SRX22336966 0C1 SRP469787 PRJNA1032716 DNeasy PowerSoil Pro Kit (Qiagen, Germany) was used to extract genomic DNA from the soil samples according to the manufacturer's protocol. DNA quality and quantity were measured using a NanoDrop UV-Vis spectrophotometer and a Qubit fluorometer 2.0 (Thermo Fisher Scientific, USA). An NGS library was prepared by amplifying the V4-V5 region of the small subunit ribosomal RNA (16S rRNA) gene for bacteria using 515F (ACA CTC TTT CCC TAC ACG ACG CTC TTC CGA TCT GTG NCA GCB GCC GCG GTR A) and 907R (GTG ACT GGA GTT CAG ACG TGT GCT CTT CCG ATC CGY CWA TTY HTT TRA GTT T) primers. Library quality was evaluated using an Agilent 2100 Bioanalyzer (Agilent Technology, USA). Lastly, sequencing was carried out at the next-generation sequencing (NGS) core facility of Kyungpook National University (Daegu, South Korea) and using an Illumina MiSeq platform (Illumina, USA) with single-end 250 bp reads. SRS19386767 SAMN37986915 0C1 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX22336967 0C2 SRP469787 PRJNA1032716 DNeasy PowerSoil Pro Kit (Qiagen, Germany) was used to extract genomic DNA from the soil samples according to the manufacturer's protocol. DNA quality and quantity were measured using a NanoDrop UV-Vis spectrophotometer and a Qubit fluorometer 2.0 (Thermo Fisher Scientific, USA). An NGS library was prepared by amplifying the V4-V5 region of the small subunit ribosomal RNA (16S rRNA) gene for bacteria using 515F (ACA CTC TTT CCC TAC ACG ACG CTC TTC CGA TCT GTG NCA GCB GCC GCG GTR A) and 907R (GTG ACT GGA GTT CAG ACG TGT GCT CTT CCG ATC CGY CWA TTY HTT TRA GTT T) primers. Library quality was evaluated using an Agilent 2100 Bioanalyzer (Agilent Technology, USA). Lastly, sequencing was carried out at the next-generation sequencing (NGS) core facility of Kyungpook National University (Daegu, South Korea) and using an Illumina MiSeq platform (Illumina, USA) with single-end 250 bp reads. SRS19386769 SAMN37986916 0C2 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX22336968 15T2 SRP469787 PRJNA1032716 DNeasy PowerSoil Pro Kit (Qiagen, Germany) was used to extract genomic DNA from the soil samples according to the manufacturer's protocol. DNA quality and quantity were measured using a NanoDrop UV-Vis spectrophotometer and a Qubit fluorometer 2.0 (Thermo Fisher Scientific, USA). An NGS library was prepared by amplifying the V4-V5 region of the small subunit ribosomal RNA (16S rRNA) gene for bacteria using 515F (ACA CTC TTT CCC TAC ACG ACG CTC TTC CGA TCT GTG NCA GCB GCC GCG GTR A) and 907R (GTG ACT GGA GTT CAG ACG TGT GCT CTT CCG ATC CGY CWA TTY HTT TRA GTT T) primers. Library quality was evaluated using an Agilent 2100 Bioanalyzer (Agilent Technology, USA). Lastly, sequencing was carried out at the next-generation sequencing (NGS) core facility of Kyungpook National University (Daegu, South Korea) and using an Illumina MiSeq platform (Illumina, USA) with single-end 250 bp reads. SRS19386768 SAMN37986925 15T2 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX22336969 15T3 SRP469787 PRJNA1032716 DNeasy PowerSoil Pro Kit (Qiagen, Germany) was used to extract genomic DNA from the soil samples according to the manufacturer's protocol. DNA quality and quantity were measured using a NanoDrop UV-Vis spectrophotometer and a Qubit fluorometer 2.0 (Thermo Fisher Scientific, USA). An NGS library was prepared by amplifying the V4-V5 region of the small subunit ribosomal RNA (16S rRNA) gene for bacteria using 515F (ACA CTC TTT CCC TAC ACG ACG CTC TTC CGA TCT GTG NCA GCB GCC GCG GTR A) and 907R (GTG ACT GGA GTT CAG ACG TGT GCT CTT CCG ATC CGY CWA TTY HTT TRA GTT T) primers. Library quality was evaluated using an Agilent 2100 Bioanalyzer (Agilent Technology, USA). Lastly, sequencing was carried out at the next-generation sequencing (NGS) core facility of Kyungpook National University (Daegu, South Korea) and using an Illumina MiSeq platform (Illumina, USA) with single-end 250 bp reads. SRS19386771 SAMN37986926 15T3 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX22336970 30C1 SRP469787 PRJNA1032716 DNeasy PowerSoil Pro Kit (Qiagen, Germany) was used to extract genomic DNA from the soil samples according to the manufacturer's protocol. DNA quality and quantity were measured using a NanoDrop UV-Vis spectrophotometer and a Qubit fluorometer 2.0 (Thermo Fisher Scientific, USA). An NGS library was prepared by amplifying the V4-V5 region of the small subunit ribosomal RNA (16S rRNA) gene for bacteria using 515F (ACA CTC TTT CCC TAC ACG ACG CTC TTC CGA TCT GTG NCA GCB GCC GCG GTR A) and 907R (GTG ACT GGA GTT CAG ACG TGT GCT CTT CCG ATC CGY CWA TTY HTT TRA GTT T) primers. Library quality was evaluated using an Agilent 2100 Bioanalyzer (Agilent Technology, USA). Lastly, sequencing was carried out at the next-generation sequencing (NGS) core facility of Kyungpook National University (Daegu, South Korea) and using an Illumina MiSeq platform (Illumina, USA) with single-end 250 bp reads. SRS19386770 SAMN37986927 30C1 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX22336971 30C2 SRP469787 PRJNA1032716 DNeasy PowerSoil Pro Kit (Qiagen, Germany) was used to extract genomic DNA from the soil samples according to the manufacturer's protocol. DNA quality and quantity were measured using a NanoDrop UV-Vis spectrophotometer and a Qubit fluorometer 2.0 (Thermo Fisher Scientific, USA). An NGS library was prepared by amplifying the V4-V5 region of the small subunit ribosomal RNA (16S rRNA) gene for bacteria using 515F (ACA CTC TTT CCC TAC ACG ACG CTC TTC CGA TCT GTG NCA GCB GCC GCG GTR A) and 907R (GTG ACT GGA GTT CAG ACG TGT GCT CTT CCG ATC CGY CWA TTY HTT TRA GTT T) primers. Library quality was evaluated using an Agilent 2100 Bioanalyzer (Agilent Technology, USA). Lastly, sequencing was carried out at the next-generation sequencing (NGS) core facility of Kyungpook National University (Daegu, South Korea) and using an Illumina MiSeq platform (Illumina, USA) with single-end 250 bp reads. SRS19386772 SAMN37986928 30C2 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX22336972 30C3 SRP469787 PRJNA1032716 DNeasy PowerSoil Pro Kit (Qiagen, Germany) was used to extract genomic DNA from the soil samples according to the manufacturer's protocol. DNA quality and quantity were measured using a NanoDrop UV-Vis spectrophotometer and a Qubit fluorometer 2.0 (Thermo Fisher Scientific, USA). An NGS library was prepared by amplifying the V4-V5 region of the small subunit ribosomal RNA (16S rRNA) gene for bacteria using 515F (ACA CTC TTT CCC TAC ACG ACG CTC TTC CGA TCT GTG NCA GCB GCC GCG GTR A) and 907R (GTG ACT GGA GTT CAG ACG TGT GCT CTT CCG ATC CGY CWA TTY HTT TRA GTT T) primers. Library quality was evaluated using an Agilent 2100 Bioanalyzer (Agilent Technology, USA). Lastly, sequencing was carried out at the next-generation sequencing (NGS) core facility of Kyungpook National University (Daegu, South Korea) and using an Illumina MiSeq platform (Illumina, USA) with single-end 250 bp reads. SRS19386773 SAMN37986929 30C3 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX22336973 30T1 SRP469787 PRJNA1032716 DNeasy PowerSoil Pro Kit (Qiagen, Germany) was used to extract genomic DNA from the soil samples according to the manufacturer's protocol. DNA quality and quantity were measured using a NanoDrop UV-Vis spectrophotometer and a Qubit fluorometer 2.0 (Thermo Fisher Scientific, USA). An NGS library was prepared by amplifying the V4-V5 region of the small subunit ribosomal RNA (16S rRNA) gene for bacteria using 515F (ACA CTC TTT CCC TAC ACG ACG CTC TTC CGA TCT GTG NCA GCB GCC GCG GTR A) and 907R (GTG ACT GGA GTT CAG ACG TGT GCT CTT CCG ATC CGY CWA TTY HTT TRA GTT T) primers. Library quality was evaluated using an Agilent 2100 Bioanalyzer (Agilent Technology, USA). Lastly, sequencing was carried out at the next-generation sequencing (NGS) core facility of Kyungpook National University (Daegu, South Korea) and using an Illumina MiSeq platform (Illumina, USA) with single-end 250 bp reads. SRS19386774 SAMN37986930 30T1 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX22336974 30T2 SRP469787 PRJNA1032716 DNeasy PowerSoil Pro Kit (Qiagen, Germany) was used to extract genomic DNA from the soil samples according to the manufacturer's protocol. DNA quality and quantity were measured using a NanoDrop UV-Vis spectrophotometer and a Qubit fluorometer 2.0 (Thermo Fisher Scientific, USA). An NGS library was prepared by amplifying the V4-V5 region of the small subunit ribosomal RNA (16S rRNA) gene for bacteria using 515F (ACA CTC TTT CCC TAC ACG ACG CTC TTC CGA TCT GTG NCA GCB GCC GCG GTR A) and 907R (GTG ACT GGA GTT CAG ACG TGT GCT CTT CCG ATC CGY CWA TTY HTT TRA GTT T) primers. Library quality was evaluated using an Agilent 2100 Bioanalyzer (Agilent Technology, USA). Lastly, sequencing was carried out at the next-generation sequencing (NGS) core facility of Kyungpook National University (Daegu, South Korea) and using an Illumina MiSeq platform (Illumina, USA) with single-end 250 bp reads. SRS19386775 SAMN37986931 30T2 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX22336975 30T3 SRP469787 PRJNA1032716 DNeasy PowerSoil Pro Kit (Qiagen, Germany) was used to extract genomic DNA from the soil samples according to the manufacturer's protocol. DNA quality and quantity were measured using a NanoDrop UV-Vis spectrophotometer and a Qubit fluorometer 2.0 (Thermo Fisher Scientific, USA). An NGS library was prepared by amplifying the V4-V5 region of the small subunit ribosomal RNA (16S rRNA) gene for bacteria using 515F (ACA CTC TTT CCC TAC ACG ACG CTC TTC CGA TCT GTG NCA GCB GCC GCG GTR A) and 907R (GTG ACT GGA GTT CAG ACG TGT GCT CTT CCG ATC CGY CWA TTY HTT TRA GTT T) primers. Library quality was evaluated using an Agilent 2100 Bioanalyzer (Agilent Technology, USA). Lastly, sequencing was carried out at the next-generation sequencing (NGS) core facility of Kyungpook National University (Daegu, South Korea) and using an Illumina MiSeq platform (Illumina, USA) with single-end 250 bp reads. SRS19386776 SAMN37986932 30T3 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX22336976 0C1F SRP469787 PRJNA1032716 DNeasy PowerSoil Pro Kit (Qiagen, Germany) was used to extract genomic DNA from the soil samples according to the manufacturer's protocol. DNA quality and quantity were measured using a NanoDrop UV-Vis spectrophotometer and a Qubit fluorometer 2.0 (Thermo Fisher Scientific, USA). For the fungal community, the ITS2 region of the ITS nuclear region was amplified using ITS86F (5-ACA CTC TTT CCC TAC ACG ACG CTC TTC CGA TCT GTG AAT CAT CGA ATC TTT GAA-3) and ITS4 (5-GTG ACT GGA GTT CAG ACG TGT GCT CTT CCG ATC TCC TCC GCT TAT TGA TAT GC-3) primers. Library quality was evaluated using an Agilent 2100 Bioanalyzer (Agilent Technology, USA). Lastly, sequencing was carried out at the next-generation sequencing (NGS) core facility of Kyungpook National University (Daegu, South Korea) and using an Illumina MiSeq platform (Illumina, USA) with single-end 250 bp reads. SRS19386778 SAMN37986933 0C1F AMPLICON METAGENOMIC PCR Illumina MiSeq SRX22336977 0C2F SRP469787 PRJNA1032716 DNeasy PowerSoil Pro Kit (Qiagen, Germany) was used to extract genomic DNA from the soil samples according to the manufacturer's protocol. DNA quality and quantity were measured using a NanoDrop UV-Vis spectrophotometer and a Qubit fluorometer 2.0 (Thermo Fisher Scientific, USA). For the fungal community, the ITS2 region of the ITS nuclear region was amplified using ITS86F (5-ACA CTC TTT CCC TAC ACG ACG CTC TTC CGA TCT GTG AAT CAT CGA ATC TTT GAA-3) and ITS4 (5-GTG ACT GGA GTT CAG ACG TGT GCT CTT CCG ATC TCC TCC GCT TAT TGA TAT GC-3) primers. Library quality was evaluated using an Agilent 2100 Bioanalyzer (Agilent Technology, USA). Lastly, sequencing was carried out at the next-generation sequencing (NGS) core facility of Kyungpook National University (Daegu, South Korea) and using an Illumina MiSeq platform (Illumina, USA) with single-end 250 bp reads. SRS19386777 SAMN37986934 0C2F AMPLICON METAGENOMIC PCR Illumina MiSeq SRX22336978 0C3 SRP469787 PRJNA1032716 DNeasy PowerSoil Pro Kit (Qiagen, Germany) was used to extract genomic DNA from the soil samples according to the manufacturer's protocol. DNA quality and quantity were measured using a NanoDrop UV-Vis spectrophotometer and a Qubit fluorometer 2.0 (Thermo Fisher Scientific, USA). An NGS library was prepared by amplifying the V4-V5 region of the small subunit ribosomal RNA (16S rRNA) gene for bacteria using 515F (ACA CTC TTT CCC TAC ACG ACG CTC TTC CGA TCT GTG NCA GCB GCC GCG GTR A) and 907R (GTG ACT GGA GTT CAG ACG TGT GCT CTT CCG ATC CGY CWA TTY HTT TRA GTT T) primers. Library quality was evaluated using an Agilent 2100 Bioanalyzer (Agilent Technology, USA). Lastly, sequencing was carried out at the next-generation sequencing (NGS) core facility of Kyungpook National University (Daegu, South Korea) and using an Illumina MiSeq platform (Illumina, USA) with single-end 250 bp reads. SRS19386779 SAMN37986917 0C3 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX22336979 0C3F SRP469787 PRJNA1032716 DNeasy PowerSoil Pro Kit (Qiagen, Germany) was used to extract genomic DNA from the soil samples according to the manufacturer's protocol. DNA quality and quantity were measured using a NanoDrop UV-Vis spectrophotometer and a Qubit fluorometer 2.0 (Thermo Fisher Scientific, USA). For the fungal community, the ITS2 region of the ITS nuclear region was amplified using ITS86F (5-ACA CTC TTT CCC TAC ACG ACG CTC TTC CGA TCT GTG AAT CAT CGA ATC TTT GAA-3) and ITS4 (5-GTG ACT GGA GTT CAG ACG TGT GCT CTT CCG ATC TCC TCC GCT TAT TGA TAT GC-3) primers. Library quality was evaluated using an Agilent 2100 Bioanalyzer (Agilent Technology, USA). Lastly, sequencing was carried out at the next-generation sequencing (NGS) core facility of Kyungpook National University (Daegu, South Korea) and using an Illumina MiSeq platform (Illumina, USA) with single-end 250 bp reads. SRS19386780 SAMN37986935 0C3F AMPLICON METAGENOMIC PCR Illumina MiSeq SRX22336980 0T1F SRP469787 PRJNA1032716 DNeasy PowerSoil Pro Kit (Qiagen, Germany) was used to extract genomic DNA from the soil samples according to the manufacturer's protocol. DNA quality and quantity were measured using a NanoDrop UV-Vis spectrophotometer and a Qubit fluorometer 2.0 (Thermo Fisher Scientific, USA). For the fungal community, the ITS2 region of the ITS nuclear region was amplified using ITS86F (5-ACA CTC TTT CCC TAC ACG ACG CTC TTC CGA TCT GTG AAT CAT CGA ATC TTT GAA-3) and ITS4 (5-GTG ACT GGA GTT CAG ACG TGT GCT CTT CCG ATC TCC TCC GCT TAT TGA TAT GC-3) primers. Library quality was evaluated using an Agilent 2100 Bioanalyzer (Agilent Technology, USA). Lastly, sequencing was carried out at the next-generation sequencing (NGS) core facility of Kyungpook National University (Daegu, South Korea) and using an Illumina MiSeq platform (Illumina, USA) with single-end 250 bp reads. SRS19386781 SAMN37986936 0T1F AMPLICON METAGENOMIC PCR Illumina MiSeq SRX22336981 0T2F SRP469787 PRJNA1032716 DNeasy PowerSoil Pro Kit (Qiagen, Germany) was used to extract genomic DNA from the soil samples according to the manufacturer's protocol. DNA quality and quantity were measured using a NanoDrop UV-Vis spectrophotometer and a Qubit fluorometer 2.0 (Thermo Fisher Scientific, USA). For the fungal community, the ITS2 region of the ITS nuclear region was amplified using ITS86F (5-ACA CTC TTT CCC TAC ACG ACG CTC TTC CGA TCT GTG AAT CAT CGA ATC TTT GAA-3) and ITS4 (5-GTG ACT GGA GTT CAG ACG TGT GCT CTT CCG ATC TCC TCC GCT TAT TGA TAT GC-3) primers. Library quality was evaluated using an Agilent 2100 Bioanalyzer (Agilent Technology, USA). Lastly, sequencing was carried out at the next-generation sequencing (NGS) core facility of Kyungpook National University (Daegu, South Korea) and using an Illumina MiSeq platform (Illumina, USA) with single-end 250 bp reads. SRS19386782 SAMN37986937 0T2F AMPLICON METAGENOMIC PCR Illumina MiSeq SRX22336982 0T3F SRP469787 PRJNA1032716 DNeasy PowerSoil Pro Kit (Qiagen, Germany) was used to extract genomic DNA from the soil samples according to the manufacturer's protocol. DNA quality and quantity were measured using a NanoDrop UV-Vis spectrophotometer and a Qubit fluorometer 2.0 (Thermo Fisher Scientific, USA). For the fungal community, the ITS2 region of the ITS nuclear region was amplified using ITS86F (5-ACA CTC TTT CCC TAC ACG ACG CTC TTC CGA TCT GTG AAT CAT CGA ATC TTT GAA-3) and ITS4 (5-GTG ACT GGA GTT CAG ACG TGT GCT CTT CCG ATC TCC TCC GCT TAT TGA TAT GC-3) primers. Library quality was evaluated using an Agilent 2100 Bioanalyzer (Agilent Technology, USA). Lastly, sequencing was carried out at the next-generation sequencing (NGS) core facility of Kyungpook National University (Daegu, South Korea) and using an Illumina MiSeq platform (Illumina, USA) with single-end 250 bp reads. SRS19386783 SAMN37986938 0T3F AMPLICON METAGENOMIC PCR Illumina MiSeq SRX22336983 15C1F SRP469787 PRJNA1032716 DNeasy PowerSoil Pro Kit (Qiagen, Germany) was used to extract genomic DNA from the soil samples according to the manufacturer's protocol. DNA quality and quantity were measured using a NanoDrop UV-Vis spectrophotometer and a Qubit fluorometer 2.0 (Thermo Fisher Scientific, USA). For the fungal community, the ITS2 region of the ITS nuclear region was amplified using ITS86F (5-ACA CTC TTT CCC TAC ACG ACG CTC TTC CGA TCT GTG AAT CAT CGA ATC TTT GAA-3) and ITS4 (5-GTG ACT GGA GTT CAG ACG TGT GCT CTT CCG ATC TCC TCC GCT TAT TGA TAT GC-3) primers. Library quality was evaluated using an Agilent 2100 Bioanalyzer (Agilent Technology, USA). Lastly, sequencing was carried out at the next-generation sequencing (NGS) core facility of Kyungpook National University (Daegu, South Korea) and using an Illumina MiSeq platform (Illumina, USA) with single-end 250 bp reads. SRS19386784 SAMN37986939 15C1F AMPLICON METAGENOMIC PCR Illumina MiSeq SRX22336984 15C2F SRP469787 PRJNA1032716 DNeasy PowerSoil Pro Kit (Qiagen, Germany) was used to extract genomic DNA from the soil samples according to the manufacturer's protocol. DNA quality and quantity were measured using a NanoDrop UV-Vis spectrophotometer and a Qubit fluorometer 2.0 (Thermo Fisher Scientific, USA). For the fungal community, the ITS2 region of the ITS nuclear region was amplified using ITS86F (5-ACA CTC TTT CCC TAC ACG ACG CTC TTC CGA TCT GTG AAT CAT CGA ATC TTT GAA-3) and ITS4 (5-GTG ACT GGA GTT CAG ACG TGT GCT CTT CCG ATC TCC TCC GCT TAT TGA TAT GC-3) primers. Library quality was evaluated using an Agilent 2100 Bioanalyzer (Agilent Technology, USA). Lastly, sequencing was carried out at the next-generation sequencing (NGS) core facility of Kyungpook National University (Daegu, South Korea) and using an Illumina MiSeq platform (Illumina, USA) with single-end 250 bp reads. SRS19386785 SAMN37986940 15C2F AMPLICON METAGENOMIC PCR Illumina MiSeq SRX22336985 15C3F SRP469787 PRJNA1032716 DNeasy PowerSoil Pro Kit (Qiagen, Germany) was used to extract genomic DNA from the soil samples according to the manufacturer's protocol. DNA quality and quantity were measured using a NanoDrop UV-Vis spectrophotometer and a Qubit fluorometer 2.0 (Thermo Fisher Scientific, USA). For the fungal community, the ITS2 region of the ITS nuclear region was amplified using ITS86F (5-ACA CTC TTT CCC TAC ACG ACG CTC TTC CGA TCT GTG AAT CAT CGA ATC TTT GAA-3) and ITS4 (5-GTG ACT GGA GTT CAG ACG TGT GCT CTT CCG ATC TCC TCC GCT TAT TGA TAT GC-3) primers. Library quality was evaluated using an Agilent 2100 Bioanalyzer (Agilent Technology, USA). Lastly, sequencing was carried out at the next-generation sequencing (NGS) core facility of Kyungpook National University (Daegu, South Korea) and using an Illumina MiSeq platform (Illumina, USA) with single-end 250 bp reads. SRS19386786 SAMN37986941 15C3F AMPLICON METAGENOMIC PCR Illumina MiSeq SRX22336986 15T1F SRP469787 PRJNA1032716 DNeasy PowerSoil Pro Kit (Qiagen, Germany) was used to extract genomic DNA from the soil samples according to the manufacturer's protocol. DNA quality and quantity were measured using a NanoDrop UV-Vis spectrophotometer and a Qubit fluorometer 2.0 (Thermo Fisher Scientific, USA). For the fungal community, the ITS2 region of the ITS nuclear region was amplified using ITS86F (5-ACA CTC TTT CCC TAC ACG ACG CTC TTC CGA TCT GTG AAT CAT CGA ATC TTT GAA-3) and ITS4 (5-GTG ACT GGA GTT CAG ACG TGT GCT CTT CCG ATC TCC TCC GCT TAT TGA TAT GC-3) primers. Library quality was evaluated using an Agilent 2100 Bioanalyzer (Agilent Technology, USA). Lastly, sequencing was carried out at the next-generation sequencing (NGS) core facility of Kyungpook National University (Daegu, South Korea) and using an Illumina MiSeq platform (Illumina, USA) with single-end 250 bp reads. SRS19386787 SAMN37986942 15T1F AMPLICON METAGENOMIC PCR Illumina MiSeq SRX22336987 15T2F SRP469787 PRJNA1032716 DNeasy PowerSoil Pro Kit (Qiagen, Germany) was used to extract genomic DNA from the soil samples according to the manufacturer's protocol. DNA quality and quantity were measured using a NanoDrop UV-Vis spectrophotometer and a Qubit fluorometer 2.0 (Thermo Fisher Scientific, USA). For the fungal community, the ITS2 region of the ITS nuclear region was amplified using ITS86F (5-ACA CTC TTT CCC TAC ACG ACG CTC TTC CGA TCT GTG AAT CAT CGA ATC TTT GAA-3) and ITS4 (5-GTG ACT GGA GTT CAG ACG TGT GCT CTT CCG ATC TCC TCC GCT TAT TGA TAT GC-3) primers. Library quality was evaluated using an Agilent 2100 Bioanalyzer (Agilent Technology, USA). Lastly, sequencing was carried out at the next-generation sequencing (NGS) core facility of Kyungpook National University (Daegu, South Korea) and using an Illumina MiSeq platform (Illumina, USA) with single-end 250 bp reads. SRS19386788 SAMN37986943 15T2F AMPLICON METAGENOMIC PCR Illumina MiSeq SRX22336988 15T3F SRP469787 PRJNA1032716 DNeasy PowerSoil Pro Kit (Qiagen, Germany) was used to extract genomic DNA from the soil samples according to the manufacturer's protocol. DNA quality and quantity were measured using a NanoDrop UV-Vis spectrophotometer and a Qubit fluorometer 2.0 (Thermo Fisher Scientific, USA). For the fungal community, the ITS2 region of the ITS nuclear region was amplified using ITS86F (5-ACA CTC TTT CCC TAC ACG ACG CTC TTC CGA TCT GTG AAT CAT CGA ATC TTT GAA-3) and ITS4 (5-GTG ACT GGA GTT CAG ACG TGT GCT CTT CCG ATC TCC TCC GCT TAT TGA TAT GC-3) primers. Library quality was evaluated using an Agilent 2100 Bioanalyzer (Agilent Technology, USA). Lastly, sequencing was carried out at the next-generation sequencing (NGS) core facility of Kyungpook National University (Daegu, South Korea) and using an Illumina MiSeq platform (Illumina, USA) with single-end 250 bp reads. SRS19386789 SAMN37986944 15T3F AMPLICON METAGENOMIC PCR Illumina MiSeq SRX22336989 0T1 SRP469787 PRJNA1032716 DNeasy PowerSoil Pro Kit (Qiagen, Germany) was used to extract genomic DNA from the soil samples according to the manufacturer's protocol. DNA quality and quantity were measured using a NanoDrop UV-Vis spectrophotometer and a Qubit fluorometer 2.0 (Thermo Fisher Scientific, USA). An NGS library was prepared by amplifying the V4-V5 region of the small subunit ribosomal RNA (16S rRNA) gene for bacteria using 515F (ACA CTC TTT CCC TAC ACG ACG CTC TTC CGA TCT GTG NCA GCB GCC GCG GTR A) and 907R (GTG ACT GGA GTT CAG ACG TGT GCT CTT CCG ATC CGY CWA TTY HTT TRA GTT T) primers. Library quality was evaluated using an Agilent 2100 Bioanalyzer (Agilent Technology, USA). Lastly, sequencing was carried out at the next-generation sequencing (NGS) core facility of Kyungpook National University (Daegu, South Korea) and using an Illumina MiSeq platform (Illumina, USA) with single-end 250 bp reads. SRS19386790 SAMN37986918 0T1 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX22336990 30C1F SRP469787 PRJNA1032716 DNeasy PowerSoil Pro Kit (Qiagen, Germany) was used to extract genomic DNA from the soil samples according to the manufacturer's protocol. DNA quality and quantity were measured using a NanoDrop UV-Vis spectrophotometer and a Qubit fluorometer 2.0 (Thermo Fisher Scientific, USA). For the fungal community, the ITS2 region of the ITS nuclear region was amplified using ITS86F (5-ACA CTC TTT CCC TAC ACG ACG CTC TTC CGA TCT GTG AAT CAT CGA ATC TTT GAA-3) and ITS4 (5-GTG ACT GGA GTT CAG ACG TGT GCT CTT CCG ATC TCC TCC GCT TAT TGA TAT GC-3) primers. Library quality was evaluated using an Agilent 2100 Bioanalyzer (Agilent Technology, USA). Lastly, sequencing was carried out at the next-generation sequencing (NGS) core facility of Kyungpook National University (Daegu, South Korea) and using an Illumina MiSeq platform (Illumina, USA) with single-end 250 bp reads. SRS19386791 SAMN37986945 30C1F AMPLICON METAGENOMIC PCR Illumina MiSeq SRX22336991 30C2F SRP469787 PRJNA1032716 DNeasy PowerSoil Pro Kit (Qiagen, Germany) was used to extract genomic DNA from the soil samples according to the manufacturer's protocol. DNA quality and quantity were measured using a NanoDrop UV-Vis spectrophotometer and a Qubit fluorometer 2.0 (Thermo Fisher Scientific, USA). For the fungal community, the ITS2 region of the ITS nuclear region was amplified using ITS86F (5-ACA CTC TTT CCC TAC ACG ACG CTC TTC CGA TCT GTG AAT CAT CGA ATC TTT GAA-3) and ITS4 (5-GTG ACT GGA GTT CAG ACG TGT GCT CTT CCG ATC TCC TCC GCT TAT TGA TAT GC-3) primers. Library quality was evaluated using an Agilent 2100 Bioanalyzer (Agilent Technology, USA). Lastly, sequencing was carried out at the next-generation sequencing (NGS) core facility of Kyungpook National University (Daegu, South Korea) and using an Illumina MiSeq platform (Illumina, USA) with single-end 250 bp reads. SRS19386792 SAMN37986946 30C2F AMPLICON METAGENOMIC PCR Illumina MiSeq SRX22336992 30C3F SRP469787 PRJNA1032716 DNeasy PowerSoil Pro Kit (Qiagen, Germany) was used to extract genomic DNA from the soil samples according to the manufacturer's protocol. DNA quality and quantity were measured using a NanoDrop UV-Vis spectrophotometer and a Qubit fluorometer 2.0 (Thermo Fisher Scientific, USA). For the fungal community, the ITS2 region of the ITS nuclear region was amplified using ITS86F (5-ACA CTC TTT CCC TAC ACG ACG CTC TTC CGA TCT GTG AAT CAT CGA ATC TTT GAA-3) and ITS4 (5-GTG ACT GGA GTT CAG ACG TGT GCT CTT CCG ATC TCC TCC GCT TAT TGA TAT GC-3) primers. Library quality was evaluated using an Agilent 2100 Bioanalyzer (Agilent Technology, USA). Lastly, sequencing was carried out at the next-generation sequencing (NGS) core facility of Kyungpook National University (Daegu, South Korea) and using an Illumina MiSeq platform (Illumina, USA) with single-end 250 bp reads. SRS19386793 SAMN37986947 30C3F AMPLICON METAGENOMIC PCR Illumina MiSeq SRX22336993 30T1F SRP469787 PRJNA1032716 DNeasy PowerSoil Pro Kit (Qiagen, Germany) was used to extract genomic DNA from the soil samples according to the manufacturer's protocol. DNA quality and quantity were measured using a NanoDrop UV-Vis spectrophotometer and a Qubit fluorometer 2.0 (Thermo Fisher Scientific, USA). For the fungal community, the ITS2 region of the ITS nuclear region was amplified using ITS86F (5-ACA CTC TTT CCC TAC ACG ACG CTC TTC CGA TCT GTG AAT CAT CGA ATC TTT GAA-3) and ITS4 (5-GTG ACT GGA GTT CAG ACG TGT GCT CTT CCG ATC TCC TCC GCT TAT TGA TAT GC-3) primers. Library quality was evaluated using an Agilent 2100 Bioanalyzer (Agilent Technology, USA). Lastly, sequencing was carried out at the next-generation sequencing (NGS) core facility of Kyungpook National University (Daegu, South Korea) and using an Illumina MiSeq platform (Illumina, USA) with single-end 250 bp reads. SRS19386794 SAMN37986948 30T1F AMPLICON METAGENOMIC PCR Illumina MiSeq SRX22336994 30T2F SRP469787 PRJNA1032716 DNeasy PowerSoil Pro Kit (Qiagen, Germany) was used to extract genomic DNA from the soil samples according to the manufacturer's protocol. DNA quality and quantity were measured using a NanoDrop UV-Vis spectrophotometer and a Qubit fluorometer 2.0 (Thermo Fisher Scientific, USA). For the fungal community, the ITS2 region of the ITS nuclear region was amplified using ITS86F (5-ACA CTC TTT CCC TAC ACG ACG CTC TTC CGA TCT GTG AAT CAT CGA ATC TTT GAA-3) and ITS4 (5-GTG ACT GGA GTT CAG ACG TGT GCT CTT CCG ATC TCC TCC GCT TAT TGA TAT GC-3) primers. Library quality was evaluated using an Agilent 2100 Bioanalyzer (Agilent Technology, USA). Lastly, sequencing was carried out at the next-generation sequencing (NGS) core facility of Kyungpook National University (Daegu, South Korea) and using an Illumina MiSeq platform (Illumina, USA) with single-end 250 bp reads. SRS19386795 SAMN37986949 30T2F AMPLICON METAGENOMIC PCR Illumina MiSeq SRX22336995 30T3F SRP469787 PRJNA1032716 DNeasy PowerSoil Pro Kit (Qiagen, Germany) was used to extract genomic DNA from the soil samples according to the manufacturer's protocol. DNA quality and quantity were measured using a NanoDrop UV-Vis spectrophotometer and a Qubit fluorometer 2.0 (Thermo Fisher Scientific, USA). For the fungal community, the ITS2 region of the ITS nuclear region was amplified using ITS86F (5-ACA CTC TTT CCC TAC ACG ACG CTC TTC CGA TCT GTG AAT CAT CGA ATC TTT GAA-3) and ITS4 (5-GTG ACT GGA GTT CAG ACG TGT GCT CTT CCG ATC TCC TCC GCT TAT TGA TAT GC-3) primers. Library quality was evaluated using an Agilent 2100 Bioanalyzer (Agilent Technology, USA). Lastly, sequencing was carried out at the next-generation sequencing (NGS) core facility of Kyungpook National University (Daegu, South Korea) and using an Illumina MiSeq platform (Illumina, USA) with single-end 250 bp reads. SRS19386796 SAMN37986950 30T3F AMPLICON METAGENOMIC PCR Illumina MiSeq SRX22336996 0T2 SRP469787 PRJNA1032716 DNeasy PowerSoil Pro Kit (Qiagen, Germany) was used to extract genomic DNA from the soil samples according to the manufacturer's protocol. DNA quality and quantity were measured using a NanoDrop UV-Vis spectrophotometer and a Qubit fluorometer 2.0 (Thermo Fisher Scientific, USA). An NGS library was prepared by amplifying the V4-V5 region of the small subunit ribosomal RNA (16S rRNA) gene for bacteria using 515F (ACA CTC TTT CCC TAC ACG ACG CTC TTC CGA TCT GTG NCA GCB GCC GCG GTR A) and 907R (GTG ACT GGA GTT CAG ACG TGT GCT CTT CCG ATC CGY CWA TTY HTT TRA GTT T) primers. Library quality was evaluated using an Agilent 2100 Bioanalyzer (Agilent Technology, USA). Lastly, sequencing was carried out at the next-generation sequencing (NGS) core facility of Kyungpook National University (Daegu, South Korea) and using an Illumina MiSeq platform (Illumina, USA) with single-end 250 bp reads. SRS19386797 SAMN37986919 0T2 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX22336997 0T3 SRP469787 PRJNA1032716 DNeasy PowerSoil Pro Kit (Qiagen, Germany) was used to extract genomic DNA from the soil samples according to the manufacturer's protocol. DNA quality and quantity were measured using a NanoDrop UV-Vis spectrophotometer and a Qubit fluorometer 2.0 (Thermo Fisher Scientific, USA). An NGS library was prepared by amplifying the V4-V5 region of the small subunit ribosomal RNA (16S rRNA) gene for bacteria using 515F (ACA CTC TTT CCC TAC ACG ACG CTC TTC CGA TCT GTG NCA GCB GCC GCG GTR A) and 907R (GTG ACT GGA GTT CAG ACG TGT GCT CTT CCG ATC CGY CWA TTY HTT TRA GTT T) primers. Library quality was evaluated using an Agilent 2100 Bioanalyzer (Agilent Technology, USA). Lastly, sequencing was carried out at the next-generation sequencing (NGS) core facility of Kyungpook National University (Daegu, South Korea) and using an Illumina MiSeq platform (Illumina, USA) with single-end 250 bp reads. SRS19386798 SAMN37986920 0T3 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX22336998 15C1 SRP469787 PRJNA1032716 DNeasy PowerSoil Pro Kit (Qiagen, Germany) was used to extract genomic DNA from the soil samples according to the manufacturer's protocol. DNA quality and quantity were measured using a NanoDrop UV-Vis spectrophotometer and a Qubit fluorometer 2.0 (Thermo Fisher Scientific, USA). An NGS library was prepared by amplifying the V4-V5 region of the small subunit ribosomal RNA (16S rRNA) gene for bacteria using 515F (ACA CTC TTT CCC TAC ACG ACG CTC TTC CGA TCT GTG NCA GCB GCC GCG GTR A) and 907R (GTG ACT GGA GTT CAG ACG TGT GCT CTT CCG ATC CGY CWA TTY HTT TRA GTT T) primers. Library quality was evaluated using an Agilent 2100 Bioanalyzer (Agilent Technology, USA). Lastly, sequencing was carried out at the next-generation sequencing (NGS) core facility of Kyungpook National University (Daegu, South Korea) and using an Illumina MiSeq platform (Illumina, USA) with single-end 250 bp reads. SRS19386799 SAMN37986921 15C1 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX22336999 15C2 SRP469787 PRJNA1032716 DNeasy PowerSoil Pro Kit (Qiagen, Germany) was used to extract genomic DNA from the soil samples according to the manufacturer's protocol. DNA quality and quantity were measured using a NanoDrop UV-Vis spectrophotometer and a Qubit fluorometer 2.0 (Thermo Fisher Scientific, USA). An NGS library was prepared by amplifying the V4-V5 region of the small subunit ribosomal RNA (16S rRNA) gene for bacteria using 515F (ACA CTC TTT CCC TAC ACG ACG CTC TTC CGA TCT GTG NCA GCB GCC GCG GTR A) and 907R (GTG ACT GGA GTT CAG ACG TGT GCT CTT CCG ATC CGY CWA TTY HTT TRA GTT T) primers. Library quality was evaluated using an Agilent 2100 Bioanalyzer (Agilent Technology, USA). Lastly, sequencing was carried out at the next-generation sequencing (NGS) core facility of Kyungpook National University (Daegu, South Korea) and using an Illumina MiSeq platform (Illumina, USA) with single-end 250 bp reads. SRS19386800 SAMN37986922 15C2 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX22337000 15C3 SRP469787 PRJNA1032716 DNeasy PowerSoil Pro Kit (Qiagen, Germany) was used to extract genomic DNA from the soil samples according to the manufacturer's protocol. DNA quality and quantity were measured using a NanoDrop UV-Vis spectrophotometer and a Qubit fluorometer 2.0 (Thermo Fisher Scientific, USA). An NGS library was prepared by amplifying the V4-V5 region of the small subunit ribosomal RNA (16S rRNA) gene for bacteria using 515F (ACA CTC TTT CCC TAC ACG ACG CTC TTC CGA TCT GTG NCA GCB GCC GCG GTR A) and 907R (GTG ACT GGA GTT CAG ACG TGT GCT CTT CCG ATC CGY CWA TTY HTT TRA GTT T) primers. Library quality was evaluated using an Agilent 2100 Bioanalyzer (Agilent Technology, USA). Lastly, sequencing was carried out at the next-generation sequencing (NGS) core facility of Kyungpook National University (Daegu, South Korea) and using an Illumina MiSeq platform (Illumina, USA) with single-end 250 bp reads. SRS19386801 SAMN37986923 15C3 AMPLICON METAGENOMIC PCR Illumina MiSeq SRX22337001 15T1 SRP469787 PRJNA1032716 DNeasy PowerSoil Pro Kit (Qiagen, Germany) was used to extract genomic DNA from the soil samples according to the manufacturer's protocol. DNA quality and quantity were measured using a NanoDrop UV-Vis spectrophotometer and a Qubit fluorometer 2.0 (Thermo Fisher Scientific, USA). An NGS library was prepared by amplifying the V4-V5 region of the small subunit ribosomal RNA (16S rRNA) gene for bacteria using 515F (ACA CTC TTT CCC TAC ACG ACG CTC TTC CGA TCT GTG NCA GCB GCC GCG GTR A) and 907R (GTG ACT GGA GTT CAG ACG TGT GCT CTT CCG ATC CGY CWA TTY HTT TRA GTT T) primers. Library quality was evaluated using an Agilent 2100 Bioanalyzer (Agilent Technology, USA). Lastly, sequencing was carried out at the next-generation sequencing (NGS) core facility of Kyungpook National University (Daegu, South Korea) and using an Illumina MiSeq platform (Illumina, USA) with single-end 250 bp reads. SRS19386802 SAMN37986924 15T1 AMPLICON METAGENOMIC PCR Illumina MiSeq