Difference between revisions of "Part:BBa K3739038"
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This part contains a ''Vibrio natriegens''-optimized GFP coding sequence, and the GFP is fused at N-terminal with his-tag in order to let us purify the protein. His-GFP is fused with secretory peptide from Aly01.We use <partinfo>BBa_K3739038</partinfo> to construct the expression system and help prove the function of some signal peptide. | This part contains a ''Vibrio natriegens''-optimized GFP coding sequence, and the GFP is fused at N-terminal with his-tag in order to let us purify the protein. His-GFP is fused with secretory peptide from Aly01.We use <partinfo>BBa_K3739038</partinfo> to construct the expression system and help prove the function of some signal peptide. | ||
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===Biology=== | ===Biology=== | ||
Aly01 | Aly01 | ||
− | Aly01 is alginate lyase from ''Vibrio natriegens'' SK42.001, which is secreted out and able to digest alginate to unsaturated alginate oligosaccharide. Its signal peptide (named Aly01 in our parts), which is fused with heterogenous protein, is performed well in E. coli. It is implied that the heterogenous protein fused with Aly01 signal peptide may be also secreted efficiently. | + | Aly01 is alginate lyase from ''Vibrio natriegens'' SK42.001, which is secreted out and able to digest alginate to unsaturated alginate oligosaccharide. Its signal peptide (named Aly01 in our parts), which is fused with heterogenous protein, is performed well in ''E. coli''. It is implied that the heterogenous protein fused with Aly01 signal peptide may be also secreted efficiently. |
GFP | GFP | ||
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===Usage=== | ===Usage=== | ||
− | Here, we used <partinfo>BBa_K3739038</partinfo> to construct the expression system and obtained the composite part BBa_Kxxxx. We transformed the constructed plasmid on the expression vector pET-28a (+) into V. natriegens to extract the protein. This protein work together with those from <partinfo> | + | Here, we used <partinfo>BBa_K3739038</partinfo> to construct the expression system and obtained the composite part BBa_Kxxxx. We transformed the constructed plasmid on the expression vector pET-28a (+) into V. natriegens to extract the protein. This protein work together with those from <partinfo>BBa_K3739041</partinfo> and <partinfo>BBa_K3739043</partinfo> to verify the function of our secretory peptides Aly01 and LMT. |
===Characterization=== | ===Characterization=== | ||
===Reference=== | ===Reference=== | ||
− | 1. Meng, Q. ''et al''. Characterization and enhanced extracellular overexpression of a new salt-activated alginate lyase. ''Journal of the science of food and agriculture'' '''101''', 5154-5162, doi:10.1002/jsfa.11161 (2021). | + | 1.Meng, Q. ''et al''. Characterization and enhanced extracellular overexpression of a new salt-activated alginate lyase. ''Journal of the science of food and agriculture'' '''101''', 5154-5162, doi:10.1002/jsfa.11161 (2021). |
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Revision as of 20:46, 21 October 2021
J23100-B0030-Aly01-his-GFP-B0010
This part contains a Vibrio natriegens-optimized GFP coding sequence, and the GFP is fused at N-terminal with his-tag in order to let us purify the protein. His-GFP is fused with secretory peptide from Aly01.We use BBa_K3739038 to construct the expression system and help prove the function of some signal peptide.
Biology
Aly01 Aly01 is alginate lyase from Vibrio natriegens SK42.001, which is secreted out and able to digest alginate to unsaturated alginate oligosaccharide. Its signal peptide (named Aly01 in our parts), which is fused with heterogenous protein, is performed well in E. coli. It is implied that the heterogenous protein fused with Aly01 signal peptide may be also secreted efficiently.
GFP Protein tags are peptides genetically fused to the proteins of interest. There are many different kinds of tags developed for for different purposes. For labeling experiments, normally the proteins of interest are tagged directly by fluorescent tags. Green fluorescent protein (GFP) make it easier to study protein localization, interactions and dynamics when fusing with other peptides and proteins.
Usage
Here, we used BBa_K3739038 to construct the expression system and obtained the composite part BBa_Kxxxx. We transformed the constructed plasmid on the expression vector pET-28a (+) into V. natriegens to extract the protein. This protein work together with those from BBa_K3739041 and BBa_K3739043 to verify the function of our secretory peptides Aly01 and LMT.
Characterization
Reference
1.Meng, Q. et al. Characterization and enhanced extracellular overexpression of a new salt-activated alginate lyase. Journal of the science of food and agriculture 101, 5154-5162, doi:10.1002/jsfa.11161 (2021).
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 7
Illegal NheI site found at 30 - 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal AgeI site found at 137
- 1000INCOMPATIBLE WITH RFC[1000]Illegal SapI.rc site found at 215