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The Hydrogenase Chip: a tiling oligonucleotide DNA microarray technique for characterizing hydrogen-producing and -consuming microbes in microbial communities

机译:氢化酶芯片:一种平铺寡核苷酸DNA微阵列技术用于表征微生物群落中产氢和消耗氢的微生物

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摘要

We developed a broad-ranging method for identifying key hydrogen-producing and consuming microorganisms through analysis of hydrogenase gene content and expression in complex anaerobic microbial communities. The method is based on a tiling hydrogenase gene oligonucleotide DNA microarray (Hydrogenase Chip), which implements a high number of probes per gene by tiling probe sequences across genes of interest at 1.67 × –2 × coverage. This design favors the avoidance of false positive gene identification in samples of DNA or RNA extracted from complex microbial communities. We applied this technique to interrogate interspecies hydrogen transfer in complex communities in (i) lab-scale reductive dehalogenating microcosms enabling us to delineate key H2-consuming microorganisms, and (ii) hydrogen-generating microbial mats where we found evidence for significant H2 production by cyanobacteria. Independent quantitative PCR analysis on selected hydrogenase genes showed that this Hydrogenase Chip technique is semiquantitative. We also determined that as microbial community complexity increases, specificity must be traded for sensitivity in analyzing data from tiling DNA microarrays.
机译:我们开发了广泛的方法,通过分析复杂的厌氧微生物群落中的氢化酶基因含量和表达来鉴定关键的产氢和耗氢微生物。该方法基于平铺加氢酶基因寡核苷酸DNA微阵列(Hydrogengenase Chip),该芯片通过在1.67×–2×覆盖范围内对感兴趣的基因进行平铺探针序列来实现每个基因的大量探针。这种设计有助于避免从复杂微生物群落中提取的DNA或RNA样品中的假阳性基因鉴定。我们应用了该技术在(i)实验室规模的还原性脱卤微观世界中探究复杂社区中的种间氢转移,这使我们能够描绘出消耗H2的关键微生物,以及(ii)产生氢的微生物垫,我们在其中发现了由H2大量产生H2的证据蓝细菌。对所选氢化酶基因的独立定量PCR分析表明,该氢化酶芯片技术是半定量的。我们还确定,随着微生物群落复杂性的增加,在分析来自切片DNA微阵列的数据时必须交换特异性以提高灵敏度。

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