Abstract
In this study, a direct detection system for triazine derivative herbicides was developed using the photosynthetic reaction center (RC) from the purple bacterium,Rhodobacter sphaeroides, and surface plasmon resonance (SPR) apparatus. The histidine-tagged RCs were immobilized on an SPR gold chip using nickel-nitrilotriacetic acid groups as a binder for one of the triazine herbicide, atrazine. The SPR responses were proportional to the sample concentrations of atrazine in the range 0.1–1 μg/mL. The sensitivity of the direct detection of atrazine using the RC-assembled sensor chip was higher than that using the antibody-immobilized chip. The other types of herbicides, DCMU or MCPP, were not detected with such high sensitivity. The results indicated the high binding selectivity of the RC complex.
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Abbreviations
- DCMU:
-
N'-(3,4-Dichlorophenyl)-N,N-dimethylurea
- ELISA:
-
Enzyme-linked immunosorbent assay
- HHisRC:
-
Heavy-subunit-histidine-tagged RC
- IgG:
-
Immunoglobulin G
- MCPP:
-
2-(2-Methyl-4-chlorophenoxy) propionic acid
- Ni-NTA:
-
Nickel-nitrilotriacetic acid
- PSII:
-
Photosystem II
- QB :
-
Secondary quinone of PSII or RC
- RC:
-
Photosynthetic reaction center
- SPR:
-
Surface plasmon resonance
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Nakamura, C., Hasegawa, M., Shimada, K. et al. Direct triazine herbicide detection using a self-assembled photosynthetic reaction center from purple bacterium. Biotechnol. Bioprocess Eng. 5, 413–417 (2000). https://doi.org/10.1007/BF02931940
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DOI: https://doi.org/10.1007/BF02931940