Department of Chemistry, University of Illinois at Chicago, Chicago, IL 60607-7061, USA.
Analyst. 2013 Nov 21;138(22):6844-51. doi: 10.1039/c3an01389h.
7.87 to 10.5 eV vacuum ultraviolet (VUV) photon energies were used in laser desorption postionization mass spectrometry (LDPI-MS) to analyze biofilms comprised of binary cultures of interacting microorganisms. The effect of photon energy was examined using both tunable synchrotron and laser sources of VUV radiation. Principal components analysis (PCA) was applied to the MS data to differentiate species in Escherichia coli-Saccharomyces cerevisiae coculture biofilms. PCA of LDPI-MS also differentiated individual E. coli strains in a biofilm comprised of two interacting gene deletion strains, even though these strains differed from the wild type K-12 strain by no more than four gene deletions each out of approximately 2000 genes. PCA treatment of 7.87 eV LDPI-MS data separated the E. coli strains into three distinct groups, two "pure" groups, and a mixed region. Furthermore, the "pure" regions of the E. coli cocultures showed greater variance by PCA at 7.87 eV photon energies compared to 10.5 eV radiation. This is consistent with the expectation that the 7.87 eV photoionization selects a subset of low ionization energy analytes while 10.5 eV is more inclusive, detecting a wider range of analytes. These two VUV photon energies therefore give different spreads via PCA and their respective use in LDPI-MS constitute an additional experimental parameter to differentiate strains and species.
7.87 至 10.5 eV 的真空紫外(VUV)光子能量被用于激光解吸后电离质谱(LDPI-MS)分析由相互作用的微生物二元培养物组成的生物膜。使用可调谐同步辐射和 VUV 辐射激光源研究了光子能量的影响。主成分分析(PCA)被应用于 MS 数据,以区分大肠杆菌-酿酒酵母共培养生物膜中的物种。LDPI-MS 的 PCA 还区分了由两个相互作用的基因缺失菌株组成的生物膜中的单个大肠杆菌菌株,尽管这些菌株与野生型 K-12 菌株的差异不超过每个大约 2000 个基因中的四个基因缺失。7.87 eV LDPI-MS 数据的 PCA 处理将大肠杆菌菌株分为三个不同的组,两个“纯”组和一个混合区域。此外,与 10.5 eV 辐射相比,7.87 eV 光子能量的 PCA 使大肠杆菌共培养物的“纯”区域的方差更大。这与 7.87 eV 光致电离选择低电离能分析物子集的预期一致,而 10.5 eV 则更具包容性,检测到更广泛的分析物。因此,这两种 VUV 光子能量通过 PCA 给出了不同的分布,它们在 LDPI-MS 中的各自使用构成了区分菌株和物种的另一个实验参数。