Difference between revisions of "Part:BBa K2380005"

Revision as of 13:47, 28 October 2017

Chitinase A1

Chitinase A1 (ChiA1) is a hydrolase isolated from the organism Bacillus circulans WL-12. The chiA gene is 1983 base pairs long and translates into an enzyme with a molecular weight of approximately 69 kDa. ChiA1's main function is to break down glycosidic bonds between N-Acetylglucosamine (GlcNAc) units in a chitin oligomer.

Usage and Biology

Chitin is a molecule found in fungal cell walls [1]. Many plants possess enzymes, so-called chitinases, which are able to break down chitin and thus help along with its digestion. These enzymes play a role in defense mechanisms of plants, in case of fungal infections [2]. Even in human tissues chitinases appear, where they defend us against parasites [3]. Chitinases break down the glycosidic bonds between chitin monomer units, and are classified as hydrolases.
Its enzymatic activity has also previously been tested on chitin pentamers. ChiA1 breaks down these chitin pentamers in two dimers and one N-acetylglucosamine (GlcNAc) unit [4].
The N-terminal domain in the ChiA1 is responsible for its catalytic activity. The C-terminal domain plays an important role in the hydrolysis of chitin, and is the reason ChiA1 has such a high affinity to the substrate[4].
For more informations about this Part, visit the Wiki: http://2017.igem.org/Team:TU_Darmstadt/project/chitinase

Results

Fig. 5: SDS-Page
Lane 1: 24 hours after induction
Lane 2: 3 hours after induction
Lane 3: Before induction
Lane 4: Empty BL21 cells

To verify if ChiA1 is produced in BL21 cells containing the pSB1C3-AraC-chiA, a SDS-Page was performed. As we have described before, the page shows the expected results and proves that ChiA1 was successfully produced in E.coli BL21 cells.

References

[1] Stefanie Nicole Hamer, Stefan Cord-Landwehr, Xevi Biarnés, Antoni Planas, Hendrik Waegeman, Bruno Maria Moerschbacher, and Staphan Kolkenbrock (2015) Enzymatic production of defined chitosan oligomers with a specific pattern of acetylation using a combination of chitin oligosaccharide deacetylases DOI: 10.1038/srep08716
[2] John G. Verburg and Q. Khai Huynh (1990) Purification and Characterization of an Antifungal Chitinase from Arabidopsis thaliana. Plant Physiol. 95, 450-455 DOI: https://doi.org/10.1104/pp.95.2.450
[3] Paoletti MG, Norberto L., Damini R., and Musumeci S. (2007) Human gastric juice contains chitinase that can degrade chitin DOI: 10.1159/000104144
[4] Sylvain Cottaz, Eric Samain (2005) Genetic engineering of Escherichia coli for the production of NI,NII-diacetylchitobiose (chitinbiose) and its utilization as a primer for the synthesis of complex carbohydrates. Metabolic Engineering 7, 311–317

Sequence and Features