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Bound detergent molecules in bacterial reaction centers facilitate detection of tetryl explosive.

Author(s): Modafferi D, Zazubovich V, Kálmán L

Photosynth Res. 2020 Jul 06;: Authors: Modafferi D, Zazubovich V, Kálmán L

Article GUID: 32632533
Comparison of bacterial reaction centers and photosystem II.

Author(s): Kálmán L, Williams JC, Allen JP

Photosynth Res. 2008 Oct-Dec;98(1-3):643-55 Authors: Kálmán L, Williams JC, Allen JP

Article GUID: 18853275
A simple and efficient method to prepare pure dimers and monomers of the cytochrome b 6 f complex from spinach.

Author(s): Luján MA, Lorente P, Zazubovich V, Picorel R

Photosynth Res. 2017 Jun;132(3):305-309 Authors: Luján MA, Lorente P, Zazubovich V, Picorel R

Article GUID: 28374305
Title:Bound detergent molecules in bacterial reaction centers facilitate detection of tetryl explosive.
Authors:Modafferi D,  Zazubovich V,  Kálmán L
Link:https://www.ncbi.nlm.nih.gov/pubmed/32632533?dopt=Abstract
DOI:10.1007/s11120-020-00770-7
Category:Photosynth Res
PMID:32632533
Dept Affiliation: PHYSICS
1 Department of Physics, Concordia University, 7141 Sherbrooke Street West, Montreal, QC, H4B 1R6, Canada.
2 Department of Chemical Engineering, McGill University, Montreal, QC, Canada.
3 Department of Physics, Concordia University, 7141 Sherbrooke Street West, Montreal, QC, H4B 1R6, Canada. valter.zazubovits@concordia.ca.
4 Department of Physics, Concordia University, 7141 Sherbrooke Street West, Montreal, QC, H4B 1R6, Canada. laszlo.kalman@concordia.ca.

Description:

Bound detergent molecules in bacterial reaction centers facilitate detection of tetryl explosive.

Photosynth Res. 2020 Jul 06;:

Authors: Modafferi D, Zazubovich V, Kálmán L

Abstract

Bacterial reaction centers (BRC) from Rhodobacter sphaeroides were found to accelerate, about 100-fold, the reaction between tetryl (2,4,6-trinitrophenylmethylnitramine) explosive and n-lauryl-N-N-dimethylamine-N-oxide (LDAO) that results in the formation of picric acid-like product with characteristic UV-VIS absorption spectrum with peaks at 345 and 415 nm. Moreover, this product also affects the spectra of BRC cofactors in the NIR spectral region and stabilizes the conformational changes associated with slow charge recombination. The evolution of the NIR absorption changes correlated with the kinetics of the product formation. Comparison between the wild-type and the R26 carotenoid-less strain indicates that tetryl-LDAO reaction is roughly five times faster for R26, which allows for identifying the carotenoid binding site as the optimal reaction site. Another, less-defined reaction site is located in the BRC's hydrophobic cavity. These effects are highly selective for tetryl and not observed for several other widespread nitric explosives; slowed-down charge recombination allows for distinguishing between tetryl and QB-site herbicides. The current limit of detection is in the ppb range or?~?100 nM. Details of the molecular mechanisms of the reactions and perspectives of using these effects in bioassays or biosensors for explosives detection are also discussed.

PMID: 32632533 [PubMed - as supplied by publisher]