scholarly journals Molecular Basis of ChvE Function in Sugar Binding, Sugar Utilization, and Virulence in Agrobacterium tumefaciens

2009 ◽  
Vol 191 (18) ◽  
pp. 5802-5813 ◽  
Author(s):  
Fanglian He ◽  
Gauri R. Nair ◽  
Cinque S. Soto ◽  
Yehchung Chang ◽  
Lillian Hsu ◽  
...  

ABSTRACT ChvE is a chromosomally encoded protein in Agrobacterium tumefaciens that mediates a sugar-induced increase in virulence (vir) gene expression through the activities of the VirA/VirG two-component system and has also been suggested to be involved in sugar utilization. The ChvE protein has homology to several bacterial periplasmic sugar-binding proteins, such as the ribose-binding protein and the galactose/glucose-binding protein of Escherichia coli. In this study, we provide direct evidence that ChvE specifically binds the vir gene-inducing sugar d-glucose with high affinity. Furthermore, ChvE mutations resulting in altered vir gene expression phenotypes have been isolated and characterized. Three distinct categories of mutants have been identified. Strains expressing the first class are defective in both virulence and d-glucose utilization as a result of mutations to residues lining the sugar-binding cleft. Strains expressing a second class of mutants are not adversely affected in sugar binding but are defective in virulence, presumably due to impaired interactions with the sensor kinase VirA. A subset of this second class of mutants includes variants of ChvE that also result in defective sugar utilization. We propose that these mutations affect not only interactions with VirA but also interactions with a sugar transport system. Examination of a homology model of ChvE shows that the mutated residues associated with the latter two phenotypes lie in two overlapping solvent-exposed sites adjacent to the sugar-binding cleft where conformational changes associated with the binding of sugar might have a maximal effect on ChvE's interactions with its distinct protein partners.

2015 ◽  
Vol 82 (4) ◽  
pp. 1136-1146 ◽  
Author(s):  
Jinlei Zhao ◽  
Andrew N. Binns

ABSTRACTMonosaccharides capable of serving as nutrients for the soil bacteriumAgrobacterium tumefaciensare also inducers of thevirregulon present in the tumor-inducing (Ti) plasmid of this plant pathogen. One such monosaccharide is galacturonate, the predominant monomer of pectin found in plant cell walls. This ligand is recognized by the periplasmic sugar binding protein ChvE, which interacts with the VirA histidine kinase that controlsvirgene expression. Although ChvE is also a member of the ChvE-MmsAB ABC transporter involved in the utilization of many neutral sugars, it is not involved in galacturonate utilization. In this study, a putative tripartite ATP-independent periplasmic (TRAP) transporter, GaaPQM, is shown to be essential for the utilization of galacturonic acid; we show that residue R169 in the predicted sugar binding site of the GaaP is required for activity. The gene upstream ofgaaPQM(gaaR) encodes a member of the GntR family of regulators. GaaR is shown to repress the expression ofgaaPQM, and the repression is relieved in the presence of the substrate for GaaPQM. Moreover, GaaR is shown to bind putative promoter regions in the sequences required for galacturonic acid utilization. Finally,A. tumefaciensstrains carrying a deletion ofgaaPQMare more sensitive to galacturonate as an inducer ofvirgene expression, while the overexpression ofgaaPQMresults in strains being less sensitive to thisvirinducer. This supports a model in which transporter activity is crucial in ensuring thatvirgene expression occurs only at sites of high ligand concentration, such as those at a plant wound site.


1991 ◽  
Vol 266 (24) ◽  
pp. 16188-16192 ◽  
Author(s):  
M.E. Lee ◽  
D.H. Temizer ◽  
J.A. Clifford ◽  
T. Quertermous

2006 ◽  
Vol 281 (36) ◽  
pp. 25882-25892 ◽  
Author(s):  
Kerstin Meyer-Lipp ◽  
Natacha Séry ◽  
Constanta Ganea ◽  
Cécile Basquin ◽  
Klaus Fendler ◽  
...  

Planta ◽  
2021 ◽  
Vol 253 (2) ◽  
Author(s):  
Elysabeth K. Barnes ◽  
Moonhyuk Kwon ◽  
Connor L. Hodgins ◽  
Yang Qu ◽  
Seon-Won Kim ◽  
...  

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