Polymer Nanocomposites of Selenium Biofabricated Using Fungi
Abstract
:1. Introduction
2. On the Definitions of Nanocomposites
3. Fungal Features to Be Recruited in Se-Nanomaterial Synthesis
4. Synthesis and Mycosynthesis of Polymer Nanocomposites
4.1. Macromolecular Building Blocks for Nanocomposites
4.1.1. Chemically Synthesized Polymer Matrices
4.1.2. Biogenic Polymer Matrices
4.2. Nanoscale Building Blocks for Selenium Nanocomposites
4.2.1. Selenium Intrinsic Properties Decisive in Nanophase Selection
4.2.2. Mechanisms Underlying the Occurrence of Selenium Nanophase
4.2.3. Points for Physicochemical Characterization of Culture Conditions and Resultant SeNPs
5. Conclusions and Challenges
Author Contributions
Funding
Informed Consent Statement
Data Availability Statement
Conflicts of Interest
References
- Gade, A.; Ingle, A.; Whiteley, C.; Rai, M. Mycogenic metal nanoparticles: Progress and applications. Biotechnol. Lett. 2010, 32, 593–600. [Google Scholar] [CrossRef] [PubMed]
- Wadhwani, S.A.; Shedbalkar, U.U.; Singh, R.; Chopade, B.A. Biogenic selenium nanoparticles: Current status and future prospects. Appl. Microbiol. Biotechnol. 2016, 100, 2555–2566. [Google Scholar] [CrossRef] [PubMed]
- Castro, L.; Blázquez, M.L.; Muñoz, J.A.; González, F.G.; Ballester, A. Mechanism and Applications of Metal Nanoparticles Prepared by Bio-Mediated Process. Rev. Adv. Sci. Eng. 2014, 3, 199–216. [Google Scholar] [CrossRef]
- Pathakoti, K.; Manubolu, M.; Hwang, H.-M. Nanostructures: Current uses and future applications in food science. J. Food Drug Anal. 2017, 25, 245–253. [Google Scholar] [CrossRef] [Green Version]
- Wilson, P.; Ke, P.C.; Davis, T.P.; Kempe, K. Poly(2-oxazoline)-based micro- and nanoparticles: A review. Eur. Polym. J. 2017, 88, 486–515. [Google Scholar] [CrossRef]
- Singla, R.; Abidi, S.M.S.; Dar, A.; Acharya, A. Nanomaterials as potential and versatile platform for next generation tissue engineering applications. J. Biomed. Mater. Res. Part B Appl. Biomater. 2019, 107, 2433–2449. [Google Scholar] [CrossRef]
- Oguz, O.; Simsek, E.; Soz, C.K.; Heinz, O.K.; Yilgor, E.; Yilgor, I.; Menceloglu, Y.Z. Effect of filler content on the structure-property behavior of poly(ethylene oxide) based polyurethaneurea-silica nanocomposites. Polym. Eng. Sci. 2018, 58, 1097–1107. [Google Scholar] [CrossRef]
- Gatadi, S.; Madhavi, Y.V.; Nanduri, S. Nanoparticle drug conjugates treating microbial and viral infections: A mini-review. J. Mol. Struct. 2021, 1228, 129750. [Google Scholar] [CrossRef]
- Vera, P.; Echegoyen, Y.; Canellas, E.; Nerín, C.; Palomo, M.; Madrid, Y.; Cámara, C. Nano selenium as antioxidant agent in a multilayer food packaging material. Anal. Bioanal. Chem. 2016, 408, 6659–6670. [Google Scholar] [CrossRef]
- Divya, K.; Kurian, L.C.; Vijayan, S.; Manakulam Shaikmoideen, J. Green synthesis of silver nanoparticles by Escherichia coli: Analysis of antibacterial activity. J. Water Environ. Nanotechnol. 2016, 1, 63–74. [Google Scholar]
- Huang, Z.-H.; Yin, Y.-N.; Zhang, Y. Preparation of a novel positively charged nanofiltration composite membrane incorpo-rated with silver nanoparticles for pharmaceuticals and personal care product rejection and antibacterial properties. Water Sci. Technol. 2016, 73, 1910–1919. [Google Scholar] [CrossRef]
- Talib, S.H.; Challab, M.K.; Alhameedawi, F.A.H. Using Nano Composites to Purify Water from Phenol Pollutants. J. Phys. Conf. Ser. 2021, 1818, 012180. [Google Scholar] [CrossRef]
- Colino, C.I.; Lanao, J.M.; Gutierrez-Millan, C. Recent advances in functionalized nanomaterials for the diagnosis and treatment of bacterial infections. Mater. Sci. Eng. C 2021, 121, 111843. [Google Scholar] [CrossRef]
- Martínez, G.; Merinero, M.; Pérez-Aranda, M.; Pérez-Soriano, E.; Ortiz, T.; Villamor, E.; Begines, B.; Alcudia, A. Environmental Impact of Nanoparticles’ Application as an Emerging Technology: A Review. Materials 2020, 14, 166. [Google Scholar] [CrossRef]
- Wang, E.; Wang, A.Z. Nanoparticles and their applications in cell and molecular biology. Integr. Biol. 2014, 6, 9–26. [Google Scholar] [CrossRef] [Green Version]
- Rónavári, A.; Igaz, N.; Adamecz, D.; Szerencsés, B.; Molnar, C.; Kónya, Z.; Pfeiffer, I.; Kiricsi, M. Green Silver and Gold Nanoparticles: Biological Synthesis Approaches and Potentials for Biomedical Applications. Molecules 2021, 26, 844. [Google Scholar] [CrossRef]
- Salunke, B.K.; Sawant, S.S.; Lee, S.-I.; Kim, B.S. Microorganisms as efficient biosystem for the synthesis of metal nanoparticles: Current scenario and future possibilities. World J. Microbiol. Biotechnol. 2016, 32, 1–16. [Google Scholar] [CrossRef] [PubMed]
- Wang, Q.; Wang, F.; Xu, Z.; Ding, Z. Bioactive Mushroom Polysaccharides: A Review on Monosaccharide Composition, Biosynthesis and Regulation. Molecules 2017, 22, 955. [Google Scholar] [CrossRef] [Green Version]
- Geetha, N.; Bhavya, G.; Abhijith, P.; Shekhar, R.; Dayananda, K.; Jogaiah, S. Insights into nanomycoremediation: Secretomics and mycogenic biopolymer nanocomposites for heavy metal detoxification. J. Hazard. Mater. 2021, 409, 124541. [Google Scholar] [CrossRef] [PubMed]
- Oréfice, R.L.; Hench, L.L.; Brennan, A.B. Effect of particle morphology on the mechanical and thermo-mechanical behavior of polymer composites. J. Braz. Soc. Mech. Sci. 2001, 23, 1–8. [Google Scholar] [CrossRef]
- Morgan, A.B.; Chu, L.L.; Harris, J.D. A flammability performance comparison between synthetic and natural clays in poly-styrene nanocomposites. Fire Mater Int. J. 2005, 29, 213–229. [Google Scholar] [CrossRef]
- Khan, M.A.; Razak, S.A.; Al Arjan, W.; Nazir, S.; Anand, T.S.; Mehboob, H.; Amin, R. Recent Advances in Biopolymeric Composite Materials for Tissue Engineering and Regenerative Medicines: A Review. Molecules 2021, 26, 619. [Google Scholar] [CrossRef] [PubMed]
- Zan, G.; Wu, Q. Biomimetic and Bioinspired Synthesis of Nanomaterials/Nanostructures. Adv. Mater. 2016, 28, 2099–2147. [Google Scholar] [CrossRef]
- Priyadarshini, E.; Priyadarshini, S.S.; Cousins, B.G.; Pradhan, N. Metal-Fungus interaction: Review on cellular processes underlying heavy metal detoxification and synthesis of metal nanoparticles. Chemosphere 2021, 274, 129976. [Google Scholar] [CrossRef]
- Hulkoti, N.I.; Taranath, T.C. Biosynthesis of nanoparticles using microbes—A review. Colloids Surf. B Biointerfaces 2014, 121, 474–483. [Google Scholar] [CrossRef]
- Li, G.; He, D.; Qian, Y.; Guan, B.; Gao, S.; Cui, Y.; Yokoyama, K.; Wang, L. Fungus-mediated green synthesis of silver na-noparticles using Aspergillus terreus. Int. J. Mol. Sci. 2012, 13, 466–476. [Google Scholar] [CrossRef] [Green Version]
- Pantidos, N.; Horsfall, L.E. Biological synthesis of metallic nanoparticles by bacteria, fungi and plants. J. Nanomed. Nanotechnol. 2014, 5, 233. [Google Scholar] [CrossRef]
- Taherzadeh, M.J.; Fox, M.; Hjorth, H.; Edebo, L. Production of mycelium biomass and ethanol from paper pulp sulfite liquor by Rhizopus oryzae. Bioresour. Technol. 2003, 88, 167–177. [Google Scholar] [CrossRef]
- Su, Y.; Chen, L.; Yang, F.; Cheung, P.C.K. Beta-d-glucan-based drug delivery system and its potential application in tar-geting tumor associated macrophages. Carbohydr. Polym. 2021, 253, 117258. [Google Scholar] [CrossRef] [PubMed]
- Bhavya, G.; Belorkar, S.A.; Mythili, R.; Geetha, N.; Shetty, H.S.; Udikeri, S.S.; Jogaiah, S. Remediation of emerging environ-mental pollutants: A review based on advances in the uses of eco-friendly biofabricated nanomaterials. Chemosphere 2021, 275, 129975. [Google Scholar] [CrossRef] [PubMed]
- Poluboyarinov, P.A.; Vikhreva, V.A.; Leshchenko, P.P.; Aripovskii, A.V.; Likhachev, A.N. Elemental selenium formation upon destruction of the organoselenium compound DAFS-25 molecule by growing fungal mycelium. Mosc. Univ. Biol. Sci. Bull. 2009, 64, 164–168. [Google Scholar] [CrossRef]
- Afzal, B.; Yasin, D.; Husain, S.; Zaki, A.; Srivastava, P.; Kumar, R.; Fatma, T. Screening of cyanobacterial strains for the selenium nanoparticles synthesis and their anti-oxidant activity. Biocatal. Agric. Biotechnol. 2019, 21, 101307. [Google Scholar] [CrossRef]
- Liang, X.; Perez, M.A.M.-J.; Nwoko, K.C.; Egbers, P.; Feldmann, J.; Csetenyi, L.; Gadd, G.M. Fungal formation of selenium and tellurium nanoparticles. Appl. Microbiol. Biotechnol. 2019, 103, 7241–7259. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Mukherjee, P.; Ahmad, A.; Mandal, D.; Senapati, S.; Sainkar, S.R.; Khan, M.I.; Parishcha, R.; Ajaykumar, P.V.; Alam, M.; Kumar, R.; et al. Fungus-Mediated Synthesis of Silver Nanoparticles and Their Immobilization in the Mycelial Matrix: A Novel Biological Approach to Nanoparticle Synthesis. Nano Lett. 2001, 1, 515–519. [Google Scholar] [CrossRef]
- Priyabrata, M.; Ahmad, A.; Deendayal, M.; Satyajyoti, S.; Sudhakar, R.S.; Mohammad, I.K.; Renu, P.; Ajaykumar, P.V.; Mansoor, A.; Rajiv, K.; et al. Fungus mediated synthesis of silver nanoparticles and their immobilization in the mycelial matrix: A novel biological approach to nanoparticle synthesis. Nano Lett. 2001, 1, 515–519. [Google Scholar]
- Estevez, M.B.; Raffaelli, S.; Mitchell, S.G.; Faccio, R.; Alborés, S. Biofilm Eradication Using Biogenic Silver Nanoparticles. Molecules 2020, 25, 2023. [Google Scholar] [CrossRef]
- Crisan, C.M.; Mocan, T.; Manolea, M.; Lasca, L.I.; Tăbăran, F.-A.; Mocan, L. Review on Silver Nanoparticles as a Novel Class of Antibacterial Solutions. Appl. Sci. 2021, 11, 1120. [Google Scholar] [CrossRef]
- Sharma, G.; Nam, J.S.; Sharma, A.R.; Lee, S.S. Antimicrobial potential of silver nanoparticles synthesized using medicinal herb coptidis rhizome. Molecules 2018, 23, 2268. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Vamanu, E.; Ene, M.; Bita, B.; Ionescu, C.; Craciun, L.; Sarbu, I. In Vitro Human Microbiota Response to Exposure to Silver Nanoparticles Biosynthesized with Mushroom Extract. Nutrients 2018, 10, 607. [Google Scholar] [CrossRef] [Green Version]
- Kitching, M.; Ramani, M.; Marsili, E. Fungal biosynthesis of gold nanoparticles: Mechanism and scale up. Microb. Biotechnol. 2015, 8, 904–917. [Google Scholar] [CrossRef]
- Zhang, S.; Pang, G.; Chen, C.; Qin, J.; Yu, H.; Liu, Y.; Zhang, X.; Song, Z.; Zhao, J.; Wang, F.; et al. Effective cancer immunotherapy by Ganoderma lucidum polysaccharide-gold nanocomposites through dendritic cell activation and memory T cell response. Carbohydr. Polym. 2019, 205, 192–202. [Google Scholar] [CrossRef]
- Rai, M.; Bonde, S.; Golinska, P.; Trzcińska-Wencel, J.; Gade, A.; Abd-Elsalam, K.; Shende, S.; Gaikwad, S.; Ingle, A. Fusarium as a Novel Fungus for the Synthesis of Nanoparticles: Mechanism and Applications. J. Fungi 2021, 7, 139. [Google Scholar] [CrossRef]
- Siddiqi, K.S.; Husen, A. Fabrication of metal nanoparticles from fungi and metal salts: Scope and application. Nanoscale Res. Lett. 2016, 11, 1–15. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Khandel, P.; Shahi, S.K. Mycogenic nanoparticles and their bio-prospective applications: Current status and future challenges. J. Nanostruct. Chem. 2018, 8, 369–391. [Google Scholar] [CrossRef] [Green Version]
- Khan, A.U.; Malik, N.; Khan, M.; Cho, M.H.; Khan, M.M. Fungi-assisted silver nanoparticle synthesis and their applications. Bioprocess Biosyst. Eng. 2018, 41, 1–20. [Google Scholar] [CrossRef]
- Salunke, B.K.; Sawant, S.S.; Lee, S.I.; Kim, B.S. Comparative study of MnO2 nanoparticle synthesis by marine bacterium Sac-charophagus degradans and yeast Saccharomyces cerevisiae. Appl. Microbiol. Biotechnol. 2015, 99, 5419–5427. [Google Scholar] [CrossRef]
- Athira, K.; Gurrala, L.; Kumar, D.V.R. Biosurfactant-mediated biosynthesis of CuO nanoparticles and their antimicrobial activity. Appl. Nanosci. 2021, 11, 1447–1457. [Google Scholar] [CrossRef]
- Zare, B.; Babaie, S.; Setayesh, N.; Shahverdi, A.R. Isolation and characterization of a fungus for extracellular synthesis of small selenium nanoparticles. Nanomedicine 2013, 11, 13–19. [Google Scholar]
- Mosallam, F.M.; Gharieb, S.; EleSayyad, G.S.; Fathy, R.M.; EleBatal, A.I. Biomoleculesemediated synthesis of selenium na-noparticles using Aspergillus oryzae fermented Lupin extract and gamma radiation for hindering the growth of some mul-tidrugeresistant bacteria and pathogenic fungi. Microb. Pathog. 2018, 122, 108e116. [Google Scholar] [CrossRef]
- Agnihotri, M.; Joshi, S.; Kumar, A.R.; Zinjarde, S.; Kulkarni, S. Biosynthesis of gold nanoparticles by the tropical marine yeast Yarrowia lipolytica NCIM 3589. Mater. Lett. 2009, 63, 1231–1234. [Google Scholar] [CrossRef]
- Haq, M.; Rathod, V.; Singh, D.; Singh, A.K.; Ninganagouda, S.; Hiremath, J. Dried mushroom Agaricus bisporus mediated synthesis of silver nanoparticles from Bandipora District (Jammu and Kashmir) and their efficacy against methicillin resistant Staphylococcus aureus (MRSA) strains. Nanosci. Nanotechnol. Int. J. 2015, 5, 1–8. [Google Scholar]
- Chang, S.-T.; Wasser, S.P. The Role of Culinary-Medicinal Mushrooms on Human Welfare with a Pyramid Model for Human Health. Int. J. Med. Mushrooms 2012, 14, 95–134. [Google Scholar] [CrossRef] [PubMed]
- Chang, S.T.; Miles, P.G. Mushroom biology—A new discipline. Mycologist 1992, 6, 64–65. [Google Scholar] [CrossRef]
- Lindequist, U.; Niedermeyer, T.H.J.; Jülich, W.-D. The Pharmacological Potential of Mushrooms. Evid.-Based Complement. Altern. Med. 2005, 2, 285–299. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Sharifi-Rad, J.; Butnariu, M.; Ezzat, S.M.; Adetunji, C.O.; Imran, M.; Sobhani, S.R.; Tufail, T.; Hosseinabadi, T.; Ramírez-Alarcón, K.; Martorell, M.; et al. Mushrooms-Rich Preparations on Wound Healing: From Nutritional to Medicinal Attributes. Front. Pharmacol. 2020, 11, 567518. [Google Scholar] [CrossRef]
- Vamanu, E.; Pelinescu, D. Effects of mushroom consumption on the microbiota of different target groups–Impact of poly-phenolic composition and mitigation on the microbiome fingerprint. LWT-Food Sci. Technol. 2017, 85, 262–268. [Google Scholar] [CrossRef]
- Vamanu, E.; Nita, S. Biological activity of fluidized bed ethanol extracts from several edible mushrooms. Food Sci. Biotechnol. 2014, 23, 1483–1490. [Google Scholar] [CrossRef]
- Vamanu, E. Bioactive capacity of some Romanian wild edible mushrooms consumed mainly by local communities. Nat. Prod. Res. 2017, 32, 440–443. [Google Scholar] [CrossRef]
- Gergely, V.; Kubachka, K.M.; Mounicou, S.; Fodor, P.; Caruso, J.A. Selenium speciation in Agaricus bisporus and Lentinula edodes mushroom proteins using multi-dimensional chromatography coupled to inductively coupled plasma mass spectrometry. J. Chromatogr. A 2006, 1101, 94–102. [Google Scholar] [CrossRef]
- Falandysz, J. Selenium in Edible Mushrooms. J. Environ. Sci. Health Part C 2008, 26, 256–299. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Klimaszewska, M.; Górska, S.; Dawidowski, M.; Podsadni, P.; Turło, J. Biosynthesis of Se-methyl-seleno-L-cysteine in Ba-sidiomycetes fungus Lentinula edodes (Berk.) Pegler. SpringerPlus 2016, 5, 733–740. [Google Scholar] [CrossRef] [Green Version]
- Maseko, T.; Callahan, D.L.; Dunshea, F.; Doronila, A.; Kolev, S.; Ng, K. Chemical characterisation and speciation of organic selenium in cultivated selenium-enriched Agaricus bisporus. Food Chem. 2013, 141, 3681–3687. [Google Scholar] [CrossRef]
- Turło, J.; Gutkowska, B.; Malinowska, E. Relationship between the selenium, selenomethionine, and selenocysteine content of submerged cultivated mycelium of Lentinula edodes (Berk.). Acta Chromatogr. 2007, 18, 36–48. [Google Scholar]
- Egressy-Molnár, O.; Ouerdane, L.; Győrfi, J.; Dernovics, M. Analogy in selenium enrichment and selenium speciation between selenized yeast Saccharomyces cerevisiae and Hericium erinaceous (lion’s mane mushroom). LWT 2016, 68, 306–312. [Google Scholar] [CrossRef]
- Turło, J.; Gutkowska, B.; Herold, F.; Gajzlerska, W.; Dawidowski, M.; Dorociak, A.; Zobel, A. Biological Availability and Preliminary Selenium Speciation in Selenium-Enriched Mycelium ofLentinula edodes (Berk.). Food Biotechnol. 2011, 25, 16–29. [Google Scholar] [CrossRef]
- Espinosa-Ortiz, E.J.; Gonzalez-Gil, G.; Saikaly, P.E.; Van Hullebusch, E.D.; Lens, P.N.L. Effects of selenium oxyanions on the white-rot fungus Phanerochaete chrysosporium. Appl. Microbiol. Biotechnol. 2014, 99, 2405–2418. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Niedzielski, P.; Mleczek, M.; Siwulski, M.; Gąsecka, M.; Kozak, L.; Rissmann, I.; Mikołajczak, P. Efficacy of supplementation of selected medicinal mushrooms with inorganic selenium salts. J. Environ. Sci. Health Part B 2014, 49, 929–937. [Google Scholar] [CrossRef]
- Milovanović, I.N. Ability of Selenium Absorption and Biological Activity of Mycelial Extracts of Selected Basidiomycotina Species. Ph.D. Thesis, University of Belgrade, Belgrade, Serbia, June 2014; p. 84. [Google Scholar]
- Turło, J.; Gutkowska, B.; Herold, F. Effect of selenium enrichment on antioxidant activities and chemical composition of Lentinula edodes (Berk.) Pegl. mycelial extracts. Food Chem. Toxicol. 2010, 48, 1085–1091. [Google Scholar] [CrossRef]
- Gharieb, M.M.; Wilkinson, S.C.; Gadd, G.M. Reduction of selenium oxyanions by unicellular, polymorphic and filamentous fungi: Cellular location of reduced selenium and implications for tolerance. J. Ind. Microbiol. Biotechnol. 1995, 14, 300–311. [Google Scholar] [CrossRef]
- Milovanović, I.; Brčeski, I.; Stajić, M.; Korać, A.; Vukojević, J.; Knežević, A. Potential of Pleurotus ostreatus Mycelium for Se-lenium Absorption. Sci. World J. 2014, 2014, 681834. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Goyal, A.; Kalia, A.; Sodhi, H.S. Selenium stress in Ganoderma lucidum: A scanning electron microscopy appraisal. Afr. J. Microbiol. Res. 2015, 9, 855–862. [Google Scholar]
- Muñoz, A.H.S.; Kubachka, K.; Wrobel, K.; Corona, J.F.G.; Yathavakilla, S.K.V.; Caruso, J.A.; Wrobel, K. Se-Enriched Mycelia ofPleurotus ostreatus: Distribution of Selenium in Cell Walls and Cell Membranes/Cytosol. J. Agric. Food Chem. 2006, 54, 3440–3444. [Google Scholar] [CrossRef]
- Milovanovic, I.; Brceski, I.; Stajic, M.; Knezevic, A.; Vukojevic, J. Potential Enrichment of Medicinal Mushrooms with Selenium to Obtain New Dietary Supplements. Int. J. Med. Mushrooms 2013, 15, 449–455. [Google Scholar] [CrossRef] [PubMed]
- Thiry, C.; Ruttens, A.; De Temmerman, L.; Schneider, Y.-J.; Pussemier, L. Current knowledge in species-related bioavailability of selenium in food. Food Chem. 2012, 130, 767–784. [Google Scholar] [CrossRef]
- Vinceti, M.; Maraldi, T.; Bergomi, M.; Malagoli, C. Risk of Chronic Low-Dose Selenium Overexposure in Humans: Insights From Epidemiology and Biochemistry. Rev. Environ. Health 2009, 24, 231–248. [Google Scholar] [CrossRef]
- Hazane-Puch, F.; Champelovier, P.; Arnaud, J.; Garrel, C.; Ballester, B.; Faure, P.; Laporte, F. Long-term selenium supple-mentation in HaCaT cells: Importance of chemical form for antagonist (protective versus toxic) activities. Biol. Trace Elem. Res. 2013, 154, 288–298. [Google Scholar] [CrossRef] [PubMed]
- Drevko, B.I.; Drevko, R.I.; Antipov, V.A.; Chernukha, B.A.; Yakovlev, A.N. Remedy for Treatment and Prophylactics of In-fectious Diseases and Poisonings of Animals and Poultry Enhancing Their Productivity and Vitality (in Russian). Russian Federation Patent No. 2171110; MPK 7 A 61 K 33/04, Filed 26.05.1999, No. 99111064/13, 27 July 2001. [Google Scholar]
- Pankratov, A.N.; Loshchinina, E.A.; Tsivileva, O.M.; Burashnikova, M.M.; Kazarinov, I.A.; Bylinkina, N.N.; Nikitina, V.E. Effects of xenobiotic organoselenium compound on the growth and metabolism of basidiomycete Lentinula edodes culture. Izv. Saratov Univ. New Series. Ser. Chem. Biol. Ecol. 2012, 12, 11–17. [Google Scholar]
- Tsivileva, O.M.; Loshchinina, E.A.; Pankratov, A.N.; Burashnikova, M.; Yurasov, N.A.; Bylinkina, N.N.; Kazarinov, I.A.; Nikitina, V.E. Biodegradation of an Organoselenium Compound to Elemental Selenium by Lentinula edodes (Shiitake) Mushroom. Biol. Trace Element Res. 2012, 149, 97–101. [Google Scholar] [CrossRef]
- Drevko, Y.B.; Sitnikova, T.S.; Burov, A.M.; Drevko, B.I.; Shchegolev, S.Y. Reduction of diacetophenonyl selenide (DAPS-25 formulation) to acetophenone with the formation of selenium micro-and nanoparticles in the presence of Saccharomyces cerevisiae culture. Appl. Biochem. Microbiol. 2016, 52, 776–781. [Google Scholar] [CrossRef]
- Tsivileva, O.M.; Perfileva, A.I. Selenium compounds biotransformed by mushrooms: Not only dietary sources, but also toxicity mediators. Curr. Nutr. Food Sci. 2017, 13, 82–96. [Google Scholar] [CrossRef]
- Behera, M.; Ram, S. Inquiring the mechanism of formation, encapsulation, and stabilization of gold nanoparticles by poly(vinyl pyrrolidone) molecules in 1-butanol. Appl. Nanosci. 2014, 4, 247–254. [Google Scholar] [CrossRef] [Green Version]
- Ahmadi, Y.; Ahmad, S. Recent progress in the synthesis and property enhancement of waterborne polyurethane nanocom-posites: Promising and versatile macromolecules for advanced applications. Polym. Rev. 2020, 60, 226–266. [Google Scholar] [CrossRef]
- Tao, A.R.; Habas, S.; Yang, P. Shape Control of Colloidal Metal Nanocrystals. Small 2008, 4, 310–325. [Google Scholar] [CrossRef]
- Fayaz, A.M.; Balaji, K.; Girilal, M.; Yadav, R.; Kalaichelvan, P.T.; Venketesan, R. Biogenic synthesis of silver nanoparticles and their synergistic effect with antibiotics: A study against gram-positive and gram-negative bacteria. Nanomed. Nanotechnol. Biol. Med. 2010, 6, 103–109. [Google Scholar] [CrossRef] [PubMed]
- Aktürk, A.; Erol Taygun, M.; Karbancıoglu Güler, F.; Goller, G.; Küçükbayrak, S. Fabrication of antibacterial polyvinylalcohol nanocomposite mats with soluble starch coated silver nanoparticles. Colloids Surf. A Physicochem. Eng. Asp. 2019, 562, 255–262. [Google Scholar] [CrossRef]
- Wei, X.; Cai, J.; Lin, S.; Li, F.; Tian, F. Controlled release of monodisperse silver nanoparticles via in situ cross-linked polyvinyl alcohol as benign and antibacterial electrospun nanofibers. Colloids Surf. B Biointerfaces 2021, 197, 111370. [Google Scholar] [CrossRef] [PubMed]
- Siddiqui, N.; Bhardwaj, A.; Hada, R.; Yadav, V.S.; Goyal, D. Synthesis, characterization and antimicrobial study of poly (methyl methacrylate)/Ag nanocomposites. Vacuum 2018, 153, 6–11. [Google Scholar] [CrossRef]
- Philip, P.; Jose, T.; Parameswaran, M.; Thankaraj, S. Structurally modified poly(methyl methacrylate) electrospun nanofibers as better host matrix for noble metal nanoparticles. J. Appl. Polym. Sci. 2021, 138, 50210. [Google Scholar] [CrossRef]
- Jatoi, A.W. Polyurethane nanofibers incorporated with ZnAg composite nanoparticles for antibacterial wound dressing applications. Compos. Commun. 2020, 19, 103–107. [Google Scholar] [CrossRef]
- Kasi, G.; Viswanathan, K.; Sadeghi, K.; Seo, J. Optical, thermal, and structural properties of polyurethane in Mg-doped zinc oxide nanoparticles for antibacterial activity. Prog. Org. Coatings 2019, 133, 309–315. [Google Scholar] [CrossRef]
- Jafari, A.; Hassanajili, S.; Karimi, M.B.; Emami, A.; Ghaffari, F.; Azarpira, N. Effect of organic/inorganic nanoparticles on performance of polyurethane nanocomposites for potential wound dressing applications. J. Mech. Behav. Biomed. Mater. 2018, 88, 395–405. [Google Scholar] [CrossRef] [PubMed]
- Alippilakkotte, S.; Kumar, S.; Sreejith, L. Fabrication of PLA/Ag nanofibers by green synthesis method using Momordica charantia fruit extract for wound dressing applications. Colloids Surf. A Physicochem. Eng. Asp. 2017, 529, 771–782. [Google Scholar] [CrossRef]
- Zhang, H.Y.; Jiang, H.B.; Kim, J.-E.; Zhang, S.; Kim, K.-M.; Kwon, J.-S. Bioresorbable magnesium-reinforced PLA membrane for guided bone/tissue regeneration. J. Mech. Behav. Biomed. Mater. 2020, 112, 104061. [Google Scholar] [CrossRef] [PubMed]
- Sportelli, M.C.; Picca, R.A.; Cioffi, N. Recent advances in the synthesis and characterization of nano-antimicrobials. TrAC Trends Anal. Chem. 2016, 84, 131–138. [Google Scholar] [CrossRef]
- Ditaranto, N.; van der Werf, I.D.; Picca, R.A.; Sportelli, M.C.; Giannossa, L.C.; Bonerba, E.; Tantillo, G.; Sabbatini, L. Charac-terization and behaviour of ZnO-based nanocomposites designed for the control of biodeterioration of patrimonial stone-works. New J. Chem. 2015, 39, 6836–6843. [Google Scholar] [CrossRef]
- Zare, E.N.; Makvandi, P.; Borzacchiello, A.; Tay, F.R.; Ashtari, K.; Padil, V.V.T. Antimicrobial gum bio-based nanocomposites and their industrial and biomedical applications. Chem. Commun. 2019, 55, 14871–14885. [Google Scholar] [CrossRef] [PubMed]
- Stevanović, M.; Filipović, N.; Djurdjević, J.; Lukić, M.; Milenković, M.; Boccaccini, A. 45S5Bioglass®-based scaffolds coated with selenium nanoparticles or with poly (lactide-co-glycolide)/selenium particles: Processing, evaluation and antibacterial ac-tivity. Colloids Surf. B Biointerfaces 2015, 132, 208–215. [Google Scholar] [CrossRef] [Green Version]
- Ermakova, T.G.; Kuznetsova, N.P.; Pozdnyakov, A.S.; Larina, L.; Korzhova, S.A.; Mazyar, I.V.; Shcherbakova, V.S.; Ivanov, A.V.; Mikhaleva, A.I.; Prozorova, G.F. 1-Vinyl-1,2,4-triazole in copolymerization reaction with 1-vinyl-4,5,6,7-tetrahydroindole: Synthesis and properties of copolymers. Russ. Chem. Bull. 2016, 65, 485–489. [Google Scholar] [CrossRef]
- Fernández-Ortuño, D.; Torés, J.A.; de Vicente, A.; Pérez-García, A. Mechanisms of resistance to QoI fungicides in phyto-pathogenic fungi. Int. Microbiol. 2008, 11, 1–9. [Google Scholar] [PubMed]
- Shcherbakova, L.A. Fungicide resistance of plant pathogenic fungi and their chemosensitization as a tool to increase an-ti-disease effects of triazoles and strobilurines. Sel’skokhozyaistvennaya Biol. [Agric. Biol. ] 2019, 54, 875–891. [Google Scholar]
- Pobezhimova, T.P.; Siberian Institute of Plant Physiology and Biochemistry SB RAS; Korsukova, A.V.; Dorofeev, N.; Grabelnych, O.I. Physiological effects of triazole fungicides in plants. Proc. Univ. Appl. Chem. Biotechnol. 2019, 3, 461–476. [Google Scholar] [CrossRef] [Green Version]
- Yin, B.; Ma, H.; Wang, S.; Chen, S. Electrochemical Synthesis of Silver Nanoparticles under Protection of Poly(N-vinylpyrrolidone). J. Phys. Chem. B 2003, 107, 8898–8904.105. [Google Scholar] [CrossRef]
- Kvitek, L.; Panáček, A.; Soukupova, J.; Kolar, M.; Vecerova, R.; Prucek, R.; Holecová, M.; Zboril, R. Effect of surfactants and polymers on stability and antibacterial activity of silver nanoparticles (NPs). J. Phys. Chem. C 2008, 112, 5825–5834. [Google Scholar] [CrossRef]
- Sintubin, L.; De Windt, W.; Dick, J.; Mast, J.; Van Der Ha, D.; Verstraete, W.; Boon, N. Lactic acid bacteria as reducing and capping agent for the fast and efficient production of silver nanoparticles. Appl. Microbiol. Biotechnol. 2009, 84, 741–749. [Google Scholar] [CrossRef]
- Bakshi, P.S.; Selvakumar, D.; Kadirvelu, K.; Kumar, N.S. Chitosan as an environment friendly biomaterial–a review on recent modifications and applications. Int. J. Biol. Macromol. 2020, 150, 1072–1083. [Google Scholar] [CrossRef] [PubMed]
- Chen, S.-F.; Zhang, H. Aggregation kinetics of nanosilver in diferent water conditions. Adv. Nat. Sci. Nanosci. Nanotechnol. 2012, 3, 035006. [Google Scholar] [CrossRef]
- Zhang, C.; Hu, Z.; Deng, B. Silver nanoparticles in aquatic environments: Physiochemical behavior and antimicrobial mechanisms. Water Res. 2016, 88, 403–427. [Google Scholar] [CrossRef] [Green Version]
- Alexandridis, P. Gold Nanoparticle Synthesis, Morphology Control, and Stabilization Facilitated by Functional Polymers. Chem. Eng. Technol. 2010, 34, 15–28. [Google Scholar] [CrossRef]
- Ermakova, T.G.; Shaulina, L.P.; Kuznetsova, N.P.; Prozorova, G.F. Synthesis and sorption activity of copolymers of vinyl-triazole with diethylene glycol divinyl ether. Russ. Chem. Bull. 2017, 66, 2298–2302. [Google Scholar] [CrossRef]
- Ermakova, T.G.; Shaulina, L.P.; Kuznetsova, N.P.; Ratovskii, G.V.; Soboleva, I.N.; Pozdnyakov, A.S.; Prozorova, G.F. Sorption recovery of noble metal ions with a copolymer of 1-vinyl-1,2,4-triazole with acrylonitrile. Russ. J. Appl. Chem. 2012, 85, 1289–1295. [Google Scholar] [CrossRef]
- Ermakova, T.G.; Shaulina, L.P.; Kuznetsova, N.P.; Volkova, L.I.; Pozdnyakov, A.S.; Prozorova, G.F. Sorption of noble metal compounds by cross-linked copolymer of 1-vinyl-1,2,4-triazole with acrylic acid. Russ. J. Appl. Chem. 2012, 85, 35–40. [Google Scholar] [CrossRef]
- Aslan, A.; Bozkurt, A. Development and characterization of polymer electrolyte membranes based on ionical cross-linked poly(1-vinyl-1,2,4 triazole) and poly(vinylphosphonic acid). J. Power Sources 2009, 191, 442–447. [Google Scholar] [CrossRef]
- Dzhardimalieva, G.I.; Uflyand, I.E. Synthetic Methodologies for Chelating Polymer Ligands: Recent Advances and Future Development. ChemistrySelect 2018, 3, 13234–13270. [Google Scholar] [CrossRef]
- Tikhonov, N.I.; Khutsishvili, S.S.; Larina, L.; Pozdnyakov, A.S.; Emel’Yanov, A.I.; Prozorova, G.F.; Vashchenko, A.V.; Vakul’Skaya, T.I. Silver polymer complexes as precursors of nanocomposites based on polymers of 1-vinyl-1,2,4-triazole. J. Mol. Struct. 2019, 1180, 272–279. [Google Scholar] [CrossRef]
- Tsivileva, O.M.; Perfileva, A.I.; Ivanova, A.A.; Pozdnyakov, A.S.; Prozorova, G.F. The Effect of Selenium- or Met-al-Nanoparticles Incorporated Nanocomposites of Vinyl Triazole Based Polymers on Fungal Growth and Bactericidal Properties. J. Polym. Environ. 2021, 29, 1287–1297. [Google Scholar] [CrossRef]
- Jamróz, E.; Kulawik, P.; Kopel, P. The Effect of Nanofillers on the Functional Properties of Biopolymer-Based Films: A Review. Polymers 2019, 11, 675. [Google Scholar] [CrossRef] [Green Version]
- John, M.J.; Thomas, S. Biofibres and biocomposites. Carbohydr. Polym. 2008, 71, 343–364. [Google Scholar] [CrossRef]
- Trache, D.; Hussin, M.H.; Chuin, C.T.H.; Sabar, S.; Fazita, M.N.; Taiwo, O.F.; Hassan, T.; Haafiz, M.M. Microcrystalline cellulose: Isolation, characterization and bio-composites application—A review. Int. J. Biol. Macromol. 2016, 93, 789–804. [Google Scholar] [CrossRef]
- Khan, M.U.A.; Haider, S.; Haider, A.; Kadir, M.R.A.; Abd Razak, S.I.; Shah, S.A.; Javad, A.; Shakir, I.; Al-Zahrani, A.A. Devel-opment of Porous, Antibacterial and Biocompatible GO/n-HAp/Bacterial Cellulose/β-Glucan Biocomposite Scaffold for Bone Tissue Engineering. Arab. J. Chem. 2020, 14, 102924. [Google Scholar] [CrossRef]
- Frank, L.A.; Onzi, G.R.; Morawski, A.S.; Pohlmann, A.R.; Guterres, S.S.; Contri, R.V. Chitosan as a coating material for na-noparticles intended for biomedical applications. React. Funct. Polym. 2020, 147, 104459. [Google Scholar] [CrossRef]
- Amine, R.; Tarek, C.; Hassane, E.; Noureddine, E.H.; Khadija, O. Chemical Proprieties of Biopolymers (Chitin/Chitosan) and their Synergic Effects with Endophytic Bacillus Species: Unlimited Applications in Agriculture. Molecules 2021, 26, 1117. [Google Scholar] [CrossRef] [PubMed]
- Baxter, A.; Dillon, M.; Taylor, K.A.; Roberts, G.A. Improved method for i.r. determination of the degree of N-acetylation of chitosan. Int. J. Biol. Macromol. 1992, 14, 166–169. [Google Scholar] [CrossRef]
- Chen, W.; Li, Y.; Yang, S.; Yue, L.; Jiang, Q.; Xia, W. Synthesis and antioxidant properties of chitosan and carboxymethyl chitosan-stabilized selenium nanoparticles. Carbohydr. Polym. 2015, 132, 574–581. [Google Scholar] [CrossRef] [PubMed]
- Kumar, M.N.V.R.; Muzzarelli, R.A.A.; Muzzarelli, C.; Sashiwa, H.; Domb, A.J. Chitosan chemistry and pharmaceutical per-spectives. Chem. Rev. 2004, 104, 6017–6084. [Google Scholar] [CrossRef]
- Chen, X.-G.; Park, H.-J. Chemical characteristics of O-carboxymethyl chitosans related to the preparation conditions. Carbohydr. Polym. 2003, 53, 355–359. [Google Scholar] [CrossRef]
- Jaiswal, L.; Shankar, S.; Rhim, J.-W.; Hahm, D.-H. Lignin-mediated green synthesis of AgNPs in carrageenan matrix for wound dressing applications. Int. J. Biol. Macromol. 2020, 159, 859–869. [Google Scholar] [CrossRef] [PubMed]
- Jiang, Y.; Huang, J.; Wu, X.; Ren, Y.; Li, Z.; Ren, J. Controlled release of silver ions from AgNPs using a hydrogel based on konjac glucomannan and chitosan for infected wounds. Int. J. Biol. Macromol. 2020, 149, 148–157. [Google Scholar] [CrossRef]
- Lesnichaya, M.V.; Aleksandrova, G.P.; Feoktistova, L.P.; Sapozhnikov, A.N.; Fadeeva, T.V.; Sukhov, B.G.; Trofimov, B.A. Silver-containing nanocomposites based on galactomannan and carrageenan: Synthesis, structure, and antimicrobial properties. Russ. Chem. Bull. 2010, 59, 2323–2328. [Google Scholar] [CrossRef]
- Lesnichaya, M.V.; Aleksandrova, G.P.; Sukhov, B.; Rokhin, A.V. Molecular-weight characteristics of galactomannan and carrageenan. Chem. Nat. Compd. 2013, 49, 405–410. [Google Scholar] [CrossRef]
- Rao, K.M.; Suneetha, M.; Zo, S.; Duck, K.H.; Han, S.S. One-pot synthesis of ZnO nanobelt-like structures in hyaluronan hy-drogels for wound dressing applications. Carbohydr. Polym. 2019, 223, 115124. [Google Scholar] [CrossRef]
- Perfileva, A.I.; Nozhkina, O.A.; Graskova, I.A.; Sidorov, A.V.; Lesnichaya, M.V.; Aleksandrova, G.P.; Dolmaa, G.; Klimenkov, I.V.; Sukhov, B. Synthesis of selenium and silver nanobiocomposites and their influence on phytopathogenic bacterium Clavibacter michiganensis subsp. sepedonicus. Russ. Chem. Bull. 2018, 67, 157–163. [Google Scholar] [CrossRef]
- Lv, H.; Cui, S.; Yang, Q.; Song, X.; Wang, D.; Hu, J.; Zhou, Y.; Liu, Y. AgNPs-incorporated nanofiber mats: Relationship between AgNPs size/content, silver release, cytotoxicity, and antibacterial activity. Mater. Sci. Eng. C 2021, 118, 111331. [Google Scholar] [CrossRef]
- Soubhagya, A.; Moorthi, A.; Prabaharan, M. Preparation and characterization of chitosan/pectin/ZnO porous films for wound healing. Int. J. Biol. Macromol. 2020, 157, 135–145. [Google Scholar] [CrossRef] [PubMed]
- Hileuskaya, K.; Ladutska, A.; Kulikouskaya, V.; Kraskouski, A.; Novik, G.; Kozerozhets, I.; Kozlovskiy, A.; Agabekov, V. ‘Green’ approach for obtaining stable pectin-capped silver nanoparticles: Physico-chemical characterization and antibacterial activity. Colloids Surf. A Physicochem. Eng. Asp. 2020, 585, 124141. [Google Scholar] [CrossRef]
- Trofimov, B.A.; Sukhov, B.G.; Aleksandrova, G.P.; Medvedeva, S.A.; Grishchenko, L.A.; Mal’Kina, A.G.; Feoktistova, L.P.; Sapozhnikov, A.N.; Dubrovina, V.I.; Martynovich, E.; et al. Nanocomposites with Magnetic, Optical, Catalytic, and Biologically Active Properties Based on Arabinogalactan. Dokl. Chem. 2003, 393, 287–288. [Google Scholar] [CrossRef]
- Grishchenko, L.A.; Medvedeva, S.A.; Aleksandrova, G.P.; Feoktistova, L.P.; Sapozhnikov, A.N.; Sukhov, B.G.; Trofimov, B.A. Redox reactions of arabinogalactan with silver ions and formation of nanocomposites. Russ. J. Gen. Chem. 2006, 76, 1111–1116. [Google Scholar] [CrossRef]
- Graskova, I.A.; Zhivet’Yev, M.A.; Borovskii, G.B.; Sukhov, B.G. Bactericide impact of polymer-stabilized multi-functional nano-composites. J. Stress Physiol. Biochem. 2012, 8, S33. [Google Scholar]
- Papkina, A.V.; Perfileva, A.I.; Zhivetev, M.A.; Borovskiy, G.B.; Graskova, I.A.; Lesnichaya, M.V.; Klimenkov, I.V.; Sukhov, B.G.; Trofimov, B.A. Effect of selenium and arabinogalactan nanocomposite on viability of the phytopathogen Clavibacter michi-ganensis subsp. sepedonicus. Dokl. Biol. Sci. 2015, 461, 89–91. [Google Scholar] [CrossRef]
- Papkina, A.V.; Perfileva, A.I.; Zhivet’yev, M.A.; Borovskii, G.B.; Graskova, I.A.; Klimenkov, I.V.; Lesnichaya, M.V.; Sukhov, B.G.; Trofimov, B.A. Complex effects of selenium-arabinogalactan nanocomposite on both phytopathogen Clavibacter michi-ganensis subsp. sepedonicus and potato plants. Nanotechn. Russ. 2015, 10, 484–491. [Google Scholar] [CrossRef]
- Kolesnikova, L.; Karpova, E.A.; Vlasov, B.Y.; Sukhov, B.G.; Mov, B.A.T. Lipid Peroxidation–Antioxidant Defense System during Toxic Liver Damage and Its Correction with a Composite Substance Containing Selenium and Arabinogalactan. Bull. Exp. Biol. Med. 2015, 159, 225–228. [Google Scholar] [CrossRef]
- Shurygina, I.A.; Rodionova, L.V.; Shurygin, M.; Sukhov, B.; Kuznetsov, S.V.; Popova, L.G.; Dremina, N.N. Using confocal microscopy to study the effect of an original pro-enzyme Se/arabinogalactan nanocomposite on tissue regeneration in a skeletal system. Bull. Russ. Acad. Sci. Phys. 2015, 79, 256–258. [Google Scholar] [CrossRef]
- Rodionova, L.V.; Shurygina, I.A.; Sukhov, B.G.; Popova, L.G.; Shurygin, M.; Artem’Ev, A.V.; Pogodaeva, N.N.; Kuznetsov, S.V.; Gusarova, N.K.; Trofimov, B. Nanobiocomposite based on selenium and arabinogalactan: Synthesis, structure, and application. Russ. J. Gen. Chem. 2015, 85, 485–487. [Google Scholar] [CrossRef]
- Lesnichaya, M.V.; Sukhov, B.; Aleksandrova, G.P.; Gasilova, E.R.; Vakul’Skaya, T.I.; Khutsishvili, S.S.; Sapozhnikov, A.N.; Klimenkov, I.V.; Trofimov, B. Chiroplasmonic magnetic gold nanocomposites produced by one-step aqueous method using κ-carrageenan. Carbohydr. Polym. 2017, 175, 18–26. [Google Scholar] [CrossRef] [PubMed]
- Lesnichaya, M.V.; Shendrik, R.; Sukhov, B.G. Relation between excitation dependent luminescence and particle size distri-butions for the selenium nanoparticles in κ-carrageenan shell. J. Lumin. 2019, 211, 305–313. [Google Scholar] [CrossRef]
- Zhu, C.; Zhang, S.; Song, C.; Zhang, Y.; Ling, Q.; Hoffmann, P.R.; Li, J.; Chen, T.; Zheng, W.; Huang, Z. Selenium nanoparticles decorated with Ulva lactuca polysaccharide potentially attenuate colitis by inhibiting NF-κB mediated hyper inflammation. J. Nanobiotechnol. 2017, 15, 20. [Google Scholar] [CrossRef] [Green Version]
- Wang, J.; Zhang, Y.; Yuan, Y.; Yue, T. Immunomodulatory of selenium nano-particles decorated by sulfated Ganoderma lucidum polysaccharides. Food Chem. Toxicol. 2014, 68, 183–189. [Google Scholar] [CrossRef] [PubMed]
- Perinelli, D.R.; Fagioli, L.; Campana, R.; Lam, J.K.; Baffone, W.; Palmieri, G.F.; Casettari, L.; Bonacucina, G. Chitosan-based nanosystems and their exploited antimicrobial activity. Eur. J. Pharm. Sci. 2018, 117, 8–20. [Google Scholar] [CrossRef]
- Tamer, T.M.; Hassan, M.A.; Omer, A.M.; Valachová, K.; Eldin, M.M.; Collins, M.N.; Šoltés, L. Antibacterial and antioxidative activity of O-amine functionalized chitosan. Carbohydr. Polym. 2017, 169, 441–450. [Google Scholar] [CrossRef]
- Liang, Y.; Faik, A.; Kieliszewski, M.; Tan, L.; Xu, W.L.; Showalter, A.M. Identification and characterization of in vitro galacto-syltransferase activities involved in arabinogalactan-protein glycosylation in tobacco and Arabidopsis. Plant Physiol. 2010, 154, 632–642. [Google Scholar] [CrossRef] [Green Version]
- Kagimura, F.Y.; da Cunha, M.A.A.; Barbosa, A.M.; Dekker, R.F.; Malfatti, C.R.M. Biological activities of derivatized d-glucans: A review. Int. J. Biol. Macromol. 2015, 72, 588–598. [Google Scholar] [CrossRef]
- Kaur, R.; Sharma, M.; Ji, D.; Xu, M.; Agyei, D. Structural Features, Modification, and Functionalities of Beta-Glucan. Fibers 2019, 8, 1. [Google Scholar] [CrossRef] [Green Version]
- Chen, L.; Ge, M.-D.; Zhu, Y.-J.; Song, Y.; Cheung, P.C.; Zhang, B.-B.; Liu, L.-M. Structure, bioactivity and applications of natural hyperbranched polysaccharides. Carbohydr. Polym. 2019, 223, 115076. [Google Scholar] [CrossRef]
- Legentil, L.; Paris, F.; Ballet, C.; Trouvelot, S.; Daire, X.; Vetvicka, V.; Ferrières, V. Molecular interactions of β-(1→ 3)-glucans with their receptors. Molecules 2015, 20, 9745–9766. [Google Scholar] [CrossRef]
- Tao, Y.; Zhang, L. Determination of molecular size and shape of hyperbranched polysaccharide in solution. Biopolymers 2006, 83, 414–423. [Google Scholar] [CrossRef] [PubMed]
- Zeng, J.; Wang, R.; Zhang, S.; Fang, J.; Liu, S.; Sun, G.; Xu, B.; Xiao, Y.; Fu, D.; Zhang, W.; et al. Hydro-gen-bonding-assisted exogenous nucleophilic reagent effect for β-selective glycosylation of rare 3-amino sugars. J. Am. Chem. Soc. 2019, 141, 8509–8515. [Google Scholar] [CrossRef] [PubMed]
- Li, X.; Cheung, P.C.K. Application of natural β-d-glucans as biocompatible functional nanomaterials. Food Sci. Hum. Wellness 2019, 8, 315–319. [Google Scholar] [CrossRef]
- Lau, B.F.; Abdullah, N.; Aminudin, N. Chemical Composition of the Tiger’s Milk Mushroom, Lignosus rhinocerotis (Cooke) Ryvarden, from Different Developmental Stages. J. Agric. Food Chem. 2013, 61, 4890–4897. [Google Scholar] [CrossRef] [PubMed]
- Liu, C.; Choi, M.W.; Li, X.; Cheung, P.C. Immunomodulatory effect of structurally-characterized mushroom sclerotial polysaccharides isolated from Polyporus rhinocerus on human monoctyes THP-1. J. Funct. Foods 2018, 41, 90–99. [Google Scholar] [CrossRef]
- Liu, C.; Choi, M.W.; Xue, X.; Cheung, P.C. Immunomodulatory effect of structurally characterized mushroom sclerotial polysaccharides isolated from Polyporus rhinocerus on bone marrow dendritic cells. J. Agric. Food Chem. 2019, 67, 12137–12143. [Google Scholar] [CrossRef]
- Han, X.-Q.; Chan, B.C.L.; Dong, C.-X.; Yang, Y.-H.; Ko, C.H.; Yue, G.G.-L.; Chen, D.; Wong, C.-K.; Lau, C.; Tu, P.-F.; et al. Isolation, Structure Characterization, and Immunomodulating Activity of a Hyperbranched Polysaccharide from the Fruiting Bodies of Ganoderma sinense. J. Agric. Food Chem. 2012, 60, 4276–4281. [Google Scholar] [CrossRef]
- Zhang, Y.; Wang, J.; Zhang, L. Creation of Highly Stable Selenium Nanoparticles Capped with Hyperbranched Polysaccharide in Water. Langmuir 2010, 26, 17617–17623. [Google Scholar] [CrossRef]
- Chen, W.; Zhao, Z.; Li, Y. Simultaneous increase of mycelial biomass and intracellular polysaccharide from Fomes fomentarius and its biological function of gastric cancer intervention. Carbohydr. Polym. 2011, 85, 369–375. [Google Scholar] [CrossRef]
- Ruthes, A.C.; Smiderle, F.; Iacomini, M. d-Glucans from edible mushrooms: A review on the extraction, purification and chemical characterization approaches. Carbohydr. Polym. 2015, 117, 753–761. [Google Scholar] [CrossRef] [PubMed]
- Wasser, S.P. Current findings, future trends, and unsolved problems in studies of medicinal mushrooms. Appl. Microbiol. Biotechnol. 2011, 89, 1323–1332. [Google Scholar] [CrossRef]
- Corrêa, R.C.G.; Brugnari, T.; Bracht, A.; Peralta, R.M.; Ferreira, I.C. Biotechnological, nutritional and therapeutic uses of Pleurotus spp. (Oyster mushroom) related with its chemical composition: A review on the past decade findings. Trends Food Sci. Technol. 2016, 50, 103–117. [Google Scholar] [CrossRef] [Green Version]
- Perfileva, A.I.; Tsivileva, O.M.; Koftin, O.V.; Anis’Kov, A.A.; Ibragimova, D.N. Selenium-Containing Nanobiocomposites of Fungal Origin Reduce the Viability and Biofilm Formation of the Bacterial Phytopathogen Clavibacter michiganensis subsp. sepedonicus. Nanotechnol. Russ. 2018, 13, 268–276. [Google Scholar] [CrossRef]
- Kim, J.; Van der Bruggen, B. The use of nanoparticles in polymeric and ceramic membrane structures: Review of manufacturing procedures and performance improvement for water treatment. Environ. Poll. 2010, 158, 2335–2349. [Google Scholar] [CrossRef]
- Videira-Quintela, D.; Martin, O.; Montalvo, G. Recent advances in polymer-metallic composites for food packaging applica-tions. Trends Food Sci. Technol. 2021, 109, 230–244. [Google Scholar] [CrossRef]
- Shakibaie, M.; Forootanfar, H.; Golkari, Y.; Mohammadi-Khorsand, T.; Shakibaie, M.R. Anti-biofilm activity of biogenic selenium nanoparticles and selenium dioxide against clinical isolates of Staphylococcus aureus, Pseudomonas aeruginosa, and Proteus mirabilis. J. Trace Elements Med. Biol. 2015, 29, 235–241. [Google Scholar] [CrossRef] [PubMed]
- Tran, P.A.; Webster, T.J. Antimicrobial selenium nanoparticle coatings on polymeric medical devices. Nanotechnology 2013, 24, 155101. [Google Scholar] [CrossRef]
- Zhang, Q.; Chen, L.; Guo, K.; Zheng, L.; Liu, B.; Yu, W.; Guo, C.; Liu, Z.; Chen, Y.; Tang, Z. Effects of Different Selenium Levels on Gene Expression of a Subset of Selenoproteins and Antioxidative Capacity in Mice. Biol. Trace Element Res. 2013, 154, 255–261. [Google Scholar] [CrossRef] [Green Version]
- Mennini, N.; Furlanetto, S.; Cirri, M.; Mura, P. Quality by design approach for developing chitosan-Ca-alginate microspheres for colon delivery of celecoxib-hydroxy-propyl-b-cyclodextrin-PVP complex. Eur. J. Pharm. Biopharm. 2012, 80, 67–75. [Google Scholar] [CrossRef] [PubMed]
- Khiralla, G.M.; El-Deeb, B.A. Antimicrobial and antibiofilm effects of selenium nanoparticles on some foodborne pathogens. LWT 2015, 63, 1001–1007. [Google Scholar] [CrossRef]
- Xu, H.; Cao, W.; Zhang, X. Selenium-Containing Polymers: Promising Biomaterials for Controlled Release and Enzyme Mimics. Accounts Chem. Res. 2013, 46, 1647–1658. [Google Scholar] [CrossRef]
- Xia, Y.; You, P.; Xu, F.; Liu, J.; Xing, F. Novel Functionalized Selenium Nanoparticles for Enhanced Anti-Hepatocarcinoma Activity In vitro. Nanoscale Res. Lett. 2015, 10, 349. [Google Scholar] [CrossRef] [Green Version]
- Zheng, W.; Cao, C.; Liu, Y.; Yu, Q.; Zheng, C.; Sun, D.; Ren, X.; Liu, J. Multifunctional polyamidoamine-modified selenium nanoparticles dual-delivering siRNA and cisplatin to A549/DDP cells for reversal multidrug resistance. Acta Biomater. 2015, 11, 368–380. [Google Scholar] [CrossRef]
- Poluboyarinov, P.A.; Elistratov, D.G.; Moiseeva, I.J. Antitumor Activity of Selenium and Search Parameters for Its New Po-tentially Active Derivatives. Russ. J. Bioorgan. Chem. 2020, 46, 989–1003. [Google Scholar] [CrossRef]
- Liu, T.; Zeng, L.; Jiang, W.; Fu, Y.; Zheng, W.; Chen, T. Rational design of cancer-targeted selenium nanoparticles to antagonize multidrug resistance in cancer cells. Nanomed. Nanotechnol. Biol. Med. 2015, 11, 947–958. [Google Scholar] [CrossRef] [PubMed]
- Sun, D.; Liu, Y.; Yu, Q.; Qin, X.; Yang, L.; Zhou, Y.; Chen, L.; Liu, J. Inhibition of tumor growth and vasculature and fluorescence imaging using functionalized ruthenium-thiol protected selenium nanoparticles. Biomaterials 2014, 35, 1572–1583. [Google Scholar] [CrossRef] [PubMed]
- Shivaramakrishnan, B.; Gurumurthy, B.; Balasubramanian, A. Potential biomedical applications of metallic nanobiomaterials: A review. Int. J. Pharm. Sci. Res. 2017, 8, 985–1000. [Google Scholar]
- Medhi, R.; Srinoi, P.; Ngo, N.; Tran, H.-V.; Lee, T.R. Nanoparticle-Based Strategies to Combat COVID-19. ACS Appl. Nano Mater. 2020, 3, 8557–8580. [Google Scholar] [CrossRef]
- Lin, Z.; Li, Y.; Guo, M.; Xiao, M.; Wang, C.; Zhao, M.; Xu, T.; Xia, Y.; Zhu, B. Inhibition of H1N1 influenza virus by selenium nanoparticles loaded with zanamivir through p38 and JNK signaling pathways. RSC Adv. 2017, 7, 35290–35296. [Google Scholar] [CrossRef] [Green Version]
- Li, Y.; Lin, Z.; Guo, M.; Xia, Y.; Zhao, M.; Wang, C.; Xu, T.; Chen, T.; Zhu, B. Inhibitory activity of selenium nanoparticles functionalized with oseltamivir on H1N1 influenza virus. Int. J. Nanomed. 2017, 12, 5733–5743. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Li, Y.; Lin, Z.; Guo, M.; Zhao, M.; Xia, Y.; Wang, C.; Xu, T.; Zhu, B. Inhibition of H1N1 influenza virus-induced apoptosis by functionalized selenium nanoparticles with amantadine through ROS-mediated AKT signaling pathways. Int. J. Nanomed. 2018, ume 13, 2005–2016. [Google Scholar] [CrossRef] [Green Version]
- Lin, Z.; Li, Y.; Gong, G.; Xia, Y.; Wang, C.; Chen, Y.; Hua, L.; Zhong, J.; Tang, Y.; Liu, X.; et al. Restriction of H1N1 influenza virus infection by selenium nanoparticles loaded with ribavirin via resisting caspase-3 apoptotic pathway. Int. J. Nanomed. 2018, ume 13, 5787–5797. [Google Scholar] [CrossRef] [Green Version]
- Li, Y.; Lin, Z.; Gong, G.; Guo, M.; Xu, T.; Wang, C.; Zhao, M.; Xia, Y.; Tang, Y.; Zhong, J.; et al. Inhibition of H1N1 influenza virus-induced apoptosis by selenium nanoparticles functionalized with arbidol through ROS-mediated signaling pathways. J. Mater. Chem. B 2019, 7, 4252–4262. [Google Scholar] [CrossRef]
- Iranifam, M.; Fathinia, M.; Rad, T.S.; Hanifehpour, Y.; Khataee, A.; Joo, S. A novel selenium nanoparticles-enhanced chemiluminescence system for determination of dinitrobutylphenol. Talanta 2013, 107, 263–269. [Google Scholar] [CrossRef] [PubMed]
- Chen, T.; Wong, Y.-S.; Zheng, W.; Bai, Y.; Huang, L. Selenium nanoparticles fabricated in Undaria pinnatifida polysaccharide solutions induce mitochondria-mediated apoptosis in A375 human melanoma cells. Colloids Surf. B Biointerfaces 2008, 67, 26–31. [Google Scholar] [CrossRef]
- Huang, Y.; He, L.; Liu, W.; Fan, C.; Zheng, W.; Wong, Y.-S.; Chen, T. Selective cellular uptake and induction of apoptosis of cancer-targeted selenium nanoparticles. Biomaterials 2013, 34, 7106–7116. [Google Scholar] [CrossRef] [PubMed]
- Wu, H.; Li, X.; Liu, W.; Chen, T.; Li, Y.; Zheng, W.; Man, C.W.-Y.; Wong, M.-K.; Wong, K.-H. Surface decoration of selenium nanoparticles by mushroom polysaccharides–protein complexes to achieve enhanced cellular uptake and antiproliferative activity. J. Mater. Chem. 2012, 22, 9602–9610. [Google Scholar] [CrossRef]
- Yang, Y.; Mathieu, J.M.; Chattopadhyay, S.; Miller, J.T.; Wu, T.; Shibata, T.; Guo, W.; Alvarez, P.J. Defense mechanisms of Pseudomonas aeruginosa PAO1 against quantum dots and their released heavy metals. ACS Nano 2012, 6, 6091–6098. [Google Scholar] [CrossRef]
- Wu, H.; Zhu, H.; Li, X.; Liu, Z.; Zheng, W.; Chen, T.; Yu, B.; Wong, K.-H. Induction of Apoptosis and Cell Cycle Arrest in A549 Human Lung Adenocarcinoma Cells by Surface-Capping Selenium Nanoparticles: An Effect Enhanced by Polysaccharide–Protein Complexes from Polyporus rhinocerus. J. Agric. Food Chem. 2013, 61, 9859–9866. [Google Scholar] [CrossRef]
- Yu, B.; Zhang, Y.; Zheng, W.; Fan, C.; Chen, T. Positive Surface Charge Enhances Selective Cellular Uptake and Anticancer Efficacy of Selenium Nanoparticles. Inorg. Chem. 2012, 51, 8956–8963. [Google Scholar] [CrossRef]
- Zhang, Y.; Li, X.; Huang, Z.; Zheng, W.; Fan, C.; Chen, T. Enhancement of cell permeabilization apoptosis-inducing activity of selenium nanoparticles by ATP surface decoration. Nanomed. Nanotechnol. Biol. Med. 2013, 9, 74–84. [Google Scholar] [CrossRef]
- Khurana, A.; Tekula, S.; Saifi, M.A.; Venkatesh, P.; Godugu, C. Therapeutic applications of selenium nanoparticles. Biomed. Pharmacother. 2019, 111, 802–812. [Google Scholar] [CrossRef]
- Ramamurthy, C.; Sampath, K.S.; Arunkumar, P.; Kumar, M.S.; Sujatha, V.; Premkumar, K.; Thirunavukkarasu, C. Green synthesis and characterization of selenium nanoparticles and its augmented cytotoxicity with doxorubicin on cancer cells. Bioprocess Biosyst. Eng. 2013, 36, 1131–1139. [Google Scholar] [CrossRef] [PubMed]
- Kumar, S.; Tomar, M.S.; Acharya, A. Carboxylic group-induced synthesis and characterization of selenium nanoparticles and its anti-tumor potential on Dalton’s lymphoma cells. Colloids Surf. B Biointerfaces 2015, 126, 546–552. [Google Scholar] [CrossRef] [PubMed]
- Ren, J.; Liao, W.; Zhang, R.; Dong, C.; Yu, Z. Novel walnut peptide–selenium hybrids with enhanced anticancer synergism: Facile synthesis and mechanistic investigation of anticancer activity. Int. J. Nanomed. 2016, 11, 1305–1321. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Wadhwani, S.A.; Gorain, M.; Banerjee, P.; Shedbalkar, U.U.; Singh, R.; Kundu, G.C.; Chopade, B.A. Green synthesis of selenium nanoparticles using Acinetobacter sp. SW30: Optimization, characterization and its anticancer activity in breast cancer cells. Int. J. Nanomed. 2017, 12, 6841–6855. [Google Scholar] [CrossRef] [Green Version]
- Xu, C.; Qiao, L.; Guo, Y.; Ma, L.; Cheng, Y. Preparation, characteristics and antioxidant activity of polysaccharides and pro-teins-capped selenium nanoparticles synthesized by Lactobacillus casei ATCC 393. Carbohydr. Polym. 2018, 195, 576–585. [Google Scholar] [CrossRef]
- Tabibi, M.; Agaei, S.S.; Amoozegar, M.A.; Nazari, R.; Zolfaghari, M.R. Antibacterial, Antioxidant, and Anticancer Activities of Biosynthesized Selenium Nanoparticles Using Two Indigenous Halophilic Bacteria. Arch. Hyg. Sci. 2020, 9, 275–286. [Google Scholar]
- Goud, K.G.; Veldurthi, N.K.; Vithal, M.; Reddy, G. Characterization and evaluation of biological and photocatalytic activities of selenium nanoparticles synthesized using yeast fermented broth. J. Mater. Nanosci. 2016, 3, 33–40. [Google Scholar]
- El-Sayed, E.S.R.; Abdelhakim, H.K.; Zakaria, Z. Extracellular biosynthesis of cobalt ferrite nanoparticles by Monascus pur-pureus and their antioxidant, anticancer and antimicrobial activities: Yield enhancement by gamma irradiation. Mater. Sci. Eng. C 2020, 107, 110318. [Google Scholar] [CrossRef] [PubMed]
- Vahidi, H.; Barabadi, H.; Saravanan, M. Emerging Selenium Nanoparticles to Combat Cancer: A Systematic Review. J. Clust. Sci. 2020, 31, 301–309. [Google Scholar] [CrossRef]
- Huang, T.-S.; Shyu, Y.-C.; Chen, H.-Y.; Lin, L.-M.; Lo, C.-Y.; Yuan, S.-S.; Chen, P.-J. Effect of Parenteral Selenium Supplementation in Critically Ill Patients: A Systematic Review and Meta-Analysis. PLoS ONE 2013, 8, e54431. [Google Scholar] [CrossRef]
- Wang, Z.; Jing, J.; Ren, Y.; Guo, Y.; Tao, N.; Zhou, Q.; Zhang, H.; Ma, Y.; Wang, Y. Preparation and application of selenium nanoparticles in a lateral flow immunoassay for clenbuterol detection. Mater. Lett. 2019, 234, 212–215. [Google Scholar] [CrossRef]
- Sonkusre, P.; Nanduri, R.; Gupta, P.; Cameotra, S.S. Improved Extraction of Intracellular Biogenic Selenium Nanoparticles and their Specificity for Cancer Chemoprevention. J. Nanomed. Nanotechnol. 2014, 5, 194. [Google Scholar] [CrossRef] [Green Version]
- Saif, S.; Tahir, A.; Chen, Y. Green Synthesis of Iron Nanoparticles and Their Environmental Applications and Implications. Nanomaterials 2016, 6, 209. [Google Scholar] [CrossRef] [Green Version]
- Rajeshkumar, S.; Bharath, L. Mechanism of plant-mediated synthesis of silver nanoparticles – A review on biomolecules involved, characterisation and antibacterial activity. Chem. Interact. 2017, 273, 219–227. [Google Scholar] [CrossRef]
- Sharma, D.; Kanchi, S.; Bisetty, K. Biogenic synthesis of nanoparticles: A review. Arab. J. Chem. 2019, 12, 3576–3600. [Google Scholar] [CrossRef] [Green Version]
- Singh, P.; Kim, Y.-J.; Zhang, D.; Yang, D.-C. Biological Synthesis of Nanoparticles from Plants and Microorganisms. Trends Biotechnol. 2016, 34, 588–599. [Google Scholar] [CrossRef] [PubMed]
- Zhao, X.; Zhou, L.; Rajoka, M.S.R.; Yan, L.; Jiang, C.; Shao, D.; Zhu, J.; Shi, J.; Huang, Q.; Yang, H.; et al. Fungal silver na-noparticles, synthesis, application and challenges. Crit. Rev. Biotechnol. 2018, 38, 817e835. [Google Scholar] [CrossRef]
- Habibullah, G.; Viktorova, J.; Ruml, T. Current Strategies for Noble Metal Nanoparticle Synthesis. Nanoscale Res. Lett. 2021, 16, 1–12. [Google Scholar] [CrossRef]
- Borase, H.P.; Salunke, B.K.; Salunkhe, R.B.; Patil, C.D.; Hallsworth, J.E.; Kim, B.S.; Patil, S.V. Plant extract: A promising bi-omatrix for ecofriendly, controlled synthesis of silver nanoparticles. Appl. Biochem. Biotech. 2014, 173, 1–29. [Google Scholar] [CrossRef]
- Govindappa, M.; Farheen, H.; Chandrappa, C.P.; Channabasava; Rai, R.V.; Raghavendra, V.B. Mycosynthesis of silver nanoparticles using extract of endophytic fungi, Penicillium species of Glycosmis mauritiana, and its antioxidant, antimicrobial, anti-inflammatory and tyrokinase inhibitory activity. Adv. Nat. Sci. Nanosci. Nanotechnol. 2016, 7, 035014. [Google Scholar] [CrossRef]
- Kang, X.; Kirui, A.; Muszyński, A.; Widanage, M.C.D.; Chen, A.; Azadi, P.; Wang, P.; Mentink-Vigier, F.; Wang, T. Molecular architecture of fungal cell walls revealed by solid-state NMR. Nat. Commun. 2018, 9, 1–12. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Das, S.K.; Liang, J.; Schmidt, M.; Laffir, F.; Marsili, E. Biomineralization Mechanism of Gold by Zygomycete Fungi Rhizopous oryzae. ACS Nano 2012, 6, 6165–6173. [Google Scholar] [CrossRef] [PubMed]
- Mukherjee, P.; Ahmad, A.; Mandal, D.; Senapati, S.; Sainkar, S.R.; Khan, M.I.; Ramani, R.; Parischa, R.; Ajayakumar, P.V.; Alam, M.; et al. Bioreduction of AuCl4− ions by the fungus, Verticillium sp. and surface trapping of the gold nanoparticles formed. Angew. Chem. Int. Ed. 2001, 40, 3585–3588. [Google Scholar] [CrossRef]
- Debieux, C.M.; Dridge, E.J.; Mueller, C.M.; Splatt, P.; Paszkiewicz, K.; Knight, I.; Florance, H.; Love, J.; Titball, R.W.; Lewis, R.J.; et al. A bacterial process for selenium nanosphere assembly. Proc. Natl. Acad. Sci. USA 2011, 108, 13480–13485. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Zhang, L.; Li, D.; Gao, P. Expulsion of selenium/protein nanoparticles through vesicle-like structures by Saccharomyces cerevisiae under microaerophilic environment. World J. Microbiol. Biotechnol. 2012, 28, 3381–3386. [Google Scholar] [CrossRef]
- Srivastava, S.K.; Yamada, R.; Ogino, C.; Kondo, A. Biogenic synthesis and characterization of gold nanoparticles by Escherichia coli K12 and its heterogeneous catalysis in degradation of 4-nitrophenol. Nanoscale Res. Lett. 2013, 8, 70. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Balakumaran, M.; Ramachandran, R.; Balashanmugam, P.; Mukeshkumar, D.; Kalaichelvan, P. Mycosynthesis of silver and gold nanoparticles: Optimization, characterization and antimicrobial activity against human pathogens. Microbiol. Res. 2016, 182, 8–20. [Google Scholar] [CrossRef] [PubMed]
- Shahverdi, A.R.; Fakhimi, A.; Shahverdi, H.R.; Minaian, S. Synthesis and effect of silver nanoparticles on the antibacterial activity of different antibiotics against Staphylococcus aureus and Escherichia coli. Nanomed. Nanotechnol. Biol. Med. 2007, 3, 168–171. [Google Scholar] [CrossRef] [PubMed]
- Prabhu, S.; Poulose, E.K. Silver nanoparticles: Mechanism of antimicrobial action, synthesis, medical applications, and toxicity effects. Int. Nano Lett. 2012, 2, 32. [Google Scholar] [CrossRef] [Green Version]
- Krishnaraj, C.; Jagan, E.; Rajasekar, S.; Selvakumar, P.; Kalaichelvan, P.; Mohan, N. Synthesis of silver nanoparticles using Acalypha indica leaf extracts and its antibacterial activity against water borne pathogens. Colloids Surf. B Biointerfaces 2010, 76, 50–56. [Google Scholar] [CrossRef]
- Iravani, S. Green synthesis of metal nanoparticles using plants. Green Chem. 2011, 13, 2638–2650. [Google Scholar] [CrossRef]
- Zhang, J.; Taylor, E.W.; Wan, X.; Peng, D. Impact of heat treatment on size, structure, and bioactivity of elemental selenium nanoparticles. Int. J. Nanomed. 2012, 7, 815–825. [Google Scholar] [CrossRef] [Green Version]
- Kashyap, P.L.; Kumar, S.; Srivastava, A.K.; Sharma, A.K. Myconanotechnology in agriculture: A perspective. World J. Microbiol. Biotechnol. 2012, 29, 191–207. [Google Scholar] [CrossRef]
- Durán, N.; Marcato, P.D.; Alves, O.L.; De Souza, G.I.H.; Esposito, E. Mechanistic aspects of biosynthesis of silver nanoparticles by several Fusarium oxysporum strains. J. Nanobiotechnol. 2005, 3, 8. [Google Scholar] [CrossRef] [Green Version]
- Medentsev, A.; Akimenko, V. Naphthoquinone metabolites of the fungi. Phytochemistry 1998, 47, 935–959. [Google Scholar] [CrossRef]
- Baker, R.A.; Tatum, J.H. Novel anthraquinones from stationary cultures of Fusarium oxysporum. J. Ferment. Bioeng. 1998, 85, 359–361. [Google Scholar] [CrossRef]
- Durán, N.; Teixeira, M.F.S.; De Conti, R.; Esposito, E. Ecological-Friendly Pigments From Fungi. Crit. Rev. Food Sci. Nutr. 2002, 42, 53–66. [Google Scholar] [CrossRef] [PubMed]
- Bell, A.A.; Wheeler, M.H.; Liu, J.; Stipanovic, R.D.; Puckhaber, L.S.; Orta, H. United States Department of Agricul-ture—Agricultural Research Service studies on polyketide toxins of Fusarium oxysporum f sp vasinfectum: Potential targets for disease control. Pest Manag. Sci. Former. Pestic. Sci. 2003, 59, 736–747. [Google Scholar] [CrossRef]
- Jha, A.K.; Prasad, K. Understanding biosynthesis of metallic/oxide nanoparticles: A biochemical perspective. In Biocompatible Nanomaterials Synthesis, Characterization and Applications; Kumar, S.A., Thiagarajan, S., Wang, S.F., Eds.; NOVA Science Publishers Inc.: Hauppauge, NY, USA, 2010. [Google Scholar]
- Salunkhe, R.B.; Patil, S.V.; Patil, C.D.; Salunke, B.K. Larvicidal potential of silver nanoparticles synthesized using fungus Cochliobolus lunatus against Aedes aegypti (Linnaeus, 1762) and Anopheles stephensi Liston (Diptera; Culicidae). Parasitol. Res. 2011, 109, 823–831. [Google Scholar] [CrossRef]
- El-Seedi, H.R.; El-Shabasy, R.M.; Khalifa, S.A.M.; Saeed, A.; Shah, A.; Shah, R.; Iftikhar, F.J.; Abdel-Daim, M.M.; Abdelfatteh, O.; Hajrahand, N.H.; et al. Metal nanoparticles fabricated by green chemistry using natural extracts: Biosynthesis, mechanisms, and applications. RSC Adv. 2019, 9, 24539–24559. [Google Scholar] [CrossRef] [Green Version]
- Mukherjee, P.; Senapati, S.; Mandal, D.; Ahmad, A.; Khan, M.I.; Kumar, R.; Sastry, M. Extracellular synthesis of gold nano-particles by the fungus Fusarium oxysporum. ChemBioChem 2002, 3, 461–463. [Google Scholar] [CrossRef]
- Ahmad, A.; Mukherjee, P.; Senapati, S.; Mandal, D.; Khan, M.I.; Kumar, R.; Sastry, M. Extracellular biosynthesis of silver nanoparticles using the fungus Fusarium oxysporum. Colloids Surf. B Biointerfaces 2003, 28, 313–318. [Google Scholar] [CrossRef]
- Basavaraja, S.; Balaji, S.D.; Lagashetty, A.; Rajasab, A.H.; Venkataraman, A. Extracellular biosynthesis of silver nanoparticles using the fungus Fusarium semitectum. Mater. Res. Bull. 2008, 43, 1164–1170. [Google Scholar] [CrossRef]
- Andreescu, D.; Sau, T.K.; Goia, D.V. Stabilizer-free nanosized gold sols. J. Colloid Interface Sci. 2006, 298, 742–751. [Google Scholar] [CrossRef] [PubMed]
- Molnár, Z.; Bódai, V.; Szakacs, G.; Erdélyi, B.; Fogarassy, Z.; Sáfrán, G.; Varga, T.; Kónya, Z.; Tóth-Szeles, E.; Szűcs, R.; et al. Green synthesis of gold nanoparticles by thermophilic filamentous fungi. Sci. Rep. 2018, 8, 1–12. [Google Scholar] [CrossRef]
- Mukherjee, P.; Roy, M.; Mandal, B.P.; Dey, G.K.; Mukherjee, P.K.; Ghatak, J.; Tyagi, A.K.; Kale, S.P. Green synthesis of highly stabilized nanocrystalline silver particles by a non-pathogenic and agriculturally important fungus T. asperellum. Nanotechnology 2008, 19, 075103. [Google Scholar] [CrossRef]
- Sanghi, R.; Verma, P. Biomimetic synthesis and characterization of protein capped silver nanoparticles. Biores. Technol. 2009, 100, 501e504. [Google Scholar] [CrossRef] [PubMed]
- Poluboyarinov, P.A.; Leshchenko, P.P. A qualitative reaction for cysteine, reduced glutathione, and diacetophenonyl selenide. J. Anal. Chem. 2013, 68, 949–952. [Google Scholar] [CrossRef]
- Pankratov, A.N.; Tsivileva, O.M. In silico Confirmation of the More Active Player Involved in Sulpho-to-seleno Amino Acid Transformations in Mushrooms. Curr. Phys. Chem. 2016, 6, 210–223. [Google Scholar] [CrossRef]
- Lloyd, J.R. Microbial reduction of metals and radionuclides. FEMS Microbiol. Rev. 2003, 27, 411–425. [Google Scholar] [CrossRef]
- Hansda, A.; Kumar, V. Anshumali A comparative review towards potential of microbial cells for heavy metal removal with emphasis on biosorption and bioaccumulation. World J. Microbiol. Biotechnol. 2016, 32, 170. [Google Scholar] [CrossRef]
- Javanbakht, V.; Alavi, S.A.; Zilouei, H. Mechanisms of heavy metal removal using microorganisms as biosorbent. Water Sci. Technol. 2013, 69, 1775–1787. [Google Scholar] [CrossRef]
- Perrone, G.; Susca, A.; Cozzi, G.; Ehrlich, K.; Varga, J.; Frisvad, J.; Meijer, M.; Noonim, P.; Mahakarnchanakul, W.; Samson, R.A. Biodiversity of Aspergillus species in some important agricultural products. Stud. Mycol. 2007, 59, 53–66. [Google Scholar] [CrossRef]
- Poluboyarinov, P.A.; Leshchenko, P.P.; Moiseeva, I.Y.; Kolesnikova, S.G.; Epshtein, N.B. Mechanism of reaction of selenium elimination in diacetophenonyl selenide under the action of reduced glutathione. J. Anal. Chem. 2017, 72, 739–744. [Google Scholar] [CrossRef]
- Burleson, D.J.; Driessen, M.D.; Penn, R.L. On the characterization of environmental nanoparticles. J. Environ. Sci. Health Part A 2004, 39, 2707–2753. [Google Scholar] [CrossRef]
- Kamnev, A.; Dyatlova, Y.; Kenzhegulov, O.; Vladimirova, A.; Mamchenkova, P.; Tugarova, A. Fourier Transform Infrared (FTIR) Spectroscopic Analyses of Microbiological Samples and Biogenic Selenium Nanoparticles of Microbial Origin: Sample Preparation Effects. Molecules 2021, 26, 1146. [Google Scholar] [CrossRef] [PubMed]
- Tugarova, A.V.; Mamchenkova, P.V.; Khanadeev, V.A.; Kamnev, A.A. Selenite reduction by the rhizobacterium Azospirillum brasilense, synthesis of extracellular selenium nanoparticles and their characterisation. New Biotechnol. 2020, 58, 17–24. [Google Scholar] [CrossRef]
- Grønbæk-Thorsen, F.; Hansen, R.H.; Østergaard, J.; Gammelgaard, B.; Møller, L.H. Analysis of selenium nanoparticles in human plasma by capillary electrophoresis hyphenated to inductively coupled plasma mass spectrometry. Anal. Bioanal. Chem. 2021, 413, 2247–2255. [Google Scholar] [CrossRef]
- Gómez-Gómez, B.; Sanz-Landaluce, J.; Pérez-Corona, M.T.; Madrid, Y. Fate and effect of in-house synthesized tellurium based nanoparticles on bacterial biofilm biomass and architecture. Challenges for nanoparticles characterization in living systems. Sci. Total. Environ. 2020, 719, 137501. [Google Scholar] [CrossRef]
- Bartosiak, M.; Giersz, J.; Jankowski, K. Analytical monitoring of selenium nanoparticles green synthesis using photochemical vapor generation coupled with MIP-OES and UV–Vis spectrophotometry. Microchem. J. 2019, 145, 1169–1175. [Google Scholar] [CrossRef]
- Wu, S.; Sun, K.; Wang, X.; Wang, D.; Wan, X.; Zhang, J. Protonation of Epigallocatechin-3-gallate (EGCG) Results in Massive Aggregation and Reduced Oral Bioavailability of EGCG-Dispersed Selenium Nanoparticles. J. Agric. Food Chem. 2013, 61, 7268–7275. [Google Scholar] [CrossRef] [PubMed]
- Akçay, F.A.; Avcı, A. Effects of process conditions and yeast extract on the synthesis of selenium nanoparticles by a novel indigenous isolate Bacillus sp. EKT1 and characterization of nanoparticles. Arch. Microbiol. 2020, 202, 2233–2243. [Google Scholar] [CrossRef]
- Kuroda, M.; Notaguchi, E.; Sato, A.; Yoshioka, M.; Hasegawa, A.; Kagami, T.; Narita, T.; Yamashita, M.; Sei, K.; Soda, S.; et al. Characterization of Pseudomonas stutzeri NT-I capable of removing soluble selenium from the aqueous phase under aerobic conditions. J. Biosci. Bioeng. 2011, 112, 259–264. [Google Scholar] [CrossRef]
- Zhang, H.; Zhou, H.; Bai, J.; Li, Y.; Yang, J.; Ma, Q.; Qu, Y. Biosynthesis of selenium nanoparticles mediated by fungus Mariannaea sp. HJ and their characterization. Colloids Surf. A Physicochem. Eng. Asp. 2019, 571, 9–16. [Google Scholar] [CrossRef]
- Diko, C.S.; Zhang, H.; Lian, S.; Fan, S.; Li, Z.; Qu, Y. Optimal synthesis conditions and characterization of selenium nanopar-ticles in Trichoderma sp. WL-Go culture broth. Mater. Chem. Phys. 2020, 246, 122583. [Google Scholar] [CrossRef]
- Rosenfeld, C.E.; Kenyon, J.A.; James, B.R.; Santelli, C.M. Selenium (IV, VI) reduction and tolerance by fungi in an oxic envi-ronment. Geobiology 2017, 15, 441–452. [Google Scholar] [CrossRef] [PubMed]
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Tsivileva, O.; Pozdnyakov, A.; Ivanova, A. Polymer Nanocomposites of Selenium Biofabricated Using Fungi. Molecules 2021, 26, 3657. https://doi.org/10.3390/molecules26123657
Tsivileva O, Pozdnyakov A, Ivanova A. Polymer Nanocomposites of Selenium Biofabricated Using Fungi. Molecules. 2021; 26(12):3657. https://doi.org/10.3390/molecules26123657
Chicago/Turabian StyleTsivileva, Olga, Alexander Pozdnyakov, and Anastasiya Ivanova. 2021. "Polymer Nanocomposites of Selenium Biofabricated Using Fungi" Molecules 26, no. 12: 3657. https://doi.org/10.3390/molecules26123657