Larsson L, Valero-Guillén P, Martin-Luengo F, Pacheco F
Acta Pathol Microbiol Immunol Scand B. 1985 Oct;93(5):353-7. doi: 10.1111/j.1699-0463.1985.tb02900.x.
Cellular fatty acids of four rapid-growing mycobacterial species (Mycobacterium chelonei, M. fortuitum, M. phlei, and M. smegmatis) were analysed by packed and capillary column gas chromatography after one, three, four, six, eight, and twelve days of incubation on Löwenstein-Jensen and Sauton agar media. Variations in incubation time did not affect the chromatograms except in the case of twelve-day incubated M. smegmatis. Mycobacteria cultivated on Sauton agar medium contained more tuberculostearic and less oleic acid compared with Löwenstein-Jensen. For informative and reproducible analytical results, we recommend using a chemically defined culture medium and splitless injection on a capillary column capable of separating not only the methyl esters of the cellular fatty acids but also the diagnostically important secondary alcohols containing 18 and 20 carbon atoms.
在罗氏培养基和苏通琼脂培养基上培养1天、3天、4天、6天、8天和12天后,采用填充柱和毛细管柱气相色谱法分析了四种快速生长分枝杆菌(龟分枝杆菌、偶然分枝杆菌、草分枝杆菌和耻垢分枝杆菌)的细胞脂肪酸。培养时间的变化对色谱图没有影响,除了培养12天的耻垢分枝杆菌。与罗氏培养基相比,在苏通琼脂培养基上培养的分枝杆菌含有更多的结核硬脂酸和更少的油酸。为了获得信息丰富且可重复的分析结果,我们建议使用化学成分明确的培养基,并在能够分离细胞脂肪酸甲酯以及含有18和20个碳原子的具有诊断重要性的仲醇的毛细管柱上进行不分流进样。