Nanoparticle biosynthesis using unicellular and subcellular supports
Source abstract
Abstract
Modern life is becoming increasingly sophisticated because of products engineered using designs inspired by nature. Fifty years ago, the burdock plant motivated Swiss scientists to invent Velcro, which was a simple but widely applied design that is still considered the greatest biomimetic invention yet. In nanotechnology, interest in biosynthesis of nanoparticles is increasing, particularly in the use of unicellular and subcellular supports. However, the polydispersity of the resultant structure, limited opportunity for product control and commercial applications of biosynthesized nanoparticles remain as challenges. Using different approaches, studies have attempted to understand nanoparticle biosynthesis and control of particle size and uniformity. In the biotechnological approach, gene sequences that were identified in one organism via gene silencing and were critical for nanoparticle synthesis were introduced and expressed in a different organism or overexpressed by promoters in the same organism to enhance productivity. In contrast, physical and chemical approaches were used for the control of nanoparticle synthesis. To provide a comprehensive understanding of nanoparticle biosynthesis using unicellular and subcellular supports, this review discusses recent studies and experimental evidence in the following categories: synthesis of metal, quantum dot, magnetic and bacterial protein nanoparticles. Genetic engineering is emerging as a key tool for improving the production of high-quality inorganic nanoparticles from microorganisms. Chen-Sheng Yeh and colleagues from National Cheng Kung University in Taiwan review recent strategies for synthesizing tiny metallic and magnetic crystals, quantum dots and protein nanostructures from cellular supports such as plasmids and viruses. While early biosynthetic efforts yielded nanoparticles with inhomogeneous shapes and sizes, techniques such as gene silencing and gene introduction have helped researchers better understand the natural mechanisms at work in cells. For example, proteins identified as participating in biosynthesis can be isolated and their functions executed controllably using microfluidic devices or cell extracts encapsulated by polymers. Nanoparticle applications ranging from drug delivery to molecular-scale robotics should benefit from the biocompatibility and precision offered by biosynthetic platforms. Formation of nanoparticles have shown significant improvement in quality of size, shape and dispersity based on recent advanced biosynthesis approaches by understanding the natural mechanisms underlying nanoparticles synthesis. Considering the biocompatibility, cost effectiveness and eco-friendliness, bio-associated synthesis of nanoparticles may provide the promising solutions to the challenge faced in the applications of industry and biomedicine.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Microbial Community Ecology and Physiology · Microbial Fuel Cells and Bioremediation · Bacteriophages and microbial interactions
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (44)
Show source-provided references
1. Pronk, J. T., Liem, K. P., Bos, J. & Kuenen, G. Energy transduction by anaerobic ferric iron respiration in Thiobacillus ferrooxidans. Appl. Environ. Microbiol. 57, 2063–2068 (1991).10.1128/AEM.57.7.2063-2068.1991 ↗
2. Klaus, T., Joerger, R., Olsson, E. & Granqvist, C.-G. Silver-based crystalline nanoparticles, microbially fabricated. Proc. Natl Acad. Sci. USA 96, 13611–13614 (1999).10.1073/pnas.96.24.13611 ↗
3. Bansal, V., Rautaray, D., Bharde, A., Ahire, K., Sanyal, A., Ahmad, A. & Sastry, M. Fungus-mediated biosynthesis of silica and titania particles. J. Mater. Chem. 15, 2583–2589 (2005).10.1039/b503008k ↗
4. Jung, J. H., Park, T. J., Lee, S. Y. & Seo, T. S. Homogeneous biogenic paramagnetic nanoparticle synthesis based on a microfluidic droplet generator. Angew. Chem. Int. Ed. 51, 5634–5637 (2012).10.1002/anie.201108977 ↗
5. Li, Y., Cui, R., Zhang, P., Chen, B.-B., Tian, Z.-Q., Li, L., Hu., B., Pang, D.-W. & Xie, Z.-X. Mechanism-oriented controllability of intracellular quantum dots formation: the role of glutathione metabolic pathway. ACS Nano. 7, 2240–2248 (2013).10.1021/nn305346a ↗
6. Kolinko, I., Lohße, A., Borg, S., Raschdorf, O., Jogler, C., Tu, Q., Pósfai, M., Tompa., E., Plitzko, J. M., Brachmann, A., Wanner, G., Müller, R., Zhang, Y. & Schüler, D. Biosynthesis of magnetic nanostructures in a foreign organism by transfer of bacterial magnetosome gene clusters. Nat. Nanotechnol 9, 193–197 (2014).10.1038/nnano.2014.13 ↗
7. Park, T. J., Lee, S. Y., Heo, N. S. & Seo, T. S. In vivo synthesis of diverse metal nanoparticles by recombinant Escherichia coli. Angew. Chem. Int. Ed. 17, 7019–7024 (2012).
8. Murawala, P., Phadnis, S. M., Bhonde, R. R. & Prasad, B. L. V. In situ synthesis of water dispersible bovine serum albumin capped gold and silver nanoparticles and their cytocompatibility studies. Colloids Surf. B Biointerfaces 73, 224–228 (2009).10.1016/j.colsurfb.2009.05.029 ↗
9. Ramanathan, R., Field, M. R., O'Mullane, A. P., Smooker, P. M., Bhargava, S. K. & Bansal, V. Aqueous phase synthesis of copper nanoparticles: a link between heavy metal resistance and nanoparticle synthesis ability in bacterial systems. Nanoscale 5, 2300–2306 (2013).10.1039/C2NR32887A ↗
10. Salvadori, M. R., Ando, R. A., Oller do Nascimento, C. A. & Corrêa, B. Intracellular Biosynthesis and removal of copper nanoparticles by dead biomass of yeast isolated from the wastewater of a mine in the Brazilian Amazonia. PLoS ONE 9, e87968 (2014).10.1371/journal.pone.0087968 ↗
11. Liu, J., Zhang, X., Yu, M., Li, S. & Zhang, J. Photoinduced silver nanoparticles/nanorings on plasmid DNA scaffolds. Small 8, 310–316 (2012).10.1002/smll.201101423 ↗
12. Wörner, M., Lioubashevski, O., Basel, M. T., Niebler, S., Gogritchiani, E., Egner, N., Heinz, C., Hoferer, J., Cipolloni, M., Janik, K., Katz, E., Braun, A. M., Willner, I., Niederweis, M. & Bossmann, S. H. Characterization of nanostructured surfaces generated by reconstitution of the porin MspA from Mycobacterium smegmatis. Small 3, 1084–1097 (2007).10.1002/smll.200600559 ↗
13. Lin, I. W.-S., Lok, C.-N. & Che, C.-M. Biosynthesis of silver nanoparticles from silver(I) reduction by the periplasmic nitrate reductase c-type cytochrome subunit NapC in a silver-resistant E. coli. Chem. Sci 5, 3144–3150 (2014).10.1039/C4SC00138A ↗
14. Correa-Llantén, D. N., Muñoz-Ibacache, S. A., Castro, M. E., Muñoz, P. A. & Blamey, J. M. Gold nanoparticles synthesized by Geobacillus sp. strain ID17 a thermophilic bacterium isolated from Deception Island, Antarctica. Microb. Cell Fact. 12, 75 (2013).10.1186/1475-2859-12-75 ↗
15. Johnston, C. W., Wyatt, M. A., Li, X., Ibrahim, A., Shuster, J., Southam, G. & Magarvey, N. A. Gold biomineralization by a metallophore from a gold-associated microbe. Nat. Chem. Biol. 9, 241–243 (2013).10.1038/nchembio.1179 ↗
16. Fayaza, A. M., Girilal, M., Rahmanb, M., Venkatesanc, R. & Kalaichelvana, P. T. Biosynthesis of silver and gold nanoparticles using thermophilic bacterium Geobacillus stearothermophilus. Process Biochem. 46, 1958–1962 (2011).10.1016/j.procbio.2011.07.003 ↗
17. Khan, S. A. & Ahmad, A. Enzyme mediated synthesis of water-dispersible, naturally protein capped, monodispersed gold nanoparticles; their characterization and mechanistic aspects. RSC Adv 4, 7729–7734 (2014).10.1039/c3ra43888k ↗
18. Zhang, M.-X., Cui, R., Tian, Z.-Q., Zhang, Z.-L. & Pang, D.-W. Kinetics-controlled formation of gold clusters using a quasi-biological system. Adv. Funct. Mater. 20, 3673–3677 (2010).10.1002/adfm.201001185 ↗
19. Ma, X., Chen, H., Yang, L., Wang, K., Guo, Y. & Yuan, L. Construction and potential applications of a functionalized cell with an intracellular mineral scaffold. Angew. Chem. Int. Ed. 50, 7414–7417 (2011).10.1002/anie.201100126 ↗
20. Dhoondia, Z. H. & Chakraborty, H. Lactobacillus mediated synthesis of silver oxide nanoparticles. Nanomater. Nanotechnol 2, 2012 (2012).10.5772/55741 ↗
21. Dameron, C. T., Reese, R. N., Mehra, R. K., Kortan, A. R., Carroll, P. J., Stteierwald, M.L., Burs, L.E. & Winge, D.R. Biosynthesis of cadmium sulphide quantum semiconductor crystallites. Nature 338, 596–597 (1989).10.1038/338596a0 ↗
22. Cui, R., Liu, H. H., Xie, H. Y., Zhang, Z. L., Yang, Y. R., Pang, D. W., Xie, Z. X., Chen, B. B., Hu, B. & Shen, P. Living yeast cells as a controllable biosynthesizer for fluorescent quantum dots. Adv. Funct. Mater. 19, 2359–2364 (2009).10.1002/adfm.200801492 ↗
23. Luo, Q.-Y., Lin, Y., Li, Y., Xiong, L.-H., Cui, R., Xie, Z.-X. & Pang, D.-W. Nanomechanical analysis of yeast cells in CdSe quantum dot biosynthesis. Small 4, 699–704 (2014).10.1002/smll.201301940 ↗
24. Monrás, J. P., Díaz, V., Bravo, D., Montes, R. A., Chasteen, T. G., Osorio-Román, I.O., Vásquez, C. C. & Pérez-Donoso, J. M. Enhanced glutathione content allows the in vivo synthesis of fluorescent CdTe nanoparticles by Escherichia coli. PLoS ONE 7, e48657 (2012).10.1371/journal.pone.0048657 ↗
25. Gu, Y.-P., Cui, R., Zhang, Z.-L., Xie, Z.-X. & Pang, D.-W. Ultrasmall near-infrared Ag2Se quantum dots with tunable fluorescence for in vivo imaging. J. Am. Chem. Soc. 134, 79–82 (2012).10.1021/ja2089553 ↗
26. Xiong, L.-H., Cui, R., Zhang, Z.-L., Yu, X., Xie, Z., Shi, Y.-B. & Pang, D.-W. Uniform fluorescent nanobioprobes for pathogen detection. ACS Nano. 8, 5116–5124 (2014).10.1021/nn501174g ↗
27. Cui, R., Gu, Y.-P., Zhang., Z.-L., Xie, Z.-X., Tiana, Z.-Q. & Pang, D.-W. Controllable synthesis of PbSe nanocubes in aqueous phase using a quasi-biosystem. J. Mater. Chem. 22, 3713–3716 (2012).10.1039/c2jm15691a ↗
28. Lee, K. G., Hong, J., Wang, K. W., Heo, N. S., Kim, D. H., Lee, S. Y., Lee, S. J. & Park, T.J. In vitro biosynthesis of metal nanoparticles in microdroplets. ACS Nano. 6, 6998–7008 (2012).10.1021/nn302043q ↗
29. Taherkhani, S., Mohammadi, M., Daoud, J., Martel, S. & Tabrizian, M. Covalent binding of nanoliposomes to the surface of magnetotactic bacteria for the synthesis of self-propelled therapeutic agents. ACS Nano. 8, 5049–5060 (2014).10.1021/nn5011304 ↗
30. Coker, V. S., Telling, N. D., van der Laan, G., Pattrick, R. A. D., Pearce., C. I., Arenholz, E., Tuna, F., Winpenny, R. E. P. & Lloyd, J. R. Harnessing the extracellular bacterial production of nanoscale cobalt ferrite with exploitable magnetic properties. ACS Nano. 3, 1922–1928 (2009).10.1021/nn900293d ↗
31. Byrne, J. M., Coker, V. S., Cespedes, E., Wincott, P. L., Vaughan, D. J., Pattrick., R. A. D., van der Laan, G., Arenholz, E., Tuna, F., Bencsik, M., Lloyd, J. R. & Telling, N. D. Biosynthesis of zinc substituted magnetite nanoparticles with enhanced magnetic properties. Adv. Funct. Mater. 24, 2518–2529 (2013).10.1002/adfm.201303230 ↗
32. Courchesne, N.-M. D., Klug, M. T., Chen, P.-Y., Kooi, S. E., Yun, D. S., Hong, N., Fang, N.X., Belcher, A.M. & Hammond, P.T. Assembly of a bacteriophage-based template for the organization of materials into nanoporous networks. Adv. Mater. 26, 3398–3404 (2014).10.1002/adma.201305928 ↗
33. Jeong, C. K., Kim, I., Park, K.-I., Oh, M. H., Paik, H., Hwang, G.-T., No, K., Nam, Y. S. & Lee, K. J. Virus-directed design of a flexible BaTiO3 nanogenerator. ACS Nano. 7, 11016–11025 (2013).10.1021/nn404659d ↗
34. Ghosh, D., Lee, Y., Thomas, S., Kohli, A. G., Yun, D. S., Belcher, A. M. & Kelly, K. A. M13-templated magnetic nanoparticles for targeted in vivo imaging of prostate cancer. Nat. Nanotechnol 7, 677–682 (2012).10.1038/nnano.2012.146 ↗
35. Butchosa, N., Brown, C., Larsson, P. T., Berglund, L. A., Bulone, V. & Zhou, Q. Nanocomposites of bacterial cellulose nanofibers and chitin nanocrystals: fabrication, characterization and bactericidal activity. Green Chem. 15, 3404–3413 (2013).10.1039/c3gc41700j ↗
36. Yamanaka, S. & Sugiyama, J. Structural modification of bacterial cellulose. Cellulose 7, 213–225 (2000).10.1023/A:1009208022957 ↗
37. Shi, P., Lin, Y.-A., Pastuszka, M., Cui, H. & MacKay, J. A. Triggered sorting and co-assembly of genetically engineered protein microdomains in the cytoplasm. Adv. Mater. 26, 449–454 (2014).10.1002/adma.201303356 ↗
38. Daube, S. S., Arad, T. & Bar-Ziv, R. Cell-free co-synthesis of protein nanoassemblies: tubes, rings, and doughnuts. Nano Lett. 7, 638–641 (2007).10.1021/nl062560n ↗
39. Hernandez-Garcia, A., Werten, M. W. T., Stuart, M. C., de Wolf, F. A. & de Vries, R. Coating of single DNA molecules by genetically engineered protein diblock copolymers. Small 8, 3491–3501 (2012).10.1002/smll.201200939 ↗
40. Behkam, B. & Sitti, M. Bacterial flagella-based propulsion and on/off motion control of microscale objects. Appl. Phys. Lett. 90, 023902 (2007).10.1063/1.2431454 ↗
41. Martel, S., Mohammadi, M., Felfoul, O., Lu, Z. & Pouponneau, P. Flagellated magnetotactic bacteria as controlled MRI-trackable propulsion and steering systems for medical nanorobots operating in the human microvasculature. Int. J. Rob. Res 28, 571–582 (2009).10.1177/0278364908100924 ↗
42. Muscat, R. A., Bath, J. & Turberfield, A. J. A programmable molecular robot. Nano Lett. 11, 982–987 (2011).10.1021/nl1037165 ↗
43. Chen, W.-Y., Lin, J.-Y., Chen, W.-J., Luo, L., Diau, E. W.-G. & Chen, Y.-C. Functional gold nanoclusters as antimicrobial agents for antibiotic-resistant bacteria. Nanomedicine 5, 755–764 (2010).10.2217/nnm.10.43 ↗
44. Matsunaga, T., Hashimoto, K., Nakamura, N., Nakamura, K. & Hashimoto, S. Phagocytosis of bacterial magnetite by leucocytes. Appl. Microbiol. Biotechnol. 31, 401–405 (1989).10.1007/BF00257612 ↗