Platinum nanoparticles stabilized by N-heterocyclic thiones. Synthesis and catalytic activity in mono- and di-hydroboration of alkynes

N-Heterocyclic Thiones (NHT) proved to be efficient ligands for the stabilization of small platinum nanoparticles (1.3-1.7 nm), synthesized by decomposition of [Pt(dba)2], under a H2 atmosphere, in the presence of variable sub-stoichiometric amounts of the NHT. Full characterization by means of TEM, HR-TEM, NMR, ICP, TGA and XPS have been carried out, providing information about the nature of the metal nanoparticles and the interaction of the NHT ligands to the metal surface. Importantly, DFT calculations indicate that some NHT ligands interact with the metal through the C[double bond, length as m-dash]C double bond of the imidazole fragment in addition to the sulfur atom, thus providing additional stabilization to the nanoparticles. According to XPS, TGA and ICP techniques, the surface coverage by the ligand increases by decreasing the size of the substituents on the nitrogen atom. The platinum nanoparticles have been used as catalyst in the hydroboration of alkynes. The most active system is that with a less covered surface area lacking an interaction of the ligand by means of the C[double bond, length as m-dash]C double bond. This catalyst hydroborates alkynes with excellent selectivities towards the monoborylated anti-Markovnikov product (vinyl-boronate) when one equiv. of borane is used. Very interestingly, aliphatic alkynes undergo a second hydroborylation process leading to the corresponding 1,1- and 1,2-diboroylated species with good selectivities towards the former.España MINECO (Projects CTQ2016-76267-P, CTQ2016-80814-R and CTQ2016- 81797-REDC)España Junta de Andalucía Project FQM-212

Characterization and genomic analysis of a new phage infecting Helicobacter pylori

Helicobacter pylori, a significant human gastric pathogen, has been demonstrating increased antibiotic resistance, causing difficulties in infection treatment. It is therefore important to develop alternatives or complementary approaches to antibiotics to tackle H. pylori infections, and (bacterio)phages have proven to be effective antibacterial agents. In this work, prophage isolation was attempted using H. pylori strains and UV radiation. One phage was isolated and further characterized to assess potential phage-inspired therapeutic alternatives to H. pylori infections. HPy1R is a new podovirus prophage with a genome length of 31,162 bp, 37.1% GC, encoding 36 predicted proteins, of which 17 were identified as structural. Phage particles remained stable at 37 °C, from pH 3 to 11, for 24 h in standard assays. Moreover, when submitted to an in vitro gastric digestion model, only a small decrease was observed in the gastric phase, suggesting that it is adapted to the gastric tract environment. Together with its other characteristics, its capability to suppress H. pylori population levels for up to 24 h post-infection at multiplicities of infection of 0.01, 0.1, and 1 suggests that this newly isolated phage is a potential candidate for phage therapy in the absence of strictly lytic phages.This study was supported by the Portuguese Foundation for Science and Technology (FCT), under the scope of the strategic funding of the UIDB/04469/2020 unit, and Project Helicophage PTDC/SAU-PUB/29182/2017 (POCI-01-0145-FEDER-029182). R.F. and R.F.S.G. acknowledge the FCT grants SFRH/BD/146496/2019 and SFRH/BD/140182/2018, respectivelyinfo:eu-repo/semantics/publishedVersio

H. pylori phages: from genome release to hope for use as therapy

The increasing antibiotic-resistant Helicobacter pylori infections worldwide and the ineffectiveness of treatments led the World Health Organization to designate clarithromycin-resistant H. pylori as a high-priority bacterium for antibiotic research and development. (Bacterio)phages, viruses that infect bacteria, showing effectiveness in the treatment of pathogenic bacteria, could be a promising alternative strategy in the fight against H. pylori infections. Material and methods In this work, a collection of 74 Portuguese H. pylori-clinical strains was used to screen for the presence of phage genes, using a new PCR-based method. Selected strains were subsequently sequenced and prophage isolation was attempted using UV radiation. Three phages were isolated, one of which was further characterized genetically and biologically. Results PCR-based detection indicated the presence of target phage sequences in 14 strains, and the induction strategies resulted in the release of a new phage. It presents a genome length of 31,162 bp with a G+C content of 37.1 %. This podovirus showed capability to form phage plaques in five strains, was stable under an in vitro gastric digestion model, and was able to maintain a H. pylori population at low levels for up to 24h post-infection. Conclusion The new PCR screening method proved to be very effective in the selection of strains carrying prophages, resulting in the isolation of a new H. pylori phage. This phage presented very promising characteristics in terms of stability and efficacy, being therefore a small step towards the future use of phage therapy in the fight against H. pylori infections.info:eu-repo/semantics/publishedVersio

Stabilisation of gold nanoparticles by N-Heterocyclic thiones

Gold nanoparticles (Au-NPs) have been prepared using N-heterocyclic thiones (NHTs) as ligand stabilisers. These Au-NPs have been shown to be very stable, even in air, and have been characterized by a combination of several techniques (TEM, HR-TEM, STEM-HAADF, EDX, DLS, elemental analysis and 1H NMR). These nanoparticles are active in the catalytic reduction of nitroarenes to anilines.Financial support (FEDER contribution) from the MINECO (Projects CTQ2016-76267-P, CTQ2016-80814-R and CTQ2014-51912-REDC) and the Junta de Andalucía (Project FQM-2126) is gratefully acknowledged. P. L thanks the Spanish MINECO for a Juan de la Cierva contract. R. C. F thanks Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq-CsF) and Fundación Carolina for financial support. L. C. M. thanks the CAPES Foundation, Ministry of Education of Brazil (CAPES-CsF 13465-13-9) for a doctoral grant

Carbon nanotube/dendrimer hybrids as electrodes for supercapacitors

Carbon nanotubes (CNTs) were surface-modified by a glycodendrimer with four glucose units (4-Gl). Electrodes for supercapacitors based on CNT/4-Gl hybrids were used for the first time in this work. The preparation was conducted by casting eight alternating bilayers of two types of modified multiwalled carbon nanotubes (MWCNTs), MWCNT-COOH/4-Gl and MWCNT-NH/4-Gl, from aqueous dispersions (pH = 6). The electrodes showed good cohesion, dimensional stability, and a homogeneous nanoscale structure because the carbon nanotube/dendrimer layers interact electrostatically. The supercapacitor was stacked with a separator embedded with a 1-ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide ionic liquid electrolyte. The device with 20 wt% of dendrimer with respect to CNT content in the electrodes achieved a remarkable increase of 600 % in capacitance compared with the capacitance without the dendrimer.The authors are grateful to Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)—Brazil for the scholarship of João Paulo Campos Trigueiro and to the Centro de Microscopia/UFMG for the images provided. Pró-Reitoria de Pesquisa from UFMG (PRPq/UFMG) is acknowledged for financial support of the English revision. Rute C. Figueiredo extends gratitude to the Carolina Foundation for its scholarship program for the mobility of Brazilian teachers

Stabilisation of gold nanoparticles by N-heterocyclic thiones.

Gold nanoparticles (Au-NPs) have been prepared using N-heterocyclic thiones (NHTs) as ligand stabilisers. These Au-NPs have been shown to be very stable, even in air, and have been characterized by a combination of several techniques (TEM, HR-TEM, STEM-HAADF, EDX, DLS, elemental analysis and 1H NMR). These nanoparticles are active in the catalytic reduction of nitroarenes to anilines

Straightforward synthesis of Man9, the relevant epitope of the high-mannose oligosaccharide

The high-mannose oligosaccharide (or its corresponding Man9 epitope) is the most abundant structure present in pathogen envelope glycoproteins. These glycans play a key role in the pathogenesis of several pathogens and also in the communication with the immune system. Understanding the mechanism of action of these glycans requires the access to pure and chemically well-defined structures in reasonable amounts. The synthesis of these complex branched oligosaccharides is not trivial and few syntheses are reported in the literature with several synthetic and purification steps and low overall yields. In this work, we described a very efficient synthetic alternative to access this relevant Man9 epitope in a very straightforward manner.This work was supported by the Ministerio de Economía y Competitividad (MINECO) project CTQ2014-52328-P, co-financed by the European Regional Development Funds (ERDF). JJR thanks the CSIC for a JAEdoc contract, JRS and NC thank the MINECO for FPI fellowships. RCF acknowledges the Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq-CsF) and the Fundación Carolina for financial support