Cappuccio Jenny A, Falso Miranda J Sarachine, Kashgarian Michaele, Buchholz Bruce A
Biosciences & Biotechnology Division, Lawrence Livermore National Laboratory, Livermore, CA 94551, United States.
Center for Accelerator Mass Spectrometry, Lawrence Livermore National Laboratory, Livermore, CA 94551, United States.
Forensic Sci Int. 2014 Jul;240:54-60. doi: 10.1016/j.forsciint.2014.04.003. Epub 2014 Apr 13.
Investigators of bioagent incidents or interdicted materials need validated, independent analytical methods that will allow them to distinguish between recently made bioagent samples versus material drawn from the archives of a historical program. Heterotrophic bacteria convert the carbon in their food sources, growth substrate or culture media, into the biomolecules they need. The F(14)C (fraction modern radiocarbon) of a variety of media, Bacillus spores, and separated proteins from Bacillus spores was measured by accelerator mass spectrometry (AMS). AMS precisely measures F(14)C values of biological materials and has been used to date the synthesis of biomaterials over the bomb pulse era (1955 to present). The F(14)C of Bacillus spores reflects the radiocarbon content of the media in which they were grown. In a survey of commercial media we found that the F(14)C value indicated that carbon sources for the media were alive within about a year of the date of manufacture and generally of terrestrial origin. Hence, bacteria and their products can be dated using their (14)C signature. Bacillus spore samples were generated onsite with defined media and carbon free purification and also obtained from archived material. Using mechanical lysis and a variety of washes with carbon free acids and bases, contaminant carbon was removed from soluble proteins to enable accurate (14)C bomb-pulse dating. Since media is contemporary, (14)C bomb-pulse dating of isolated soluble proteins can be used to distinguish between historical archives of bioagents and those produced from recent media.
生物制剂事件或被拦截材料的调查人员需要经过验证的独立分析方法,以便能够区分近期制备的生物制剂样本与从历史项目档案中提取的材料。异养细菌将其食物来源、生长底物或培养基中的碳转化为它们所需的生物分子。通过加速器质谱法(AMS)测量了多种培养基、芽孢杆菌孢子以及从芽孢杆菌孢子中分离出的蛋白质的F(14)C(现代放射性碳分数)。AMS能精确测量生物材料的F(14)C值,并已被用于确定炸弹脉冲时代(1955年至今)生物材料的合成时间。芽孢杆菌孢子的F(14)C反映了其生长培养基中的放射性碳含量。在对商业培养基的调查中,我们发现F(14)C值表明培养基的碳源在制造日期后约一年内是有生命的,且一般来源于陆地。因此,细菌及其产物可以利用其(14)C特征进行年代测定。芽孢杆菌孢子样本在现场用特定培养基和无碳纯化方法制备,也从存档材料中获取。通过机械裂解以及用无碳酸碱进行多种洗涤,从可溶性蛋白质中去除了污染碳,以实现准确的(14)C炸弹脉冲年代测定。由于培养基是当代的,对分离出的可溶性蛋白质进行(14)C炸弹脉冲年代测定可用于区分生物制剂的历史档案和近期培养基产生的档案。