Influence of Pd:Bi ratio on Pd-Bi/Al2O3 catalysts: structure, surface and activity in glucose oxidation

2021 ◽  
Author(s):  
Mariya Petrovna Sandu ◽  
Mikhail Andreevich Kovtunov ◽  
Vladimir S. Baturin ◽  
Irina Kurzina ◽  
Artem R. Oganov
Keyword(s):  
Gluconic Acid ◽  
Acid Production ◽  
Oxidation Reaction ◽  
Glucose Oxidation ◽  
High Efficiency ◽  
Bismuth Content ◽  
Structure Surface ◽  
Glucose Oxidation Reaction ◽  
Bi Nanoparticles ◽  
Gluconic Acid Production

Pd-Bi nanoparticles show high efficiency in catalyzing gluconic acid production by glucose oxidation reaction. Although this type of catalysts was studied for some time, the correlation between bismuth content and...

γ-MnOOH Nanowires Hydrothermally Reduced by Leaves for High-Efficiency Electrocatalysis of the Glucose Oxidation Reaction

2019 ◽  
Vol 7 (9) ◽  
pp. 8972-8978 ◽  
Author(s):  
Yuqing Luo ◽  
Xiaotian Guo ◽  
Meijuan Yuan ◽  
Yan Yan ◽  
Changyun Chen ◽  
...  
Keyword(s):  
Oxidation Reaction ◽  
Glucose Oxidation ◽  
High Efficiency ◽  
Glucose Oxidation Reaction

Gluconic acid production at high concentrations by Aspergillus niger immobilized on a nonwoven fabric

1989 ◽  
Vol 67 (6) ◽  
pp. 404-408 ◽  
Author(s):  
Hiroshi Sakurai ◽  
Hang Woo Lee ◽  
Seigo Sato ◽  
Sukekuni Mukataka ◽  
Joji Takahashi
Keyword(s):  
Aspergillus Niger ◽  
Gluconic Acid ◽  
Acid Production ◽  
Nonwoven Fabric ◽  
High Concentrations ◽  
Gluconic Acid Production

Size-Dependent Electrocatalytic Activity of Free Gold Nanoparticles for the Glucose Oxidation Reaction

ChemPhysChem ◽  
2016 ◽  
Vol 17 (10) ◽  
pp. 1454-1462 ◽  
Author(s):  
Seydou Hebié ◽  
Teko W. Napporn ◽  
Cláudia Morais ◽  
K. Boniface Kokoh
Keyword(s):  
Gold Nanoparticles ◽  
Electrocatalytic Activity ◽  
Oxidation Reaction ◽  
Glucose Oxidation ◽  
Size Dependent ◽  
Free Gold ◽  
Glucose Oxidation Reaction

scholarly journals Role of Gluconic Acid Production in the Regulation of Biocontrol Traits of Pseudomonas fluorescens CHA0

2009 ◽  
Vol 75 (12) ◽  
pp. 4162-4174 ◽  
Author(s):  
Patrice de Werra ◽  
Maria Péchy-Tarr ◽  
Christoph Keel ◽  
Monika Maurhofer
Keyword(s):  
Pseudomonas Fluorescens ◽  
Gluconic Acid ◽  
Acid Production ◽  
Disease Suppression ◽  
Gaeumannomyces Graminis ◽  
Antifungal Compounds ◽  
Enhanced Production ◽  
Biocontrol Activity ◽  
Gluconic Acid Production

ABSTRACT The rhizobacterium Pseudomonas fluorescens CHA0 promotes the growth of various crop plants and protects them against root diseases caused by pathogenic fungi. The main mechanism of disease suppression by this strain is the production of the antifungal compounds 2,4-diacetylphloroglucinol (DAPG) and pyoluteorin (PLT). Direct plant growth promotion can be achieved through solubilization of inorganic phosphates by the production of organic acids, mainly gluconic acid, which is one of the principal acids produced by Pseudomonas spp. The aim of this study was to elucidate the role of gluconic acid production in CHA0. Therefore, mutants were created with deletions in the genes encoding glucose dehydrogenase (gcd) and gluconate dehydrogenase (gad), required for the conversion of glucose to gluconic acid and gluconic acid to 2-ketogluconate, respectively. These enzymes should be of predominant importance for rhizosphere-colonizing biocontrol bacteria, as major carbon sources provided by plant root exudates are made up of glucose. Our results show that the ability of strain CHA0 to acidify its environment and to solubilize mineral phosphate is strongly dependent on its ability to produce gluconic acid. Moreover, we provide evidence that the formation of gluconic acid by CHA0 completely inhibits the production of PLT and partially inhibits that of DAPG. In the Δgcd mutant, which does not produce gluconic acid, the enhanced production of antifungal compounds was associated with improved biocontrol activity against take-all disease of wheat, caused by Gaeumannomyces graminis var. tritici. This study provides new evidence for a close association of gluconic acid metabolism with antifungal compound production and biocontrol activity in P. fluorescens CHA0.

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