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Purification of Histidine-Tagged T4 RNA Ligase from E. coli
Author(s) -
Qing S. Wang,
Peter J. Unrau
Publication year - 2002
Publication title -
biotechniques
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.617
H-Index - 131
eISSN - 1940-9818
pISSN - 0736-6205
DOI - 10.2144/02336st03
Subject(s) - rna ligase , dna ligase , rna , biology , escherichia coli , histidine , genetics , biochemistry , computational biology , microbiology and biotechnology , chemistry , dna , enzyme , gene
Here we report the construction of a histidine-tagged T4 RNA ligase expression plasmid (pRHT4). The construct, when overexpressed in BL21 (DE3) cells, allows the preparation of large quantities of T4 RNA ligase in high purity using only a single purification column. The histidine affinity tag does not inhibit enzyme function, and we were able to purify 1-3 mg pure protein/g cell pellet. A simple purification procedure ensures that the enzyme is de-adenylated to levels comparable to those found for many commercial preparations. The purified protein has very low levels of RNase contamination and functioned normally in a variety of activity assays.

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