Affiliation:
1. Laboratory of Bioluminescent Biotechnologies, Department of Biophysics, Institute of Fundamental Biology and Biotechnology Siberian Federal University 79 Svobodny Prospect Krasnoyarsk Russia
2. Department of Biomedical Science, Acharya Narendra Dev College University of Delhi, Govindpuri, Kalkaji New Delhi India
3. Institute of Biophysics SB RAS Federal Research Center ‘Krasnoyarsk Science Center SB RAS’ Akademgorodok 50/50 Krasnoyarsk Russia
Abstract
AbstractBioluminescent bacteria in the form of a cell suspension for on‐site hazard analysis are not suitable as in vivo luminescence in free cells fluctuates and may lead to erroneous results. Furthermore, the culture broth cannot be stored for long durations to continue sensing analytes as the luminescence ceases over time. Factors that affect luminescence response include growth dynamism, and ambient environmental conditions. The present study investigated the effect of storage conditions such as temperature (25 ± 2°C, room temperature; 4°C; and −20°C) and ambient aqueous environment (M1: sucrose, 1.02 M; M2, bioluminescent media [tryptone, 10 g L−1; NaCl, 28.5 g L−1; MgCl2.7H2O, 4.5 g L−1; CaCl2, 0.5 g L−1; KCl 0.5 g L−1; yeast extract, 1 g L−1; H2O, 1 L]; M3, bioluminescent media and 95% glycerol, 1:1 ratio) on the luminescence emission from the calcium alginate‐immobilized Photobacterium phosphoreum (Sb) against the cells in free suspension for an extended period. The results indicated that both the parameters that were undertaken markedly affected the luminescence. In the study, Sb showed an enhanced luminescence emission than the control up to 18.5‐fold and for a prolonged period which can be efficiently utilized for rapid biosensing of hazardous materials.
Subject
Chemistry (miscellaneous),Biophysics