Development of a bioluminescent cyanobacterial reporter strain for detection of arsenite, arsenate and antimonite

Loredana Peca1,2, Csaba Istvan Nagy1,3, Attila Ordog4, Imre Vass1, P ter Balazs Kos1,5

1 Institute of Plant Biology, Biological Research Center of the Hungarian Academy of Sciences, Temesv ri krt 62., H-6726 Szeged, Hungary
2 National Institute of Research and Development for Biological Sciences, Institute of Biological Research Cluj-Napoca, 400015 Romania
3 Molecular Plant Biology, Department of Biochemistry, University of Turku, 20014 Turun Yliopisto, Finland
4 Department of Plant Biology, Faculty of Science and Informatics, Unversity of Szeged, K z p fasor 52., H-6726 Szeged, Hungary
5 Department Biotechnology, Faculty of Science and Informatics,Unversity of Szeged, K z p fasor 52., H-6726 Szeged, Hungary

Abstract


In the present study the potential of a gene fusion between the arsB promoter from Synechocystis 6803 and the bacterial luxAB genes was evaluated to be used as a cyanobacterial bioreporter for monitoring the bioavailability of inorganic arsenic species. A whole-cell bioreporter strain, designated arsLux, was constructed based on this fusion. In concert with the specificity of the promoter presented earlier, luminescent signal could be detected upon exposure to arsenite, arsenate and antimonite, in a concentration-dependent manner, following an incubation period of 14 hours. The detection range of arsLux was 4 M to 1 mM for As(III) and Sb(III), and 150 M to 150 mM for As(V). However, arsLux activity was inhibited by Cu2+ and Zn2+ with a half maximal inhibitory concentration (IC50) of about 8 M and 16 M, respectively. The bioreporter performance was tested using water samples from a thermal spring and from the River Tisza, both of them supplemented with arsenite. In the first case the bioluminescent signal was comparable with the signal of the standard solution, whereas in the second case the signal was much lower, presumably due to inhibitors present in the river water. Our data show the arsB promoter has the potential for whole cell bioreporter applications with some further improvements that are also discussed.

Keywords


antimony; arsenic; bioluminescent bioreporter; cyanobacteria; Synechocystis PCC 6803

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