106 research outputs found
Interaction of desulfovibrio desulfuricans biofilms with stainless steel surface and its impact on bacterial metabolism
Aims: To study the influence of some metallic elements of stainless steel 304 (SS 304) on the development and activity of a sulfate-reducing bacterial biofilm, using as comparison a reference nonmetallic material polymethylmethacrylate (PMMA).
Methods and Results: Desulfovibrio desulfuricans biofilms were developed on SS
304 and on a reference nonmetallic material, PMMA, in a flow cell system.
Steady-state biofilms were metabolically more active on SS 304 than on PMMA. Activity tests with bacteria from both biofilms at steady state also showed that the doubling time was lower for bacteria from SS 304 biofilms.
The influence of chromium and nickel, elements of SS 304 composition, was
also tested on a cellular suspension of Des. desulfuricans. Nickel decreased the bacterial doubling time, while chromium had no significant effect.
Conclusions: The following mechanism is hypothesized: a Des. desulfuricans
biofilm grown on a SS 304 surface in anaerobic conditions leads to the weakening
of the metal passive layer and to the dissolution in the bulk phase of nickel ions that have a positive influence on the sulfate-reducing bacteria metabolism.
This phenomenon may enhance the biocorrosion process.
Significance and Impact of the Study: A better understanding of the interactions between metallic surfaces such as stainless steel and bacteria commonly implied in the corrosion phenomena which is primordial to fight biocorrosion.Programme Praxis XXI; University of Santiago de
Compostela
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The Effect of Ion Implanting on Hydrogen Entry into Metals
The effectiveness of platinum ion implanting in mitigating hydrogen entry into 4340 steel is measured and quantified. Data are presented to compare the extent of hydrogen absorption by the substrate during electrolytic hydrogen charging of platinum ion-implanted and unimplanted 4340 steel substrates. Several implanting conditions were used in processing the samples, and the surface-limited mass-transfer coefficient was calculated for each case and used to quantify the effectiveness of each treatment in reducing hydrogen absorption. It is shown that the underlying mechanism for reducing hydrogen absorption by platinum ion-implanted substrates is the catalytic effect of platinum that favors hydrogen evolution at the steel\u27s surface over hydrogen absorption by the metal. Although scattering experiments with low energy helium ions suggest that the platinum content in the first monolayer of platinum-implanted steels is small, the ability of Pt to catalyze the hydrogen evolution reaction is still strong enough to significantly reduce the quantity of hydrogen that enters the metal
DNA from Plant leaf Extracts: A Review for Emerging and Promising Novel Green Corrosion Inhibitors.
With growing global awareness and concern for environmental protection through
the use of less hazardous and environmentally-friendly extracts of plant origin,
there has been a plethora of green corrosion inhibitors research with far reaching
contributions to the science of corrosion prevention and control. Attention has
increasingly turned towards green corrosion inhibitors, compounds of natural
origin with anti-oxidant activity towards metals and their alloys. Green inhibitors
have been investigated for their corrosion and adsorption properties with good
results. The findings from these research works provide evidence of the
adsorption behavior of green inhibitors which was confirmed by the adsorption
isotherms that were proposed. Adsorption is the first step of any surface reaction
and since corrosion is a surface phenomenon the effectiveness of green corrosion
inhibitors is related to their ability to adsorb on metal surfaces. This review
proposes the potential of plant dna as an emerging and promising novel inhibitor
for mild steel. It begins with a list of plants that have been used in studies to
determine corrosion inhibition properties and moves on to establish the adsorption
behavior of bio macromolecules; protein, polysaccharides (chitosan) and dna. It
reviews studies and investigation of dna interaction and adsorption on inorganic
surfaces before focusing on the use of salmon (fish) sperm dna and calf thymus
gland dna as green corrosion inhibitors for mild steel. It concludes that plant dna
is a promising candidate for green corrosion inhibitor given the similarity between
the plant and animal dna structure and function, and the fact that the use of plant
is more environmentally sustainable than animal-based produc
Corrosion Inhibitors for Sour Oilfield Environment (H2S Corrosion)
Lower-grade steel materials are the most commonly used construction materials for oil and gas wells
due to their low cost and high performance. However, they are susceptible to corrosion when they
come in contact with corrosive environments that are highly acidic. In oil wells, particularly deep oil
wells, hydrogen sulfide (H2S) is commonly found. The dissolution of H2S gas in produced water
makes the fluid corrosive. The use of corrosion inhibitors is perhaps the most practical and costeffective
means of controlling corrosion of low carbon steels in the sour environment. In this chapter,
typical corrosion inhibitors used in oil and gas fields to control the internal corrosion of oilfield
equipment caused by H2S are being examined. The inhibitors found to be effective are polar
functional compounds, with many being based on nitrogen-containing compounds, such as amines,
imidazolines, and quaternary ammonium salts. Drawbacks of these compounds in practical
applications and potentials of future developments are discussed
Study of doubly strange systems using stored antiprotons
Bound nuclear systems with two units of strangeness are still poorly known despite their importance for many strong interaction phenomena. Stored antiprotons beams in the GeV range represent an unparalleled factory for various hyperon-antihyperon pairs. Their outstanding large production probability in antiproton collisions will open the floodgates for a series of new studies of systems which contain two or even more units of strangeness at the P‾ANDA experiment at FAIR. For the first time, high resolution γ-spectroscopy of doubly strange ΛΛ-hypernuclei will be performed, thus complementing measurements of ground state decays of ΛΛ-hypernuclei at J-PARC or possible decays of particle unstable hypernuclei in heavy ion reactions. High resolution spectroscopy of multistrange Ξ−-atoms will be feasible and even the production of Ω−-atoms will be within reach. The latter might open the door to the |S|=3 world in strangeness nuclear physics, by the study of the hadronic Ω−-nucleus interaction. For the first time it will be possible to study the behavior of Ξ‾+ in nuclear systems under well controlled conditions
Dominant-negative mutations in human IL6ST underlie hyper-IgE syndrome
Autosomal dominant hyper-IgE syndrome (AD-HIES) is typically caused by dominant-negative (DN) STAT3 mutations. Patients suffer from cold staphylococcal lesions and mucocutaneous candidiasis, severe allergy, and skeletal abnormalities. We report 12 patients from 8 unrelated kindreds with AD-HIES due to DN IL6ST mutations. We identified seven different truncating mutations, one of which was recurrent. The mutant alleles encode GP130 receptors bearing the transmembrane domain but lacking both the recycling motif and all four STAT3-recruiting tyrosine residues. Upon overexpression, the mutant proteins accumulate at the cell surface and are loss of function and DN for cellular responses to IL-6, IL-11, LIF, and OSM. Moreover, the patients’ heterozygous leukocytes and fibroblasts respond poorly to IL-6 and IL-11. Consistently, patients with STAT3 and IL6ST mutations display infectious and allergic manifestations of IL-6R deficiency, and some of the skeletal abnormalities of IL-11R deficiency. DN STAT3 and IL6ST mutations thus appear to underlie clinical phenocopies through impairment of the IL-6 and IL-11 response pathways
Erratum: Dominant-negative mutations in human IL6ST underlie hyper-IgE syndrome (J. Exp. Med. (2020) 217:6 Doi:10.1084/jem.20191804)
The authors regret that in the original version of Table S1, the column for patient 12 was mistakenly duplicated in the column for patient 8. The online Table S1 PDF has been corrected. The error appears only in PDFs downloaded before June 4, 2020
The impact of inversions across 33,924 families with rare disease from a national genome sequencing project
Detection of structural variants (SVs) is currently biased toward those that alter copy number. The relative contribution of inversions toward genetic disease is unclear. In this study, we analyzed genome sequencing data for 33,924 families with rare disease from the 100,000 Genomes Project. From a database hosting >500 million SVs, we focused on 351 genes where haploinsufficiency is a confirmed disease mechanism and identified 47 ultra-rare rearrangements that included an inversion (24 bp to 36.4 Mb, 20/47 de novo). Validation utilized a number of orthogonal approaches, including retrospective exome analysis. RNA-seq data supported the respective diagnoses for six participants. Phenotypic blending was apparent in four probands. Diagnostic odysseys were a common theme (>50 years for one individual), and targeted analysis for the specific gene had already been performed for 30% of these individuals but with no findings. We provide formal confirmation of a European founder origin for an intragenic MSH2 inversion. For two individuals with complex SVs involving the MECP2 mutational hotspot, ambiguous SV structures were resolved using long-read sequencing, influencing clinical interpretation. A de novo inversion of HOXD11-13 was uncovered in a family with Kantaputra-type mesomelic dysplasia. Lastly, a complex translocation disrupting APC and involving nine rearranged segments confirmed a clinical diagnosis for three family members and resolved a conundrum for a sibling with a single polyp. Overall, inversions play a small but notable role in rare disease, likely explaining the etiology in around 1/750 families across heterogeneous clinical cohorts
Large-scale sequencing identifies multiple genes and rare variants associated with Crohn's disease susceptibility
Genome-wide association studies (GWASs) have identified hundreds of loci associated with Crohn's disease (CD). However, as with all complex diseases, robust identification of the genes dysregulated by noncoding variants typically driving GWAS discoveries has been challenging. Here, to complement GWASs and better define actionable biological targets, we analyzed sequence data from more than 30,000 patients with CD and 80,000 population controls. We directly implicate ten genes in general onset CD for the first time to our knowledge via association to coding variation, four of which lie within established CD GWAS loci. In nine instances, a single coding variant is significantly associated, and in the tenth, ATG4C, we see additionally a significantly increased burden of very rare coding variants in CD cases. In addition to reiterating the central role of innate and adaptive immune cells as well as autophagy in CD pathogenesis, these newly associated genes highlight the emerging role of mesenchymal cells in the development and maintenance of intestinal inflammation.Large-scale sequence-based analyses identify novel risk variants and susceptibility genes for Crohn's disease, and implicate mesenchymal cell-mediated intestinal homeostasis in disease etiology.Cellular mechanisms in basic and clinical gastroenterology and hepatolog
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