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Estimation of Bacterial Cell Numbers in Humic Acid-Rich Salt Marsh Sediments with Probes Directed to 16S Ribosomal DNA

机译:腐殖酸丰富的盐沼沉积物中的细菌细胞数与针对16S核糖体DNA的探针的估计。

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摘要

The feasibility of using probes directed towards ribosomal DNAs (rDNAs) as a quantitative approach to estimating cell numbers was examined and applied to study the structure of a bacterial community in humic acid-rich salt marsh sediments. Hybridizations were performed with membrane-bound nucleic acids by using seven group-specific DNA oligonucleotide probes complementary to 16S rRNA coding regions. These included a general eubacterial probe and probes encompassing most members of the gram-negative, mesophilic sulfate-reducing bacteria (SRB). DNA was extracted from sediment samples, and contaminating materials were removed by a series of steps. Efficiency of DNA extraction was 48% based on the recovery of tritiated plasmid DNA added to samples prior to extraction. Reproducibility of the extraction procedure was demonstrated by hybridizations to replicate samples. Numbers of target cells in samples were estimated by comparing the amount of hybridization to extracted DNA obtained with each probe to that obtained with a standard curve of genomic DNA for reference strains included on the same membrane. In June, numbers of SRB detected with an SRB-specific probe ranged from 6.0 × 107 to 2.5 × 109 (average, 1.1 × 109 ± 5.2 × 108) cells g of sediment−1. In September, numbers of SRB detected ranged from 5.4 × 108 to 7.3 × 109 (average, 2.5 × 109 ± 1.5 × 109) cells g of sediment−1. The capability of using rDNA probes to estimate cell numbers by hybridization to DNA extracted from complex matrices permits initiation of detailed studies on community composition and changes in communities based on cell numbers in formerly intractable environments.
机译:研究了使用针对核糖体DNA(rDNA)的探针作为定量估算细胞数量的定量方法的可行性,并将其用于研究富含腐殖酸的盐沼沉积物中细菌群落的结构。通过使用与16S rRNA编码区互补的七个组特异性DNA寡核苷酸探针,与膜结合核酸进行杂交。这些包括通用的真细菌探针和涵盖大多数革兰氏阴性,嗜温硫酸盐还原细菌(SRB)成员的探针。从沉积物样品中提取DNA,并通过一系列步骤除去污染物质。根据提取前样品中tri化质粒DNA的回收率,DNA提取效率为48%。提取复制品的杂交证明了提取方法的可重复性。通过将与每个探针获得的提取DNA的杂交量与同一膜上所含参考菌株的基因组DNA的标准曲线获得的杂交量进行比较,从而估算样品中靶细胞的数量。 6月,使用SRB专用探针检测到的SRB数量从6.0×10 7 到2.5×10 9 (平均1.1×10 9 ±5.2×10 8 )细胞g沉积物 -1 。 9月,检测到的SRB数量从5.4×10 8 到7.3×10 9 (平均2.5×10 9 ±1.5×10 9 )个沉积物 -1 的细胞g。通过使用rDNA探针与从复杂基质中提取的DNA进行杂交来估计细胞数的能力,使得可以开始对群落组成和基于先前难治的环境中的细胞数进行群落变化的详细研究。

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