Pacific Northwest National Laboratory, P.O. Box 999, MS P7-50, Richland, Washington 99352, USA.
Anal Chem. 2010 Feb 15;82(4):1200-6. doi: 10.1021/ac901491c.
Presented here is an analytical method to detect residual agar from a bacterial spore sample as an indication of culturing on an agar plate. This method is based on the resolubilization of agar polysaccharide from a bacterial spore sample, enzymatic digestion, followed by electrospray ionization tandem mass spectrometry (ESI-MS(n)) analysis for detection of a specific agar fragment ion. A range of Bacillus species and strains were selected to demonstrate the effectiveness of this approach. The characteristic agar fragment ion was detected in the spores grown on agar that were washed from 1 to 5 times, irradiated or nonirradiated, and not in the spores grown in broth. A sample containing approximately 10(8) spores is currently needed for confident detection of residual agar from culture on agar plates in the presence of bacterial spores with a limit of detection of approximately 1 ppm agar spiked into a broth-grown spore sample. The results of a proficiency test with 42 blinded samples are presented demonstrating the utility of this method with no false positives and only three false negatives for samples that were below the detection level of the method as documented.
这里介绍了一种分析方法,用于检测细菌孢子样品中的残留琼脂,以作为在琼脂平板上培养的指示。该方法基于从细菌孢子样品中重新溶解琼脂多糖,酶解,然后进行电喷雾电离串联质谱(ESI-MS(n))分析,以检测特定的琼脂片段离子。选择了一系列芽孢杆菌属的物种和菌株来证明该方法的有效性。在从琼脂上洗下的孢子中,无论是否辐照,都检测到了特征性的琼脂片段离子,而在肉汤中生长的孢子中则没有。目前,对于在存在细菌孢子的情况下,从琼脂平板上的培养物中检测残留琼脂,需要大约 10^8 个孢子的样品,琼脂的检测限约为 1ppm,琼脂掺入肉汤培养的孢子样品中。提供了 42 个盲样能力验证的结果,证明了该方法的实用性,对于低于方法检测限的样品,没有假阳性,只有三个假阴性。