Difference between revisions of "Part:BBa K3078004"

Line 34: Line 34:
 
</p>
 
</p>
 
</h5>
 
</h5>
<h5>
 
 
<P style="text-indent:2em;">
 
<P style="text-indent:2em;">
 
To assess the expression of our &#946;-1,3-glucanase, Congo Red experiment was used.
 
To assess the expression of our &#946;-1,3-glucanase, Congo Red experiment was used.

Revision as of 02:40, 21 October 2019


β-1,3-glucanase

β-1,3-glucanase protein coding region. β-1,3-glucanase can degrade biofilm.

1. Usage and Biology

β-1,3-glucan is one of the primary components in C. albicans biofilm EPS, which is important for Candida biofilm formation and resistance to stresses. The enzyme β-1,3-glucanase, form Cellulosimicrobium cellulans, can degrade β-1,3-glucan. Therefore, this year, we decided use β-1,3-glucanase to disrupt the Candida biofilm matrix and increase the effect of the antimicrobial drug.


2. Characterization

We characterised β-1,3-glucanase by cloning it into pVE vector. Moreover, an signal peptide were added.

To verify the construction of pVE-β-1,3-glucanase(pVE-β-GA) which we generated, the digestion by SalI/EcoRV was performed by a standard protocol following agarose gel electrophoresis (Figure 1).

B13-1

Figure 1. Digestion and agarose gel electrophoresis of pVE-β-GA.

To assess the expression of our β-1,3-glucanase, Congo Red experiment was used.

To assess the expression of our β-1,3-glucanase, Congo Red experiment was used.

</h5>











Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal NgoMIV site found at 274
    Illegal NgoMIV site found at 483
    Illegal NgoMIV site found at 622
  • 1000
    COMPATIBLE WITH RFC[1000]