Regulation of Soluble Phosphate on the Ability of Phytate Mineralization and β-Propeller Phytase Gene Expression of Pseudomonas fluorescens JZ-DZ1, a Phytate-Mineralizing Rhizobacterium

2016 ◽  
Vol 73 (6) ◽  
pp. 915-923 ◽  
Author(s):  
Lan Shen ◽  
Xiao-Qin Wu ◽  
Qing-Wei Zeng ◽  
Hong-Bin Liu
2015 ◽  
Vol 31 (1) ◽  
pp. 39-81 ◽  
Author(s):  
María T. Gómez-Sagasti ◽  
José M. Becerril ◽  
Lur Epelde ◽  
Itziar Alkorta ◽  
Carlos Garbisu

MethodsX ◽  
2019 ◽  
Vol 6 ◽  
pp. 1181-1187
Author(s):  
Ann-Marie Fortuna ◽  
Sanjivni Sinha ◽  
Tonoy K. Das ◽  
Achintya N. Bezbaruah

2009 ◽  
Vol 22 (12) ◽  
pp. 1611-1623 ◽  
Author(s):  
Matthieu Barret ◽  
Pascale Frey-Klett ◽  
Anne-Yvonne Guillerm-Erckelboudt ◽  
Morgane Boutin ◽  
Gregory Guernec ◽  
...  

Traits contributing to the competence of biocontrol bacteria to colonize plant roots are often induced in the rhizosphere in response to plant components. These interactions have been studied using the two partners in gnotobiotic systems. However, in nature, beneficial or pathogenic fungi often colonize roots. Influence of these plant–fungus interactions on bacterial behavior remains to be investigated. Here, we have examined the influence of colonization of wheat roots by the take-all fungus Gaeumannomyces graminis var. tritici on gene expression of the biocontrol bacterium Pseudomonas fluorescens Pf29Arp. Bacteria were inoculated onto healthy, early G. graminis var. tritici-colonized and necrotic roots and transcriptomes were compared by shotgun DNA microarray. Pf29Arp decreased disease severity when inoculated before the onset of necrosis. Necrotic roots exerted a broader effect on gene expression compared with early G. graminis var. tritici-colonized and healthy roots. A gene encoding a putative type VI secretion system effector was only induced in necrotic conditions. A common pool of Pf29Arp genes differentially expressed on G. graminis var. tritici-colonized roots was related to carbon metabolism and oxidative stress, with a highest fold-change with necrosis. Overall, the data showed that the association of the pathogenic fungus with the roots strongly altered Pf29Arp adaptation with differences between early and late G. graminis var. tritici infection steps.


2008 ◽  
Vol 17 (9) ◽  
pp. 1033-1037 ◽  
Author(s):  
Ki-Hyun Park ◽  
Geun-Tae Park ◽  
Sung-Man Kim ◽  
Chung-Yeol Lee ◽  
Hong-Joo Son

2020 ◽  
Vol 11 ◽  
Author(s):  
Luciana F. Brito ◽  
Marina Gil López ◽  
Lucas Straube ◽  
Luciane M. P. Passaglia ◽  
Volker F. Wendisch

Due to the importance of phosphorus (P) in agriculture, crop inoculation with phosphate-solubilizing bacteria is a relevant subject of study. Paenibacillus sonchi genomovar Riograndensis SBR5 is a promising candidate for crop inoculation, as it can fix nitrogen and excrete ammonium at a remarkably high rate. However, its trait of phosphate solubilization (PS) has not yet been studied in detail. Here, differential gene expression and functional analyses were performed to characterize PS in this bacterium. SBR5 was cultivated with two distinct P sources: NaH2PO4 as soluble phosphate source (SPi) and hydroxyapatite as insoluble phosphate source (IPi). Total RNA of SBR5 cultivated in those two conditions was isolated and sequenced, and bacterial growth and product formation were monitored. In the IPi medium, the expression of 68 genes was upregulated, whereas 100 genes were downregulated. Among those, genes involved in carbon metabolism, including those coding for subunits of 2-oxoglutarate dehydrogenase, were identified. Quantitation of organic acids showed that the production of tricarboxylic acid cycle-derived organic acids was reduced in IPi condition, whereas acetate and gluconate were overproduced. Increased concentrations of proline, trehalose, and glycine betaine revealed active osmoprotection during growth in IPi. The cultivation with hydroxyapatite also caused the reduction in the motility of SBR5 cells as a response to Pi depletion at the beginning of its growth. SBR5 was able to solubilize hydroxyapatite, which suggests that this organism is a promising phosphate-solubilizing bacterium. Our findings are the initial step in the elucidation of the PS process in P. sonchi SBR5 and will be a valuable groundwork for further studies of this organism as a plant growth-promoting rhizobacterium.


2005 ◽  
Vol 71 (5) ◽  
pp. 2687-2694 ◽  
Author(s):  
Marta Villacieros ◽  
Clare Whelan ◽  
Martina Mackova ◽  
Jesper Molgaard ◽  
María Sánchez-Contreras ◽  
...  

ABSTRACT Rhizoremediation of organic chemicals requires high-level expression of biodegradation genes in bacterial strains that are excellent rhizosphere colonizers. Pseudomonas fluorescens F113 is a biocontrol strain that was shown to be an excellent colonizer of numerous plant rhizospheres, including alfalfa. Although a derivative of F113 expressing polychlorinated biphenyl (PCB) biodegradation genes (F113pcb) has been reported previously, this strain shows a low level of bph gene expression, limiting its rhizoremediation potential. Here, a high-level expression system was designed from rhizobial nod gene regulatory relays. Nod promoters were tested in strain F113 by using β-galactosidase transcriptional fusions. This analysis showed that nodbox 4 from Sinorhizobium meliloti has a high level of expression in F113 that is dependent on an intact nodD1 gene. A transcriptional fusion of a nodbox cassette containing the nodD1 gene and nodbox 4 fused to a gfp gene was expressed in the alfalfa rhizosphere. The bph operon from Burkholderia sp. strain LB400 was cloned under the control of the nodbox cassette and was inserted as a single copy into the genome of F113, generating strain F113L::1180. This new genetically modified strain has a high level of BphC activity and grows on biphenyl as a sole carbon and energy source at a growth rate that is more than three times higher than that of F113pcb. Degradation of PCBs 3, 4, 5, 17, and 25 was also much faster in F113L::1180 than in F113pcb. Finally, the modified strain cometabolized PCB congeners present in Delor103 better than strain LB400, the donor of the bph genes used.


2010 ◽  
Vol 165 (4) ◽  
pp. 329-335 ◽  
Author(s):  
Ruiyu Zuo ◽  
Juan Chang ◽  
Qingqiang Yin ◽  
Liying Chen ◽  
Qixin Chen ◽  
...  

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