scholarly journals The chromosomal virulence gene, chvE, of Agrobacterium tumefaciens is regulated by a LysR family member.

1993 ◽  
Vol 175 (24) ◽  
pp. 7880-7886 ◽  
Author(s):  
S L Doty ◽  
M Chang ◽  
E W Nester
1989 ◽  
Vol 3 (9) ◽  
pp. 1237-1246 ◽  
Author(s):  
P. Morel ◽  
B. S. Powell ◽  
P. M. Rogowsky ◽  
C. I. Kado

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.


2001 ◽  
Vol 183 (12) ◽  
pp. 3704-3711 ◽  
Author(s):  
Scott M. Lohrke ◽  
Hongjiang Yang ◽  
Shouguang Jin

ABSTRACT The ability to utilize Escherichia coli as a heterologous system in which to study the regulation ofAgrobacterium tumefaciens virulence genes and the mechanism of transfer DNA (T-DNA) transfer would provide an important tool to our understanding and manipulation of these processes. We have previously reported that the rpoA gene encoding the alpha subunit of RNA polymerase is required for the expression of lacZ gene under the control of virB promoter (virBp::lacZ) in E. colicontaining a constitutively active virG gene [virG(Con)]. Here we show that an RpoA hybrid containing the N-terminal 247 residues from E. coli and the C-terminal 89 residues from A. tumefaciens was able to significantly express virBp::lacZ in E. coli in a VirG(Con)-dependent manner. Utilization oflac promoter-driven virA and virGin combination with the A. tumefaciens rpoA construct resulted in significant inducer-mediated expression of thevirBp::lacZ fusion, and the level ofvirBp::lacZ expression was positively correlated to the copy number of the rpoA construct. This expression was dependent on VirA, VirG, temperature, and, to a lesser extent, pH, which is similar to what is observed in A. tumefaciens. Furthermore, the effect of sugars on virgene expression was observed only in the presence of thechvE gene, suggesting that the glucose-binding protein ofE. coli, a homologue of ChvE, does not interact with the VirA molecule. We also evaluated other phenolic compounds in induction assays and observed significant expression with syringealdehyde, a low level of expression with acetovanillone, and no expression with hydroxyacetophenone, similar to what occurs in A. tumefaciens strain A348 from which the virA clone was derived. These data support the notion that VirA directly senses the phenolic inducer. However, the overall level of expression of thevir genes in E. coli is less than what is observed in A. tumefaciens, suggesting that additional gene(s) from A. tumefaciens may be required for the full expression of virulence genes in E. coli.


2013 ◽  
Vol 59 (2) ◽  
pp. 136-139 ◽  
Author(s):  
Bin Pei ◽  
Yuning Wang ◽  
David S. Katzianer ◽  
Hui Wang ◽  
Hui Wu ◽  
...  

Vibrio cholerae is the causative agent of the devastating diarrheal disease cholera. A number of regulatory pathways are involved in V. cholerae pathogenesis and antibiotic resistance. For example, there are over 40 LysR-family proteins in the V. cholerae genome, but most of their functions are unknown. In this study, we examine the role of VC2323 (TehAVc) and its divergently transcribed LysR-family regulator VC2324 (TehRVc) in V. cholerae pathogenesis. We found that in V. cholerae C6706, the expression of tehAVcis dependent on TehRVc. VC2323 (TehAVc), homologous to the Escherichia coli tellurite resistance protein (TehAEc), differs from TehAEcin that TehAVchas no noticeable role in tellurite resistance but instead contributes to chloramphenicol resistance. Interestingly, both tehAVcand tehRVcmutants were defective in colonization of infant mice. Though the expression of a key virulence gene tcpA was not affected in either of these mutants, tehAVcmutants failed to attach to mouse intestinal surfaces in the presence of crude bile, suggesting a new role of the TehAVc–TehRVcpair in V. cholerae pathogenesis.


Structure ◽  
1997 ◽  
Vol 5 (8) ◽  
pp. 1017-1032 ◽  
Author(s):  
Richard Tyrrell ◽  
Koen HG Verschueren ◽  
Eleanor J Dodson ◽  
Garib N Murshudov ◽  
Christine Addy ◽  
...  

1991 ◽  
Vol 39 (9) ◽  
pp. 2347-2350 ◽  
Author(s):  
Yan-Nong SONG ◽  
Masaaki SHIBUYA ◽  
Yutaka EBIZUKA ◽  
Ushio SANKAWA

1987 ◽  
Vol 9 (6) ◽  
pp. 635-645 ◽  
Author(s):  
Leo S. Melchers ◽  
Dave V. Thompson ◽  
Ken B. Idler ◽  
Saskia T. C. Neuteboom ◽  
Ruud A. de Maagd ◽  
...  

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