Browsing by Author "Öncel, SS"

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    Green synthesis of metal nanoparticles by microalgae
    (EGE UNIV, FAC FISHERIES) Mutaf, T; Caliskan, G; Öncel, SS; Elibol, M
    Green synthesis of metal nanoparticles through biological resources has attracted attention in recent years. The main reason for that, a lot of toxic chemicals as reducing and stabilizing agents are used in physical and chemical methods which are known as conventional methods. Organisms such as plants, fungi, bacteria, and algae are alternative sources for green nanoparticle synthesis because of their more eco-friendly nature and not be a threat to human health. Microalgae as aquatic microorganisms have been added into the formulations of food, cosmetics, and pharmaceutical for many years, due to their high value-added metabolites such as proteins, vitamins, pigments, fatty acids, intracellular and extracellular polysaccharides. In addition, microalgae have a high potential in biogenic nanoparticle synthesis because of their metal ions accumulation capability, phytoremediation potential, and rich in intracellular and extracellular metabolites that will reduce metal ions to elemental state. In recent years, the number of studies, focused on silver, gold, titanium, zinc, iron, etc. nanoparticle synthesis from many microalgae species by intracellular and extracellular pathways has increased. This review article aims to provide a brief outline of microalgae and cyanobacteria species studied in the context of nanoparticle synthesis, different approaches for nanoparticle synthesis from microalgae, the mechanism of nanoparticle synthesis, and basic characterization principles and antimicrobial activities of nanoparticles produced by green synthesis.
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    Green synthesis of titanium nanoparticles using a sustainable microalgal metabolite solution for potential biotechnological activities
    (WILEY) Mutaf, T; Caliskan, G; Ozel, H; Akagac, G; Öncel, SS; Elibol, M
    In this study, green synthesis of titanium nanoparticles using liquids metabolites of microalgae, Porphyridium cruentum, was performed to evaluate potential biotechnological activity. The rising rates of multidrug-resistant bacteria and the number of cancer patients are driving the search for novel antimicrobial and anticancer agents to combat this threat. In recent years, with the increasing number of studies, nanomaterials are starting to be better understood and are emerging as a solution to this problem. Especially, green synthesized nanoparticles with anticancer, antioxidant, and antimicrobial activities have potential in biomedical applications because of their eco-friendly and biocompatible nature. Scanning electron microscopy (SEM) images revealed that spherical shaped Ti-NPs' size ranged from 62 to 133 nm. This study aimed to assess the effectiveness of antibacterial activity of Ti-NPs and chitosan-coated Ti-NPs against Escherichia coli and Staphylococcus aureus using disc diffusion assay. It demonstrated the concentration-dependent cytotoxic effect of Ti-NPs of human prostate adenocarcinoma (PC-3), human alveolar adenocarcinoma (A549), and human mammary gland adenocarcinoma (MDA-MB) cancer cell lines. This present study shows promising outcomes for possible future applications of synthesized Ti-NPs as a novel antibacterial and cytotoxic agent for biomedical applications such as drug delivery, biosensor, and hyperthermia.
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    Production, purification and characterization of a proteolytic enzyme from Streptomyces sp. 2M21
    (TAYLOR & FRANCIS LTD) Deniz, I; Zihnioglu, F; Öncel, SS; Hames, EE; Vardar-Sukan, F
    The recent application studies on keratinase lead to new application areas for the enzyme to be used in novel industries such as pharmaceuticals and biodegradable composites. Thus, designing an economical and environmentally friendly keratinase production and purification with new features turned into an intriguing objective for its commercialization. In this study, keratinase enzyme was produced using a bioreactor of 5 L by a native Streptomyces sp. 2M21 and purified by ion exchange chromatography using step-wise gradient with 24.1-fold purification. Purified keratinase showed optimum activity at pH 9 and 30 degrees C. The enzyme was shown to be able to decompose different complex substrates such as chicken feather, wool and nail. Moreover, the addition of DTT enhanced the hydrolysis of wool and chicken feather to 3.4- and 3.2-fold, respectively. The potential of Streptomyces sp. to produce significant levels of keratinase using feathers as a substrate might establish cleaner applications for the production of high value-added products and degrading of keratin-containing wastes.