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1.
J Environ Biol ; 2008 Sep; 29(5): 743-6
Artículo en Inglés | IMSEAR | ID: sea-113542

RESUMEN

Aspergillus sp PS 104, a soil isolate had excellent potential to solubilize rock phosphate in vitro. The process was influenced by the presence of various concentrations of local loess (red soil). The simultaneous occurrence, in our experiment, of high levels of solubilized phosphate and synthesized citric acid, together with the lowest reached pH values, confirmed the role of citric acid in the phosphate solubilization mechanism. When the soil was present, phosphate release was better correlated than citrate synthesis with H+ concentration. Changes in soluble phosphate concentration did not follow a sigmoid pattern. The ability of organism to release phosphatase was also studied. An interesting relationship was observed between the two processes of phosphate mobilization: citric acid synthesis and phosphatase production.


Asunto(s)
Aspergillus/metabolismo , Ácido Cítrico/química , Concentración de Iones de Hidrógeno , Fosfatos/química , Monoéster Fosfórico Hidrolasas/metabolismo , Microbiología del Suelo , Solubilidad
2.
Indian J Exp Biol ; 2003 Dec; 41(12): 1442-6
Artículo en Inglés | IMSEAR | ID: sea-59557

RESUMEN

Maximum colony growth inhibition was observed due to Pseudomonas PS2 (74%) as compared to PS1 (71%) on trypticase soy agar (TSM) plates after 5 days of incubation. Light and scanning electron microscopic examination showed hyphal coiling, vacuolation, coagulation and granulation of cytoplasm resulting in lysis of hyphae of M. phaseolina by pseudomonads. Cell free culture filtrates of strains PS1 and PS2 restricted the growth of mycelium of M. phaseolina. PS1 and PS2 caused maximum colony growth inhibition by 57 and 61% respectively at 20% concentration of culture filtrate after 4 days of incubation. Volatile substances produced by PS1 and PS2 also inhibited the colony growth of M. phaseolina by 25 and 32%, respectively. Inhibitory effect of volatile substances, however, decreased with advancing in incubation period. Colony growth of M. phaseolina was significantly decreased by PS1 and PS2 as compared to control both in iron- sufficient and iron-deficient conditions. PS2 showed higher antagonistic activity than PS1, as evidenced by pronounced colony growth inhibition.


Asunto(s)
Basidiomycota/fisiología , Fluorescencia , Microscopía Electrónica , Enfermedades de las Plantas/microbiología , Pseudomonas/fisiología
3.
Indian J Exp Biol ; 2003 Oct; 41(10): 1160-4
Artículo en Inglés | IMSEAR | ID: sea-56094

RESUMEN

Rhizobia promote the growth of plants either directly through N2 fixation, supply of nutrients, synthesis of phytohormones and solubilization of minerals, or indirectly as a biocontrol agent by inhibiting the growth of pathogens. The biocontrol effect of rhizobia is due to the secretion of secondary metabolites such as antibiotics and HCN. Siderophore production in iron stress conditions provides rhizobia an added advantage, resulting in exclusion of pathogens due to iron starvation.


Asunto(s)
Hongos/crecimiento & desarrollo , Hierro/metabolismo , Control Biológico de Vectores , Enfermedades de las Plantas/microbiología , Rhizobium/fisiología , Sideróforos/metabolismo , Microbiología del Suelo
4.
Indian J Exp Biol ; 2001 Dec; 39(12): 1318-21
Artículo en Inglés | IMSEAR | ID: sea-63002

RESUMEN

Pseudomonas aeruginosa (GRC1) isolated from potato rhizosphere, grew better on succinate medium than tryptic soy medium and produced hydroxamate type of siderophore in iron-deficient succinate medium. When the strain GRC1 was grown in the presence of different metal ion compounds, viz. ZnSO4, MnSO4, MnCl2 and FeCl3 at 6 and 12 microM concentrations individually, ZnSO4 (12 microM) promoted siderophore production but suppressed the growth and protein content of test organism. MnCl2 and FeCl3 (12 microM) enhanced the growth, whereas MnCl2 and MnSO4 (12 microM) induced protein contents of strain GRC1.


Asunto(s)
Proteínas Bacterianas/biosíntesis , Metales/farmacología , Pseudomonas aeruginosa/efectos de los fármacos , Sideróforos/biosíntesis
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