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微克至亚纳克量葡萄糖的细菌生物测定法。

Bacterial bioassay of microgram to subnanogram quantities of glucose.

作者信息

Nishigaki K, Yamada T, Watanabe T, Husimi Y, Tanaka T

机构信息

Department of Environmental Chemistry, Faculty of Engineering, Saitama University, Japan.

出版信息

Biotechnol Appl Biochem. 1988 Oct;10(5):428-34.

PMID:3058151
Abstract

A simple and highly sensitive bioassay for the measurement of glucose is described. The method is based on the fact that the yields of cultured bacteria depend on the amount of glucose input, which is a limiting factor in Davis minimal medium. The number of cells cultured under fixed conditions was shown to be dependent on the amount of glucose in the culture medium. Therefore, the concentration of glucose can be measured by counting the cell number after culturing the bacteria. With Davis medium depleted of sodium citrate, we used this method to detect a subnanogram level of glucose, although with the accuracy of order of magnitude estimation. In the microgram per milliliter range of glucose, the cell number can be measured optically, with proliferation being proportional to the input glucose. The high selectivity for glucose of this method is based on the preferential usage of glucose as a carbon and energy source by the bacteria adopted. The feasibility of applying this method to other substances is discussed.

摘要

本文描述了一种用于测量葡萄糖的简单且高灵敏度的生物测定法。该方法基于这样一个事实:培养细菌的产量取决于葡萄糖的输入量,而葡萄糖是戴维斯基本培养基中的一个限制因素。在固定条件下培养的细胞数量被证明取决于培养基中葡萄糖的含量。因此,可以通过在培养细菌后计数细胞数量来测量葡萄糖的浓度。使用不含柠檬酸钠的戴维斯培养基,我们用这种方法检测到了亚纳克级水平的葡萄糖,不过其准确性为数量级估计。在葡萄糖每毫升微克范围内,可以通过光学方法测量细胞数量,细胞增殖与输入的葡萄糖成正比。该方法对葡萄糖的高选择性基于所采用的细菌优先将葡萄糖用作碳源和能源。文中还讨论了将该方法应用于其他物质的可行性。

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