Difference between revisions of "Part:BBa K3114009"
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<partinfo>BBa_K3114009 short</partinfo> | <partinfo>BBa_K3114009 short</partinfo> | ||
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+ | ===Usage and Biology=== | ||
7-Hydroxymethyl chlorophyll a reductase (7-HCAR) is a naturally occurring plant enzyme prominent in the chlorophyll degradation pathway. 7-HCAR and cofactor Ferredoxin<sub>reduced</sub> catalyze the conversion of 7-Hydroxymethyl Chlorophyll a to Chlorophyll a (Meguro et al. 2011). | 7-Hydroxymethyl chlorophyll a reductase (7-HCAR) is a naturally occurring plant enzyme prominent in the chlorophyll degradation pathway. 7-HCAR and cofactor Ferredoxin<sub>reduced</sub> catalyze the conversion of 7-Hydroxymethyl Chlorophyll a to Chlorophyll a (Meguro et al. 2011). | ||
+ | BBa_K3114009 is a golden gate compatible part which allows insertion of the gene encoding 7-HCAR into genetic circuits to express the enzyme. In creating this part, iGEM Calgary wished to allow the golden gate cloning of this plant enzyme into <i>E.coli</i> for other teams to use in projects involving degradation of chlorophyll. This part was designed to be golden-gate compatible based on the Mo-Clo standard (Weber et al., 2011). It is also compatible with the BioBrick RFC[10] standard. | ||
− | + | This part is compatible with other golden gate parts created by iGEM Calgary including the following: | |
− | + | <ul> | |
+ | <li>DsbA signal peptide [https://parts.igem.org/Part:BBa_K3114000 (BBa_K3114000)]</li> | ||
+ | <li>MalE signal peptide [https://parts.igem.org/Part:BBa_K3114001 (BBa_K3114001)]</li> | ||
+ | <li>OmpA signal peptide [https://parts.igem.org/Part:BBa_K3114002 (BBa_K3114002)]</li> | ||
+ | <li>PhoA signal peptide [https://parts.igem.org/Part:BBa_K3114003 (BBa_K3114003)]</li> | ||
+ | <li>TorA signal peptide [https://parts.igem.org/Part:BBa_K3114005 (BBa_K3114005)]</li> | ||
+ | <li>YcbK signal peptide [https://parts.igem.org/Part:BBa_K3114004 (BBa_K3114004)]</li> | ||
+ | <li>Double Terminator [https://parts.igem.org/Part:BBa_K3114013 (BBa_K3114013)]</li> | ||
+ | <li>Universal Spacer with 6XHis tag and Double Terminator [https://parts.igem.org/Part:BBa_K3114014 (BBa_k3114014)]</li> | ||
− | ==His Tag Purification== | + | |
+ | </ul> | ||
+ | |||
+ | |||
+ | ===His Tag Purification=== | ||
Meguro et al. 2011 purified 7-HCAR using a his-tag/nickel column, but the recombinant protein did not exhibit enzymatic activity. The authors conjectured that the "His tag at the N terminus disturbed the HCAR activity" (Meguro et al. 2011). | Meguro et al. 2011 purified 7-HCAR using a his-tag/nickel column, but the recombinant protein did not exhibit enzymatic activity. The authors conjectured that the "His tag at the N terminus disturbed the HCAR activity" (Meguro et al. 2011). | ||
The 2019 Calgary iGEM team set out to get around this problem. The team modelled the electrostatic interactions of 7-HCAR and discovered that 7-HCAR has a highly electronegative core, which is likely interfering with the positively charged His tag. iGEM Calgary developed a universal spacer sequence (https://parts.igem.org/Part:BBa_K3114014) which permitted successful His tag purification. | The 2019 Calgary iGEM team set out to get around this problem. The team modelled the electrostatic interactions of 7-HCAR and discovered that 7-HCAR has a highly electronegative core, which is likely interfering with the positively charged His tag. iGEM Calgary developed a universal spacer sequence (https://parts.igem.org/Part:BBa_K3114014) which permitted successful His tag purification. | ||
− | === | + | |
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− | + | ===Sequences and Features | |
− | + | <partinfo>BBa_K3114009 SequenceAndFeatures</partinfo> | |
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===References=== | ===References=== | ||
Meguro, M., Ito, H., Takabayashi, A., Tanaka, R., & Tanaka, A. (2011). Identification of the 7-hydroxymethyl chlorophyll a reductase of the chlorophyll cycle in Arabidopsis. The Plant Cell, 23(9), 3442-3453. | Meguro, M., Ito, H., Takabayashi, A., Tanaka, R., & Tanaka, A. (2011). Identification of the 7-hydroxymethyl chlorophyll a reductase of the chlorophyll cycle in Arabidopsis. The Plant Cell, 23(9), 3442-3453. | ||
− | + | Weber, E., Engler, C., Gruetzner, R., Werner, S., & Marillonnet, S. (2011). A modular cloning system for standardized assembly of multigene constructs. <i>PLoS ONE</i>, 6(2). https://doi.org/10.1371/journal.pone.0016765 | |
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Revision as of 23:48, 18 October 2019
7-Hydroxymethyl Chlorophyll A Reductase (7-HCAR)
Usage and Biology
7-Hydroxymethyl chlorophyll a reductase (7-HCAR) is a naturally occurring plant enzyme prominent in the chlorophyll degradation pathway. 7-HCAR and cofactor Ferredoxinreduced catalyze the conversion of 7-Hydroxymethyl Chlorophyll a to Chlorophyll a (Meguro et al. 2011).
BBa_K3114009 is a golden gate compatible part which allows insertion of the gene encoding 7-HCAR into genetic circuits to express the enzyme. In creating this part, iGEM Calgary wished to allow the golden gate cloning of this plant enzyme into E.coli for other teams to use in projects involving degradation of chlorophyll. This part was designed to be golden-gate compatible based on the Mo-Clo standard (Weber et al., 2011). It is also compatible with the BioBrick RFC[10] standard.
This part is compatible with other golden gate parts created by iGEM Calgary including the following:
- DsbA signal peptide (BBa_K3114000)
- MalE signal peptide (BBa_K3114001)
- OmpA signal peptide (BBa_K3114002)
- PhoA signal peptide (BBa_K3114003)
- TorA signal peptide (BBa_K3114005)
- YcbK signal peptide (BBa_K3114004)
- Double Terminator (BBa_K3114013)
- Universal Spacer with 6XHis tag and Double Terminator (BBa_k3114014)
His Tag Purification
Meguro et al. 2011 purified 7-HCAR using a his-tag/nickel column, but the recombinant protein did not exhibit enzymatic activity. The authors conjectured that the "His tag at the N terminus disturbed the HCAR activity" (Meguro et al. 2011).
The 2019 Calgary iGEM team set out to get around this problem. The team modelled the electrostatic interactions of 7-HCAR and discovered that 7-HCAR has a highly electronegative core, which is likely interfering with the positively charged His tag. iGEM Calgary developed a universal spacer sequence (https://parts.igem.org/Part:BBa_K3114014) which permitted successful His tag purification.
===Sequences and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal XhoI site found at 4
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 869
Illegal AgeI site found at 293
Illegal AgeI site found at 386 - 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 1
Illegal BsaI.rc site found at 1403
References
Meguro, M., Ito, H., Takabayashi, A., Tanaka, R., & Tanaka, A. (2011). Identification of the 7-hydroxymethyl chlorophyll a reductase of the chlorophyll cycle in Arabidopsis. The Plant Cell, 23(9), 3442-3453.
Weber, E., Engler, C., Gruetzner, R., Werner, S., & Marillonnet, S. (2011). A modular cloning system for standardized assembly of multigene constructs. PLoS ONE, 6(2). https://doi.org/10.1371/journal.pone.0016765