2022
DOI: 10.1007/s11104-022-05491-5
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Responses of functional genes involved in nitrogen cycling to green manuring in different paddy soils in south China

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Cited by 12 publications
(5 citation statements)
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“…In addition, long‐term GM resulted in the highest absolute abundance of AMF (as a helper of N fixation) which could form hyphae to provide highly efficient transport corridors for chemical compounds (especially P) to support the BNF by diazotrophs [ 27 , 31 ]. These results agree with the previous findings of Li et al [ 49 ] and Guo et al [ 50 ] that green manure or legume in agriculture system has the advantage of enriching diazotrophs and AMF, which indicate that the potential effects of biotic factors (such as GM root exudates) on the microbial community may be larger than the variations in the soil environment.…”
Section: Discussionsupporting
confidence: 93%
“…In addition, long‐term GM resulted in the highest absolute abundance of AMF (as a helper of N fixation) which could form hyphae to provide highly efficient transport corridors for chemical compounds (especially P) to support the BNF by diazotrophs [ 27 , 31 ]. These results agree with the previous findings of Li et al [ 49 ] and Guo et al [ 50 ] that green manure or legume in agriculture system has the advantage of enriching diazotrophs and AMF, which indicate that the potential effects of biotic factors (such as GM root exudates) on the microbial community may be larger than the variations in the soil environment.…”
Section: Discussionsupporting
confidence: 93%
“…qPCR was conducted using a three-step thermal cycling method that included pre-denaturation at 95 °C for 5 min, 35 cycles of denaturation at 95 °C for 30 s, annealing at 58 °C for 30 s, and an extension at 72 °C for 1 min. ( Li et al, 2022 ). To create standard curves, the plasmid pMD18-T was used with seven functional genes and 10-fold dilution gradients.…”
Section: Methodsmentioning
confidence: 99%
“…Each qPCR reaction was run in triplicate for each set of primers, and the non-template control served as a negative control. Furthermore, q-PCR was carried out using a three-step thermal cycling method that involved 35 cycles of 95°C pre-denaturation for 5 min, 95°C denaturation for 30 s, 58°C annealing for 30 s, and 72°C extension for 1 min (Li et al, 2022). Standard curves were created by diluting pMD18-T, a plasmid for five functional genes, in a 10-fold gradient.…”
Section: Real-time Fluorescence Quantitative Pcrmentioning
confidence: 99%