Abstract. In this paper we report the biological synthesis of gold nanoparticles (GNPs) by the reduction of gold ions using a suspension and supernatant of P. aeruginosa. The biosynthesis method was straightforward and yielded good results without using toxic chemicals. The size distribution of the gold nanoparticles synthesized by P. aeruginosa at higher temperatures was larger than that synthesized at lower temperatures. The GNPs morphology was isotropic at various temperatures. With an increase in the temperature, the stability of the GNPs decreased. The absorption and fluorescence spectra accorded well with the size distribution of the particles, with the nanoparticle size increasing as the absorption and fluorescence increased too. The optical properties of the GNPs observed in the study accorded well with the scanning electron microscopy (SEM) observations. The visible photoluminescence (PL) around 435 nm indicated the possible use of the obtained colloids, which consisted of GNPs and capping biomaterial, in therapeutic applications. Moreover, the synthesized GNPs showed good antibacterial activity toward E. coli indicating their potential in biological applications.

Recently, the biosynthesis of gold nanoparticles (AuNPs) has been widely studied and described. In the age of bacterial drug resistance, an intensive search for new agents with antibacterial properties or a new form of antibiotics with effective action is necessary. As a result, the antibacterial activity of AuNPs functionalized with natural compounds is being investigated more frequently. AuNPs biosynthesized with plant extract or functionalized with bioactive compounds isolated from plants could be particularly useful for pharmaceutical applications. The biosynthesized AuNPs are stabilized by an envelope, which may consist of flavonoids, phenolic acids, lipids and proteins as well as carbohydrates and vitamins. The composition of the natural coating affects the size, shape and stability of the AuNPs and is also responsible for interactions with the bacterial cell wall. Recently, several mechanisms of AuNP interactions with bacterial cells have been identified. Nevertheless, they are not yet well understood, due to the large diversity of plants and biosynthesized AuNPs. Understanding the antibacterial mechanisms allows for the creation of pharmaceutical formulations in the most useful form. Utilizing AuNPs functionalized with plant compounds as antibacterial agents is still a new concept. However, the unique physicochemical and biological properties of AuNPs emphasises their potential for a broad range of applications in the future.

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Gold nanoparticles (GNPs) are well-known nanomaterials that can be used for multiple biomedical applications. There are various methods for synthesis of GNPs using microorganisms and plants, particularly through the use of fruit extracts. Their use is due to the fact that fruit extracts are the natural concentrate of substances that possesses therapeutic properties. In this review, we aim to compare the recent studies concerning the methods for synthesis of GNPs from fruit extracts, the methods used to characterize the properties of GNPs and capping biomaterial and the potential applications of GNPs. The most frequently used methods to characterize GNPs and capping biomaterial are UV-visible spectroscopy, transmission or scanning electron microscopy, dynamic light scattering and Fourier transformation infrared spectroscopy techniques. Because of GNPs' optoelectronic properties, biocompatibility, stability and oxidation resistance, they can be used in areas such as electronics, chemical and biological sensing, tumour imaging, drug delivery and phototherapy.

Transmembrane translocation of polyion homopolymers takes place in the case of polyanionic polysialic acid (polySia), polyanionic polynucleotides and polycationic polypeptides. The purpose of this work was to determine the role of membrane electrical parameters on the kinetics of polyion translocation, the influence of polysialic acid on ion adsorption on positively charged membrane surface and the dynamics of the phospholipid hydrocarbon chains and choline group by using 1H-NMR. The analysis of polyion translocation was performed by using the electrical equivalent circuit of the membrane for the initial membrane potential equal to zero. The changes in polysialic acid flux was up to 75% after 1 ms in comparison with the zero-time flux. Both a decrease of membrane conductance and an increase of polyion chain length resulted in the diminution of this effect. An increase of praseodymium ions adsorption to positively charged liposomes and an increase of the rate of segmental movement of the -CH2 and -CH3 groups, and the choline headgrup of lipid molecules, was observed in the presence of polySia. The results show that the direction of the vectorial polyion translocation depends both on the membrane electrical properties and the degree of polymerization of the polymer, and that polysialic acid can modulate the degree of ion adsorption and the dynamics of membrane lipids.