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1.
PLoS One ; 13(3): e0193659, 2018.
Article in English | MEDLINE | ID: mdl-29509801

ABSTRACT

Low-cost biosorbents (ginkgo leaf, osmanthus leaf, banyan leaf, magnolia leaf, holly leaf, walnut shell, and grapefruit peel) were evaluated in the simultaneous removal of La3+, Ce3+, Pr3+, Nd3+, Sm3+, Eu3+, Gd3+, Yb3+, Lu3+, UO22+, Th4+, Y3+, Co2+, Zn2+, Ni2+, and Sr2+ from aqueous solutions. In single metal systems, all adsorbents exhibited good to excellent adsorption capacities toward lanthanides and actinides. In a simulated multicomponent mixed solution study, higher selectivity and efficiency were observed for Th4+ over other metal cations, with ginkgo leaves providing the highest adsorptivity (81.2%) among the seven biosorbents. Through optimization studies, the selectivity of Th4+ biosorption on ginkgo leaf was found to be highly pH-dependent, with optimum Th4+ removal observed at pH 4. Th4+ adsorption was found to proceed rapidly with an equilibrium time of 120 min and conform to pseudo-second-order kinetics. The Langmuir isotherm model best described Th4+ biosorption, with a maximum monolayer adsorption capacity of 103.8 mg g-1. Thermodynamic calculations indicated that Th4+ biosorption was spontaneous and endothermic. Furthermore, the physical and chemical properties of the adsorbent were determined by scanning electron microscopy, Brunauer-Emmett-Teller, X-ray powder diffraction, and Fourier transform infrared analysis. The biosorption of Th from a real sample (monazite mineral) was studied and an efficiency of 90.4% was achieved from nitric acid at pH 4 using ginkgo leaves.


Subject(s)
Ginkgo biloba/chemistry , Plant Leaves/chemistry , Thorium/chemistry , Water/chemistry , Adsorption , Citrus paradisi/chemistry , Computer Simulation , Environmental Restoration and Remediation , Ficus/chemistry , Hydrogen-Ion Concentration , Ilex/chemistry , Juglans/chemistry , Kinetics , Magnolia/chemistry , Models, Theoretical , Nitric Acid/chemistry , Oleaceae/chemistry , Powders/chemistry , Solutions/chemistry , Spectroscopy, Fourier Transform Infrared , Temperature , Thorium/isolation & purification , Water Pollutants, Chemical/chemistry , Water Pollutants, Chemical/isolation & purification , X-Ray Diffraction
2.
Mol Plant Microbe Interact ; 21(9): 1242-8, 2008 Sep.
Article in English | MEDLINE | ID: mdl-18700828

ABSTRACT

Fusarium head blight (FHB) or scab of wheat is a devastating disease in warm and humid regions at wheat-flowering periods worldwide. Natural resistance against FHB pathogens is inadequate and the development of FHB-resistant wheat cultivars has been a challenge. Expression of pathogen-specific antibodies in plants has been proposed as a strategy for crop protection. In this study, an antibody fusion protein comprising a Fusarium-specific recombinant antibody derived from chicken and an antifungal peptide from Aspergillus giganteus was expressed in wheat as a method for protecting plants against FHB pathogens. Plants expressing the antibody fusion displayed a very significantly enhanced resistance in T2 and T3 generations upon single-floret inoculation with the macroconidia of Fusarium asiaticum, the predominant species causing FHB in China, indicating a type II resistance. Spraying inoculation further revealed an enhanced type I resistance in the transgenic wheat plants. Remarkably, more grains were produced in the transgenic plants than the nontransgenic controls. Our results demonstrated that the antibody fusion protein may be used as an effective tool for the protection of crops against FHB pathogens.


Subject(s)
Fusarium/immunology , Genetic Engineering/methods , Recombinant Fusion Proteins/genetics , Triticum/genetics , Triticum/microbiology , Animals , Antibodies, Fungal/genetics , Antibodies, Fungal/physiology , Blotting, Southern , Blotting, Western , Chickens , Fungal Proteins/genetics , Fungal Proteins/physiology , Fusarium/growth & development , Immunity, Innate/genetics , Plant Diseases/genetics , Plant Diseases/microbiology , Plants, Genetically Modified/genetics , Plants, Genetically Modified/microbiology , Polymerase Chain Reaction , Recombinant Fusion Proteins/physiology , Reverse Transcriptase Polymerase Chain Reaction
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