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1.
Folia Microbiol (Praha) ; 63(4): 433-441, 2018 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-29305688

RESUMEN

The study evaluates the survivability and storage stability of seven Trichoderma strains belonging to the species: T. harzianum (1), T. atroviride (4), and T. virens (2) after the lyophilization of their solid state cultures on wheat straw. Biomass of Trichoderma strains was freeze-dried with and without the addition of maltodextrin. Furthermore, in order to determine the ability of tested Trichoderma strains to preserve selected technological features, the biosynthesis of extracellular hydrolases (cellulases, xylanases, and polygalacturonases) after a 3-month storage of lyophilizates was investigated. Strains of T. atroviride (except TRS40) and T. harzianum TRS85 showed the highest viability after lyophilization process (up to 100%). After 3 months of storage, T. atroviride TRS14 exhibited the highest stability (95.23%); however, the number of active conidia remained at high level of 106-107 cfu/g for all tested T. atroviride strains and T. harzianum TRS85. Interestingly, after a 3-month storage of lyophilized formulations, most of the tested Trichoderma strains exhibited higher cellulolytic and xylanolytic activities compared to the control, i.e., before freeze-drying process. The highest activities of these enzymes exhibited the following: T. atroviride TRS14-2.37 U/g and T. atroviride TRS25-21.47 U/g, respectively, whereas pectinolytic activity was weak for all tested strains, with the highest value of 0.64 U/g registered for T. virens TRS109.


Asunto(s)
Liofilización , Hidrolasas/metabolismo , Viabilidad Microbiana , Trichoderma/crecimiento & desarrollo , Biomasa , Almacenaje de Medicamentos , Fermentación , Esporas Fúngicas/crecimiento & desarrollo , Factores de Tiempo , Trichoderma/clasificación , Trichoderma/fisiología , Triticum/metabolismo
2.
Food Microbiol ; 61: 93-101, 2017 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-27697174

RESUMEN

The antagonistic effects of Debaryomyces hansenii KI2a, D. hansenii MI1a and Wickerhamomyces anomalus BS91 were tested against Monilinia fructigena and Monilinia fructicola in in vitro and in vivo trials. All yeast strains demonstrated antifungal activity at different levels depending on species, strain and pathogen. D hansenii KI2a and W. anomalus BS91 showed the highest biocontrol activity in vitro; the production of hydrolytic enzymes, killer toxins and volatile organic compounds (VOCs) were hypothesized as their main mechanisms of action against pathogens. D hansenii KI2a and W. anomalus BS91 significantly reduced brown rot incidence and severity on peach and plum fruits artificially inoculated with M. fructigena and M. fructicola, especially when applied 24 h before pathogen inoculation. On the opposite, D. hansenii MI1a exhibited weak antagonistic activity towards M. fructigena on peach and plum fruits and was ineffective against M. fructicola. The noticeable ability of W. anomalus BS91 to control brown rot could be also correlated with its high capacity to colonize the wound tissue and to increase its population density. Accordingly, the antagonistic strains of D. hansenii and W. anomalus could be proposed as active ingredients for the development of biofungicides against Monilinia species that are responsible for considerable economic losses in stone fruit crops.


Asunto(s)
Antibiosis , Ascomicetos/fisiología , Candida/fisiología , Frutas/microbiología , Factores Asesinos de Levadura/metabolismo , Enfermedades de las Plantas/prevención & control , Prunus/microbiología , Saccharomyces cerevisiae/fisiología , Ascomicetos/efectos de los fármacos , Agentes de Control Biológico/química , Candida/química , Microbiología de Alimentos , Enfermedades de las Plantas/microbiología , Prunus domestica/microbiología , Saccharomyces cerevisiae/química , Compuestos Orgánicos Volátiles/farmacología
3.
Acta Crystallogr C ; 62(Pt 7): o419-22, 2006 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-16823219

RESUMEN

In the structures of decafluorodiphenylamine, C(12)HF(10)N, and its 1:1 cocrystal with diphenylamine, C(12)HF(10)NxC(12)H(11)N, the molecules are located on special positions of C(2) symmetry. The NH groups are not involved in hydrogen bonding and the usual face-to-face stacking interactions between phenyl and pentafluorophenyl rings are not observed in the cocrystal.

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