43 research outputs found
In vitro antimicrobial activity and characterization of mangrove isolates of streptomycetes effective against bacteria and fungi of nosocomial origin
Microbial Inoculants-Assisted Phytoremediation for Sustainable Soil Management.
Agricultural soil Pollution refers to its accumulation of heavy metals and related compounds which could be from natural or anthropogenic sources. This threatens food quality, food security and environmental health. The traditional physico-chemical technologies soil washing used for soil remediation render the land useless as a medium for plant growth, as they remove all biological activities. Others are labour intensive and have high maintenance cost. Phytoremediation, sustainable and cheaper in situ remediation techniques was therefore considered. However plants do not have the capability to degrade many soil pollutants especially the organic pollutant. It is therefore imperative to take advantage of the degrading ability of soil microorganisms. This chapter therefore focuses on phytoremediation techniques augmented by microbial inoculants
ohrR and ohr Are the Primary Sensor/Regulator and Protective Genes against Organic Hydroperoxide Stress in Agrobacterium tumefaciens
The genes involved in organic hydroperoxide protection in Agrobacterium tumefaciens were functionally evaluated. Gene inactivation studies and functional analyses have identified ohr, encoding a thiol peroxidase, as the gene primarily responsible for organic hydroperoxide protection in A. tumefaciens. An ohr mutant was sensitive to organic hydroperoxide killing and had a reduced capacity to metabolize organic hydroperoxides. ohr is located next to, and is divergently transcribed from, ohrR, encoding a sensor and transcription regulator of organic hydroperoxide stress. Transcription of both ohr and ohrR was induced by exposure to organic hydroperoxides but not by exposure to other oxidants. This induction required functional ohrR. The results of gel mobility shift and DNase I footprinting assays with purified OhrR, combined with in vivo promoter deletion analyses, confirmed that OhrR regulated both ohrR and ohr by binding to a single OhrR binding box that overlapped the ohrR and ohr promoters. ohrR and ohr are both required for the establishment of a novel cumene hydroperoxide-induced adaptive response. Inactivation or overexpression of other Prx family genes (prx1, prx2, prx3, bcp1, and bcp2) did not affect either the resistance to, or the ability to degrade, organic hydroperoxide. Taken together, the results of biochemical, gene regulation and physiological studies support the role of ohrR and ohr as the primary system in sensing and protecting A. tumefaciens from organic hydroperoxide stress
Phytoextraction of Heavy Metals Induced by Bioaugmentation of a Phosphate Solubilizing Bacterium
Chemicobiological Insight into Anti-phytopathogenic Properties of Rhizospheric Serratia plymuthica R51
Effective plant-endophyte interplay can improve the cadmium hyperaccumulation in Brachiaria mutica
Tuna Condensate Waste with Molasses as a Renewable Substrate for Antifungal Compounds by Streptomyces philanthi RL-1-178 Against Aflatoxingenic B1 (AFB1) Aspergillus flavus
Induction of Chitinase and Brown Spot Disease Resistance by Oligochitosan and Nanosilica–Oligochitosan in Dragon Fruit Plants
Production of Antifungal Chitinase by Aspergillus niger LOCK 62 and Its Potential Role in the Biological Control
Agrobacterium tumefaciens estC, Encoding an Enzyme Containing Esterase Activity, Is Regulated by EstR, a Regulator in the MarR Family
Analysis of the A. tumefaciens genome revealed estC, which encodes an esterase located next to its transcriptional regulator estR, a regulator of esterase in the MarR family. Inactivation of estC results in a small increase in the resistance to organic hydroperoxides, whereas a high level of expression of estC from an expression vector leads to a reduction in the resistance to organic hydroperoxides and menadione. The estC gene is transcribed divergently from its regulator, estR. Expression analysis showed that only high concentrations of cumene hydroperoxide (CHP, 1 mM) induced expression of both genes in an EstR-dependent manner. The EstR protein acts as a CHP sensor and a transcriptional repressor of both genes. EstR specifically binds to the operator sites OI and OII overlapping the promoter elements of estC and estR. This binding is responsible for transcription repression of both genes. Exposure to organic hydroperoxide results in oxidation of the sensing cysteine (Cys16) residue of EstR, leading to a release of the oxidized repressor from the operator sites, thereby allowing transcription and high levels of expression of both genes. The estC is the first organic hydroperoxide-inducible esterase-encoding gene in alphaproteobacteria
