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ORIGINAL ARTICLE/SHORT PAPER

Microbial populations in various paddy soils respond differently to denitrification-inducing conditions, albeit background bacterial populations are similar

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Pages 220-224 | Received 14 Oct 2009, Accepted 31 Dec 2009, Published online: 21 Dec 2010

Figures & data

Table 1 Physicochemical characteristics of the soil samples

Figure 1 Bacterial community structures assessed by denaturing gradient gel electrophoresis (DGGE) analysis. (a) The DGGE banding profiles of the six soil samples and three treatments. Lanes 1–3, soil sample collected from the continuous rice field from Niigata (NC); lanes 4–6, soil sample collected from the rice–soybean rotation field from Niigata (NR); lanes 7–9, soil sample collected from the continuous rice field from Yamagata (YC); lanes 10–12, soil sample collected from the rice–soybean rotation field from Yamagata (YR); lanes 13–15, soil sample collected from the continuous rice field from Kumamoto (KC); lanes 16–18, soil sample collected from the rice–soybean rotation field from Kumamoto (KR); BA, samples without incubation; SU, samples incubated with added succinate; NS, samples incubated with added nitrate and succinate. (b) Principal component analysis (PCA) plot based on the DGGE profile. The normalized location and intensity of each DGGE band were used in the PCA analysis. The numbers in the plot correspond to the lane numbers in (a). The numbers in parentheses are the percentages of variation explained by each component.

Figure 1 Bacterial community structures assessed by denaturing gradient gel electrophoresis (DGGE) analysis. (a) The DGGE banding profiles of the six soil samples and three treatments. Lanes 1–3, soil sample collected from the continuous rice field from Niigata (NC); lanes 4–6, soil sample collected from the rice–soybean rotation field from Niigata (NR); lanes 7–9, soil sample collected from the continuous rice field from Yamagata (YC); lanes 10–12, soil sample collected from the rice–soybean rotation field from Yamagata (YR); lanes 13–15, soil sample collected from the continuous rice field from Kumamoto (KC); lanes 16–18, soil sample collected from the rice–soybean rotation field from Kumamoto (KR); BA, samples without incubation; SU, samples incubated with added succinate; NS, samples incubated with added nitrate and succinate. (b) Principal component analysis (PCA) plot based on the DGGE profile. The normalized location and intensity of each DGGE band were used in the PCA analysis. The numbers in the plot correspond to the lane numbers in (a). The numbers in parentheses are the percentages of variation explained by each component.

Table 2 Taxonomic assignment of the clones obtained from the excised denaturing gradient gel electrophoresis bands

Figure 2 Neighbor-joining tree showing the phylogenetic relationship between the clones obtained from the excised denaturing gradient gel electrophoresis band shown in Fig. 1. Bootstrap values (%) were generated from 1,000 replicates and only values >70% are shown. α, Alphaproteobacteria; β, Betaproteobacteria; B, Bacilli.

Figure 2 Neighbor-joining tree showing the phylogenetic relationship between the clones obtained from the excised denaturing gradient gel electrophoresis band shown in Fig. 1. Bootstrap values (%) were generated from 1,000 replicates and only values >70% are shown. α, Alphaproteobacteria; β, Betaproteobacteria; B, Bacilli.

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