Difference between revisions of "Part:BBa K3122007"
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<partinfo>BBa_K3122007 short</partinfo> | <partinfo>BBa_K3122007 short</partinfo> | ||
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| − | + | Vibrio cholerae’s ompT gene sequence was adapted to Golden Gate and MoClo assembly system, and expressed in this construct. The aim of it is to be the target for aptamers in the SELEX process, until developing a specific library against it. Unfortunately, we have not been able to clone this part for the moment. We expect future iGEM teams to resume our work from this point. | |
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| − | < | + | <h2> Biology </h2> |
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| − | <partinfo> | + | OmpT is described as a member of the family of outer membrane proteases called omptins (L. Vandeputte-Rutten, 2001). Moreover, other studies show a correlation between this protein and the regulation of cholera toxins, such as ToxR, and the presence of OmpT is directly connected to the sensitivity of the pathogen to host bile, hindering the colonization by the pathogen (E. Krukonis, 2003). |
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| + | <h2> Characterization </h2> | ||
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| + | Characterization of this part was meant to be conducted by building a transcriptional unit <partinfo>BBa_K3122013</partinfo> and performing western blotting assays. | ||
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<partinfo>BBa_K3122007 parameters</partinfo> | <partinfo>BBa_K3122007 parameters</partinfo> | ||
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| + | <h2>References</h2> | ||
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| + | L. Vandeputte-Rutten, R. Kramer, J. Kroon, N. Dekker, M. Egmond and P. Gros, "Crystal structure of the outer membrane protease OmpT from Escherichia coli suggests a novel catalytic site", The EMBO Journal, vol. 20, no. 18, pp. 5033-5039, 2001. Available: 10.1093/emboj/20.18.5033 [Accessed 19 October 2019]. | ||
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| + | E. Krukonis and V. DiRita, "From motility to virulence: sensing and responding to environmental signals in Vibrio cholerae", Current Opinion in Microbiology, vol. 6, no. 2, pp. 186-190, 2003. Available: 10.1016/s1369-5274(03)00032-8 [Accessed 19 October 2019]. | ||
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Revision as of 03:32, 22 October 2019
Outer membrane protein T (Vibrio cholerae) (TypeIIS adapted)
Vibrio cholerae’s ompT gene sequence was adapted to Golden Gate and MoClo assembly system, and expressed in this construct. The aim of it is to be the target for aptamers in the SELEX process, until developing a specific library against it. Unfortunately, we have not been able to clone this part for the moment. We expect future iGEM teams to resume our work from this point.
Biology
OmpT is described as a member of the family of outer membrane proteases called omptins (L. Vandeputte-Rutten, 2001). Moreover, other studies show a correlation between this protein and the regulation of cholera toxins, such as ToxR, and the presence of OmpT is directly connected to the sensitivity of the pathogen to host bile, hindering the colonization by the pathogen (E. Krukonis, 2003).
Characterization
Characterization of this part was meant to be conducted by building a transcriptional unit BBa_K3122013 and performing western blotting assays.
References
L. Vandeputte-Rutten, R. Kramer, J. Kroon, N. Dekker, M. Egmond and P. Gros, "Crystal structure of the outer membrane protease OmpT from Escherichia coli suggests a novel catalytic site", The EMBO Journal, vol. 20, no. 18, pp. 5033-5039, 2001. Available: 10.1093/emboj/20.18.5033 [Accessed 19 October 2019].
E. Krukonis and V. DiRita, "From motility to virulence: sensing and responding to environmental signals in Vibrio cholerae", Current Opinion in Microbiology, vol. 6, no. 2, pp. 186-190, 2003. Available: 10.1016/s1369-5274(03)00032-8 [Accessed 19 October 2019].