Coding

Part:BBa_K4242004

Designed by: zongheng Wei   Group: iGEM22_CUG-China   (2022-09-29)
Revision as of 08:45, 1 October 2024 by Crisxy (Talk | contribs)


yedQ

This part sequence originated from Escherichia coli encodes YedQ protein. YedQ is diguanylate cyclase.

Usage and Biology

YedQ can work with the phosphodiesterase (YhjH) modulated the in vivo c-di-GMP levels. The expression of the yedQ gene increased the intracellular c-di-GMP concentration and resulted in the enhanced secretion of EPS[1]. So, The protein YedQ can promote bacterial self-aggregation and adhesion onto negatively charged surfaces. In E. coli, extracellular DNA (eDNA) was increased as expected for the deletions of yedQ. As a result of the significantly enhanced motility, but contrary to current models of decreased biofilm formation with decreased diguanylate cyclase activity, early biofilm formation increased dramatically for the deletions of yedQ[2].

The quantification of intracellular c-di-GMP

YedQ.png
Fig. 1. The quantification of intracellular c-di-GMP in C. testosteroni WDL7/pYedQ2, the wild-type strain and WDL7/YhjH. nd, not determined (a). Crystal violet staining of WDL7/pYedQ2, WDL7 and WDL7/YhjH strains for quantifying relative biofilm biomass (b). * indicates significantly difference when compared with the WDL7 wild type strain, * p < 0.05, *** p < 0.001[1].

CUG-China 2024--Contribution

YedQ is a diguanylate cyclase from Escherichia coli.<i> It is registered in 2022 by CUG-China, which works with the phosphodiesterase (YhjH) modulated the in vivo c-di-GMP levels. The expression of the <i>yedQ<i> gene increased the intracellular c-di-GMP concentration and resulted in the enhanced secretion of EPS. We design the expression vector “pYDT-<i>Ptac<i>-<i>yedQ<i>” in <i>E.coli<i> BL21 and <i>Acidithiobacillus ferrooxidans<i> to characterize its function.

c1.png
Fig 1. The gene circuit of expression vector “pYDT-<i>Ptac<i>-<i>yedQ<i>”

We examined the role of <i>yedQ<i> by overexpressing <i>yedQ<i> and measuring biofilm formation in overexpressing engineered bacteria versus c-di-GMP content in bacteria.

<center>c2.png
Fig 2.(A) <i>Acidithiobacillus ferrooxidans<i> pore plate biofilm formation column.(B) <i>Escherichia coli<i> pore plate biofilm formation column.(C) Schematic diagram of c-di-GMP content of engineered <i>E.coli<i> BL21 pYDT-0053, pYDT-1379, pYDT-1373, pYDT-yedQ. (D) Indicates the standard curve of c-di-GMP.

By overexpressing the <i>yedQ<i> gene, we found that <i>A. ferrooxidans<i> and <i>E. coli BL21<i> formed thicker biofilms. <i>yedQ<i> also showed the highest concentration of c-di-GMP in <i>E. coli<i> BL21 strains, suggesting that high levels of c-di-GMP can regulate the formation of thicker biofilms.

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 AgeI site found at 1591
  • 1000
    COMPATIBLE WITH RFC[1000]

References

[1] Yang S, Wu Y, Qu C, et al. Quantitative analysis of the surficial and adhesion properties of the Gram-negative bacterial species Comamonas testosteroni modulated by c-di-GMP[J]. Colloids Surf B Biointerfaces, 2021,198:111497.

[2] Sanchez-Torres V, Hu H, Wood T K. GGDEF proteins YeaI, YedQ, and YfiN reduce early biofilm formation and swimming motility in Escherichia coli[J]. Appl Microbiol Biotechnol, 2011,90(2):651-658.

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