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首页> 外文期刊>European food research and technology =: Zeitschrift fur Lebensmittel-Untersuchung und -Forschung. A >Effect of glycerol and dihydroxyacetone concentrations in the culture medium on the growth of acetic acid bacteria Gluconobacter oxydans ATCC 621
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Effect of glycerol and dihydroxyacetone concentrations in the culture medium on the growth of acetic acid bacteria Gluconobacter oxydans ATCC 621

机译:培养基中甘油和二羟基丙酮的浓度对醋酸细菌氧化葡糖杆菌ATCC 621生长的影响

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Bacteria of the species Gluconobacter oxydans are applied in the industrial production of dihydroxyacetone (DHA) via glycerol oxidation. The major problem of this biotransformation involves process inhibition by substrate and/or product. Improper initial concentration of glycerol and increasing DHA concentration may inhibit the metabolic activity of bacterial cells and impede further course of the reaction. An attempt was, therefore, undertaken in this study to determine which concentrations of glycerol (30, 50, 70, 100 g L-1) and DHA (10-100 g L-1) may inhibit the growth of acetic acid bacteria of G. oxydans ATCC 621 species. Cultures of this strain were run in the Bioscreen C MBR apparatus on experimental culture media with various initial concentrations of glycerol and DHA. Analyses were also carried out to examine the impact of pH (5.0, 7.0, 8.0) of glycerol-containing culture media on cell growth of the analyzed strain G. oxydans. None of the applied substrate concentrations was inhibiting cellular divisions of G. oxydans bacteria. The initial glycerol concentrations that enabled rapid cellular divisions reached 50 g L-1 in the medium with pH 5.0 (coefficient of specific growth rate mu = 0.0550) and 70 g L-1 in the medium with pH 7.0 (mu = 0.0556). DHA was shown to inhibit the mitotic activity of G. oxydans bacteria even at low concentrations (20-30 g L-1), whereas at the concentration of 70 g L-1, it made cell divisions impossible. The applied pH values of the culture media did not inhibit the growth of G. oxydans strain
机译:氧化葡糖杆菌属的细菌通过甘油氧化被用于二羟基丙酮(DHA)的工业生产中。这种生物转化的主要问题涉及底物和/或产物的过程抑制。甘油初始浓度不当和DHA浓度增加可能会抑制细菌细胞的代谢活性,并阻碍反应的进一步进程。因此,本研究试图确定甘油(30、50、70、100 g L-1)和DHA(10-100 g L-1)的浓度可能会抑制G的乙酸细菌的生长。 oxydans ATCC 621种该菌株的培养物在Bioscreen C MBR设备中在具有各种初始浓度的甘油和DHA的实验培养基上进行。还进行了分析以检查含甘油的培养基的pH(5.0、7.0、8.0)对被分析的氧化单孢菌的细胞生长的影响。所施加的底物浓度均没有抑制氧化单歧杆菌的细胞分裂。能够使细胞快速分裂的初始甘油浓度在pH 5.0(比生长系数μ= 0.0550)的培养基中达到50 g L-1,在pH 7.0(mu = 0.0556)的培养基中达到70 g L-1。已显示DHA即使在低浓度(20-30 g L-1)下也能抑制氧化单歧杆菌的有丝分裂活性,而在70 g L-1的浓度下DHA使细胞分裂成为不可能。施加的培养基pH值不会抑制氧化单歧杆菌的生长

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