Type‐specific quantification of particulate methane monooxygenase gene of methane‐oxidizing bacteria at the oxic–anoxic interface of a surface paddy soil by digitalPCR

Abstract

AbstractAerobic methane‐oxidizing bacteria (MOB) play an important role in mitigating methane emissions from paddy fields. In this study, we developed a differential quantification method for the copy number ofpmoAgenes of type Ia, Ib, and IIa MOB in paddy field soil using chip‐based digital PCR. Three probes specific to thepmoAof type Ia, Ib, and IIa MOB worked well in digital PCR quantification when genomic DNA of MOB isolates and PCR‐amplified DNA fragments ofpmoAwere examined as templates. WhenpmoAgenes in the surface soil layer of a flooded paddy were quantified by digital PCR, the copy numbers of type Ia, Ib, and IIa MOB were 105–106, 105–106, and 107copies g−1dry soil, respectively, with the highest values in the top 0–2‐mm soil layer. Especially, the copy numbers of type Ia and Ib MOB increased by 240% and 380% at the top layer after soil flooding, suggesting that the soil circumstances at the oxic–anoxic interfaces were more preferential for growth of type I MOB than type II MOB. Thus, type I MOB likely play an important role in the methane consumption at the surface paddy soil.