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首页> 外文期刊>European food research and technology =: Zeitschrift fur Lebensmittel-Untersuchung und -Forschung. A >A study on Saccharomyces cerevisiae and Candida utilis cell wall capacity for binding magnesium.
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A study on Saccharomyces cerevisiae and Candida utilis cell wall capacity for binding magnesium.

机译:酿酒酵母和假丝酵母念珠菌细胞壁结合镁的能力研究。

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摘要

The capacity for binding magnesium by bakery's yeast strain Saccharomyces cerevisiae No. 102 (Pure Culture Collection, Faculty Food Technology, Warsaw) and fodder yeast strain Candida utilis (ATCC 9950) was investigated in media supplemented with that element. The capacities of C. utilis (ATCC 9950) and S. cerevisiae (No. 102) biomass for binding magnesium were not statistically different in the first 24 h. In the next 24 h of cultivation the cells of C. utilis (ATCC 9950) were still able to bind magnesium ions, whereas those of S. cerevisiae (No. 102) released a part of previously bound magnesium to the medium. The major part of magnesium bound by the cells of C. utilis (ATCC 9950) was accumulated in cytosole. It was opposite to the cells of bakery yeast S. cerevisiae (No. 102) that accumulated magnesium mainly in the cell wall. The cells of C. utilis (ATCC 9950) yeast were smaller and their cell walls were thinner as compared to those of S. cerevisiae (No. 102) yeast. The thickness of the external mannoprotein layers was similar in both strains analyzed.
机译:在补充有该元素的培养基中,研究了面包房的酵母菌株Saccharomyces cerevisiae No.102(纯培养物保藏中心,Faculty Food Technology,华沙)和饲料酵母菌株Candida utilis(ATCC 9950)结合镁的能力。在最初的24小时内,草梭菌(ATCC 9950)和酿酒酵母(No. 102)生物量结合镁的能力在统计学上没有差异。在接下来的24小时培养中,util。C. utilis(ATCC 9950)的细胞仍然能够结合镁离子,而S. cerevisiae(No. 102)的细胞则将一部分先前结合的镁释放到培养基中。铜绿假单胞菌(ATCC 9950)的细胞结合的镁的大部分积累在细胞底中。与面包酵母S. cerevisiae(No. 102)的细胞相反,后者主要在细胞壁中积累镁。与酿酒酵母(No. 102)相比,util。C. utilis(ATCC 9950)酵母的细胞更小,细胞壁更薄。在所分析的两个菌株中,外部甘露蛋白层的厚度相似。

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