Difference between revisions of "Part:BBa K4247022"
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| − | ===Orf438 tyrosinase cofactor [Streptomyces antibioticus] | + | ===Orf438 tyrosinase cofactor [Streptomyces antibioticus]=== |
This basic part codes for the orf438 of Streptomyces antibioticus, copper cofactor of the tyrosinase enzyme. Orf438 is indispensable for the functioning of S. antibioticus tyrosinase according to Bernan et al., 1985 and was used by Choi et al., 2012 to activate the same enzyme (basic part BBa_K4247023) in a co-expression system. The part is codon optimised for E.coli. | This basic part codes for the orf438 of Streptomyces antibioticus, copper cofactor of the tyrosinase enzyme. Orf438 is indispensable for the functioning of S. antibioticus tyrosinase according to Bernan et al., 1985 and was used by Choi et al., 2012 to activate the same enzyme (basic part BBa_K4247023) in a co-expression system. The part is codon optimised for E.coli. | ||
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The enzyme tyrosinase is an oxidase found across taxa, it contains copper and is well known for its tyrosine modifying step that gives melanin. Our project specifically focused on converting the tyrosines of mfp151 (parts BBa_K4247020, BBa_K4247021) into DOPA in E.coli, a post-translational modification that makes mfp sticky. A way to achieve this dopaquinone conversion is by first producing mfp in vitro and then expose it to tyrosinase, but it has the limitations of having to purify the enzymes and of not allowing the dopa modification to occur in all the tyrosines that are not exposed to the enzyme. For this reason, we focused on a co-expression system where E.coli would have mfp151 on a plasmid and tyrosinase with its copper cofactor (orf438) on another. By inducing with IPTG, the tyrosines incorporated in the mfp151 protein have been hydroxylated to DOPA. | The enzyme tyrosinase is an oxidase found across taxa, it contains copper and is well known for its tyrosine modifying step that gives melanin. Our project specifically focused on converting the tyrosines of mfp151 (parts BBa_K4247020, BBa_K4247021) into DOPA in E.coli, a post-translational modification that makes mfp sticky. A way to achieve this dopaquinone conversion is by first producing mfp in vitro and then expose it to tyrosinase, but it has the limitations of having to purify the enzymes and of not allowing the dopa modification to occur in all the tyrosines that are not exposed to the enzyme. For this reason, we focused on a co-expression system where E.coli would have mfp151 on a plasmid and tyrosinase with its copper cofactor (orf438) on another. By inducing with IPTG, the tyrosines incorporated in the mfp151 protein have been hydroxylated to DOPA. | ||
| − | [[File: Tyrosinase.jpeg]] | + | [[File: Tyrosinase.jpeg|px400|]] |
Revision as of 15:53, 29 September 2022
Orf438 tyrosinase cofactor [Streptomyces antibioticus]
This basic part codes for the orf438 of Streptomyces antibioticus, copper cofactor of the tyrosinase enzyme. Orf438 is indispensable for the functioning of S. antibioticus tyrosinase according to Bernan et al., 1985 and was used by Choi et al., 2012 to activate the same enzyme (basic part BBa_K4247023) in a co-expression system. The part is codon optimised for E.coli.
Usage and Biology
The enzyme tyrosinase is an oxidase found across taxa, it contains copper and is well known for its tyrosine modifying step that gives melanin. Our project specifically focused on converting the tyrosines of mfp151 (parts BBa_K4247020, BBa_K4247021) into DOPA in E.coli, a post-translational modification that makes mfp sticky. A way to achieve this dopaquinone conversion is by first producing mfp in vitro and then expose it to tyrosinase, but it has the limitations of having to purify the enzymes and of not allowing the dopa modification to occur in all the tyrosines that are not exposed to the enzyme. For this reason, we focused on a co-expression system where E.coli would have mfp151 on a plasmid and tyrosinase with its copper cofactor (orf438) on another. By inducing with IPTG, the tyrosines incorporated in the mfp151 protein have been hydroxylated to DOPA.
