Difference between revisions of "Part:BBa K1529150"
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[[File:T--CAU_China--PathA30.png|600px|thumb|center|]]
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<p style="text-align: center;"><b>Fig.1 Genetic circuit for ObcA verification (the excitation light of 488nm and emission light of 507nm)
  
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<p>We build the gene circuit by ClonExpress II one-step cloning kit (Vazyme Biotech, China). And for the T7 promoter, T7 terminator and lac operator, we just followed the structure that came with pET30a.</p>
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<p>After sequencing and amplifying, that vector as well as unmodified pET30a were transferred into <i>E.coli</i> BL21 (DE3) separately and cultivated on plates. After cultivating them in the LB liquid culture medium at 200 rpm, 37 ℃ for 12 h, the OD<SUB>600</SUB> of the two bacteria were adjusted to nearly the same (nearly 1.3) using ddH<SUB>2</SUB>O, then they were induced by IPTG. Before induction, half of the two bacterial solutions were divided into the control group without induction, which were use as a blank control for colorimetric method. After a cultivation at 120 rpm, 28 ℃ for 8 h, the bacterial solution was collected and then centrifuged at 8000 xg for 1 min. The precipitate was resuspended in a ratio of 200ul of water per 3 ml of product of the bacterial solution, and ultrasonic crushing for 10 minutes, according to the ultrasonic 3 seconds pause 3 seconds, Amp1 30% parameters. we measured its oxalic acid concentration by Oxalic Acid Content Detection Kit (BOXBIO, Beijing, China), a kit for the determination of oxalic acid concentration by salicylic acid iron colorimetric method. We tested the absorbance at OD<SUB>520</SUB> and convert it into the concentration of oxalic acid inside the thallus. Data are shown below:</p>
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<span class='h3bb'>Sequence and Features</span>
 
<span class='h3bb'>Sequence and Features</span>
 
<partinfo>BBa_K1529150 SequenceAndFeatures</partinfo>
 
<partinfo>BBa_K1529150 SequenceAndFeatures</partinfo>

Revision as of 08:25, 28 September 2022


PT7_obcA

1


Contribution From CAU_China 2022

Group: CAU_China, 2022 https://2022.igem.org/Team:CAU_China

Author: Liu Muhua

Summary: Verified that this composite Part can produce oxalic acid in Escherichia coli

Characterization

CAU_China 2022 used the CDS sequence in their oxalate secretion pathway and the expression product of obcA is one of the main enzyme in this pathway. It canact together with ObcB to catalyze oxaloacetic acid (OAA) and citric acid to form oxalic acid (OA). When there is only ObcA, it has a low ability to form oxalic acidin our project.

Hence, we aim to verify that the gene obcA, originally from Burkholderia glumae, can be regulated by PT7 and lac operator and properly expressed downstream to produce oxalic acid in Escherichia coli.


File:T--CAU China--PathA30.png

Fig.1 Genetic circuit for ObcA verification (the excitation light of 488nm and emission light of 507nm)
<p>We build the gene circuit by ClonExpress II one-step cloning kit (Vazyme Biotech, China). And for the T7 promoter, T7 terminator and lac operator, we just followed the structure that came with pET30a.</p> <p>After sequencing and amplifying, that vector as well as unmodified pET30a were transferred into E.coli BL21 (DE3) separately and cultivated on plates. After cultivating them in the LB liquid culture medium at 200 rpm, 37 ℃ for 12 h, the OD600 of the two bacteria were adjusted to nearly the same (nearly 1.3) using ddH2O, then they were induced by IPTG. Before induction, half of the two bacterial solutions were divided into the control group without induction, which were use as a blank control for colorimetric method. After a cultivation at 120 rpm, 28 ℃ for 8 h, the bacterial solution was collected and then centrifuged at 8000 xg for 1 min. The precipitate was resuspended in a ratio of 200ul of water per 3 ml of product of the bacterial solution, and ultrasonic crushing for 10 minutes, according to the ultrasonic 3 seconds pause 3 seconds, Amp1 30% parameters. we measured its oxalic acid concentration by Oxalic Acid Content Detection Kit (BOXBIO, Beijing, China), a kit for the determination of oxalic acid concentration by salicylic acid iron colorimetric method. We tested the absorbance at OD520 and convert it into the concentration of oxalic acid inside the thallus. Data are shown below:</p>

Sequence and Features


Assembly Compatibility:
  • 10
    INCOMPATIBLE WITH RFC[10]
    Illegal PstI site found at 276
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal PstI site found at 276
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BglII site found at 1420
    Illegal XhoI site found at 183
    Illegal XhoI site found at 1307
    Illegal XhoI site found at 1751
  • 23
    INCOMPATIBLE WITH RFC[23]
    Illegal PstI site found at 276
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal PstI site found at 276
    Illegal NgoMIV site found at 268
    Illegal NgoMIV site found at 599
    Illegal NgoMIV site found at 627
    Illegal NgoMIV site found at 663
    Illegal NgoMIV site found at 893
    Illegal NgoMIV site found at 1670
    Illegal NgoMIV site found at 1721
    Illegal AgeI site found at 205
  • 1000
    COMPATIBLE WITH RFC[1000]