Mekuto Lukhanyo, Ntwampe Seteno K O, Mudumbi John B N, Akinpelu Enoch A, Mewa-Ngongang Maxwell
Bioresource Engineering Research Group (BioERG), Department of Biotechnology, Cape Peninsula University of Technology, P.O. Box 652, Cape Town, 8000 South Africa.
Data Brief. 2017 Jul 4;13:738-741. doi: 10.1016/j.dib.2017.06.049. eCollection 2017 Aug.
The data presented in this article contains the bacterial community structure of the free cyanide (CN) and thiocyanate (SCN) degrading organisms that were isolated from electroplating wastewater and synthetic SCN containing wastewater. PCR amplification of the 16S rRNA V1-V3 regions was undertaken using the 27F and 518R oligonucleotide primers following the metacommunity DNA extraction procedure. The PCR amplicons were processed using the illumina® reaction kits as per manufacturer׳s instruction and sequenced using the illumina® MiSeq-2000, using the MiSeq V3 kit. The data was processed using bioinformatics tools such as QIIME and the raw sequence files are available via NCBI׳s Sequence Read Archive (SRA) database.
本文所呈现的数据包含从电镀废水和含硫氰酸盐的合成废水中分离出的游离氰化物(CN)和硫氰酸盐(SCN)降解微生物的细菌群落结构。在进行宏群落DNA提取后,使用27F和518R寡核苷酸引物对16S rRNA V1 - V3区域进行PCR扩增。PCR扩增产物按照制造商的说明使用illumina®反应试剂盒进行处理,并使用MiSeq V3试剂盒在illumina® MiSeq - 2000上进行测序。数据使用QIIME等生物信息学工具进行处理,原始序列文件可通过NCBI的序列读取存档(SRA)数据库获取。