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Biochemical properties of Bacillus Calmette Guerin ribonuclease III
Author(s) -
Yang Lei,
Wang YanLi,
Dai JinChuan,
Liu Min,
Li Xin,
Tang Hua
Publication year - 2016
Publication title -
journal of basic microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.58
H-Index - 54
eISSN - 1521-4028
pISSN - 0233-111X
DOI - 10.1002/jobm.201500360
Subject(s) - rna , rnase p , ribonuclease , microbiology and biotechnology , ribonuclease iii , rna silencing , rnase h , cleavage (geology) , biology , ribosomal rna , biochemistry , chemistry , gene , rna interference , paleontology , fracture (geology)
Double‐stranded RNA (dsRNA) is discovered to participate in the regulation of gene expression in both bacterial and eukaryotic cells. Members of ribonuclease III (RNase III) family recognize RNA motifs and cleave substrates at specific sites in a divalent‐metal‐ion‐dependent manner. In this study, we find the RNase III from Bacillus Calmette Guerin (BCG‐RNase III) cleaves small hairpin RNA based on the conserved stem structure associated with Mycobacterium 16S ribosomal RNA precursor at specific sites which are not determined. To evaluate the influence of remnant endogenous ribonucleases from expression host on RNA cleavage assays for RNase III, we use E44A and D48A mutant of the enzyme to perform RNA cleavage assays and find that remnant ribonucleases have no effect on cleavage assays. The RNA cleavage activity of the enzyme can be supported by Mg 2+ , Mn 2+ , and Co 2+ and enhanced with the increasing salt concentration. The catalytic activity of the enzyme is exhibited when the temperature of the reaction buffer ranges from 30 to 55 °C and the pH of the buffer from 7.0 to 10.0. Two major cleavage sites in RNA substrate are identified using RNA Ligase Mediated Rapid Amplification of cDNA Ends (RLM‐RACE).