“…Total community DNA of the collected hot spring sediments were extracted with FastDNA Spin Kit according to the manufacturer’s instructions (MP Biomedicals, LLC, Solon, OH). Bacterial and Archaeal 16S rRNA genes were amplified with a universal primer set of 515F (5′GTGYCAGCMGCCGCGGTA-3′)/806R (5′-GGACTACVSGGGTATCTAAT-3′) according to the PCR conditions described previously ( Tamaki et al, 2011 ; Caporaso et al, 2012 ; Zhang et al, 2018 ). The hydA genes of the total community DNA in the collected hot spring sediments were PCR amplified using the primer set FeFe-272F (5′-GCHGAYMTBACHATWATGGARGA-3′, where H = A, C, T; Y = C, T; M = A, C; B = C, G, T; W = A, T; R = A, G; 432-fold degeneracy)/FeFe-427R (5′-GCNGCYTCCATDACDCCDCCNGT-3′, where N = A, C, T, G; Y = C, T; D = A, G, T; 864-fold degeneracy) ( Boyd et al, 2010 ; Sahl et al, 2011 ; Baba et al, 2014 ).…”