Difference between revisions of "Part:BBa K2539400"
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<partinfo>BBa_K2539400 short</partinfo> | <partinfo>BBa_K2539400 short</partinfo> | ||
− | This construct uses the inducible promoter PalcA (BBa_K2092002). PalcA is activated in the presence of both ethanol and a transcription factor, alcR (BBa_K2092001), and was originally isolated from the fungus Aspergillus nidulans (Panozzo <i>et al.</i>, 1997). | + | This construct uses the inducible promoter PalcA (BBa_K2092002). PalcA is activated in the presence of both ethanol and a transcription factor, alcR (BBa_K2092001), and was originally isolated from the fungus <i>Aspergillus nidulans</i> (Panozzo <i>et al.</i>, 1997). |
ALDH2*1 is the wild type form of human mitochondrial aldehyde dehydrogenase (ALDH2), which functions in alcohol metabolism to convert the toxic intermediate, acetaldehyde, into acetate (Larson <i>et al.</i>, 2005; Farrés <i>et al.</i>, 1994). | ALDH2*1 is the wild type form of human mitochondrial aldehyde dehydrogenase (ALDH2), which functions in alcohol metabolism to convert the toxic intermediate, acetaldehyde, into acetate (Larson <i>et al.</i>, 2005; Farrés <i>et al.</i>, 1994). | ||
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https://static.igem.org/mediawiki/parts/a/a2/T--TAS_Taipei--300pcr.jpg | https://static.igem.org/mediawiki/parts/a/a2/T--TAS_Taipei--300pcr.jpg | ||
− | <b>PCR check for BBa_K2539400 using VF2 and VR primers. Using these primers, PCR produced a band at the expected size of 2.9 kb.</b> | + | <b>PCR check for BBa_K2539400 (D) using VF2 and VR primers. Using these primers, PCR produced a band at the expected size of 2.9 kb.</b> |
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Panozzo C, Capuano V, Fillinger S, Felenbok B. (1997). The zinc binuclear cluster activator AlcR is able to bind to single sites but requires multiple repeated sites for synergistic activation of the alcA gene in Aspergillus nidulans. J Biol Chem. 5;272(36):22859-65. | Panozzo C, Capuano V, Fillinger S, Felenbok B. (1997). The zinc binuclear cluster activator AlcR is able to bind to single sites but requires multiple repeated sites for synergistic activation of the alcA gene in Aspergillus nidulans. J Biol Chem. 5;272(36):22859-65. | ||
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Latest revision as of 12:47, 17 October 2018
PalcA-Regulated ALDH2*1 Expression Construct
This construct uses the inducible promoter PalcA (BBa_K2092002). PalcA is activated in the presence of both ethanol and a transcription factor, alcR (BBa_K2092001), and was originally isolated from the fungus Aspergillus nidulans (Panozzo et al., 1997). ALDH2*1 is the wild type form of human mitochondrial aldehyde dehydrogenase (ALDH2), which functions in alcohol metabolism to convert the toxic intermediate, acetaldehyde, into acetate (Larson et al., 2005; Farrés et al., 1994).
Construct Design
The PalcA promoter is placed in front of a strong RBS (BBa_B0034), the human ALDH2*1 sequence (BBa_K2539150), and double terminator (BBa_B0015). This places the expression of ALDH2*1 under the control of the PalcA promoter.
PCR Check Results
The part was confirmed by PCR using the primers VF2 and VR, as well as sequencing by Tri-I Biotech.
PCR check for BBa_K2539400 (D) using VF2 and VR primers. Using these primers, PCR produced a band at the expected size of 2.9 kb.
References
Farrés J, Wang X, Takahashi K, Cunningham SJ, Wang TT, Weiner H. (1994). Effects of changing glutamate 487 to lysine in rat and human liver mitochondrial aldehyde dehydrogenase. A model to study human (Oriental type) class 2 aldehyde dehydrogenase. J Biol Chem. 13;269(19):13854-60.
Larson HN, Weiner H, Hurley TD. (2005). Disruption of the Coenzyme Binding Site and Dimer Interface Revealed in the Crystal Structure of Mitochondrial Aldehyde Dehydrogenase “Asian” Variant. J Biol Chem. 280(34):30550-6.
Panozzo C, Capuano V, Fillinger S, Felenbok B. (1997). The zinc binuclear cluster activator AlcR is able to bind to single sites but requires multiple repeated sites for synergistic activation of the alcA gene in Aspergillus nidulans. J Biol Chem. 5;272(36):22859-65.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 274
Illegal BglII site found at 2116 - 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 1174
Illegal NgoMIV site found at 1317
Illegal NgoMIV site found at 1830 - 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 1236
Illegal SapI.rc site found at 1733