Difference between revisions of "Part:BBa K1717171"
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<partinfo>BBa_K1717171 short</partinfo> | <partinfo>BBa_K1717171 short</partinfo> | ||
− | Keratinases are proteolytic enzymes which break the disulphide bonds in various keratin substrates. KERA is a basic part comprised from a synthesized KERA protein coding sequence, optimized for expression in E. coli and most active in degrading keratin in | + | Keratinases are proteolytic enzymes which break the disulphide bonds in various keratin substrates. KERA is a basic part comprised from a synthesized KERA protein coding sequence, optimized for expression in E. coli and most active in degrading keratin in feathers. |
− | This gene, when expressed in cells, can be tested for activity through looking for zones of clearing on skim milk agar plates where cells are growing, as well as by looking at degradation of keratin-containing substrates ( | + | This gene, when expressed in cells, can be tested for activity through looking for zones of clearing on skim milk agar plates where cells are growing, as well as by looking at degradation of keratin-containing substrates (feathers, hair, chemically synthesized keratin, etc.) when grown with cells. |
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Revision as of 01:29, 25 September 2015
Protein coding sequence for KeratinaseA
Keratinases are proteolytic enzymes which break the disulphide bonds in various keratin substrates. KERA is a basic part comprised from a synthesized KERA protein coding sequence, optimized for expression in E. coli and most active in degrading keratin in feathers. This gene, when expressed in cells, can be tested for activity through looking for zones of clearing on skim milk agar plates where cells are growing, as well as by looking at degradation of keratin-containing substrates (feathers, hair, chemically synthesized keratin, etc.) when grown with cells.
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 130
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal AgeI site found at 391
- 1000INCOMPATIBLE WITH RFC[1000]Illegal SapI site found at 761
Illegal SapI site found at 1064