Difference between revisions of "Part:BBa K5201000"
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<p>Long description </p> | <p>Long description </p> | ||
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<p>Biology </p> | <p>Biology </p> | ||
<p><i>pmHAS </i>encodes hyaluronan synthase (HAS) from <i>Pasteurella Multocida</i>. <i>pmHAS </i>is a class II HAS enzyme, which is a peripheral membrane protein that can function without cell membrane. </p> | <p><i>pmHAS </i>encodes hyaluronan synthase (HAS) from <i>Pasteurella Multocida</i>. <i>pmHAS </i>is a class II HAS enzyme, which is a peripheral membrane protein that can function without cell membrane. </p> | ||
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<p>We expressed <i>pmHAS</i> in <i>DH5a</i> <i>E. coli</i> under a <i>lac promoter</i> and measured the amount of HA produced. In both glucose medium and glucose + glucosamine medium, we observed a consistent increase in HA absorbance suggesting that the HAS is functional and able to synthesize HA in <i>E. coli. </i>We also observed that the addition of glucosamine, one of the precursors of HA, can further increase the HA yield. </p> | <p>We expressed <i>pmHAS</i> in <i>DH5a</i> <i>E. coli</i> under a <i>lac promoter</i> and measured the amount of HA produced. In both glucose medium and glucose + glucosamine medium, we observed a consistent increase in HA absorbance suggesting that the HAS is functional and able to synthesize HA in <i>E. coli. </i>We also observed that the addition of glucosamine, one of the precursors of HA, can further increase the HA yield. </p> | ||
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Latest revision as of 10:13, 2 October 2024
Characterisation of BBa_K5201001: HongKong-UCCKE
Long description
Biology
pmHAS encodes hyaluronan synthase (HAS) from Pasteurella Multocida. pmHAS is a class II HAS enzyme, which is a peripheral membrane protein that can function without cell membrane.
Usage and design
Our recombinant plasmid consists of pmHAS and kfiD which is expressed under promoter (BBa_R0010). We hope that the pmHAS can produce HAS enzyme for synthesis of HA. HA is widely utilized by the cosmetic industry for its significant water absorption and retention properties. And therefore, we want to further implement it for agricultural use.
Standard curve of HA
The cetyltrimethylammonium bromide (CTAB) solution will react with HA to form precipitate, which absorbs 400 nm light. 150µL of standard HA solution in range of 0g/L to 0.1g/L, 350µL acetate acid, 1mL of 2.5g/L CTAB solution at room temperature for 5 min is added in a 96-well plate. The absorbance of the precipitate at 400 nm is measured using a plate reader. The standard curve of OD400 against HA concentration is plotted.
(Part_registry_6) Fig. 6 HA calibration |
Production of HA
- Culture in glucose medium
(Part_registry_7) |
(Part_registry_8) | |
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Figs. 7, 8 OD400 of transformed and untransformed bacteria supplied with glucose |
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- Culture in glucose and glucosamine medium
(Part_registry_9) |
(Part_registry_10) | |
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Figs. 9, 10 OD400 of transformed and untransformed bacteria supplied with glucose and glucosamine |
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We expressed pmHAS in DH5a E. coli under a lac promoter and measured the amount of HA produced. In both glucose medium and glucose + glucosamine medium, we observed a consistent increase in HA absorbance suggesting that the HAS is functional and able to synthesize HA in E. coli. We also observed that the addition of glucosamine, one of the precursors of HA, can further increase the HA yield.