Swatkoski Stephen, Russell Scott C, Edwards Nathan, Fenselau Catherine
Department of Chemistry & Biochemistry, University of Maryland, College Park, Maryland 20742, USA.
Anal Chem. 2006 Jan 1;78(1):181-8. doi: 10.1021/ac051521d.
A method for the rapid identification of Bacillus spores is proposed, based on the selective release and chemical digestion of small, acid-soluble spore proteins (SASPs). Microwave-assisted acid hydrolysis of SASPs from B. anthracis str. Sterne and B. subtilis str. 168 was accomplished in a single step requiring only 90 s of heating. The peptide products of the chemical digestion were identified by postsource decay sequencing with a MALDI-TOF-MS equipped with a curved-field reflectron. The specificity of the observed SASP peptides was evaluated using a cross-species sequence search. The incomplete nature of the acid digestion under these conditions allowed detection of the digest products along with the proteins from which they originated, which increased species identification confidence. The feasibility of this approach for the rapid identification of Bacillus species was further demonstrated by analyzing a mixture of B. subtilis str. 168 and B. anthracis str. Sterne spores.
本文提出了一种基于小的酸溶性芽孢蛋白(SASP)的选择性释放和化学消化的快速鉴定芽孢杆菌芽孢的方法。炭疽芽孢杆菌斯特恩菌株和枯草芽孢杆菌168菌株的SASP的微波辅助酸水解在一步中完成,仅需90秒加热。化学消化的肽产物通过配备弯曲场反射器的基质辅助激光解吸电离飞行时间质谱仪(MALDI-TOF-MS)的源后衰变测序进行鉴定。使用跨物种序列搜索评估观察到的SASP肽的特异性。在这些条件下酸消化的不完全性允许检测消化产物及其来源的蛋白质,这增加了物种鉴定的可信度。通过分析枯草芽孢杆菌168菌株和炭疽芽孢杆菌斯特恩菌株芽孢的混合物,进一步证明了该方法用于快速鉴定芽孢杆菌属物种的可行性。