Organic Sulfur Sources Research Articles

Thiourea-Driven Mild Synthesis of Photochromic Zeolite without H2 for Transient Information Storage.

The synthesis of hackmanite has been a topic of research for nearly 100 years, but up to now, the reported synthesis methods inevitably use reducing H2 to introduce the F-center through high-temperature calcination to make it change color, which extremely hinders its energy efficient large-scale synthesis before commercial applications. Herein, we present a facile route to synthesize hackmanite by using organic sulfur source thiourea as a precursor in a mild and hydrogen-free process. The synthesized hackmanite exhibits UVC-specific response, fast response, high contrast coloring, and fast fading at room temperature. In view of its photochromic features, a proof-of-concept is presented for transient information storage and burning-after-reading protection; the written information can be automatically erased within 8 min at room temperature.

Investigating organic sulfur in estuarine and offshore environments: A combined field and cultivation approach

Estuarine-offshore sediments accumulate substantial particulate organic matter, containing organic sulfur as a key component. However, the distribution and sources of organic sulfur in such environments remain poorly understood. This study investigated organic sulfur in the Yangtze River Estuary and adjacent East China Sea. Dissolved organic sulfur varied from 0.65 to 1.99 μmol/L (molar S:C 0.006–0.018), while particulate organic sulfur ranged from 0.42 to 2.69 μmol/L (molar S:C 0.007–0.082). Sedimentary organic sulfur exhibited a similar molar S:C ratio (0.014–0.071) to particulate organic sulfur in bottom water, implying that particulate matter deposition is a potential source. Furthermore, sediments exposed to frequent hypoxia harbored significantly higher organic sulfur and S:C values compared to non-hypoxic areas. Laboratory incubation experiments revealed the underlying mechanism: sustained activity of sulfate-reducing bacteria in hypoxic sediments led to a substantial increase in sedimentary organic sulfur (from 15 to 53 μmol/g) within 600 days. This microbially driven sulfurization rendered over 90 % of the organic sulfur resistant to acid hydrolysis. Therefore, this study demonstrates that, alongside particle deposition, microbial sulfurization significantly contributes to organic sulfur enrichment and likely promotes organic matter preservation in estuarine-offshore sediments, particularly under hypoxic conditions. This finding advances our understanding of organic sulfur sources in these vital ecosystems.

Gut microbiota carbon and sulfur metabolisms support Salmonella infections.

Salmonella enterica serovar Typhimurium is a pervasive enteric pathogen and ongoing global threat to public health. Ecological studies in the Salmonella impacted gut remain underrepresented in the literature, discounting microbiome mediated interactions that may inform Salmonella physiology during colonization and infection. To understand the microbial ecology of Salmonella remodeling of the gut microbiome, we performed multi-omics on fecal microbial communities from untreated and Salmonella-infected mice. Reconstructed genomes recruited metatranscriptomic and metabolomic data providing a strain-resolved view of the expressed metabolisms of the microbiome during Salmonella infection. These data informed possible Salmonella interactions with members of the gut microbiome that were previously uncharacterized. Salmonella-induced inflammation significantly reduced the diversity of genomes that recruited transcripts in the gut microbiome, yet increased transcript mapping was observed for seven members, among which Luxibacter and Ligilactobacillus transcript read recruitment was most prevalent. Metatranscriptomic insights from Salmonella and other persistent taxa in the inflamed microbiome further expounded the necessity for oxidative tolerance mechanisms to endure the host inflammatory responses to infection. In the inflamed gut lactate was a key metabolite, with microbiota production and consumption reported amongst members with detected transcript recruitment. We also showed that organic sulfur sources could be converted by gut microbiota to yield inorganic sulfur pools that become oxidized in the inflamed gut, resulting in thiosulfate and tetrathionate that support Salmonella respiration. This research advances physiological microbiome insights beyond prior amplicon-based approaches, with the transcriptionally active organismal and metabolic pathways outlined here offering intriguing intervention targets in the Salmonella-infected intestine.

ВЛИЯНИЕ МЕТИЛСУЛЬФОНИЛМЕТАНА НА ФИЗИОЛОГИЧЕСКИЕ ПОКАЗАТЕЛИ БЕЛЫХ КРЫС ПРИ ЭКСПЕРИМЕНТАЛЬНОЙ ИНТОКСИКАЦИИ КАДМИЕМ И СВИНЦОМ

Cadmium and lead, being one of the most dangerous ecotoxicants, are entering feed in an increasing number of regions and then into livestock products, posing a danger to the body of animals and humans. Therefore, the problem of reducing the toxic effect and accumulation of cadmium and lead in the body does not lose its relevance. One of the ways to reduce the accumulation and negative effects of heavy metals (HM) is the use of biologically active substances. Since one of the mechanisms of the toxic effect of heavy metals is the binding of sulfhydry groups, sulfur and preparations containing it are often used to reduce intoxication. Methylsulfonylmethane (MSM) is a sulfur-containing compound that is a natural component of many foods (fruits, vegetables, grains). It has hepatoprotective, antioxidant and antitoxic properties, and is a source of organic sulfur. The introduction of cadmium and lead at a dose of 2,5 and 5 μg/kg into the diet of white rats for two and a half months led to the normalization of the animals’ behavioral indicators, the state of the central nervous system according to the determination of the summation-threshold index (STI), restoration of the level of immunoglobulin, and the content of chlorides in the urine , and in the blood serum – general SH groups, but the hemoglobin content remained significantly low.

Unveiling the Effect of Organic Sulfur Sources on Synthesized MoS2 Phases and Electrocatalytic Hydrogen Evolution Performances

Metallic-phase MoS2 exhibits Pt-comparable electrocatalytic hydrogen evolution reaction (HER) performance in acidic conditions. However, the controllable synthesis of metallic-phase MoS2 is quite challenging because the key factor determining the phase types of MoS2 during synthesis is still unclear. Herein, the effect of organic sulfur sources on the formed MoS2 phase is studied by use of thioacetamide (TAA), l-cysteine, and thiourea as sulfur sources. The TAA and l-cysteine produce metallic MoS2, while thiourea gives rise to semiconducting MoS2. Owing to the metallic phase and smaller size, the MoS2 prepared with TAA and l-cysteine has a higher electrocatalytic HER activity than the MoS2 obtained from thiourea. The HER overpotential of MoS2 synthesized with TAA is only 210 mV for reaching the current density of 10 mA/cm2, and the corresponding Tafel slope is 44 mV/decade. Further studies find that the decomposition temperature of sulfur precursors is the key factor for the formation of metallic MoS2. Sulfur precursors with a lower decomposition temperature release sulfur ions quickly, which in turn stabilize the metallic phase and inhibit the growth of MoS2 into large sizes. Our findings unveil the key factor for controlling the phase type of MoS2 synthesized from organic sulfur precursors and will be very helpful for the synthesis of MoS2 with high electrocatalytic activity.

Noble Metal‐Free CoSx/NiSx Heterojunction for Photo‐Assisted Methanol Electrooxidation

AbstractDesigning noble metal‐free anode catalysts for photo‐assisted direct methanol fuels cells still remains a significant challenge. In this report, CoSx/NiSx heterojunction was prepared by a two‐step method containing room temperature coordination reaction and calcination using L‐cysteine as both organic ligands and sulfur sources. The as‐prepared CoSx/NiSx heterojunction displayed a significant enhancement in the methanol electrocatalytic oxidation activity under the light irradiation by combining their electrocatalytic and photocatalytic properties. The photocatalytic process was discussed in detail to explore the photo‐assisted enhancement mechanism. The electrochemical and photochemical results indicated that, the synergistic effect of electro‐ and photocatalytic reaction contributes to the enhanced catalytic performance. This work provides a new paradigm to improve the methanol electrocatalytic activity of noble metal‐free semiconductor catalyst. Our proposed noble metal‐free CoSx/NiSx heterojunction will have potential use in photo‐assisted direct methanol fuel cells.

Construction and performance of CdS/MoO2@Mo2C-MXene photocatalyst for H2 production

Nowadays, photocatalytic technologies are regarded as promising strategies to solve energy problems, and various photocatalysts have been synthesized and explored. In this paper, a novel CdS/MoO2@Mo2C-MXene photocatalyst for H2 production was constructed by a two-step hydrothermal method, where MoO2@Mo2C-MXene acted as a binary co-catalyst. In the first hydrothermal step, MoO2 crystals with an egged shape grew on the surface of two-dimensional (2D) Mo2C MXene via an oxidation process in HCl aqueous solution. In the second hydrothermal step, CdS nanorods were uniformly assembled on the surface of MoO2@Mo2C-MXene in ethylenediamine with an inorganic cadmium source and organic sulfur source. The CdS/MoO2@Mo2C-MXene composite with MoO2@Mo2C-MXene of 5 wt% exhibits an ultrahigh visible-light photocatalytic H2 production activity of 22,672 µmol/(g·h), which is ∼21% higher than that of CdS/Mo2C-MXene. In the CdS/MoO2@Mo2C-MXene composite, the MoO2 with metallic nature separates CdS and Mo2C MXene, which acts as an electron-transport bridge between CdS and Mo2C MXene to accelerate the photoinduced electron transferring. Moreover, the energy band structure of CdS was changed by MoO2@Mo2C-MXene to suppress the recombination of photogenerated carriers. This novel compound delivers upgraded photocatalytic H2 evolution performance and a new pathway of preparing the low-cost photocatalyst to solve energy problems in the future.

Effect of the organic sulfur source on the photocatalytic activity of CdS.

By controlling the species of the organic sulfur source, CdS samples were produced with different photocatalytic performances by a low-temperature solvothermal method. Different species of the organic sulfur source were chosen as the coordination agent to control the interactions in the crystal growth process. Among them, thioacetamide was the best coordination agent. The hydrophobic chain could be good for reducing the resistance of charge transfer, and increasing the rate of surface charge transfer and the lifetime of the photoexcited electrons. Benefiting from the hydrophobic chain, CdS shows an excellent photocatalytic hydrogen evolution rate of 943.54 μmol h−1 g−1 and a rhodamine B photocatalytic degradation rate of 99.1% in 60 min, which is superior to the photocatalysis of pure CdS prepared by many other methods.

Sulfur-based mixotrophic denitrification with the stoichiometric S0/N ratio and methanol supplementation: effect of the C/N ratio on the process

The impact of the organic carbon to nitrate ratio (C/N ratio) on mixotrophic denitrification rate has been scarcely studied. Thus, this work aims to investigate the effect of the C/N ratio on the mixotrophic denitrification when methanol is used as a source of organic matter and elemental sulfur as an electron donor for autotrophic denitrification. For this, two initial concentrations of NO3 --N (50 and 25 mg/L) at a stoichiometric ratio of S0/N, and four initial C/N ratios (0, 0.6, 1.2, and 1.9 mg CH3OH/mg NO3 - -N) were used at 25 (±2) °C. The results showed that when using a C/N ratio of 0.6, the highest total nitrogen removal was obtained and the accumulation of nitrites was reduced, compared to an autotrophic system. The most significant contribution to nitrate consumption was through autotrophic denitrification (AuDeN) for a C/N ratio of 0.6 and 1.2, while for C/N = 1.9 the most significant contribution of nitrate consumption was through heterotrophic denitrification (HD). Finally, organic supplementation (methanol) served to increase the specific nitrate removal rate at high and low initial concentrations of substrate. Therefore, the best C/N ratio was 0.6 since it allowed for increasing the removal efficiency and the denitrification rate.

Plant volatile organic compound (E)-2-hexenal facilitates Botrytis cinerea infection of fruits by inducing sulfate assimilation.

Investigation into plant-fungal pathogen interactions is one of the most interesting fields in plant sciences. However, the roles of plant volatile organic compounds in the arms race are still largely unknown. Based on precise quantification of plant volatiles, we discovered that the plant volatile organic compound (E)-2-hexenal, at concentrations that were similar to or lower than those in tissues of strawberry and tomato fruits, upregulates sulfate assimilation in spores and hyphae of the phytopathogenic fungus Botrytis cinerea. This upregulation is independent of the types of sulfur sources in the plant and can be achieved in the presence of inorganic sulfate and organic sulfur sources. Using the fungal deletion mutants, we further found that sulfate assimilation is involved in the infection of tomato and strawberry fruits by B.cinerea, and that the severity of the disease is proportional to the sulfate content in the fruits. Both before and during the infection, (E)-2-hexenal induced utilisation of plant sulfate by B.cinerea facilitates its pathogenesis through enhancing its tolerance to oxidative stress. This work provides novel insights into the role of plant volatiles in plant-fungal pathogen interaction and highlights the importance of sulfur levels in the host in the prevention of grey mould disease.

DMSP synthesis genes distinguish two types of DMSP producer phenotypes.

Dimethylsulfoniopropionate (DMSP) is an important organic carbon and sulfur source in the surface ocean that fuels microbial activity and significantly impacts Earth's climate. After three decades of research, the cellular role(s) of DMSP and environmental drivers of production remain enigmatic. Recent work suggests that cellular DMSP concentrations, and changes in these concentrations in response to environmental stressors, define two major groups of DMSP producers: high DMSP producers that contain ≥ 50 mM intracellular DMSP and low DMSP producers that contain < 50 mM. Here we show that two recently described DMSP synthesis genes (DSYB and TpMT2) may differentiate these two DMSP phenotypes. A survey of prokaryotic and eukaryotic isolates found a significant correlation between the presence of DSYB and TpMT2 genes and previous measurements of high and low DMSP concentrations, respectively. Phylogenetic analysis demonstrated that DSYB and TpMT2 form two distinct clades. DSYB and TpMT2 were also found to be globally abundant in in situ surface communities, and their taxonomic annotations were similar to those observed for isolates. The strong correlation of the DSYB and TpMT2 synthesis genes with high and low producer phenotypes establishes a foundation for direct quantification of DMSP producers, enabling significantly improved predictions of DMSP in situ.

Starmera foglemanii sp. nov. and Starmera ilhagrandensis sp. nov., two novel yeast species isolated from ephemeral plant substrates.

Four isolates of two novel ascosporogenous species belonging to the clade Starmera were obtained from cactus tissues and rotting wood in Brazil. Results of analyses of the sequences of the ITS and D1/D2 domains of the large subunit rRNA gene indicated that the two isolates of the cactophilic species are related to Starmera caribaea and Starmera pilosocereana, yeasts that are associated with cacti and require an organic source of sulfur for growth. We propose the novel species Starmera foglemanii sp. nov. (CBS 16113T; MycoBank number: MB 834400) to accommodate these isolates. The other two isolates are phylogenetically related to Candida dendrica, Candida laemsonensis and Candida berthetii, also in the Starmera clade. The novel species name Starmera ilhagrandensis sp. nov. (CBS 16316T; MycoBank number: MB 834402) is proposed for this species.

Evidence for contrasting roles of dimethylsulfoniopropionate production in Emiliania huxleyi and Thalassiosira oceanica.

Summary Dimethylsulfoniopropionate (DMSP) is a globally abundant marine metabolite and a significant source of organic carbon and sulfur for marine microbial ecosystems with the potential to influence climate regulation. However, the physiological function of DMSP has remained enigmatic for >30 yr. Recent insight suggests that there are different physiological roles for DMSP based on the cellular DMSP concentrations in producers.Differential production of DMSP was tested with multiple physiological experiments that altered nitrate availability, salinity and temperature to create stressed growth and target different metabolic conditions in Emiliania huxleyi, a high DMSP producer and Thalassiosira oceanica, a low DMSP producer. Emiliania huxleyi intracellular DMSP did not respond to metabolically imbalanced conditions, while Thalassiosira oceanica intracellular DMSP was significantly correlated to stressed growth rate across all conditions tested and exhibited a plastic response on a timescale of hours in nonsteady‐state.The previous assumption that proposed DMSP mechanism(s) can be universally applied to all producers is shown to be unlikely. Rather, two distinct ecological roles for DMSP likely exist that differ by producer type, where: (1) the primary role of DMSP in high producers is a constitutive compatible solute; and (2) DMSP production in low producers is a finely tuned stress response.

Optimizing the precursor of sulfur source for hydrothermal synthesis of high performance CdS for photocatalytic hydrogen production.

Although the CdS photocatalyst has been extensively investigated, a rational hydrothermal synthesis route is still required to prepare highly active CdS for H2 evolution reaction (HER). To optimize the precursor of the sulfur source, three prevalent organic sulfur sources of thiourea (TA), thioacetamide (TAA) and l-cysteine (l-Cys) were used for hydrothermal synthesis of CdS. Their effects on the crystallographic structure, morphology, optical property, band structure, and photocatalytic HER performance of the products were then investigated systematically. The results indicated that hexagonal branched dendritic structure CdS (S-TA) could be produced in TA solution and showed the highest HER activity due to the branched 1D structure, the smallest interfacial electron transfer resistance and the most negative conduction band bottom (Ecb). Whereas in TAA, spherical CdS (S-TAA) with a mixed phase of hexagonal and cubic was obtained. The mixed phase structure and the more positive Ecb of S-TAA lead to a considerably lower HER activity than that of S-TA. Poorly crystallized hexagonal CdS nanoparticles (S-Cys) were prepared in l-Cys and showed the lowest HER performance as its Ecb is very near to H+ reduction potential. Thus, compared to T-AA and l-Cys, TA is a more suitable sulfur source for hydrothermal preparation of highly active CdS for HER.

Microbial pathway for anaerobic 5′-methylthioadenosine metabolism coupled to ethylene formation

Numerous cellular processes involving S-adenosyl-l-methionine result in the formation of the toxic by-product, 5'-methylthioadenosine (MTA). To prevent inhibitory MTA accumulation and retain biologically available sulfur, most organisms possess the "universal" methionine salvage pathway (MSP). However, the universal MSP is inherently aerobic due to a requirement of molecular oxygen for one of the key enzymes. Here, we report the presence of an exclusively anaerobic MSP that couples MTA metabolism to ethylene formation in the phototrophic bacteria Rhodospirillum rubrum and Rhodopseudomonas palustris In vivo metabolite analysis of gene deletion strains demonstrated that this anaerobic MSP functions via sequential action of MTA phosphorylase (MtnP), 5-(methylthio)ribose-1-phosphate isomerase (MtnA), and an annotated class II aldolase-like protein (Ald2) to form 2-(methylthio)acetaldehyde as an intermediate. 2-(Methylthio)acetaldehyde is reduced to 2-(methylthio)ethanol, which is further metabolized as a usable organic sulfur source, generating stoichiometric amounts of ethylene in the process. Ethylene induction experiments using 2-(methylthio)ethanol versus sulfate as sulfur sources further indicate anaerobic ethylene production from 2-(methylthio)ethanol requires protein synthesis and that this process is regulated. Finally, phylogenetic analysis reveals that the genes corresponding to these enzymes, and presumably the pathway, are widespread among anaerobic and facultatively anaerobic bacteria from soil and freshwater environments. These results not only establish the existence of a functional, exclusively anaerobic MSP, but they also suggest a possible route by which ethylene is produced by microbes in anoxic environments.

Synthesis and characterization of PbS nanoparticles in an ionic liquid using single and dual source precursors

We report a green route for the synthesis of PbS nanoparticles in an imidazolium based ionic liquid (IL) (1-ethyl-3-methylimidazolium methanesulfonate) using single source and dual source precursor methods. Lead ethyl xanthogenate complex was used as single source molecular precursor for the synthesis of PbS nanoparticles, whereas in dual source approach organic sulfur (1-dodecanethiol) and inorganic sulfur (sodium sulfide) sources were used to observe the suitability of different sulfur sources on formation of PbS nanoparticles. The results showed that the temperature has an effect on the as prepared nanoparticles for both routes. X-ray diffraction (XRD) studies confirmed formation of cubic phase of PbS from both routes. Electron microscopy techniques showed that the nanoparticle morphologies differed significantly depending on the synthetic factors such as temperature, nature of precursors and ranged from spherical to cubic shapes.

Sulfate-Binding Protein (Sbp) from Xanthomonas citri: Structure and Functional Insights.

The uptake and transport of sulfate in bacteria is mediated by an ATP-binding cassette transporter (ABC transporter) encoded by sbpcysUWA genes, whose importance has been widely demonstrated due to their relevance in cysteine synthesis and bacterial growth. In Xanthomonas citri, the causative agent of canker disease, the expression of components from this ABC transporter and others related to uptake of organic sulfur sources has been shown during in vitro growth cultures. In this work, based on gene reporter and proteomics analyses, we showed the activation of the promoter that controls the sbpcysUWA operon in vitro and in vivo and the expression of sulfate-binding protein (Sbp), a periplasmic-binding protein, indicating that this protein plays an important function during growth and that the transport system is active during Citrus sinensis infection. To characterize Sbp, we solved its three-dimensional structure bound to sulfate at 1.14 Å resolution and performed biochemical and functional characterization. The results revealed that Sbp interacts with sulfate without structural changes, but the interaction induces a significant increasing of protein thermal stability. Altogether, the results presented in this study show the evidence of the functionality of the ABC transporter for sulfate in X. citri and its relevance during infection.

Diversity of bacterial dimethylsulfoniopropionate degradation genes in surface seawater of Arctic Kongsfjorden.

Dimethylsulfoniopropionate (DMSP), which is the major source of organic sulfur in the world’s oceans, plays a significant role in the global sulfur cycle. This compound is rapidly degraded by marine bacteria either by cleavage to dimethylsulfide (DMS) or demethylation to 3-methylmercaptopropionate (MMPA). The diversity of genes encoding bacterial demethylation (dmdA) and DMS production (dddL and dddP) were measured in Arctic Kongsfjorden. Both dmdA and dddL genes were detected in all stations along a transect from the outer to the inner fjord, while dddP gene was only found in the outer and middle parts of the fjord. The dmdA gene was completely confined to the Roseobacter clade, while the dddL gene was confined to the genus Sulfitobacter. Although the dddP gene pool was also dominated by homologs from the Roseobacter clade, there were a few dddP genes showing close relationships to both Alphaproteobacter and Gammaproteobacter. The results of this study suggest that the Roseobacter clade may play an important role in DMSP catabolism via both demethylation and cleavage pathways in surface waters of Kongsfjorden during summer.

Diallyl trisulfide protects against ethanol-induced oxidative stress and apoptosis via a hydrogen sulfide-mediated mechanism

Garlic is one natural source of organic sulfur containing compounds and has shown promise in the treatment of chronic liver disease. Dietary garlic consumption is inversely correlated with the progression of alcoholic fatty liver (AFL), although the exact underlying mechanisms are not clear. Our previous studies also have shown that diallyl trisulfide (DATS), the primary organosulfur compound from Allium sativum L, displayed anti-lipid deposition and antioxidant properties in AFL. The aim of the present study was to clarify the underlying mechanisms. In the present study, we used the intragastric infusion model of alcohol administration and human normal liver cell line LO2 cultured with suitable ethanol to mimic the pathological condition of AFL. We showed that accumulation of intracellular reactive oxygen species (ROS) was lowered significantly by the administration of DATS, but antioxidant capacity was increased by DATS. Additionally, DATS inhibited hepatocyte apoptosis via down-regulating Bax expression and up-regulating Bcl-2 expression, and attenuated alcohol-induced caspase-dependent apoptosis. More importantly, using iodoacetamide (IAM) to block hydrogen sulfide (H2S) production from DATS, we noted that IAM abolished all the above effects of DATS in ethanol-treated LO2 cells. Lastly, we found DATS could increase the expressions of cystathionine gamma-lyase (CSE) and cystathionine beta-synthase (CBS), the major H2S-producing enzymes. These results demonstrate that DATS protect against alcohol-induced fatty liver via a H2S-mediated mechanism. Therefore, targeting H2S may play a therapeutic role for AFL.

Dibenzothiophene desulfurization capability and evolutionary divergence of newly isolated bacteria.

Metabolically microorganisms are diverse, and they are capable of transforming almost every known group of chemical compounds present in coal and oil in various forms. In this milieu, one of the important microbial metabolic processes is the biodesulfurization [cleavage of carbon-sulfur (C-S) bond] of thiophenic compounds, such as dibenzothiophene (DBT), which is the most abundant form of organic sulfur present in fossil fuels. In the current study, ten newly isolated bacterial isolates, designated as species of genera Gordonia, Amycolatopsis, Microbacterium and Mycobacterium, were enriched from different samples in the presence of DBT as a sole source of organic sulfur. The HPLC analysis of the DBT grown cultures indicated the consumption of DBT and accumulation of 2-hydroxybiphenyl (2-HBP). Detection of 2-HBP, a marker metabolite of 4S (sulfoxide-sulfone-sulfinate-sulfate) pathway, suggested that the newly isolated strains harbored metabolic activity for DBT desulfurization through the cleavage of C-S bond. The maximum 2-HBP formation rate was 3.5µmol/g dry cell weight (DCW)/h. The phylogenetic analysis of the new isolates showed that they had diverse distribution within the phylogenetic tree and formed distinct clusters, suggesting that they might represent strains of already reported species or they were altogether new species. Estimates of evolutionary divergence showed high level of nucleotide divergence between the isolates within the same genus. The new isolates were able to use a range of heterocyclic sulfur compounds, thus making them suitable candidates for a robust biodesulfurization system for fossil fuels.