Earthworm polysaccharide and its antibacterial function on plant-pathogen microbes in vitro

2007 ◽  
Vol 43 ◽  
pp. S135-S142 ◽  
Author(s):  
Chong Wang ◽  
Zhenjun Sun ◽  
Yanqin Liu ◽  
Dongmei Zheng ◽  
Xuelian Liu ◽  
...  
Keyword(s):  
2006 ◽  
Vol 188 (11) ◽  
pp. 4158-4162 ◽  
Author(s):  
Seiji Tsuge ◽  
Takeshi Nakayama ◽  
Shinsaku Terashima ◽  
Hirokazu Ochiai ◽  
Ayako Furutani ◽  
...  

ABSTRACT A novel regulatory gene, trh, which is involved in hrp gene expression, is identified in the plant pathogen Xanthomonas oryzae pv. oryzae. In the trh mutant, expression of HrpG, which is a key regulator for hrp gene expression, is reduced both under the in vitro hrp-inducing condition and in planta.


2016 ◽  
Vol 5 ◽  
pp. 69-77 ◽  
Author(s):  
Fatematuz Zohara ◽  
Md. Abdul Mannan Akanda ◽  
Narayan Chandra Paul ◽  
Mahfuz Rahman ◽  
Md. Tofazzal Islam

2004 ◽  
Vol 237 (2) ◽  
pp. 341-353 ◽  
Author(s):  
Alessandra A. Souza ◽  
Marco A. Takita ◽  
Helvécio D. Coletta-Filho ◽  
Camila Caldana ◽  
Giane M. Yanai ◽  
...  

Glycobiology ◽  
2019 ◽  
Vol 29 (10) ◽  
pp. 705-714 ◽  
Author(s):  
Hanke van der Wel ◽  
Elisabet Gas-Pascual ◽  
Christopher M West

Abstract Skp1 is hydroxylated by an O2-dependent prolyl hydroxylase (PhyA) that contributes to O2-sensing in the social amoeba Dictyostelium and the mammalian pathogen Toxoplasma gondii. HO-Skp1 is subject to glycosylation and the resulting pentasaccharide affects Skp1 conformation in a way that influences association of Skp1 with F-box proteins, and potentially the assembly of E3(SCF) ubiquitin ligase complexes that mediate the polyubiquitination of target proteins that are degraded in the 26S-proteasome. To investigate the conservation and specificity of these modifications, we analyzed proteins from the oomycete Pythium ultimum, an important crop plant pathogen. Putative coding sequences for Pythium’s predicted PhyA and first glycosyltransferase in the predicted five-enzyme pathway, a GlcNAc-transferase (Gnt1), predict a bifunctional enzyme (Phgt) that, when expressed in Dictyostelium, rescued a knockout of phyA but not gnt1. Though recombinant Phgt was also unable to glycosylate Dictyostelium HO-Skp1, it could hydrolyze UDP-GlcNAc and modify a synthetic hydroxypeptide from Dictyostelium Skp1. Pythium encodes two highly similar Skp1 isoforms, but only Skp1A was efficiently hydroxylated and glycosylated in vitro. While kinetic analysis revealed no evidence for processive processing of Skp1, the physical linkage of the two activities implies dedication to Skp1 in vivo. These findings indicate a widespread occurrence of the Skp1 modification pathway across protist phylogeny, suggest that both Gnt1 and PhyA are specific for Skp1 and indicate that the second Skp1 provides a bypass mechanism for O2-regulation in Pythium and other protists that conserve this gene.


mBio ◽  
2014 ◽  
Vol 5 (5) ◽  
Author(s):  
Xilan Yu ◽  
Steven P. Lund ◽  
Jessica W. Greenwald ◽  
Angela H. Records ◽  
Russell A. Scott ◽  
...  

ABSTRACTThe plant pathogenPseudomonas syringaepv. syringae B728a grows and survives on leaf surfaces and in the leaf apoplast of its host, bean (Phaseolus vulgaris). To understand the contribution of distinct regulators to B728a fitness and pathogenicity, we performed a transcriptome analysis of strain B728a and nine regulatory mutants recovered from the surfaces and interior of leaves and exposed to environmental stresses in culture. The quorum-sensing regulators AhlR and AefR influenced few genesin plantaorin vitro. In contrast, GacS and a downstream regulator, SalA, formed a large regulatory network that included a branch that regulated diverse traits and was independent of plant-specific environmental signals and a plant signal-dependent branch that positively regulated secondary metabolite genes and negatively regulated the type III secretion system. SalA functioned as a central regulator of iron status based on its reciprocal regulation of pyoverdine and achromobactin genes and also sulfur uptake, suggesting a role in the iron-sulfur balance. RetS functioned almost exclusively to repress secondary metabolite genes when the cells were not on leaves. Among the sigma factors examined, AlgU influenced many more genes than RpoS, and most AlgU-regulated genes depended on RpoN. RpoN differentially impacted many AlgU- and GacS-activated genes in cells recovered from apoplastic versus epiphytic sites, suggesting differences in environmental signals or bacterial stress status in these two habitats. Collectively, our findings illustrate a central role for GacS, SalA, RpoN, and AlgU in global regulation in B728ain plantaand a high level of plasticity in these regulators’ responses to distinct environmental signals.IMPORTANCELeaves harbor abundant microorganisms, all of which must withstand challenges such as active plant defenses and a highly dynamic environment. Some of these microbes can influence plant health. Despite knowledge of individual regulators that affect the fitness or pathogenicity of foliar pathogens, our understanding of the relative importance of various global regulators to leaf colonization is limited.Pseudomonas syringaestrain B728a is a plant pathogen and a good colonist of both the surfaces and interior of leaves. This study used global transcript profiles of strain B728a to investigate the complex regulatory network of putative quorum-sensing regulators, two-component regulators, and sigma factors in cells colonizing the leaf surface and leaf interior under stressfulin vitroconditions. The results highlighted the value of evaluating these networksin plantadue to the impact of leaf-specific environmental signals and suggested signal differences that may enable cells to differentiate surface versus interior leaf habitats.


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