Difference between revisions of "Part:BBa I742143"
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− | This part consists of the genes sam8 and sam5, encoding tyrosine ammonia lyase and 4-coumarate-3-hydroxylase, from the bacterium Saccharothrix espanaensis DSM 4429. The enzymes acting together are expected to convert tyrosine to caffeic acid. Reference: Berner, M., Krug, D., Bihlmaier, C., Vente, A., Muller, R. and Bechthold, A. 'Genes and Enzymes Involved in Caffeic Acid Biosynthesis in the Actinomycete Saccharothrix espanaensis' J. Bacteriol. 188 (7), 2666-2673 (2006). Note that there is a PstI site near the 3' end of the sam5 gene in this version. This will be removed by site directed mutagenesis in due course. This construct was prepared to test activity before undertaking the mutagenesis. | + | This part consists of the genes sam8 and sam5, encoding tyrosine ammonia lyase and 4-coumarate-3-hydroxylase, from the bacterium ''Saccharothrix espanaensis'' DSM 4429. The enzymes acting together are expected to convert tyrosine to caffeic acid. Reference: Berner, M., Krug, D., Bihlmaier, C., Vente, A., Muller, R. and Bechthold, A. 'Genes and Enzymes Involved in Caffeic Acid Biosynthesis in the Actinomycete ''Saccharothrix espanaensis''' J. Bacteriol. 188 (7), 2666-2673 (2006). Note that there is a PstI site near the 3' end of the sam5 gene in this version. This will be removed by site directed mutagenesis in due course. This construct was prepared to test activity before undertaking the mutagenesis. |
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Latest revision as of 18:28, 25 October 2007
sam8+sam5 (tyrosine ammonia lyase + coumarate hydroxylase)
This part consists of the genes sam8 and sam5, encoding tyrosine ammonia lyase and 4-coumarate-3-hydroxylase, from the bacterium Saccharothrix espanaensis DSM 4429. The enzymes acting together are expected to convert tyrosine to caffeic acid. Reference: Berner, M., Krug, D., Bihlmaier, C., Vente, A., Muller, R. and Bechthold, A. 'Genes and Enzymes Involved in Caffeic Acid Biosynthesis in the Actinomycete Saccharothrix espanaensis' J. Bacteriol. 188 (7), 2666-2673 (2006). Note that there is a PstI site near the 3' end of the sam5 gene in this version. This will be removed by site directed mutagenesis in due course. This construct was prepared to test activity before undertaking the mutagenesis.
Sequence and Features
- 10INCOMPATIBLE WITH RFC[10]Illegal PstI site found at 2994
- 12INCOMPATIBLE WITH RFC[12]Illegal PstI site found at 2994
- 21INCOMPATIBLE WITH RFC[21]Illegal BamHI site found at 808
Illegal BamHI site found at 1210 - 23INCOMPATIBLE WITH RFC[23]Illegal PstI site found at 2994
- 25INCOMPATIBLE WITH RFC[25]Illegal PstI site found at 2994
Illegal NgoMIV site found at 551
Illegal NgoMIV site found at 1595
Illegal NgoMIV site found at 1603
Illegal NgoMIV site found at 2353
Illegal NgoMIV site found at 2526
Illegal NgoMIV site found at 2928
Illegal NgoMIV site found at 2932
Illegal AgeI site found at 498
Illegal AgeI site found at 667 - 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 102
Illegal BsaI site found at 368
Illegal BsaI.rc site found at 2127