Difference between revisions of "Part:BBa K3562000"

Line 1: Line 1:
  
__NOTOC__
 
<partinfo>BBa_K3562000 short</parti
 
 
__NOTOC__
 
__NOTOC__
 
<partinfo>BBa_K3562000 short</partinfo>
 
<partinfo>BBa_K3562000 short</partinfo>
Line 31: Line 29:
 
Different AHL degrading enzymes have different substrate preferences and degradation activities.(Fig.2)
 
Different AHL degrading enzymes have different substrate preferences and degradation activities.(Fig.2)
 
[[Image:AHL-lactonase.png|frame|'''Figure 1:'''Mechanism of AHL-lactonase]]
 
[[Image:AHL-lactonase.png|frame|'''Figure 1:'''Mechanism of AHL-lactonase]]
nfo>
 
 
AHL-lactonase with AHLs (Quorum-sensing factor Acyl Homoserine Lactone) degradation activity.
 
 
<!-- -->
 
<span class='h3bb'>Sequence and Features</span>
 
<partinfo>BBa_K3562000 SequenceAndFeatures</partinfo>
 
 
 
<!-- Uncomment this to enable Functional Parameter display
 
===Functional Parameters===
 
<partinfo>BBa_K3562000 parameters</partinfo>
 
<!-- -->
 
 
===Usage and Biology===
 
Quorum sensing factor is closely related to bacterial virulence.
 
<br/>
 
Different AHL degrading enzymes have different substrate preferences and degradation activities.
 

Revision as of 15:56, 25 October 2020


AiiC (with His-tag)

AHL-lactonase with AHLs (Quorum-sensing factor Acyl Homoserine Lactone) degradation activity.

Sequence and Features


Assembly Compatibility:
  • 10
    INCOMPATIBLE WITH RFC[10]
    Illegal SpeI site found at 2071
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal SpeI site found at 2071
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    INCOMPATIBLE WITH RFC[23]
    Illegal SpeI site found at 2071
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal SpeI site found at 2071
  • 1000
    COMPATIBLE WITH RFC[1000]


Usage and Biology

AHL-lactonase is a kind of lactonase opened the homoserine lactone ring of AHL in the presence of water to produce N-acly homoserine.(Fig.1) The biological activity of degradation products will be greatly reduced.

Figure 1:Mechanism of AHL-lactonase

Quorum sensing factor is closely related to bacterial virulence. Enzymes that degrade AHL can control the concentration of AHL to silence the expression of related genes. In our project, we use these enzymes to control the virulence of Pseudomonas aeruginosa referred to existing experimental therapies.

Different AHL degrading enzymes have different substrate preferences and degradation activities.(Fig.2)

Figure 1:Mechanism of AHL-lactonase