监测金属加工液中微生物成分随时间和系统使用情况变化的初步研究。

M K Lonon, M Abanto, R H Findlay
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引用次数: 28

摘要

本文描述了一项初步研究的结果,该研究旨在检查金属加工液(MWF)生物成分的变化与使用的关系。流体样品取自两个新充电的系统,编号为BT-7415和BT-7707,每隔一周采集一次,共8周,并对无细胞上清液中存在的细菌种类和数量以及可溶性蛋白的存在进行表征。此外,采用气相色谱/质谱法检测BT-7415液中颗粒状细胞的脂质提取物中存在的磷脂脂肪酸(PLFA)的种类和相对数量。共培养鉴定出19种不同的细菌,其中超过一半(12/19)为革兰氏阴性。总菌落形成单位(CFU)在BT-7415中达到2.2 × 10(3)/mL,在BT-7707中达到2.4 × 10(5)/mL。最常见的属是假单胞菌。根据BT-7415样品中PLFA的总生物量估计,使用8周后,细胞数量为1.1 x 10(7)/mL。随着液体的使用,BT-7415中检测到的PLFA的数量和数量都增加了。色谱图以两种脂肪酸为主,其含量随时间的增加而增加。这些脂肪酸,18:2 ω - 6和18:1 ω - 9c,通常与假单胞菌无关。这表明,目前使用的培养技术尚未检测到MWF中生物联合体的重要组成部分。两种系统的样品中均未检测到可溶性蛋白。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A pilot study for monitoring changes in the microbiological component of metalworking fluids as a function of time and use in the system.

This article describes the results of a pilot study to examine changes in the biological component of metalworking fluids (MWF) as a function of use. Fluid samples were taken from two newly charged systems, designated BT-7415 and BT-7707, at 1-week intervals for 8 weeks and characterized with respect to the kinds and numbers of bacteria present and presence of soluble protein in cell-free supernatants. In addition, lipid extracts of pelleted cells from fluids in BT-7415 were examined by gas chromatography/mass spectroscopy for the kinds and relative amounts of phospholipid fatty acids (PLFA) present. A total of 19 different bacterial species was cultured and identified, more than half (12/19) of which were gram-negative. Total colony-forming units (CFU) reached levels of 2.2 x 10(3)/mL in BT-7415 and 2.4 x 10(5)/mL in BT-7707. The most common genus isolated was Pseudomonas. Estimations of cell numbers based on total biomass from PLFA in samples from BT-7415 indicated 1.1 x 10(7)/mL after 8 weeks of use. Both the numbers of PLFA identified and the amounts of each detected in BT-7415 increased as the fluids were used. The chromatograms were dominated by two fatty acids, the amounts of which increased with time. These fatty acids, 18:2 omega 6 and 18:1 omega 9c, are not commonly associated with pseudomonads. This suggests that there is an important component of the biological consortium in MWF is not being detected by currently used culture techniques. There was no soluble protein detected in any of the samples from either system.

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