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Characterization of Bacillus spore species and their mixtures using postsource decay with a curved-field reflectron

机译:使用后场衰减和弯曲场反射器表征芽孢杆菌孢子及其混合物

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A strategy is proposed for the rapid identification of Bacillus spores, which relies on the selective release of a family of proteins, referred to as small, acid-soluble spore proteins (SASPs). In this work, SASPs were selectively solubilized from Bacillus spores on the MALDI sample plate by using 10% TFA. Proteolytic digests of SASPs generated in situ from spores of B. subtilis 168, B. globigii, B. thuringiensis subs. Kurstaki HD-1, B. cereus T, and the nonpathogenic strain B. anthracis Sterne were prepared in 5-25 min by using trypsin immobilized on Agarose beads and subsequently analyzed by MALDI-TOFMS using a curved-field reflectron. Protein identification was obtained by partial sequencing of distinctive tryptic peptides from Bacillus spores via post-source decay analysis combined with genome-based database searches by Mascot Sequence Query. Various unique SASPs were identified, allowing the characterization of Bacillus species by obtaining sequence-specific information on single peptides. The applicability of this approach for the rapid identification of Bacillus species was further established by analyzing spore mixtures. [References: 59]
机译:提出了一种快速鉴定芽孢杆菌孢子的策略,该策略依赖于选择性释放一种蛋白质的家族,这种蛋白质被称为小酸溶性孢子蛋白(SASP)。在这项工作中,通过使用10%TFA,从MALDI样品板上的芽孢杆菌孢子中选择性溶解了SASP。从枯草芽孢杆菌168,globigii芽孢杆菌,苏云金芽孢杆菌subs的孢子原位产生的SASP的蛋白水解消化物。通过使用固定在琼脂糖珠上的胰蛋白酶在5-25分钟内制备Kurstaki HD-1,蜡状芽孢杆菌T和无病原性炭疽芽孢杆菌Sterne,然后使用弯曲场反射镜通过MALDI-TOFMS分析。通过源后衰变分析与Mascot Sequence Query结合基于基因组的数据库搜索,对芽孢杆菌孢子的独特胰蛋白酶肽进行部分测序,从而获得蛋白质鉴定。鉴定出各种独特的SASP,从而通过获得单个肽段上的序列特异性信息来鉴定芽孢杆菌属。通过分析孢子混合物,进一步确立了该方法在快速鉴定芽孢杆菌属中的适用性。 [参考:59]

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