نتایج جستجو برای: sorbitol dehydrogenase

تعداد نتایج: 73628  

Journal: :Applied and environmental microbiology 2008
Xue-Peng Yang Liu-Jing Wei Jin-Ping Lin Bo Yin Dong-Zhi Wei

A membrane-bound protein purified from Gluconobacter oxydans M5 was confirmed to be a pyrroloquinoline quinone-dependent D-sorbitol dehydrogenase. Gene disruption and complementation experiments demonstrated that this enzyme is responsible for the oxidation of 1-(2-hydroxyethyl) amino-1-deoxy-D-sorbitol (1NSL) to 6-(2-hydroxyethyl) amino-6-deoxy-L-sorbose (6NSE), which is the precursor of an an...

Journal: :Applied and environmental microbiology 1998
T McGonigal P Bodelle C Schopp A V Sarthy

A new inducible yeast expression vector, pXS7, was constructed by using the promoter and terminator sequences from the Saccharomyces cerevisiae SOR1 gene, which codes for the sorbitol dehydrogenase protein. We cloned the coding sequence of the Saccharomyces YEF3 gene in this vector and demonstrated an increase in YEF3 protein levels when cells were grown in the presence of the sugar sorbitol.

Journal: :Plant physiology 1999
B Shen S Hohmann R G Jensen a H Bohnert

For many organisms there is a correlation between increases of metabolites and osmotic stress tolerance, but the mechanisms that cause this protection are not clear. To understand the role of polyols, genes for bacterial mannitol-1-P dehydrogenase and apple sorbitol-6-P dehydrogenase were introduced into a Saccharomyces cerevisiae mutant deficient in glycerol synthesis. Sorbitol and mannitol pr...

Journal: :Clinical chemistry 1979
J F Dooley L J Turnquist L Racich

We describe a mechanized method for centrifugal analyzer determination of sorbitol dehydrogenase in serum, based on conversion of D-fructose to sorbitol with simultaneous oxidation of NADH, in triethanolamine buffer at pH 7.4 and 30 degrees C. The standard curve for this assay is linear to 200 U of activity per liter of serum. The mean within-run precision (CV) of the assay is 0.8%. Results cor...

Journal: :Journal of andrology 2006
Gilles Frenette Michel Thabet Robert Sullivan

Two enzymes are involved in the polyol pathway: an aldose reductase that reduces glucose in sorbitol followed by its oxidation in fructose by sorbitol dehydrogenase. It has been previously shown that both enzymes are presented in the bovine epididymis, where they are associated with membranous vesicles called epididymosomes. Based on the distribution of these enzymes, it has been hypothesized t...

2003
ALBERT T. BROWN

In recent years much interest has focused upon Streptococcus mutans as the etiological agent of smooth-surface caries in both rodents (7, 8, 10) and humans (5, 11, 12). Although similar in many respects to other homolactic streptococci found in the oral environment, a nutritional characteristic which has been used to distinguish S. mutans is its ability to utilize either mannitol or sorbitol as...

Journal: :Plant science : an international journal of experimental plant biology 2015
Ho-Youn Kim Macarena Farcuh Yuval Cohen Carlos Crisosto Avi Sadka Eduardo Blumwald

During ripening fruits undergo several physiological and biochemical modifications that influence quality-related properties, such as texture, color, aroma and taste. We studied the differences in ethylene and sugar metabolism between two genetically related Japanese plum cultivars with contrasting ripening behaviors. 'Santa Rosa' (SR) behaved as a typical climacteric fruit, while the bud sport...

2015
M. Francisca Aguayo Juan Carlos Cáceres Matías Fuentealba Rodrigo Muñoz Claudia Stange Ricardo Cabrera Michael Handford

Polyols are enzymatically-produced plant compounds which can act as compatible solutes during periods of abiotic stress. Nicotinamide adenine dinucleotide(+)-dependent SORBITOL DEHYDROGENASE (SDH, E. C. 1.1.1.14) from Arabidopsis thaliana L. sorbitol dehydrogenase (AtSDH) is capable of oxidizing several polyols including sorbitol, ribitol, and xylitol. In the present study, enzymatic assays usi...

Journal: :Clinical chemistry 1988
J C Liao M Rountree R Good J Hook C Punko

In this enzymatic method to analyze erythrocytes for D-sorbitol, the erythrocytes were separated from plasma by centrifugation, washed with isotonic saline (9 g/L NaCl), then diluted threefold with more saline. We lysed 1.5 mL of the diluted erythrocytes with chloroform and precipitated the protein with 58 g/L HClO4 solution. The resulting supernates were mixed with buffer, NAD+, and sorbitol d...

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