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− | __NOTOC__
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− | <partinfo>BBa_K4263001 short</partinfo> | + | <meta charset="UTF-8"> |
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− | ACC1 is the major member of ACCs in mammalian, mountains of documents record the roles of ACC1 in various diseases, such as cancer, diabetes, obesity. Besides, acetyl-CoA and malonyl-CoA are cofactors in protein acetylation and malonylation, respectively, so that the manipulation of acetyl-CoA and malonyl-CoA by ACC1 can also markedly influence the profile of protein post-translational modifications, resulting in alternated biological processes in mammalian cells. | + | <meta name="viewport" content="width=device-width, initial-scale=1.0"> |
− | | + | <title>K4263001</title> |
− | <!-- Add more about the biology of this part here | + | <link rel="stylesheet" href="https://2022.igem.wiki/scut-china/static/css/part-public.css"> |
− | ===Usage and Biology===
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− | <span class='h3bb'>Sequence and Features</span> | + | <h2 style="font-weight: bold;">P<sub>ACC1</sub></h2> |
− | <partinfo>BBa_K4263001 SequenceAndFeatures</partinfo> | + | <h2>Introduction</h2> |
− | | + | <p>ACC1 is the major member of ACCs in mammalian<sup>[1]</sup>.</p> |
− | | + | <h2>Characterization</h2> |
− | <!-- Uncomment this to enable Functional Parameter display | + | <p>In order to test the function of P<em><sub>ACC1</sub></em>, we construct "P<em><sub>ACC1</sub>-EGFP-</em>terminator" (Figure 1). If P<em><sub>ACC1</sub></em> is functional, we can test the fluorescence intensity of EGFP in supernatant samples obtained from the culture of recombinant <em>P.pastoris</em> GS115 strain.</p> |
− | ===Functional Parameters===
| + | <img src="https://static.igem.wiki/teams/4263/wiki/parts/image/acc1e-min.jpg" alt=""> |
− | <partinfo>BBa_K4263001 parameters</partinfo> | + | <h4>Figure 1 Gene circuit of P<em><sub>ACC1</sub>-EGFP-</em>terminator</h4> |
− | <!-- --> | + | <p>Our results matched the general expected trend (Figure 2). After fermentation experiment in BMMY medium containing 1% methanol. The fluorescence intensity of the samples of recombinant <em>P.pastoris</em> GS115 containing the <em>EGFP</em> gene gradually increased over time . At the same time, we measured the growth curve of the strains.</p> |
| + | <img src="https://static.igem.wiki/teams/4263/wiki/parts/image/pacc1-min.jpg" alt=""> |
| + | <h4>Figure 2 Fluorescence intensity and OD600 absorbance of samples obtained at different time points from the culture of corresponding recombinant <em>P.pastoris</em> GS115 containing <em>EGFP</em> gene.</h4> |
| + | <h2>Reference</h2> |
| + | <p>[1] Wang Y, Yu W, Li S, et al. Acetyl-CoA Carboxylases and Diseases[J]. Front Oncol, 2022,12:836058.</p> |
| + | </article> |
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PACC1
Introduction
ACC1 is the major member of ACCs in mammalian[1].
Characterization
In order to test the function of PACC1, we construct "PACC1-EGFP-terminator" (Figure 1). If PACC1 is functional, we can test the fluorescence intensity of EGFP in supernatant samples obtained from the culture of recombinant P.pastoris GS115 strain.
Figure 1 Gene circuit of PACC1-EGFP-terminator
Our results matched the general expected trend (Figure 2). After fermentation experiment in BMMY medium containing 1% methanol. The fluorescence intensity of the samples of recombinant P.pastoris GS115 containing the EGFP gene gradually increased over time . At the same time, we measured the growth curve of the strains.
Figure 2 Fluorescence intensity and OD600 absorbance of samples obtained at different time points from the culture of corresponding recombinant P.pastoris GS115 containing EGFP gene.
Reference
[1] Wang Y, Yu W, Li S, et al. Acetyl-CoA Carboxylases and Diseases[J]. Front Oncol, 2022,12:836058.