“…A semi-nested PCR protocol was used to amplify the %630 bp-long small subunit (SSU) region of the AMF 18S rDNA via pyrosequencing analysis (454 GS-FLX, Roche). In the first PCR run (PCRI) a Glomeromycota-specific region was amplified with the primer set GLOMERWT0/GLOMER1536 (Wubet et al, 2006), followed by the semi-nested second PCR reaction with the forward general fungal primer NS31 (Simon et al, 1992) including the A adaptor and a 10 bp multiplex identifier (1 of 60 different MIDs), and the B adaptor including the reverse modified AMF primer AM1a and AM1b (Morris et al, 2013). The first PCR was carried out at a 25 μl reaction volume with 0.5 μl of diluted DNA template (5-20 ng μl −1 ), 12.5 μl GoTaq Green Mastermix 2× (Promega, Mannheim, Germany), 1 μl of each primer (25 μM) on an Eppendorf Mastercycler DNA Engine Thermal Cycler PCR (Eppendorf, Hamburg, Germany) with the following PCR conditions: 98 C for 30 s, 5 cycles of 94 C for 30 s, 60 C (−1 C/cycle, 4 cycles) for 30 s, 72 C for 1 min and 25 cycles of 94 C for 30 s, 55 C for 30 s, 72 C for 1 min, and for extension 72 C for 5 min.…”