Research Support, Non-U.S. Gov't
- D101 is critical for the function of AttJ, a repressor of quorum quenching system in Agrobacterium tumefaciens
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Chao Wang , Chunlan Yan , Yong-Gui Gao , Lian-Hui Zhang
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J. Microbiol. 2015;53(9):623-632. Published online August 1, 2015
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DOI: https://doi.org/10.1007/s12275-015-5100-x
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Abstract
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The quorum quenching system of Agrobacterium tumefaciens
is specifically activated upon entering the stationary
phase. Evidence has shown that this system includes two key
components: the IclR-type transcriptional factor AttJ (also
named as BlcR) and the AHL-lactonase AttM (also named
as BlcC). At exponential phase, AttJ binds to the promoter
region of attM and thus suppresses the expression of attM.
At stationary phase, however, the small molecule SSA directly
binds to AttJ and relieves its inhibition of AttJ and thereby
triggers the expression of attM. While the regulation of AttM
has been extensively investigated, little is known about the
regulation of AttJ. In this study, we demonstrated the D101
amino acid of AttJ is essential for the AttJ function. In vitro,
the variant protein of AttJD101H appeared to be readily aggregated.
In vivo, the D101H mutation in AttJ entirely abolished
the inhibitory activity of AttJ and overexpressed attM in A.
tumefaciens A6. In addition, D101H mutation led to an overexpression
of attJ, indicating an auto-regulatory mechanism
for the attJ regulation. Put together, these findings demonstrate
that D101 is an important amino acid for the transcription
activity of AttJ and the transcription of attJ is regulated
by a negative feedback loop. These results expand previous
biochemical characterization of AttJ and provide new mechanistic
insights into the regulation of quorum quenching in
A. tumefaciens.
- Quorum Sensing and Quorum-Quenching Enzymes
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Yi-Hu Dong , Lian-Hui Zhang
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J. Microbiol. 2005;43(1):101-109.
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Abstract
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To gain maximal benefit in a competitive environment, single-celled bacteria have adopted a community genetic regulatory mechanism, known as quorum sensing (QS). Many bacteria use QS signaling systems to synchronize target gene expression and coordinate biological activities among a local population. N-acylhomoserine lactones (AHLs) are one family of the well-characterized QS signals in Gram-negative bacteria, which regulate a range of important biological functions, including virulence and biofilm formation. Several groups of AHL-degradation enzymes have recently been identified in a range of living organisms, including bacteria and eukaryotes. Expression of these enzymes in AHL-dependent pathogens and transgenic plants efficiently quenches the microbial QS signaling and blocks pathogenic infections. Discovery of these novel quorum quenching enzymes has not only provided a promising means to control bacterial infections, but also presents new challenges to investigate their roles in host organisms and their potential impacts on ecosystems.