Department of Biotechnology, Human Nutrition and Food Commodities, University of Life Sciences in Lublin, Skromna 8, 20-704 Lublin, Poland.
J Microbiol Biotechnol. 2011 Apr;21(4):421-9.
For precise identification of a Lactobacillus K1 isolate, LC-MS/MS analysis of the putative surface layer protein was performed. The results obtained from LTQ-FT-ICR mass spectrometry confirmed that the analyzed protein spot is the surface layer protein originating from Lb. helveticus species. Moreover, the identified protein has the highest similarity with the surface layer protein from Lb. helveticus R0052. To evaluate the proteomic study, multilocus sequence analysis of selected housekeeping gene sequences was performed. Combination of 16S rRNA sequencing with partial sequences for the genes encoding the RNA polymerase alpha subunit (rpoA), phenylalanyl-tRNA synthase alpha subunit (pheS), translational elongation factor Tu (tuf), and Hsp60 chaperonins (groEL) also allowed to classify the analyzed isolate as Lb. helveticus. Further classification at the strain level was achieved by sequencing of the slp gene. This gene showed 99.8% identity with the corresponding slp gene of Lb. helveticus R0052, which is in good agreement with data obtained by nano-HPLC coupled to an LTQ-FT-ICR mass spectrometer. Finally, LC-MS/ MS analysis of surface layer proteins extracted from three other Lactobacillus strains proved that the proposed method is the appropriate molecular tool for the identification of S-layer-possessing lactobacilli at the species and even strain levels.
为了精确鉴定乳酸杆菌 K1 分离株,对假定的表面层蛋白进行了 LC-MS/MS 分析。来自 LTQ-FT-ICR 质谱的结果证实,所分析的蛋白斑点是源自乳杆菌属的表面层蛋白。此外,鉴定出的蛋白与乳杆菌属 R0052 的表面层蛋白具有最高的相似性。为了评估蛋白质组学研究,对选定的管家基因序列进行了多位点序列分析。16S rRNA 测序与编码 RNA 聚合酶 alpha 亚基(rpoA)、苯丙氨酸-tRNA 合成酶 alpha 亚基(pheS)、翻译延伸因子 Tu(tuf)和 Hsp60 伴侣蛋白(groEL)的部分序列的组合,也可以将分析的分离株分类为乳杆菌属。通过 slp 基因的测序进一步在菌株水平上进行分类。该基因与乳杆菌属 R0052 的相应 slp 基因具有 99.8%的同一性,这与通过纳升 HPLC 与 LTQ-FT-ICR 质谱仪耦合获得的数据非常吻合。最后,从另外三种乳杆菌菌株中提取的表面层蛋白的 LC-MS/MS 分析证明,该方法是在种甚至菌株水平上鉴定具有 S 层的乳杆菌的合适分子工具。