Difference between revisions of "Part:BBa K5378001"
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+ | __NOTOC__ | ||
+ | <partinfo>BBa_K5378001 short</partinfo> | ||
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+ | Trp hydroxylase-1 (TPH1) are rate-limiting enzymes in Trp metabolism. | ||
+ | <!-- Add more about the biology of this part here | ||
+ | ===Usage and Biology=== | ||
+ | |||
+ | <!-- --> | ||
+ | <p class='h3bb'>Sequence and Features</p> | ||
+ | <partinfo>BBa_K5378001 SequenceAndFeatures</partinfo> | ||
+ | |||
+ | |||
+ | <!-- Uncomment this to enable Functional Parameter display | ||
+ | ===Functional Parameters=== | ||
+ | <partinfo>BBa_K5378001 parameters</partinfo> | ||
+ | <!-- --> | ||
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<html lang="zh"> | <html lang="zh"> | ||
<head> | <head> | ||
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<h1>Usage and Biology</h1> | <h1>Usage and Biology</h1> | ||
− | <p>A small amount of Trp is catalyzed to 5-HTP by TPH (Figure).Aromatic L-amino acid decarboxylase interacts with the cofactor pyridoxal-5’-phosphate to convert 5-HTP to 5-HT. 5-HT is a monoamine neurotransmitter in the human central nervous sys tem and is also known as serotonin because it can cause vascular smooth muscle contraction when present in the blood. The synthesis of 5-HT takes place in both the gut and brain.Peripheral 5-HT is primarily synthesized by TPH1 in the enterochromaffin cells. 5-HT is subsequently stored in platelets and contributes to various physiological functions, including the regulation of vasocontraction and proliferation of vascular smooth muscle cells. | + | <p>A small amount of Trp is catalyzed to 5-HTP by TPH (Figure).Aromatic L-amino acid decarboxylase interacts with the cofactor pyridoxal-5’-phosphate to convert 5-HTP to 5-HT. 5-HT is a monoamine neurotransmitter in the human central nervous sys tem and is also known as serotonin because it can cause vascular smooth muscle contraction when present in the blood. The synthesis of 5-HT takes place in both the gut and brain.Peripheral 5-HT is primarily synthesized by TPH1 in the enterochromaffin cells. 5-HT is subsequently stored in platelets and contributes to various physiological functions, including the regulation of vasocontraction and proliferation of vascular smooth muscle cells.</p> |
− | We learned that 5-HT can be further converted to melatonin, which further regulates the sleep-wake cycle by consulting the literature.Furthermore, 5-HT in the gut has been reported to be involved in the production of melatonin.</p> | + | <p>We learned that 5-HT can be further converted to melatonin, which further regulates the sleep-wake cycle by consulting the literature.Furthermore, 5-HT in the gut has been reported to be involved in the production of melatonin.</p> |
+ | <p>After being metabolized by gut bacteria, aromatic amino acids from food can produce monoamine false neurotransmitters, such as phenylalanine being metabolized into phenylethylamine, and tyrosine into tyramine. Tryptophan, through different metabolic pathways, can be converted into kynurenine, serotonin, and indole.</p> | ||
+ | <p>Patients who develop liver failure can not digest those aromatic amino acids properly, and this can lead to false neuro-transmitters accumulation, causing neuro system symptoms.</p> | ||
<div class="image"> | <div class="image"> | ||
<img id="image" src="https://static.igem.wiki/teams/5378/part/tph.webp" alt="示例图片" /> | <img id="image" src="https://static.igem.wiki/teams/5378/part/tph.webp" alt="示例图片" /> | ||
</div> | </div> | ||
+ | |||
+ | <h1>Design</h1> | ||
+ | <p>We designed a plasmid that can be transformed into EcN to express tryptophan hydroxylase 1 (TPH1), enabling the conversion of tryptophan (Trp) into serotonin (5-HT) and reducing excess aromatic amino acids. Since serotonin synthesized in the gut cannot cross the blood-brain barrier (BBB) or affect central nervous system function, there is no concern about adverse effects on the central nervous system.</p> | ||
<h1>Functional Verification</h1> | <h1>Functional Verification</h1> | ||
− | + | From the figure below, the size of each band of k y agarose gel electrophoresis is basically the same as the size of the target gene, indicating that the plasmid has been successfully transformed into ECN. | |
− | + | ||
− | + | <div class="image"> | |
+ | <img id="image" src="https://static.igem.wiki/teams/5378/part/tph1-1.webp" alt="示例图片" /> | ||
+ | </div> | ||
+ | |||
<h1>Reference</h1> | <h1>Reference</h1> | ||
<p>[1]Daubert, E.A., and Condron, B.G. (2010). Serotonin: a regulator of neuronal morphology and circuitry. Trends Neurosci. 33, 424–434. https://doi.org/10.1016/j.tins.2010.05.005. </p> | <p>[1]Daubert, E.A., and Condron, B.G. (2010). Serotonin: a regulator of neuronal morphology and circuitry. Trends Neurosci. 33, 424–434. https://doi.org/10.1016/j.tins.2010.05.005. </p> | ||
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<p>[3]Chen,C.Q., Fichna, J., Bashashati, M., Li, Y.Y., and Storr, M. (2011). Dis tribution, function and physiological role of melatonin in the lower gut. World J. Gastroenterol. 17, 3888–3898. https://doi.org/10.3748/wjg. v17.i34.3888.</p> | <p>[3]Chen,C.Q., Fichna, J., Bashashati, M., Li, Y.Y., and Storr, M. (2011). Dis tribution, function and physiological role of melatonin in the lower gut. World J. Gastroenterol. 17, 3888–3898. https://doi.org/10.3748/wjg. v17.i34.3888.</p> | ||
<p>[4]Xue C, Li G, Zheng Q, Gu X, Shi Q, Su Y, Chu Q, Yuan X, Bao Z, Lu J, Li L. Tryptophan metabolism in health and disease. Cell Metab. 2023 Aug 8;35(8):1304-1326. doi: 10.1016/j.cmet.2023.06.004. Epub 2023 Jun 22. PMID: 37352864.</p> | <p>[4]Xue C, Li G, Zheng Q, Gu X, Shi Q, Su Y, Chu Q, Yuan X, Bao Z, Lu J, Li L. Tryptophan metabolism in health and disease. Cell Metab. 2023 Aug 8;35(8):1304-1326. doi: 10.1016/j.cmet.2023.06.004. Epub 2023 Jun 22. PMID: 37352864.</p> | ||
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</body> | </body> | ||
</html> | </html> |
Latest revision as of 02:16, 2 October 2024
Trp hydroxylase-1 (TPH1)
Trp hydroxylase-1 (TPH1) are rate-limiting enzymes in Trp metabolism.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Usage and Biology
A small amount of Trp is catalyzed to 5-HTP by TPH (Figure).Aromatic L-amino acid decarboxylase interacts with the cofactor pyridoxal-5’-phosphate to convert 5-HTP to 5-HT. 5-HT is a monoamine neurotransmitter in the human central nervous sys tem and is also known as serotonin because it can cause vascular smooth muscle contraction when present in the blood. The synthesis of 5-HT takes place in both the gut and brain.Peripheral 5-HT is primarily synthesized by TPH1 in the enterochromaffin cells. 5-HT is subsequently stored in platelets and contributes to various physiological functions, including the regulation of vasocontraction and proliferation of vascular smooth muscle cells.
We learned that 5-HT can be further converted to melatonin, which further regulates the sleep-wake cycle by consulting the literature.Furthermore, 5-HT in the gut has been reported to be involved in the production of melatonin.
After being metabolized by gut bacteria, aromatic amino acids from food can produce monoamine false neurotransmitters, such as phenylalanine being metabolized into phenylethylamine, and tyrosine into tyramine. Tryptophan, through different metabolic pathways, can be converted into kynurenine, serotonin, and indole.
Patients who develop liver failure can not digest those aromatic amino acids properly, and this can lead to false neuro-transmitters accumulation, causing neuro system symptoms.
Design
We designed a plasmid that can be transformed into EcN to express tryptophan hydroxylase 1 (TPH1), enabling the conversion of tryptophan (Trp) into serotonin (5-HT) and reducing excess aromatic amino acids. Since serotonin synthesized in the gut cannot cross the blood-brain barrier (BBB) or affect central nervous system function, there is no concern about adverse effects on the central nervous system.
Functional Verification
From the figure below, the size of each band of k y agarose gel electrophoresis is basically the same as the size of the target gene, indicating that the plasmid has been successfully transformed into ECN.Reference
[1]Daubert, E.A., and Condron, B.G. (2010). Serotonin: a regulator of neuronal morphology and circuitry. Trends Neurosci. 33, 424–434. https://doi.org/10.1016/j.tins.2010.05.005.
[2] Watts, S.W., Morrison, S.F., Davis, R.P., and Barman, S.M. (2012). Sero tonin and blood pressure regulation. Pharmacol. Rev. 64, 359–388. https://doi.org/10.1124/pr.111.004697.
[3]Chen,C.Q., Fichna, J., Bashashati, M., Li, Y.Y., and Storr, M. (2011). Dis tribution, function and physiological role of melatonin in the lower gut. World J. Gastroenterol. 17, 3888–3898. https://doi.org/10.3748/wjg. v17.i34.3888.
[4]Xue C, Li G, Zheng Q, Gu X, Shi Q, Su Y, Chu Q, Yuan X, Bao Z, Lu J, Li L. Tryptophan metabolism in health and disease. Cell Metab. 2023 Aug 8;35(8):1304-1326. doi: 10.1016/j.cmet.2023.06.004. Epub 2023 Jun 22. PMID: 37352864.