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1.
Asia Pac J Clin Nutr ; 8(1): 36-8, 1999 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-24393734

RESUMO

The iron and vitamin C content of water spinach and rice samples from three sites in Vietnam were chemically analysed. The iron content of home-milled rice from Nghe An was higher than the iron content of machine-milled rice from Thai Binh and Hanoi. In addition, the iron content of cooked rice was lower than that of uncooked rice as iron was removed during the washing and rinsing of the rice prior to cooking. Cooked rice that was washed and rinsed less thoroughly had a higher iron content. The iron content of water spinach from different locations was very similar, although white water spinach had a much higher vitamin C content than red water spinach.

2.
Antonie Van Leeuwenhoek ; 68(3): 215-23, 1995 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-8572679

RESUMO

Arxula adeninivorans Ls3 is described as an ascomycetous, arthroconidial, anamorphic, xerotolerant yeast, which was selected from wood hydrolysates in Siberia. By using minimal salt medium or yeast-extract-peptone-medium with glucose or maltose as carbon source it was shown that this yeast is able to grow at up to 48 degrees C. Increasing temperatures induce changes in morphology from the yeast phase to mycelia depending on an altered programme of gene expression. This dimorphism is an environmentally conditioned (reversible) event and the mycelia can be induced at a cultivation temperature of 45 degrees C. Depending on the morphology of strain Ls3 (yeast phase or mycelia) the secretion behaviour as well as the spectrum of polypeptides accumulated in the culture medium changed. The activities of the accumulated extracellular enzymes glucoamylase and invertase were 2 to 3 times higher in cultures grown at 45 degrees C than in those grown at 30 degrees C. While the level of the glucoamylase protein secreted from mycelia between 45 and 70 hours did not change, biochemical activity decreased after a cultivation time of 43 hours. It was shown that this effect depended on both the catabolic repression of the glucoamylase by glucose and the thermal inactivation of this enzyme in media without or with low concentrations of starch or maltose.


Assuntos
Ascomicetos/fisiologia , Ascomicetos/ultraestrutura , Proteínas Fúngicas/metabolismo , Regulação Fúngica da Expressão Gênica , Glucana 1,4-alfa-Glucosidase/metabolismo , Glucose/metabolismo , Glicosídeo Hidrolases/metabolismo , Maltose/metabolismo , Microscopia Eletrônica de Varredura , RNA Fúngico/biossíntese , RNA Fúngico/genética , Temperatura , beta-Frutofuranosidase
3.
Microbiol Res ; 150(2): 113-20, 1995 May.
Artigo em Inglês | MEDLINE | ID: mdl-7600007

RESUMO

Seven Arxula adeninivorans strains originating from The Netherlands (CSIR 1136, CSIR 1138 and CBS 8244T), South Africa (CSIR 1147, CSIR 1148 and CSIR 1149) and Siberia (Ls3) were compared concerning their secretory glucoamylase. Within the spectrum of secretory polypeptides obtained by SDS-polyacrylamide gel electrophoresis, the glucoamylase corresponding polypeptide, could be identified by means of specific antibodies directed against the glucoamylase of strain Ls3. The molecular masses of the glucoamylases vary from 84 to 95 kDa. After endoglycosidase F treatment of the secretory proteins, the N-linked carbohydrate content for each glucoamylase could be quantified at about 25%. Glucoamylase activity staining of secretory proteins separated under nondenaturing conditions revealed one glucoamylase active protein for the Dutch strains and two active forms for the strains originating from South Africa and Siberia. Highest activities of glucoamylase can be measured at the end of the exponential growth phase for each strain. The Dutch strain CSIR 1138 secretes the highest activity. Optimum values for temperature and pH were determined and compared. By means of pulsed field gel electrophoresis and Southern analysis, the glucoamylase corresponding gene could be localized on the second of the four chromosomes of each yeast strain.


Assuntos
Glucana 1,4-alfa-Glucosidase/metabolismo , Fungos Mitospóricos/enzimologia , Anticorpos Antifúngicos/biossíntese , Mapeamento Cromossômico , Glucana 1,4-alfa-Glucosidase/genética , Glucana 1,4-alfa-Glucosidase/imunologia , Fungos Mitospóricos/genética , Fungos Mitospóricos/imunologia
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