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微生物计数的微生物学方法与物理化学方法的比较

Comparison of microbiological and physicochemical methods for enumeration of microorganisms.

作者信息

Szermer-Olearnik Bożena, Sochocka Marta, Zwolińska Katarzyna, Ciekot Jarosław, Czarny Anna, Szydzik Joanna, Kowalski Konrad, Boratyński Janusz

机构信息

Laboratory of Biomedical Chemistry "Neolek", Institute of Immunology and Experimental Therapy, Polish Academy of Sciences, Wrocław, Poland.

Laboratory of Biomedical Chemistry "Neolek", Institute of Immunology and Experimental Therapy, Polish Academy of Sciences, Wrocław, Poland; Laboratory of Virology, Institute of Immunology and Experimental Therapy, Polish Academy of Sciences, Wrocław, Poland.

出版信息

Postepy Hig Med Dosw (Online). 2014 Jan 2;68:1392-6. doi: 10.5604/17322693.1130086.

Abstract

Determination of the number of cultured bacteria is essential for scientific and industrial practice. A spread plate technique is the most common and accurate method for counting of microorganisms. However, time consuming incubation does not allow for a quick estimation of the number of bacteria in a growing culture. In the present study, the results of photometric measurements: direct optical density method (OD at 585 nm), UV absorbance at 260 and/or 280 nm of separated and lysed bacteria by sodium hydroxide and surfactant with the spread plate technique were compared. The linear regression model for bacterial strains Staphylococcus aureus, Pseudomonas aeruginosa and Escherichia coli was used to compare these three methods. The UV measurement method enabled determination of the number of bacteria with similar precision. The procedure for solubilized bacteria UV measurement is robust, and is not influenced by dispersions in the original culture medium.

摘要

确定培养细菌的数量对于科学和工业实践至关重要。平板涂布技术是计数微生物最常用且最准确的方法。然而,耗时的培养过程无法快速估算生长培养物中的细菌数量。在本研究中,比较了光度测量结果:直接光密度法(585nm处的OD值)、用氢氧化钠和表面活性剂分离并裂解细菌后在260和/或280nm处的紫外吸光度,同时采用平板涂布技术。使用金黄色葡萄球菌、铜绿假单胞菌和大肠杆菌菌株的线性回归模型来比较这三种方法。紫外测量法能够以相似的精度测定细菌数量。溶解细菌的紫外测量程序稳健,不受原始培养基中分散物的影响。

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