|
|
|
|
|
|
2D Fluorescence Spectra Measurement of 6 Kinds of Bioagents Simulants by Short-Range Lidar |
YANG Hui1, MA Xiu-bing2, SUN Yan-fei1, WANG Tie-dong1, QING Feng1, ZHAO Xue-song3 |
1. PLA Amy Academy Artillery and Air Defence, Hefei 230031, China
2. School of Life Sciences, Anhui Agricultural University, Hefei 230031, China
3. Anhui Institute of Optics and Fine Mechanics, Chinese Academy of Sciences, Hefei 230031, China |
|
|
Abstract Four kinds of bioagents simulants, Pantoea agglomerans (Pan), Staphylococcus aureus subsp. Aureus (Sta), Bacillus globigii (BG) and Escherichia coli (EH) were cultured and the strains growth curves were obtained, and the generation time were 0.99, 0.835, 1.07 and 1.909 h respectively. Two wavelengths at 266 and 355 nm of a designed short range fluorescence lidar were engaged for the measurements of two dimensional fluorescence spectra in the amino acid band and NADH band of the biological warfare agents, respectively. The simulants were diffused homogeneously inside a controlled fluorescence measurement chamber and interogated by the lidar. The 2 dimensional fluorescence spectra of four kinds of vegetative bacteria, BSA and OVA(as simulant of toxin agents) were obtained with resolution of 4 nm. The fluorescence spectra of Pan, Sta, EH and BG, BSA and OVA were consistent with the standard fluorescent component tryptophan in the amino acid band with FWHM of 60 nm, but the central wavelength of the fluorescence spectra of these simulants blue/purple shifted obviously as affected by the external biochemical environment, concentration and ratio of different bacterial internal fluorophores, so the energy level between the excited state and the ground state of the fluorescence molecule increased. Accordingly, weak NADH fluorescence spectra with 100 nm FWHM inside the four vegetative bacteria aerosols were also detected, but Raman scattering contribution of water and nitrogen could not be effectively extracted. The second-order derivative fluorescence spectra of the four simulants showed that the high-order processing and recognition of the fluorescence spectrum was feasible.
|
Received: 2017-06-26
Accepted: 2017-12-21
|
|
|
[1] Orlando Cenciarelli, Silvia Rea, Mariachiara Carestia, et al. Defence S&T Technical Bulletin, 2013, 6(2): 111.
[2] Joshi D, Kumar D, Maini A K, et al. Spectrochimica Acta Part A Molecular & Biomole., 2013, 112(4): 446.
[3] Lakowicz J R. Principles of Fluorescence Spectroscopy, 3rd Edition. Science Press, 2006, 13(2): 029901.
[4] Rustad G, Skogan G, Øystein Farsund. Biomedical Optics Express, 2012, 3(11): 2964.
[5] Thrush E, Salciccioli N, Brown D M, et al. Appl. Opt., 2012, 51(12): 1836.
[6] Deepak Kumar, Ramesh C Sharma, Anil K Maini. Spectroscopy Letters, 2013, 46(2): 147.
[7] Gupta L, Kumar S, Sharma R C, et al. Journal of Scientific & Industrial Research, 2012, 71: 800.
[8] Ho J. Analytica Chimica Acta, 2002, 457(1): 125.
[9] ZHANG Xian-da(张贤达). Modern Signal Processing(现代信号处理). Bejing:Tsinghua University Press(北京:清华大学出版社), 2002.
[10] Yin Qiwei, Liu Zhishen, Liu Binyi. Journal of Atmospheric and Enviromental Optics, 2011, 6(4):260.
[11] CHANG Jian-hua, DONG Qi-gong(常建华, 董绮功). BOPU YUANLI YU JIEXI(波谱原理及解析). Beijing: Science Press(北京: 科学出版社), 2001. 54. |
|
|
|