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Detection of microbial biomass in subseafloor sediment by pyrolysis–GC/MS

机译:利用热解 - 气相色谱/质谱联用技术检测海底沉积物中的微生物生物量

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摘要

The conventional approaches for qualitative and quantitative assessment of microbial biomass in sediments, e.g., via quantitative polymerase chain reaction or intact polar lipids analysis, are rather tedious and time-consuming. Here we present a new, optimized and simple pyrolysis-gas chromatography/mass spectrometry protocol for rapid screening of sediment samples for the presence of microbial signals and quantification of bulk population. Analysis of microbial cultures of different bacterial and archaeal lineages as well as reference substances and model compounds provided molecular fingerprints for tracking microbial biomass. The diagnostic fingerprints consist of benzyl nitrile (derived from DNA and protein), 2-furanmethanol (from DNA and peptidoglycan), indole (from peptidoglycan and protein), phenol (from DNA, peptidoglycan and protein) and pyrrole (from peptidoglycan). Detection of microbial signals through the molecular fingerprints requires a cell density of at least 106 cells/g, whereas at least 107 cells/g is necessary for quantification. The pyrolysis method was applied to marine sediments from different depths (until ∼400 m below the seafloor at the Canterbury Basin) and with different organic carbon contents (0.11–6.99%).
机译:定性和定量评估沉积物中微生物生物量的常规方法,例如,通过定量聚合酶链反应或完整的极性脂质分析,相当繁琐且耗时。在这里,我们提出了一种新的,优化的和简单的热解-气相色谱/质谱协议,用于快速筛查沉积物样品中是否存在微生物信号并定量分析总体种群。对不同细菌和古细菌谱系的微生物培养物以及参考物质和模型化合物的分析提供了用于追踪微生物生物量的分子指纹。诊断指纹包括苄腈(衍生自DNA和蛋白质),2-呋喃甲醇(衍生自DNA和肽聚糖),吲哚(衍生自肽聚糖和蛋白质),苯酚(衍生自DNA,肽聚糖和蛋白质)和吡咯(衍生自肽聚糖)。通过分子指纹检测微生物信号需要至少106个细胞/克的细胞密度,而定量至少需要107个细胞/克。热解方法适用于不同深度(直到坎特伯雷盆地海底以下至400m以下)且有机碳含量不同(0.11-6.99%)的海洋沉积物。

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