Difference between revisions of "Part:BBa K4387997"
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| − | The hemolysin A secretion machinery is a one-step secretion system (T1SS) that was originally isolated from uropathogenic E. coli strains. It is composed of 3 main peptides, the inner membrane proteins HlyB and HlyD, and the outer membrane protein TolC. Together, these 3 proteins build a continuous channel, through which originally the HlyA toxin is secreted in a one-step manner. Interestingly, the secretion signal is not found on the N-terminal site, instead it is found at the C-terminal end and the signal sequence is not removed during secretion. Scientists have identified the secretion signal and by fusing it to different proteins, were able to secrete various proteins with this secretion machinery. The very last 50 amino acids have been identified to bind to HlyB and HlyD, leading to a successful secretion. However, various lengths of HlyA fragments have been used to secrete the protein of interest, either containing the last 60 amino acids, or even longer fragments with 218 or, as shown with this part, 651 amino acids. | + | The hemolysin A secretion machinery is a one-step secretion system (T1SS) that was originally isolated from uropathogenic E. coli strains. It is composed of 3 main peptides, the inner membrane proteins HlyB and HlyD, and the outer membrane protein TolC. Together, these 3 proteins build a continuous channel, through which originally the HlyA toxin is secreted in a one-step manner. Interestingly, the secretion signal is not found on the N-terminal site, instead it is found at the C-terminal end and the signal sequence is not removed during secretion. Scientists have identified the secretion signal and by fusing it to different proteins, were able to secrete various proteins with this secretion machinery. The very last 50 amino acids have been identified to bind to HlyB and HlyD, leading to a successful secretion. However, various lengths of HlyA fragments have been used to secrete the protein of interest, either containing the last 60 amino acids, or even longer fragments with 218 or, as shown with this part, 651 amino acids. [1] |
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| + | ===References=== | ||
| + | * [1] Ruano-Gallego, D., Fraile, S., Gutierrez, C. et al. Screening and purification of nanobodies from E. coli culture supernatants using the hemolysin secretion system. Microb Cell Fact 18, 47 (2019). https://doi.org/10.1186/s12934-019-1094-0 | ||
Revision as of 15:56, 2 October 2022
HlyA-tag obtained from the hemolysin A one-step secretion system
The hemolysin A secretion machinery is a one-step secretion system (T1SS) that was originally isolated from uropathogenic E. coli strains. It is composed of 3 main peptides, the inner membrane proteins HlyB and HlyD, and the outer membrane protein TolC. Together, these 3 proteins build a continuous channel, through which originally the HlyA toxin is secreted in a one-step manner. Interestingly, the secretion signal is not found on the N-terminal site, instead it is found at the C-terminal end and the signal sequence is not removed during secretion. Scientists have identified the secretion signal and by fusing it to different proteins, were able to secrete various proteins with this secretion machinery. The very last 50 amino acids have been identified to bind to HlyB and HlyD, leading to a successful secretion. However, various lengths of HlyA fragments have been used to secrete the protein of interest, either containing the last 60 amino acids, or even longer fragments with 218 or, as shown with this part, 651 amino acids. [1]
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 565
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
References
- [1] Ruano-Gallego, D., Fraile, S., Gutierrez, C. et al. Screening and purification of nanobodies from E. coli culture supernatants using the hemolysin secretion system. Microb Cell Fact 18, 47 (2019). https://doi.org/10.1186/s12934-019-1094-0