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Quantitative Detection of Methanotrophs in Soil by Novel pmoA-Targeted Real-Time PCR Assays

机译:新型pmoA靶向实时PCR分析法定量检测土壤中的甲烷营养菌

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摘要

Methane oxidation in soils is mostly accomplished by methanotrophic bacteria. Little is known about the abundance of methanotrophs in soils, since quantification by cultivation and microscopic techniques is cumbersome. Comparison of 16S ribosomal DNA and pmoA (α subunit of the particulate methane monooxygenase) phylogenetic trees showed good correlation and revealed five distinct groups of methanotrophs within the α and γ subclasses of Proteobacteria: the Methylococcus group, the Methylobacter/Methylosarcina group, the Methylosinus group, the Methylocapsa group, and the forest clones group (a cluster of pmoA sequences retrieved from forest soils). We developed quantitative real-time PCR assays with SybrGreen for each of these five groups and for all methanotrophic bacteria by targeting the pmoA gene. Detection limits were between 101 and 102 target molecules per reaction for all assays. Real-time PCR analysis of soil samples spiked with cells of Methylococcus capsulatus, Methylomicrobium album, and Methylosinus trichosporium recovered almost all the added bacteria. Only the Methylosinus-specific assay recovered only 20% of added cells, possibly due to a lower lysis efficiency of type II methanotrophs. Analysis of the methanotrophic community structure in a flooded rice field soil showed (5.0 ± 1.4) × 106 pmoA molecules g?1 for all methanotrophs. The Methylosinus group was predominant (2.7 × 106 ± 1.1 × 106 target molecules g?1). In addition, bacteria of the Methylobacter/Methylosarcina group were abundant (2.0 × 106 ± 0.9 × 106 target molecules g of soil?1). On the other hand, pmoA affiliated with the forest clones and the Methylocapsa group was below the detection limit of 1.9 × 104 target molecules g of soil?1. Our results showed that pmoA-targeted real-time PCR allowed fast and sensitive quantification of the five major groups of methanotrophs in soil. This approach will thus be useful for quantitative analysis of the community structure of methanotrophs in nature.
机译:土壤中的甲烷氧化主要由甲烷营养细菌完成。人们对土壤中甲烷营养菌的含量知之甚少,因为通过耕种和显微技术进行定量分析非常麻烦。 16S核糖体DNA和 pmoA (颗粒甲烷单加氧酶的α亚基)系统发育树的比较显示出良好的相关性,并揭示了变形杆菌的α和γ亚类中的五个不同的甲烷营养生物。 :甲基球菌组,甲基杆菌/甲基osarcarcina 组, Methylosinus 组, Methylocapsa 组和森林克隆组(从森林土壤中检索到的 pmoA 序列簇)。我们针对这五个组以及针对所有甲烷营养细菌,利用SybrGreen开发了实时定量PCR检测方法,并以 pmoA 基因为靶标。对于所有测定,每个反应的检出限在10 1 和10 2 个目标分子之间。荚膜甲基球菌甲基微生物菌种甲基毛孢菌细胞掺入的土壤样品的实时PCR分析几乎回收了所有添加的细菌。只有 Methylosinus 特异性检测方法只能回收添加细胞的20%,这可能是由于II型甲烷营养菌的裂解效率较低。对淹水的稻田土壤甲烷营养群落结构的分析表明,所有甲烷营养菌均具有(5.0±1.4)×10 6 pmoA 分子g ?1 甲基肌苷组占主导地位(2.7×10 6 ±1.1×10 6 目标分子g ?1 )。此外,甲基细菌/甲基藻类组的细菌丰富(土壤的目标分子为2.0×10 6 ±0.9×10 6 g)。 >?1 )。另一方面,与森林无性系相关的 pmoA Methylocapsa 组的检出限低于1.9×10 4 靶分子g土?1 。我们的结果表明,以 pmoA 为靶标的实时PCR可以快速,灵敏地定量测定土壤中的五种主要甲烷甲烷营养素。因此,这种方法将对自然界中甲烷菌的群落结构进行定量分析很有用。

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