The Office for Harmonization in the Internal Market (OHIM) has issued ArcticZymes AS with Community Trade Marks for its name “ArcticZymes” in Europe. The protection covers most European countries and will help ArcticZymes distinguish their products from other companies with similar marks.
Last week a poster was presented at the Human Identification Solution conference in Madrid by our collaborators from the Forensic group at The Arctic University of Norway.
On Thursday 29 January, Norway’s most popular science TV show, “Schrödingers katt” on NRK, made a story on how enzymes from ArcticZymes can improve DNA analysis as part of the criminal investigation of rape cases.
Through interviews with Marthe Aune, bioengineer at the Center for Legal Genetics (Rettsgenetisk senter) in Tromsø, the story explains how enzymes from arctic shrimps can be used to remove the DNA in a DNA test from a rape victim, without damaging the sperm cell DNA from the rapist.
As the story points out, enzymes from ArcticZymes make such DNA analysis easier and more evident with regards to a reliable output. More evident DNA profiles will strengthen criminal investigations and evidences in rape cases.
As a student at the Arctic University of Norway, Marthe Aune has previously headed a research project in cooperation with ArcticZymes on arctic enzymes and DNA in legal genetic analysis.
We have just published our poster for “Reducing DNA content during protein purification with an easily removable nuclease” to the website. This poster was presented at PepTalk, January 19-23 2015 in San Diego, USA. Below you can read the introduction:
When purifying DNA-modifying enzymes, an essentially DNA-free product is desirable as endogenous DNA from production may contaminate down-stream applications.
While nuclease treatment of the crude cell-lysate is a common step during protein purification, its primary function is viscosity reduction for easier sample handling rather than complete DNA removal. More efficient enzymatic DNA removal could be achieved if applied to a partially purified protein sample, such as the His-trap eluate, where the majority of impurities have been removed and the volume is reduced; however the salt concentrations used in elution protocols are incompatible with the salinity optima of most commercially available nucleases. Furthermore, treatment of semi-pure protein may cause residual nuclease contamination in the purified protein which will interfere with
nucleic-acid based applications.
ArcticZymes has developed a Heat-Labile Salt Active Nuclease (HL-SAN) that is compatible with treatment of eluates: it is active at up to 1M NaCl, tolerates imidazole and can be separated from most proteins by cation exchange or inactivated by reducing agents. Here we present efficient DNA removal from recombinantly-produced T4 DNA ligase by direct treatment of the His-trap eluate with HL-SAN, and demonstrate that the final, active T4 ligase is free of contaminating HL-SAN activity.