Abstract
Biosynthesis by diatoms provides a green approach for nanoparticle (NP) production. However, reproducible and homogeneous shapes are essential for their application. To improve these characteristics during biosynthesis, the underlying synthesis mechanisms as well as involved substances need to be understood. The first essential step for suitable analyses is the purification of Au-silica-nanocomposites from organic biomass. Succesfully cleaned nanocomposites could, for example, be useful as catalysts. In combination with the biosynthesized NPs, this material presents a “green” catalyst and could contribute to the currently thriving green nanochemistry. In this work, we compare different purification agents with respect to their ability to purify cells of the diatom Stephanopyxis turris without separating the biosynthesized Au-silica-nanocomposites from the diatom cell walls. Scanning electron microscopy (SEM) and energy dispersive X-ray spectroscopy (EDX) are used to localize and identify Au-silica-nanocomposites around the cells. The amount of remaining organic compounds on the purified cell is detected by attenuated total reflection Fourier transform infrared (ATR-FTIR) spectroscopy. Furthermore, inductively coupled plasma optical emission spectrometry (ICP-OES) is used to track the “gold path” during cell growth and the different purifications steps.
Acknowledgement
The authors wish to thank A. Brünner and M. Lê Anh (Inorganic Chemistry, TU Dresden) for SEM and EDX and R. Schulze (Bioanalytical Chemistry, TU Dresden) for ICP-OES measurements and continuative discussion of the results. Furthermore, thanks are due to B. Klemmed (Physical Chemistry, TU Dresden) for TEM measurements. Financial support from the Deutsche Forschungsgemeinschaft (grants no. BR1278/22-1 and BR1278/25-3) is gratefully acknowledged.
References
1. E. V. Armbrust, J. A. Berges, C. Bowler, B. R. Green, D. Martinez, N. H. Putnam, S. Zhou, A. E. Allen, K. E. Apt, M. Bechner, M. A. Brzezinski, B. K. Chaal, A. Chiovitti, A. K. Davis, M. S. Demarest, J. C. Detter, T. Glavina, D. Goodstein, M. Z. Hadi, U. Hellsten, M. Hildebrand, B. D. Jenkins, W. W. Y. Lau, T. W. Lane, F. W. Larimer, C. J. Lippmeier, S. Lucas, A. Montsant, M. Obornik, M. S. Parker, B. Palenik, G. J. Pazour, P. M. Richardson, T. A. Rynearson, M. A. Saito, D. C. Schwartz, K. Thamatrakoln, K. Valentin, A. Vardi, F. P. Wilkerson, D. S. Rokhsar, Science 306 (2004) 79.10.1126/science.1101156Search in Google Scholar PubMed
2. D. Werner, The Biology of Diatoms, University of California Press, Berkeley and Los Angeles (1997).Search in Google Scholar
3. N. Kröger, N. Poulsen, Annu. Rev. Genet. 42 (2008) 83.10.1146/annurev.genet.41.110306.130109Search in Google Scholar PubMed
4. J. Parkinson, R. Gordon, Nanotechnology 17 (1999) 190.10.1016/S0167-7799(99)01321-9Search in Google Scholar PubMed
5. R. Ragni, S. R. Cicco, D. Vona, G. M. Farinola, Adv. Mater. 1704289 (2017) 1.Search in Google Scholar
6. C. Jeffryes, S. N. Agathos, G. Rorrer, Curr. Opin. Biotechnol. 33 (2015) 23.10.1016/j.copbio.2014.10.005Search in Google Scholar PubMed
7. C. Jeffryes, J. Campbell, H. Li, J. Jiao, G. Rorrer, Energy Environ. Sci. 4 (2011) 3930.10.1039/c0ee00306aSearch in Google Scholar
8. D. Losic, J. G. Mitchell, N. H. Voelcker, Adv. Mater. 21 (2009) 2947.10.1002/adma.200803778Search in Google Scholar
9. N. Nassif, J. Livage, Chem. Soc. Rev. 40 (2011) 849.10.1039/C0CS00122HSearch in Google Scholar PubMed
10. D. Y. Zhang, Y. Wang, J. Cai, J. F. Pan, X. G. Jiang, Y. G. Jiang, Chinese Sci. Bull. 57 (2012) 3836.10.1007/s11434-012-5410-xSearch in Google Scholar
11. S. S. Dixit, J. P. Smol, Environ. Monit. Assess. 31 (1994) 275.10.1007/BF00577258Search in Google Scholar PubMed
12. J. K. Wang, M. Seibert, Biotechnol. Biofuels 10 (2017) 1.10.1186/s13068-017-0699-ySearch in Google Scholar PubMed PubMed Central
13. M. Hildebrand, A. K. Davis, S. R. Smith, J. C. Traller, R. Abbriano, Biofuels 3 (2012) 221.10.4155/bfs.11.157Search in Google Scholar
14. M. S. Aw, S. Simovic, J. Addai-Mensah, D. Losic, Nanomedicine 6 (2011) 1159.10.2217/nnm.11.29Search in Google Scholar PubMed
15. C. Fischer, M. Adam, A. C. Mueller, E. Sperling, M. Wustmann, K.-H. Van Pée, S. Kaskel, E. Brunner, ACS Omega 1 (2016) 123.10.1021/acsomega.6b00406Search in Google Scholar PubMed PubMed Central
16. B. C. Jeffryes, R. Solanki, Y. Rangineni, W. Wang, C. Chang, G. L. Rorrer, Adv. Mater. 20 (2008) 2633.10.1002/adma.200800292Search in Google Scholar
17. F. Ren, J. Campbell, X. Wang, G. L. Rorrer, X. W. Alan, Opt. Express 21 (2013) 15308.10.1364/OE.21.015308Search in Google Scholar PubMed
18. A. Eychmüller, J. Phys. Chem. B 104 (2000) 6514.10.1021/jp9943676Search in Google Scholar
19. K. B. Narayanan, N. Sakthivel, Adv. Colloid Interface Sci. 169 (2011) 59.10.1016/j.cis.2011.08.004Search in Google Scholar PubMed
20. L. Kühn, A. K. Herrmann, B. Rutkowski, M. Oezaslan, M. Nachtegaal, M. Klose, L. Giebeler, N. Gaponik, J. Eckert, T. J. Schmidt, A. Czyrska-Filemonowicz, A. Eychmüller, Chem. Eur. J. 22 (2016) 13446.10.1002/chem.201602487Search in Google Scholar PubMed
21. W. J. Crookes-Goodson, J. M. Slocik, R. R. Naik, Chem. Soc. Rev. 37 (2008) 2403.10.1039/b702825nSearch in Google Scholar PubMed
22. H. Korbekandi, S. Iravani, S. Abbasi, Crit. Rev. Biotechnol. 29 (2009) 279.10.3109/07388550903062462Search in Google Scholar PubMed
23. G. L. Rorrer, C.-H. Chang, S.-H. Liu, C. Jeffryes, J. Jiao, J. A. Hedberg, J. Nanosci. Nanotechnol. 5 (2005) 41.10.1166/jnn.2005.005Search in Google Scholar PubMed
24. T. Qin, T. Gutu, J. Jiao, C. Chang, G. L. Rorrer, ACS Nano 2 (2008) 1296.10.1021/nn800114qSearch in Google Scholar PubMed
25. C. Jeffryes, T. Gutu, J. Jiao, G. L. Rorrer, ACS Nano 2 (2008) 2103.10.1021/nn800470xSearch in Google Scholar PubMed
26. C. Jeffryes, T. Gutu, J. Jiao, G. L. Rorrer, Mater. Sci. Eng. C 28 (2008) 107.10.1016/j.msec.2007.01.002Search in Google Scholar
27. T. Yamazaki, H. Sasanuma, S. Mayama, K. Umemura, Phys. Status Solidi C 7 (2010) 2759.10.1002/pssc.200983808Search in Google Scholar
28. J. Toster, K. S. Iyer, R. Burtovyy, S. S. O. Burgess, I. A. Luzinov, C. L. Raston, J. Am. Chem. Soc. 131 (2009) 8356.10.1021/ja901806ySearch in Google Scholar PubMed
29. A. Schröfel, G. Kratošová, M. Krautová, E. Dobročka, I. Vávra, J. Nanoparticle Res. 13 (2011) 3207.10.1007/s11051-011-0221-6Search in Google Scholar
30. A. Feurtet-Mazel, S. Mornet, L. Charron, N. Mesmer-Dudons, R. Maury-Brachet, M. Baudrimont, Environ. Sci. Pollut. Res. 23 (2016) 4334.10.1007/s11356-015-4139-xSearch in Google Scholar PubMed
31. N. Pytlik, J. Kaden, M. Finger, J. Naumann, S. Wanke, S. Machill, E. Brunner, Algal Res. 28 (2017) 9.10.1016/j.algal.2017.10.004Search in Google Scholar
32. J. Jena, N. Pradhan, B. P. Dash, P. K. Panda, B. K. Mishra, J. Saudi Chem. Soc. 19 (2015) 661.10.1016/j.jscs.2014.06.005Search in Google Scholar
33. P. Roychoudhury, C. Nandi, R. Pal, J. Appl. Phycol. 28 (2016) 2857.10.1007/s10811-016-0809-4Search in Google Scholar
34. A. Dubavik, V. Lesnyak, N. Gaponik, A. Eychmüller, Langmuir 27 (2011) 10224.10.1021/la201638tSearch in Google Scholar PubMed
35. A. A. Shemetov, I. Nabiev, A. Sukhanova, ACS Nano 6 (2012) 4585.10.1021/nn300415xSearch in Google Scholar PubMed
36. P. Harrison, R. E. Waters, F. J. R. Taylor, J. Phycol. 16 (1980) 28.10.1111/j.1529-8817.1980.tb00724.xSearch in Google Scholar
37. N. Kröger, C. Bergsdorf, M. Sumper, EMBO J. 13 (1994) 4676.10.1002/j.1460-2075.1994.tb06791.xSearch in Google Scholar PubMed PubMed Central
38. E. Van Eynde, B. Lenaerts, T. Tytgat, S. W. Verbruggen, B. Hauchecorne, R. Blust, S. Lenaerts, RSC Adv. 4 (2014) 56200.10.1039/C4RA09305DSearch in Google Scholar
39. N. Chamuah, L. Chetia, N. Zahan, S. Dutta, G. A. Ahmed, P. Nath, J. Phys. D Appl. Phys. 50 (2017) 175103.10.1088/1361-6463/aa63b0Search in Google Scholar
40. J. Chen, G. Qin, Q. Chen, J. Yu, S. Li, F. Cao, B. Yang, Y. Ren, J. Mater. Chem. C 3 (2015) 4933.10.1039/C5TC00717HSearch in Google Scholar
41. J. Toster, C. Harnagea, K. S. Iyer, C. L. Raston, Cryst. Eng. Comm. 14 (2012) 3446.10.1039/c2ce06648cSearch in Google Scholar
42. S. Hauptkorn, J. Pavel, H. Seltner, J. Anal. Chem. 370 (2001) 246.10.1007/s002160100759Search in Google Scholar PubMed
43. M. P. Andrews, A. Hajiaboli, J. Hiltz, T. Gonzalez, G. Singh, R. B. Lennox, Proc. SPIE 7946 (2011) 79461S.10.1117/12.881467Search in Google Scholar
44. Y. Li, Y. H. Gao, X. S. Li, J. Y. Yang, G. H. Que, Colloids Surf. B Biointerfaces 75 (2010) 550.10.1016/j.colsurfb.2009.09.026Search in Google Scholar PubMed
45. E. K. Payne, N. L. Rosi, C. Xue, C. A. Mirkin, Angew. Chemie – Int. Ed. 44 (2005) 5064.10.1002/anie.200500988Search in Google Scholar PubMed
46. N. Kröger, R. Deutzmann, M. Sumper, Science 286 (1999) 1129.10.1126/science.286.5442.1129Search in Google Scholar PubMed
47. J. R. Martinez, F. Ruiz, Y. V. Vorobiev, F. Perez-Robles, J. Gonzalez-Hernandez, J. Chem. Phys. 109 (1998) 7511.Search in Google Scholar
48. M. Giordano, M. Kansiz, P. Heraud, J. Beardall, B. Wood, D. McNaughton, J. Phycol. 37 (2001) 271.10.1046/j.1529-8817.2001.037002271.xSearch in Google Scholar
49. P. Innocenzi, J. Non. Cryst. Solids 316 (2003) 309.10.1016/S0022-3093(02)01637-XSearch in Google Scholar
50. A. Barth, Biochim. Biophys. Acta – Bioenerg. 1767 (2007) 1073.10.1016/j.bbabio.2007.06.004Search in Google Scholar PubMed
51. K. Stehfest, J. Toepel, C. Wilhelm, Plant Physiol. Biochem. 43 (2005) 717.10.1016/j.plaphy.2005.07.001Search in Google Scholar PubMed
52. V. Martin-Jézéquel, M. Hildebrand, M. A. Brzezinski, J. Phycol. 36 (2000) 821.10.1046/j.1529-8817.2000.00019.xSearch in Google Scholar
53. J. C. Lewin, Geochim. Cosmochim. Acta 21 (1961) 182.10.1016/S0016-7037(61)80054-9Search in Google Scholar
Supplementary Material:
The online version of this article offers supplementary material (https://doi.org/10.1515/zpch-2018-1141).
©2018 Walter de Gruyter GmbH, Berlin/Boston