|center|700px|thumb|'''Fig. 1: Metabolism pathway for anthocyanin synthesis''']]
  
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We divided the seven enzymes into two parts, 4CL, CHS and CHI catalyzed the production of naringenin one by one, and naringenin was further generated into anthocyanins in the presence of F3H, F3'5'H, DFR and ANS. The F3H, F3'5'H, DFR and ANS sequences come from (四个物种). We constructed the last four enzymes on the pRSFDuet vector, in which F3H was fused to F3'5'H and DFR was fused to ANS.
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The function of the enzymes can be listed below:
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F3H: catalyze flavanone into dihydrokaempferol
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F3’5’H: catalyze dihydrokaempferol into dihydromyricetin
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DFR: catalyze dihydromyricetin into delphinin colorless
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ANS: catalyze delphinin colorless into delphinidin
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Protocol we use:
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We asked biological company to synthesize the sequence at first. And we constructed it into pRSFDUET plasmid. Next, we transformed the plasmids into E. coli BL21(DE3).
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After the colony has grown up on the plate, we picked a single colony by a sterile tip and added it into 4 ml LB medium with the corresponding antibiotic.
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Later, we added 1 mM IPTG for induction and shook at 16℃ overnight. We also set a control group and didn’t add IPTG into it.
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Finally, we centrifuged the bacterial solution at 12000 g, discard the supernatant, and used RIPA as a lysis buffer. we added loading buffer to the supernatant which contains the protein extract, and after heating at 96℃ for 10 min, we underwent SDS-PAGE and Coomassie brilliant blue staining for expression test.
 +
We could see a clear band at the position of (请老师补充分子量大小)kD, which only appeared in the group with IPTG. The molecular weight of this band was in line with the expectation, and it was under the condition of induction, so we believed that we had successfully expressed fusion proteins combined by F3H and F3’5’H, DFR and ANS.
 +
[[Image:SHSBNU.2.gif|center|700px|thumb|'''Fig. 2: Plasmid design''']]
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[[Image:SHSBNU.3.gif|center|700px|thumb|'''Fig. 3: Plasmid design''']]
 
===User Reviews===
 
===User Reviews===
 
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<!-- DON'T DELETE --><partinfo>BBa_K4255014 StartReviews</partinfo>

Revision as of 10:26, 8 October 2022


This experience page is provided so that any user may enter their experience using this part.
Please enter how you used this part and how it worked out.

Applications of BBa_K4255014

This year our project is focused on the synthesis of anthocyanin, which has a lot of research and reporting on this canonical pathway. But due to anthocyanins are ubiquitous in plants, therefore, each enzyme can find multiple homologous proteins. To get the better yeild, we first compared enzymes in different species and selected the most suitable sequence for E.coli expression, we constructed several new parts, which has been submitted this year.

Fig. 1: Metabolism pathway for anthocyanin synthesis

We divided the seven enzymes into two parts, 4CL, CHS and CHI catalyzed the production of naringenin one by one, and naringenin was further generated into anthocyanins in the presence of F3H, F3'5'H, DFR and ANS. The F3H, F3'5'H, DFR and ANS sequences come from (四个物种). We constructed the last four enzymes on the pRSFDuet vector, in which F3H was fused to F3'5'H and DFR was fused to ANS. The function of the enzymes can be listed below: F3H: catalyze flavanone into dihydrokaempferol F3’5’H: catalyze dihydrokaempferol into dihydromyricetin DFR: catalyze dihydromyricetin into delphinin colorless ANS: catalyze delphinin colorless into delphinidin

Protocol we use: We asked biological company to synthesize the sequence at first. And we constructed it into pRSFDUET plasmid. Next, we transformed the plasmids into E. coli BL21(DE3). After the colony has grown up on the plate, we picked a single colony by a sterile tip and added it into 4 ml LB medium with the corresponding antibiotic. Later, we added 1 mM IPTG for induction and shook at 16℃ overnight. We also set a control group and didn’t add IPTG into it. Finally, we centrifuged the bacterial solution at 12000 g, discard the supernatant, and used RIPA as a lysis buffer. we added loading buffer to the supernatant which contains the protein extract, and after heating at 96℃ for 10 min, we underwent SDS-PAGE and Coomassie brilliant blue staining for expression test. We could see a clear band at the position of (请老师补充分子量大小)kD, which only appeared in the group with IPTG. The molecular weight of this band was in line with the expectation, and it was under the condition of induction, so we believed that we had successfully expressed fusion proteins combined by F3H and F3’5’H, DFR and ANS. File:SHSBNU.2.gif File:SHSBNU.3.gif

User Reviews

UNIQde1bf3fa403340b7-partinfo-00000000-QINU UNIQde1bf3fa403340b7-partinfo-00000001-QINU