Difference between revisions of "Part:BBa K5396003"
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===Usage and Biology=== | ===Usage and Biology=== | ||
− | <p>The BaCBM2-Cys fragment was generated from a PCR reaction using primers that specifically amplify the linker-BaCBM2-linker region of | + | <p>The BaCBM2-Cys fragment was generated from a PCR reaction using primers that specifically amplify the linker-BaCBM2-linker region of BBa_K5396000. The reverse primer used in this reaction adds a codon that encodes the amino acid cysteine at the end of the sequence.</p> |
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<span class='h3bb'>Sequence and Features</span> | <span class='h3bb'>Sequence and Features</span> |
Revision as of 19:47, 16 September 2024
BaCBM2-Cys
CBM2, or Carbohydrate-Binding Module 2, is a protein sourced from Bacillus anthracis. It belongs to a broader family of carbohydrate-binding modules that are crucial for the degradation of polysaccharides. These modules are important to break down complex carbohydrates, enabling microorganisms to convert them into usable energy sources.
Recent study [ ] has shown that CBM2 has the ability to bind to certain types of plastics, especially those derived from polysaccharides or exhibiting similar structural features. This binding ability is largely due to the protein's carbohydrate-binding properties, which facilitate interactions with specific functional groups found on plastic surfaces.
This CBM2 protein is modified with an additional amino acid (cysteine). This enhancement allows it to be effectively utilized in our biosensor technology.
Usage and Biology
The BaCBM2-Cys fragment was generated from a PCR reaction using primers that specifically amplify the linker-BaCBM2-linker region of BBa_K5396000. The reverse primer used in this reaction adds a codon that encodes the amino acid cysteine at the end of the sequence.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]