Difference between revisions of "Part:BBa K1216003"
(→Characterization) |
|||
Line 25: | Line 25: | ||
[[File:NagZ_colored.png|frame|right|<b>Figure 1. Cell lysate from <i>E.Coli</i> overexpressing NagZ after reacting with pNP-GlcNac.</b>]] | [[File:NagZ_colored.png|frame|right|<b>Figure 1. Cell lysate from <i>E.Coli</i> overexpressing NagZ after reacting with pNP-GlcNac.</b>]] | ||
[http://2013.igem.org/Team:ETH_Zurich ETH Zurich 2013] used NagZ in their project as reporter enzyme. | [http://2013.igem.org/Team:ETH_Zurich ETH Zurich 2013] used NagZ in their project as reporter enzyme. | ||
− | To test the functionality of the enzyme, cell lysate of <i>E.Coli</i> overexpressing NagZ was incubated with GlcNac. | + | To test the functionality of the enzyme, cell lysate of <i>E.Coli</i> overexpressing NagZ was incubated with pNP-GlcNac. |
− | [[File:nagz_color_reaction.png|thumb|center|396px|<b>Figure 2. Enzymatic reaction of NagZ with GlcNac.</b>]] | + | [[File:nagz_color_reaction.png|thumb|center|396px|<b>Figure 2. Enzymatic reaction of NagZ with pNP-GlcNac.</b>]] |
Cell lysate for the assay described below was tested for active enzyme in the same way, but with the fluorescent substrate 4-MU-N-acetyl-β-D-glucosaminide. Unforunately this did not work until the wiki freeze. | Cell lysate for the assay described below was tested for active enzyme in the same way, but with the fluorescent substrate 4-MU-N-acetyl-β-D-glucosaminide. Unforunately this did not work until the wiki freeze. | ||
[[File:nagz_fluorescent_reaction.png|frame|center|<b>Figure 4. Enzymatic reaction of NagZ with 4-MU-N-acetyl-β-D-glucosaminide.</b>]] | [[File:nagz_fluorescent_reaction.png|frame|center|<b>Figure 4. Enzymatic reaction of NagZ with 4-MU-N-acetyl-β-D-glucosaminide.</b>]] |
Revision as of 20:24, 4 October 2013
beta-N-Acetylglucosaminidase (nagZ) from Escherichia Coli
nagZ encodes β-N-Acetylglucosaminidase, a cytoplasmatic hydrolase which is involved in the murein tripeptide recycling pathway of E.coli[1].
Usage and Biology
β-N-Acetylglucosaminidase can be used as a reporter enzyme in a histochemical reaction with substrates like 5-Bromo-4-Chloro-3-Indolyl-N-Acetyl-β-D-Glucosaminide, which will after hydrolysis release a blue chromophore[2].
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 25
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal SapI.rc site found at 76
Characterization
[http://2013.igem.org/Team:ETH_Zurich ETH Zurich 2013] used NagZ in their project as reporter enzyme. To test the functionality of the enzyme, cell lysate of E.Coli overexpressing NagZ was incubated with pNP-GlcNac.
Cell lysate for the assay described below was tested for active enzyme in the same way, but with the fluorescent substrate 4-MU-N-acetyl-β-D-glucosaminide. Unforunately this did not work until the wiki freeze.
References
- Cheng et al. (2000). Molecular Characterization of the b-N-Acetylglucosaminidase of Escherichia coli and Its Role in Cell Wall Recycling. Journal of Bacteriology. 182: 4836-4840.
- [http://www.inalcopharm.com/cart.php?m=product_detail&p=6 Inalcopharm datasheet]