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1.
J Xenobiot ; 13(4): 529-543, 2023 Sep 23.
Artículo en Inglés | MEDLINE | ID: mdl-37873811

RESUMEN

The cell wall of Candida yeast grown on presence of hexadecane as a sole carbon source undergoes structural and functional changes including the formation of specific supramolecular complexes-canals. The canals contain specific polysaccharides and enzymes that provide primary oxidization of alkanes. In addition, inorganic polyphosphate (polyP) was identified in Candida maltosa canals. The aim of the work was a comparative study of the features of cell walls and extracellular structures in yeast C. maltosa, C. albicans and C. tropicalis with special attention to inorganic polyphosphates as possible part of these structures when grown on the widely used xenobiotic hexadecane (diesel fuel). Fluorescence microscopy with DAPI has shown an unusual localization of polyP on the cell surface and in the exovesicles in the three yeast species, when growing on hexadecane. Electron-scanning microscopy showed that the exovesicles were associated with the cell wall and also presented in the external environment probably as biofilm components. Treatment of hexadecane-grown cells with purified Ppx1 polyphosphatase led to the release of phosphate into the incubation medium and the disappearance of polyP in vesicles and cell wall observed using microscopic methods. The results indicate the important role of polyP in the formation of extracellular structures in the Candida yeast when consuming hexadecane and are important for the design of xenobiotic destructors based on yeast or mixed cultures.

2.
FEMS Yeast Res ; 17(3)2017 05 01.
Artículo en Inglés | MEDLINE | ID: mdl-28475763

RESUMEN

Canals are supramolecular complexes observed in the cell wall of Candida maltosa grown in the presence of hexadecane as a sole carbon source. Such structures were not observed in glucose-grown cells. Microscopic observations of cells stained with diaminobenzidine revealed the presence of oxidative enzymes in the canals. 4΄,6΄-diamino-2-phenylindole staining revealed that a substantial part of cellular polyphosphate was present in the cell wall of cells grown on hexadecane in condition of phosphate limitation. The content and chain length of polyphosphates were higher in hexadecane-grown cells than in glucose grown ones. The treatment of cells with yeast polyphosphatase PPX1 resulted in the decrease of the canal size. These data clearly indicated that polyphosphates are constituents of canals; they might play an important role in the canal structure and functioning.


Asunto(s)
Alcanos/farmacología , Candida/efectos de los fármacos , Pared Celular/efectos de los fármacos , 3,3'-Diaminobencidina , Ácido Anhídrido Hidrolasas/química , Candida/química , Candida/metabolismo , Candida/ultraestructura , Pared Celular/química , Pared Celular/metabolismo , Pared Celular/ultraestructura , Medios de Cultivo/química , Medios de Cultivo/farmacología , Diaminas , Glucosa/metabolismo , Glucosa/farmacología , Indoles , Microscopía Electrónica de Transmisión , Polifosfatos/química , Polifosfatos/metabolismo , Coloración y Etiquetado/métodos
3.
Yeast ; 33(2): 55-62, 2016 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-26833628

RESUMEN

Electron-microscopic examinations have demonstrated local modifications in the cell wall of the yeast Candida maltosa grown on hexadecane. In our earlier studies, these modified sites, observed in other yeasts grown on oil hydrocarbons, were conventionally called 'canals'. The biochemical and cytochemical studies of C. maltosa have revealed a correlation between the formation of 'canals' and decrease in the amount of cell wall polysaccharides, glucan and mannan. The ultrathin sections and surface replicas have shown that the 'canals' are destroyed by pronase, thus indicating that a significant proportion of their content is represented by proteins. This finding was compatible with our earlier data on the localization of oxidative enzymes in 'canals' and possible participation of the 'canals' in the primary oxidation of hydrocarbons. A completely unexpected and intriguing phenomenon has been the appearance of 'canals' in the yeast C. maltosa under starvation conditions. Unlike the yeasts grown on hexadecane, mannan almost disappears in starving cells, while the quantity of glucan first decreases and then is restored to its initial level. The role of 'canals' in starving cells is as yet unclear; it is assumed that they acquire exoenzymes involved in the utilization of products of cell lysis in the starving population. In the future, 'canals' of starving cells will be studied in connection with their possible participation in apoptosis.


Asunto(s)
Alcanos/metabolismo , Candida/crecimiento & desarrollo , Pared Celular/ultraestructura , Candida/metabolismo , Candida/ultraestructura , Pared Celular/química , Medios de Cultivo , Hidrolasas/metabolismo , Mananos/metabolismo , Microscopía Electrónica
4.
FEMS Yeast Res ; 12(6): 617-24, 2012 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-22591314

RESUMEN

The search for new phosphate-accumulating microorganisms is of interest in connection with the problem of excess phosphate in environment. The ability of some yeast species belonging to ascomycetes and basidiomycetes for phosphate (P (i) ) accumulation in nitrogen-deficient medium was studied. The ascomycetous Saccharomyces cerevisiae and Kuraishia capsulata and basidiomycetous Cryptococcus humicola, Cryptococcus curvatus, and Pseudozyma fusiformata were the best in P (i) removal. The cells of Cryptococcus humicola and S. cerevisiae took up 40% P (i) from the media containing P (i) and glucose (5 and 30 mM, respectively), and up to 80% upon addition of 5 mM MgSO(4) (.) The cells accumulated P (i) mostly in the form of polyphosphate (PolyP). In the presence of Mg(2+) , the content of PolyP with longer average chain length increased in both yeasts; they both had numerous inclusions fluorescing in the yellow region of the spectrum, typical of DAPI-PolyP complexes. Among the yeast species tested, Cryptococcus humicola is a new promising model organisms to study phosphorus removal from the media and biomineralization in microbial cells.


Asunto(s)
Cryptococcus/metabolismo , Nitrógeno/metabolismo , Polifosfatos/metabolismo , Saccharomycetales/metabolismo , Medios de Cultivo/química , Glucosa/metabolismo , Sulfato de Magnesio/metabolismo , Ustilaginales/metabolismo
5.
FEMS Microbiol Lett ; 315(2): 134-40, 2011 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-21182540

RESUMEN

Cytochemical staining and microscopy were used to study the trophic structures and cellular morphotypes that are produced during the colonization of oil-water interfaces by oil-degrading yeasts and bacteria. Among the microorganisms studied here, the yeasts (Schwanniomyces occidentalis, Torulopsis candida, Candida tropicalis, Candida lipolytica, Candida maltosa, Candida paralipolytica) and two representative bacteria (Rhodococcus sp. and Pseudomonas putida) produced exocellular structures composed of biopolymers during growth on petroleum hydrocarbons. Four of the yeasts including S. occidentalis, T. candida, C. tropicalis and C. maltosa excreted polymers through modified sites in their cell wall ('canals'), whereas C. lipolytica and C. paralipolytica and the two bacterial species secreted polymers over the entire cell surface. These polymers took the form of fibrils and films that clogged pores and cavities on the surfaces of the oil droplets. A three-dimensional reconstruction of the cavities using serial thin sections showed that the exopolymer films isolated the ambient aqueous medium together with microbial cells and oil to form both closed and open granules that contained pools of oxidative enzymes utilized for the degradation of the oil hydrocarbons. The formation of such granules, or 'trophosomes,' appears to be a fundamental process that facilitates the efficient degradation of oil in aqueous media.


Asunto(s)
Bacterias/crecimiento & desarrollo , Bacterias/metabolismo , Biopolímeros/metabolismo , Petróleo/metabolismo , Microbiología del Agua , Levaduras/crecimiento & desarrollo , Levaduras/metabolismo , Bacterias/citología , Biodegradación Ambiental , Biotransformación , Hidrocarburos/metabolismo , Microscopía , Levaduras/citología
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