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Infectious microbes that spread easily in healthcare facilities remain as the severe threat for the public health, especially among immunocompromised populations. Given the intricate problem of dramatic increase in resistance to common biocides, the development of safe and efficient biocide formulated agents to alleviate drug resistance is highly demanding. In this study, Schiff-base ligands were successfully formed on natural biopolymer of epsilon-poly-L-lysine (e-PL) decorated aldehyde functionalized mesoporous silica SBA-15 (CHO-SBA-15) for the selective coordination of silver ions, which was affirmed by various physicochemical methods. Besides the identified broad-spectrum antibacterial activities, the as-prepared Schiff-base silver nanocomplex (CHO-SBA-15/e-PL/Ag, CLA-1) exhibited an improved inhibitory effect on infectious pathogen growth typified by Escherichia coli and Staphylococcus aureus in comparison with two control silver complexes without Schiff-base conjugates, SBA-15/e-PL/Ag and CHO-SBA-15/Ag, respectively. In addition, CLA-1 remarkably inhibited the growth of Mycobacterium tuberculosis due to the excellent antimicrobial activity of silver species. Significantly, CLA-1 kills Candida albicans cells, inhibits biofilm formation, and eliminates preformed biofilms, with no development of resistance during continuous serial passaging. The antifungal activity is connected to disruption of bacterial cell membranes and increased levels of intracellular reactive oxygen species. In mouse models of multidrug-resistant C. albicans infection, CLA-1 exhibited efficient in vivo fungicidal efficacy superior to two antifungal drugs, amphotericin B and fluconazole. Moreover, CLA-1 treatment induces negligible toxicity against normal tissues with safety. Therefore, this study reveals the pivotal role of the molecular design of Schiff-base silver nanocomplex formation on biopolymer surface-functionalized silica mesopores as a green and efficient nanoplatform to tackle infectious microbes.

An unprecedented dimeric pimarane-derived diterpenoid (trichanthol A, 1) and a new 17-nor-(9β-H)-pimarane diterpenoid glucoside (trichanthol B, 2) together with ten known analogs (3–12) were obtained from the tuber of Icacina trichantha (Icacinaceae) in a bioassay-guided phytochemical investigation. Trichanthol A (1) is the first example of a pimarane-derived diterpenoid dimer furnished by forming an undescribed C-16–C-7′ linkage, and this is the first report of the glucosylation of a 17-nor-(9β-H)-pimarane diterpenoid (2). Their structures were elucidated by the interpretation of spectroscopic data and chemical methods in combination with calculated 13C NMR-DP4+ analysis and electronic circular dichroism methods. All isolated compounds exhibited antibacterial activity against standard and drug-resistant Helicobacter pylori strains with MIC values ranging from 8 to 64 μg mL−1. Moreover, icacinlactone B (6) showed an additive effect in combination with metronidazole or clarithromycin against H. pylori.

The prevalence of invasive aspergillosis with azole resistance is increasing, but the mechanisms underlying the development of resistance and treatment strategies are still limited. The present work is focused on finding a relationship between long-chain unsaturated fatty acids (LCUFAs), Aspergillus fumigatus development, and antifungal resistance. The effects of LCUFAs on antifungal agents in vitro were determined, and the stearic acid desaturase gene (sdeA) of A. fumigatus was characterized. In in vitro antifungal tests, LCUFAs antagonized the antifungal activity of itraconazole by extracting it from media, thereby preventing it from entering cells. The OA auxotrophic phenotype caused by an sdeA deletion confirmed that SdeA was required for OA biosynthesis in A. fumigatus. Furthermore, several low-level sdeA-overexpressing mutants with impaired vegetative growth phenotypes were successfully constructed. Additionally, an sdeA-overexpressing mutant, OEsdeA-5, showed lowered sensitivity levels to itraconazole. Moreover, RNA sequencing of OEsdeA-5 revealed that the altered gene-expression pattern. Through targeted metabolomics, decreased palmitic acid and stearic acid contents, accompanied by higher palmitoleic acid, margaroleic acid, and OA production levels, were found in OEsdeA-5. This study provides a novel insight of understanding of azole resistance and a potential target for drug development.

Unsaturated fatty acids (UFAs) are essential for functional membrane phospholipids in most bacteria. The bifunctional dehydrogenase/isomerase FabX is an essential UFA biosynthesis enzyme in the widespread human pathogen Helicobacter pylori, a bacterium etiologically related to 95% of gastric cancers. Here, we present the crystal structures of FabX alone and in complexes with an octanoyl-acyl carrier protein (ACP) substrate or with holo-ACP. FabX belongs to the nitronate monooxygenase (NMO) flavoprotein family but contains an atypical [4Fe-4S] cluster absent in all other family members characterized to date. FabX binds ACP via its positively charged α7 helix that interacts with the negatively charged α2 and α3 helices of ACP. We demonstrate that the [4Fe-4S] cluster potentiates FMN oxidation during dehydrogenase catalysis, generating superoxide from an oxygen molecule that is locked in an oxyanion hole between the FMN and the active site residue His182. Both the [4Fe-4S] and FMN cofactors are essential for UFA synthesis, and the superoxide is subsequently excreted by H. pylori as a major resource of peroxide which may contribute to its pathogenic function in the corrosion of gastric mucosa., Helicobacter pylori FabX, a dehydrogenase/isomerase flavoprotein, is required for unsaturated fatty acid synthesis. Here, the authors characterize FabX substrate recognition and catalytic mechanism, and reveal that it contains an atypical [4Fe-4S] cluster, which is essential and participates in the catalytic cycle.

SummaryPlants employ an array of intricate and hierarchical signaling cascades to perceive and transduce informational cues to synchronize and tailor adaptive responses. Systemic stress response (SSR) is a recognized complex signaling and response network quintessential to plant’s local and distal responses to environmental triggers, however, the identity of the initiating signals has remained fragmented.Here, we show that both biotic (aphids and viral pathogens) and abiotic (high-light and wounding) stresses induce accumulation of the plastidial-retrograde-signaling metabolite, methylerythritol cyclodiphosphate (MEcPP), leading to reduction of the phytohormone, auxin, and the subsequent decreased expression of the phosphatase, PP2C.D1.This enables phosphorylation of mitogen-activated protein kinases (MAPK3/6), and the consequential induction of the downstream events ultimately resulting in biosynthesis of the two SSR priming metabolites, pipecolic- and N-hydroxy-pipecolic acid.This work identifies plastids as the initiation site, and the plastidial retrograde-signal, MEcPP as the initiator of a multi-component signaling cascade potentiating the biosynthesis of SSR activators, in response to biotic and abiotic triggers.

Glycogen has long been considered to have a function in energy metabolism. However, our recent study indicated that glycogen metabolism, directed by cytosolic phosphoenolpyruvate carboxykinase Pck1, controls the formation and maintenance of CD8+ memory T (Tmem) cells by regulating redox homeostasis1. This unusual metabolic program raises the question of how Pck1 is upregulated in CD8+ Tmem cells. Here, we show that mitochondrial acetyl coenzyme A is diverted to the ketogenesis pathway, which indirectly regulates Pck1 expression. Mechanistically, ketogenesis-derived β-hydroxybutyrate is present in CD8+ Tmem cells; β-hydroxybutyrate epigenetically modifies Lys 9 of histone H3 (H3K9) of Foxo1 and Ppargc1a (which encodes PGC-1α) with β-hydroxybutyrylation, upregulating the expression of these genes. As a result, FoxO1 and PGC-1α cooperatively upregulate Pck1 expression, therefore directing the carbon flow along the gluconeogenic pathway to glycogen and the pentose phosphate pathway. These results reveal that ketogenesis acts as an unusual metabolic pathway in CD8+ Tmem cells, linking epigenetic modification required for memory development. Zhang et al. show that ketogenesis-derived β-hydroxybutyrate (BHB) epigenetically modifies H3K9 of Foxo1 and Ppargc1a to regulate Pck1, which in turn controls metabolic flux and CD8+ memory T-cell development.

The biosynthesis of the pimelate moiety of biotin in Escherichia coli requires two specialized proteins, BioC and BioH. However, the enzymes that have BioC- or BioH-like activities show remarkable sequence diversity among biotin-producing bacteria. Here, we report that the intracellular rickettsial pathogen Ehrlichia chaffeensis encodes two novel proteins, BioT and BioU, which functionally replace the E. coli BioC and BioH proteins, respectively. The desthiobiotin assays demonstrated that these two proteins make pimeloyl-acyl carrier protein (ACP) from the substrate malonyl-ACP with the aid of the FAS II pathway, through the expected pimeloyl-ACP methyl ester intermediate. BioT and BioU homologues seem restricted to the species of Ehrlichia and its close relative, Anaplasma. Taken together, the synthesis of the biotin precursor in E. chaffeensis appears to be catalyzed by two novel BioC- and BioH-like proteins.

Cellulase is an important enzyme that can be used to breakdown lignocellulose into glucose. Microbulbifer hydrolyticus IRE-31(ATCC 700072) is a kind of marine bacterium, which could grow in high salinity medium and has fast-strong growth ability. In this study, a novel strain was screened from Microbulbifer hydrolyticus IRE-31 through mutations to produce cellulase. The effect of different carbon sources on the growth as well as on the production of cellulase of the new strain was studied. Carboxymethyl-cellulase (CMCase) activity selected to represent cellulase was proven to be effectively promoted while xylose, galactose, and melibiose as well as glucose were used as carbon sources. When xylose and glucose were chosen to be further investigated, 472.57 U/L and 266.01 U/L CMCase activity were obtained from 30 g/L glucose and 10 g/L xylose, respectively. These results clarified the effect of different carbon sources on the production of cellulase, which laid a good foundation for the further research in the production of cellulase by marine bacteria.

Hypoxia is known to be commonly present in breast tumor microenvironments. Stem-like cells that repopulate breast tumors, termed tumor-repopulating cells (TRC), thrive under hypoxic conditions, but the underlying mechanism remains unclear. Here, we show that hypoxia promotes the growth of breast TRCs through metabolic reprogramming. Hypoxia mobilized transcription factors HIF1α and FoxO1 and induced epigenetic reprogramming to upregulate cytosolic phosphoenolpyruvate carboxykinase (PCK1), a key enzyme that initiates gluconeogenesis. PCK1 subsequently triggered retrograde carbon flow from gluconeogenesis to glycogenesis, glycogenolysis, and the pentose phosphate pathway. The resultant NADPH facilitated reduced glutathione production, leading to a moderate increase of reactive oxygen species that stimulated hypoxic breast TRC growth. Notably, this metabolic mechanism was absent in differentiated breast tumor cells. Targeting PCK1 synergized with paclitaxel to reduce the growth of triple-negative breast cancer (TNBC). These findings uncover an altered glycogen metabolic program in breast cancer, providing potential metabolic strategies to target hypoxic breast TRCs and TNBC. Significance: Hypoxic breast cancer cells trigger self-growth through PCK1-mediated glycogen metabolism reprogramming that leads to NADPH production to maintain a moderate ROS level.

Counter-current chromatography (CCC) is a unique liquid–liquid partition chromatography and largely relies on the partition interactions of solutes and solvents in two-phase solvents. Usually, the two-phase solvents used in CCC include a lipophilic organic phase and a hydrophilic aqueous phase. Although a large number of partition interactions have been found and used in the CCC separations, there are few studies that address the role of water on solvents and solutes in the two-phase partition. In this study, we presented a new insight that H2O (water) might be an efficient and sensible hydrophobic agent in the n-hexane-methanol-based two-phase partition and CCC separation of lipophilic compounds, i.e., anti-cancer component mollugin from Rubia cordifolia. Although the n-hexane-methanol-based four components solvent systems of n-hexane-ethyl acetate-methanol-water (HEMWat) is one of the most popular CCC solvent systems and widely used for natural products isolation, this is an interesting trial to investigate the water roles in the two-phase solutions. In addition, as an example, the bioactive component mollugin was targeted, separated, and purified by MS-guided CCC with hexane-methanol and minor water as a hydrophobic agent. It might be useful for isolation and purification of lipophilic mollugin and other bioactive compounds complex natural products and traditional Chinese medicines.

Summary Unlike in metazoans, the stepwise biogenesis of microRNAs (miRNAs) occurs within the nucleus in plants. Whether or how the major steps in miRNA biogenesis are coordinated is largely unknown. Here, we show that the plant TREX-2 complex promotes multiple steps in miRNA biogenesis, including transcription, processing and nuclear export. Core subunits of TREX-2, THP1 and SAC3A, interact and co-localize with RNA Polymerase II to promote the transcription of MIR genes in the nucleoplasm. TREX-2 interacts with the microprocessor component SERRATE and promotes the formation of Dicing bodies in the nucleoplasm. THP1 also interacts and co-localizes with the nucleoporin protein NUP1 at the nuclear envelope. NUP1 and THP1 promote the nuclear export of miRNAs and AGO1. These results suggest that TREX-2 coordinates the transcription, processing and export steps in miRNA biogenesis to ensure efficient miRNA production.

Consumption of functional juice is becoming increasingly popular. This study aimed to evaluate the effect of probiotic fermentation with Bacillus sp. DU-106; Lactobacillus planturum Lp-43 and Lactobacillus rhamnosus Lr-156 on the biochemical and functional characteristics, antioxidant activities and storage stability of Dendrobium officinale and banana (DOB) juice. The cell levels of the lactic acid bacteria reached near 9 log copies/mL after fermentation at 32 °C for 36 h and could keep in this level after storage at 4 °C for 28 days. After fermentation, total acidity, flavonoids and polysaccharide contents of DOB juice increased, while pH, dissolved oxygen, nitrite, nitrate, vitamin C, β-carotene, sugar contents and antioxidant capacity slightly decreased. Compared with nonfermented DOB juice, polyphenol oxidase (PPO) and peroxidase (POD) activities of fermented DOB decreased significantly, but the color value and the content of total phenols and vitamin C decreased slightly in fermented DOB juice during storage. Overall, the probiotic fermentation with selected strains could improve the quality the DOB juice, enhance antioxidant capacity and storage stability, and destroy accumulation of nitrite and nitrate during storage. Findings of this study would help in the development of beneficial beverages in industrial production.

Intractable or recurrent chronic itch greatly reduces the patients' QOL and impairs their daily activities. In this study, we investigated whether there are certain key signaling molecules downstream of the recently identified peptides mediating itch in the spinal cord. RNA sequencing analysis of mouse spinal cord in chronic itch models induced by squaric acid dibutylester and imiquimod showed that extracellular signal-regulated kinase (ERK) 1/2 cascade is the most significantly upregulated gene cluster in both models. In four different mouse models of chronic itch, sustained ERK phosphorylation was detected mainly in spinal neurons, and MAPK/ERK kinase inhibitors significantly inhibited chronic itch in these models. Phosphorylated ERK was observed in the interneurons expressing the receptors of different neuropeptides for itch, including gastrin-releasing peptide receptor, natriuretic peptide receptor A, neuromedin B receptor, and sst2A. Blocking gastrin-releasing peptide receptor and natriuretic peptide receptor A by genetic approaches or toxins in mice significantly attenuated or ablated spinal phosphorylated ERK. When human embryonic kidney 293T cells transfected with these receptors were exposed to their respective agonists, ERK was the most significantly activated intracellular signaling molecule. Together, our work showed that phosphorylated ERK is a unique marker for itch signal transmission in the spinal cord and an attractive target for the treatment of chronic itch.

Exquisitely regulated plastid-to-nucleus communication by retrograde signaling pathways is essential for fine-tuning of responses to the prevailing environmental conditions. The plastidial retrograde signaling metabolite methylerythritol cyclodiphosphate (MEcPP) has emerged as a stress signal transduced into a diverse ensemble of response outputs. Here we demonstrate enhanced phytochrome B protein abundance in red-light grown MEcPP-accumulating mutant (ceh1) plant relative to wild-type seedlings. We further establish MEcPP-mediated coordination of phytochrome B with auxin and ethylene signaling pathways, and uncover differential hypocotyl growth of red-light grown seedlings in response to these phytohormones. Genetic and pharmacological interference with ethylene and auxin pathways outline the hierarchy of responses, placing auxin epistatic to the ethylene signaling pathway. Collectively, our finding establishes the key role of a plastidial retrograde metabolite in orchestrating the transduction of a repertoire of signaling cascades, and positions plastids at the zenith of relaying information coordinating external signals and internal regulatory circuitry to secure organismal integrity.Two sentence summaryThe plastidial retrograde metabolite, MEcPP, orchestrates coordination of light and hormonal signaling cascade through induction of phytochrome B abundance and modulation of auxin and ethylene levels for optimal adaptive responses to light environment.

Background: Genomic DNA methylation plays an important role in both the occurrence and development of bladder cancer. Kaempferol (Kae), a natural flavonoid that is present in many fruits and vegetables, exhibits potent anti-cancer effects in bladder cancer. Similar to other flavonoids, Kae possesses a flavan nucleus in its structure. This structure was reported to inhibit DNA methylation by suppressing DNA methyltransferases (DNMTs). However, whether Kae can inhibit DNA methylation remains unclear. Methods: Nude mice bearing bladder cancer were treated with Kae for 31 days. The genomic DNA was extracted from xenografts and the methylation changes was determined using an Illumina Infinium HumanMethylation 450 BeadChip Array. The ubiquitination was detected using immuno-precipitation assay. Results: Our data indicated that Kae modulated DNA methylation in bladder cancer, inducing 103 differential DNA methylation positions (dDMPs) associated with genes (50 hyper-methylated and 53 hypo-methylated). DNA methylation is mostly relied on the levels of DNMTs. We observed that Kae specifically inhibited the protein levels of DNMT3B without altering the expression of DNMT1 or DNMT3A. However, Kae did not downregulate the transcription of DNMT3B. Interestingly, we observed that Kae induced a premature degradation of DNMT3B by inhibiting protein synthesis with cycloheximide (CHX). By blocking proteasome with MG132, we observed that Kae induced an increased ubiquitination of DNMT3B. These results suggested that Kae could induce the degradation of DNMT3B through ubiquitin-proteasome pathway. Conclusion: Our data indicated that Kae is a novel DNMT3B inhibitor, which may promote the degradation of DNMT3B in bladder cancer.

Our current understanding of how sugar metabolism affects inflammatory pathways in macrophages is incomplete. Here, we show that glycogen metabolism is an important event that controls macrophage-mediated inflammatory responses. IFN-γ/LPS treatment stimulates macrophages to synthesize glycogen, which is then channeled through glycogenolysis to generate G6P and further through the pentose phosphate pathway to yield abundant NADPH, ensuring high levels of reduced glutathione for inflammatory macrophage survival. Meanwhile, glycogen metabolism also increases UDPG levels and the receptor P2Y14 in macrophages. The UDPG/P2Y14 signaling pathway not only upregulates the expression of STAT1 via activating RARβ but also promotes STAT1 phosphorylation by downregulating phosphatase TC45. Blockade of this glycogen metabolic pathway disrupts acute inflammatory responses in multiple mouse models. Glycogen metabolism also regulates inflammatory responses in patients with sepsis. These findings show that glycogen metabolism in macrophages is an important regulator and indicate strategies that might be used to treat acute inflammatory diseases., Glycogen can be metabolized via glycogenolysis and the pentose phosphate pathway as well as into the production of UDP glucose, which when secreted can bind the P2Y14 receptor. Here the authors show how these glycogen metabolism pathways contribute to proinflammatory macrophage activation and susceptibility to sepsis.

Plant survival necessitates constant monitoring of fluctuating light and balancing growth demands with adaptive responses, tasks mediated via interconnected sensing and signaling networks. Photoreceptor phytochrome B (phyB) and plastidial retrograde signaling metabolite methylerythritol cyclodiphosphate (MEcPP) are evolutionarily conserved sensing and signaling components eliciting responses through unknown connection(s). Here, via a suppressor screen, we identify two phyB mutant alleles that revert the dwarf and high salicylic acid phenotypes of the high MEcPP containing mutant ceh1. Biochemical analyses show high phyB protein levels in MEcPP-accumulating plants resulting from reduced expression of phyB antagonists and decreased auxin levels. We show that auxin treatment negatively regulates phyB abundance. Additional studies identify CAMTA3, a MEcPP-activated calcium-dependent transcriptional regulator, as critical for maintaining phyB abundance. These studies provide insights into biological organization fundamentals whereby a signal from a single plastidial metabolite is transduced into an ensemble of regulatory networks controlling the abundance of phyB, positioning plastids at the information apex directing adaptive responses., MEcPP is an evolutionarily conserved metabolite that acts as a plastid-to-nucleus retrograde signal to regulate adaptive responses to fluctuating light. Here the authors show that MEcPP regulates seedling development by stabilizing the phyB photoreceptor in an auxin and Ca2+ dependent manner.

Cyclopropane fatty acids (CFAs) are synthetized by the addition of a methylene group from S-adenosyl-l-methionine across the carbon-carbon double bonds of unsaturated fatty acid chains of membrane phospholipids. This fatty acid cyclopropanation, catalyzed by the CFA synthase (CfaS) enzyme, occurs in many bacteria, including the human pathogen Helicobacter pylori. Although the cyclopropane modification was reported to play a key role in the adaptation in response to environmental stress, its role in H. pylori remains unknown. In this study, we showed that H. pylori HP0416 encodes a functional CfaS. The enzyme was demonstrated to be required for acid resistance, antibiotic resistance, intracellular survival and mouse gastric colonization, and cell membrane integrity. Moreover, the tool compound dioctylamine, which acts as a substrate mimic, directly inhibits the CfaS function of H. pylori, resulting into sensitivity to acid stress, increased antibiotic susceptibility, and attenuated abilities to avoid macrophage killing and to colonize mouse stomachs. These results validate CfaS as a promising antibiotic target and provide new potentials for this recognized target in future anti-H. pylori drug discovery efforts. IMPORTANCE The increasing prevalence of multidrug-resistant Helicobacter pylori strains has created an urgent need for alternative therapeutic regimens that complement the current antibiotic treatment strategies for H. pylori eradication; however, this is greatly hampered due to a lack of “druggable” targets. Although the CFAs are present in H. pylori cytoplasmic membranes at high levels, their physiological role has not been established. In this report, deletion of the CFA synthase CfaS was shown to attenuate acid and drug resistance, immune escape, and gastric colonization of H. pylori. These findings were validated by inhibition of the CfaS activity with the tool compound dioctylamine. These studies identify this enzyme as an attractive target for further drug discovery efforts against H. pylori.

Background Staphylococcal enterotoxin A (SEA) is a well-known superantigen and stimulates human peripheral blood mononuclear cells (PBMCs) involving in the pathogenesis of inflammatory disorders and cancer. Objective To better understand the biological activities of SEA and the possible intracellular mechanisms by which SEA plays its roles in conditions like staphylococcal inflammatory and/or autoimmune disorders and immunotherapy. Methods Recombinant SEA (rSEA) was expressed in a prokaryotic expression system and its effects on the cytokine and chemokine production was examined by Enzyme-linked Immunospot (ELISpot) Assay and ELISA analysis. Results In vitro experiments showed rSEA could significantly enhance secretion of a broad spectrum of cytokines and chemokines from PBMCs dose-dependently. Increased secretion of cytokines and chemokines from rSEA stimulated PBMCs was barely affected by C-C motif chemokine receptor 2 (CCR2) antagonist INCB3344. However, Src, ERK and STAT pathway inhibitors were able to successfully block the enhanced secretion of most of cytokines and chemokines produced by rSEA stimulated PBMCs. Conclusions Our work suggested that rSEA serves as a potent stimulant of PBMCs, and induces the release of cytokines and chemokines through Src, ERK and STAT pathways upon a relatively independent network. Our work also strongly supported that Src, ERK and STAT signaling inhibitors could be effective therapeutic agents against diseases like toxic shock syndrome or infection by microbes resistant to antibiotics.

Antifungal treatment is often ineffectual, partly because of biofilm formation. In this study, by using a combined forward and reverse genetic strategy, we identified that nucleus-localized AfSsn3 and its partner AfSsn8, which constitute a Cdk8-cyclin pair, are required for azole resistance in Aspergillus fumigatus . Deletion of Afssn3 led to increased absorption and utilization of glucose and amino acids. Interestingly, absorption and utilization of glucose accelerated the extracellular polysaccharide formation, while utilization of the amino acids serine, threonine, and glycine increased sphingolipid pathway intermediate accumulation. In addition, the absence of Afssn3 induced the activity of the efflux pump proteins. These factors indicate the mature biofilm is responsible for the major mechanisms of A. fumigatus resistance to azoles in the Δ Afssn3 mutant. Collectively, the loss of Afssn3 led to two “barrier” layers between the intracellular and extracellular spaces, which consequently decreased drug penetration into the cell.

Helicobacter pylori is a Gram-negative bacterium that inhabits human upper gastrointestinal tract and the presence of this pathogen in the gut microbiome increases the risk of peptic ulcers and stomach cancer. H. pylori depends on unsaturated fatty acid (UFA) biosynthesis for maintaining membrane structure and function. Although some of the H. pylori enzymes involved in UFA biosynthesis are functionally homologous with the enzymes found in Escherichia coli, we show here that an enzyme HP0773, now annotated as FabX, uses an unprecedented a backtracking mechanism to not only dehydrogenate decanoyl-acyl carrier protein (ACP) in a reaction that parallels that of acyl-CoA dehydrogenase, the first enzyme of the fatty acid β-oxidation cycle, but additionally isomerizes trans-2-decenoyl-ACP to cis-3-decenoyl-ACP, the key UFA synthetic intermediate. Thus, FabX reverses the normal fatty acid synthesis cycle in H. pylori at the C10 stage. Overall, this unusual FabX activity may offer a broader explanation for how many bacteria that lack the canonical pathway enzymes produce UFA-containing phospholipids.

The nanocomposite of titanium dioxide (TiO2) combined with graphene oxide (GO) and cerium (Ce) was successfully synthesized via sol–gel method followed by calcining at 300 °C for 2 h. The composite was characterized by X-ray diffraction, ultraviolet–visible diffuse reflectance spectroscopy, scanning electron microscopy (SEM) and Brunauer–Emmett–Teller. The photocatalytic activity was evaluated by photodegradation of methylene blue (MB) under the irradiation of xenon lamp. This study demonstrated that GO and Ce co-doped in TiO2 could broaden absorption edge to the visible light and increase surface area of samples. SEM observation showed that addition of Ce could solve the problem of the agglomeration of GO under the same experimental conditions. Moreover, the MB photocatalytic degradation rate of the composite with GO doped for 0.2 % and Ce doped for 0.6 % (mass ratio) was up to 97.7 %, which was largely attributed to the synergistic effects in the GO, Ce and TiO2 system.

In this work, carbon nano-tube/TiO2(CNTs/TiO2) nanocomposites were prepared using a conventional sol-gel method. To further obtain a uniform catalyst film, chitosan (CS) was used as a crosslinker for the CNTs/TiO2composite. The structure and property of CNTs/TiO2/CS film were characterized using XRD, FT-IR, TEM, SEM, and UV-vis. The photocatalytic activities of CNTs/TiO2/CS film were measured through the photocatalytic degradation of gaseous formaldehyde. Compared with the commercial TiO2, higher degradation was achieved with the CNTs/TiO2/CS film due to stronger absorbability and synergetic effect among CNTs, TiO2, and CS.

Introduction Sodium tanshinone sulphonates are water-soluble derivatives of tanshinones originated from Tanshen (or Danshen, Salvia miltiorrhiza Bunge), a famous Traditional Chinese Medicine, which have potent biological activities, especially in the treatment of cardiovascular disorders. However, the classical preparation processes of sodium tanshinone sulphonates often involve multiple time- and solvent-consuming steps after purification of tanshinones, resulting in relatively low yields. Objective To develop a simple protocol for direct preparation of sodium tanshinone sulphonates from the complex crude extract of the roots of S. miltiorrhiza without pre-purification of tanshinones. Methodology The 100 mg crude tanshinone extract of S. miltiorrhiza was first sulphonated in a ultrasound bath with glacial acetic acid, acetic anhydride and concentrated sulphuric acid for 20 min, and then subjected to counter-current chromatography (CCC) separation using a optimum two-phase solvent system composed of n-hexane:ethylacetate:ethanol:5% sodium chloride aqueous solution (1:8:4:10, v/v). Based on the UV detection and HPLC analyses, the sulphonated fractions were collected. Result Sodium tanshinone IIA sulphonate (7.1 mg) and sodium tanshinone I sulphonate (2.8 mg) with over 95% purity were obtained successfully for the first time by ultrasound-assisted sulphonation and following CCC purification. Conclusion The study has shown that the method combining ultrasound-assisted sulphonation and CCC purification is an efficient way to prepare tanshinone sulphonates without pre-purification of tanshinones from the complex extracts of Tanshen, and can be explored as a new protocol for wide natural product modification directly from a crude complex extracts without pre-purification. Copyright © 2011 John Wiley & Sons, Ltd.

Calcium phosphate film was prepared by electrochemical deposition technology. Subsequently, the alkaline treatment process of calcium phosphate film in 0.1 mol/L NaOH solution was monitored on real time by the piezoelectric quartz crystal impedance (PQCI) technique. The variations of morphology and composition for the alkaline treatment products were characterized by scanning electron microscopy (SEM), Fourier transform infrared (FT-IR) and X-ray diffraction (XRD), respectively. The dynamic variations of calcium phosphate can be characterized by the change of equivalent circuit parameters. The results show that the forming process of hydroxyapatite (HA) is composed of three stages: (1) acidic calcium phosphate dissolution; (2) phase transformation; and (3) HA formation. Furthermore, the correlative kinetic equations and parameters are obtained by fitting the static capacitance (Cs)—time curves.

A simple and sensitive method for the amperometric detection of trace amount of chromium(VI) using a Prussian blue modified glassy carbon electrode (PB/GCE) is described here. The Everitts salt/Prussian blue redox couple of the PB film was found to mediate the Cr(VI) reduction, and the mechanism of electrochemical reaction was investigated. The effects of PB film thickness, applied potential and electrolyte solution on the current response of Cr(VI) reduction were thoroughly studied. Under the optimized conditions, the PB/GCE provided a wide linear range for Cr(VI) analysis from 0.5 to 200 ppb with excellent sensitivity (15±0.2 nA/ppb) and low detection limit (0.15 ppb). In addition, the modified electrode showed excellent stability, reproducibility and good resistance to other metal ions and surfactants. Finally, the proposed method was applied to detect trace Cr(VI) in wastewater with satisfactory results. The great advantages of the method were characterized by the simplicity, ease of preparation, stability, short analysis time and cost-efficiency.

The main objectives were to (1) calculate the total volatile organic compounds (TVOCs) inhalation dose, (2) analyze the proportions of human’s inhaled contaminant dose from different sources, and (3) present a newly defined ratio of relative inhalation dose level (RIDL) to assess indoor air quality (IAQ). A user defined function based on CFD (computational fluid dynamics) was developed, which integrated human motion model with TVOCs emission model in a high sidewall air supply ventilation mode. Based on simulation results of 10 cases, it is shown that the spatial concentration distribution of TVOCs is affected by human motion. TVOCs diffusion characteristic of building material is the most effective way to impact the TVOCs inhalation dose. From the RIDL index, case A-2 has the most serious IAQ problem, while case D-1 is of the best IAQ.

Photo-induced polymerization is employed to prepare polyaniline (PAN) nanoparticles in ionic liquid for the first time. Photons and photoactive ionic liquid cations replace conventional oxidants and metal complexes to promote the polymerization of aniline monomer. The diameter of the resulted PAN is confirmed in nano-scale by SEM. With increase of protonic acid in medium, the yield of the PAN increased, the UV absorption of the PAN strengthened, and a blue shift of the π-polaron absorption was observed. And the conductivity of the PAN also increased with the acid content in medium. The potential mechanism of photo-induced polymerization of aniline is proposed. Moreover, after the ionic liquid is separated from the reaction mixture and reused for five times, no obvious decrease in catalytic activity could be found in photo-induced polymerization of aniline. The method may open a new pathway to prepare nano-scale conducting polymers with sunlight.

In this work, in situ microwave activation of electrochemical detection of copper(II) at a gold nanoparticles-modified Pt microelectrode (Au-NPs/Pt) was investigated. Self-focusing of the microwave radiation creates an extreme localized heating at the electrode/solution (electrolyte) interface within the diffusion layer of the electrode with an inverted thermal gradient and convective flow. The temperature at the electrode/solution interface is calibrated with reversible one electron redox system Fe ( CN ) 6 3 - / 4 - in aqueous K 2 SO 4 solution (pH 3). Significantly increased currents were observed at the Au-NPs/Pt electrode compared to that at bare Pt electrode under the low microwave power. The Cu(II) detection at the Au-NPs/Pt microelectrode by cyclic voltammetry is also shown to be strongly enhanced by microwave radiation, which triggers Cu(II) current response orders of magnitude higher than those expected values in conventional conditions. The limit of detection by cyclic voltammetry is found to be 0.1 μM and 1.0 μM with and without microwave radiation. The effect of surfactant, which blocks the electrochemical Cu(II) signal under conventional conditions, is discussed on the Cu(II) response under the in situ microwave radiation of electrochemical process.

Gold nanoparticles/carbon nanotubes (Au-NPs/CNTs) composites were rapidly synthesized by microwave radiation, and firstly applied for the determination of trace mercury(II) by anodic stripping voltammetry (ASV). The structure and composition of the synthesized Au-NPs/CNTs nanocomposites were characterized by transmission electron microscopy (TEM), energy dispersive X-ray spectroscopy (EDX), UV–vis absorption spectroscopy and cyclic voltammetry. Au-NPs/CNTs nanocomposites modified glassy carbon electrode (Au-NPs/CNTs/GCE) exhibited excellent performance for Hg(II) analysis. A wide linear range (5 × 10−10–1.25 × 10−6 mol/L) and good repeatability (relative standard deviation of 1.84%) were obtained for Hg(II) detection. The limit of detection was found to be 3 × 10−10 mol/L (0.06 μg/L) at 2 min accumulation, while the World Health Organization’s guideline value of mercury for drinking water is 1 μg/L, suggesting the proposed method may have practical utility. Keywords: Microwave-irradiated synthesis, Gold nanoparticles, Carbon nanotubes, Voltammetry, Mercury

Multiwall carbon nanotubes were dispersed in Nafion (MWCNTs-NA) solution and used in combination with bismuth (MWCNTs-NA/Bi) for fabricating composite sensors to determine trace Pb(II) and Cd(II) by differential pulse anodic stripping voltammetry (DPASV). The electrochemical properties of the MWCNTs-NA/Bi composites film modified glassy carbon electrode (GCE) were evaluated. The synergistic effect of MWCNTs and bismuth composite film was obtained for Pb(II) and Cd(II) detection with improved sensitivity and reproducibility. Linear calibration curves ranged from 0.05 to 100 μg/L for Pb(II) and 0.08 to 100 μg/L for Cd(II). The determination limits (S/N=3) were 25 ng/L for Pb and 40 ng/L for Cd, which compared favorably with previously reported methods in the area of electrochemical Pb(II) and Cd(II) detection. The MWCNTs-NA/Bi composite film electrodes were successfully applied to determine Pb(II) and Cd(II) in real sample, and the results of the present method agreed well with those of atomic absorption spectroscopy.

A novel method for the oxidative determination of trace arsenic(III) was investigated on highly ordered platinum-nanotube array electrodes (PtNTAEs). The PtNTAEs with a highly organized structure were fabricated by electrochemical deposition of platinum in a 3-aminopropyltrimethoxysilane-modified porous anodic alumina template (PAA). The morphologies and structures of PtNTAEs were characterized by scanning electron microscopy (SEM) and X-ray diffraction (XRD). Electrochemical experiments proved that the PtNTAEs exhibited better performance for As(III) analysis in comparison with platinum nanoparticles-coated GCE (Ptnano/GCE) or Pt foil electrode. The PtNTAEs showed to provide higher reproducibility and lower detection limit. The relative standard deviation (RSD) was 3.5% for 50 repeated measurements of 20 μM As(III), and the limit of detection (LOD) was 0.1 ppb, which was typically 1–2 orders of magnitude lower than that of Ptnano/GCE or Pt foil electrode. Keywords: Highly ordered platinum-nanotube array, Arsenic, Voltammetry, Porous anodic alumina template, Heavy metals

A novel analytical procedure for the determination of Pb(II) and Cd(II) in herbal medicines by differential pulse anodic stripping voltammetry (DPASV) on Nafion-coated bismuth film electrode (NCBFE) was proposed and experimentally validated. Various experimental parameters, which influenced the response of the NCBFE to these metals in real samples, were optimized. The results showed that there were well-defined peaks of Pb and Cd in herb samples at deposition potential of −1.2 V and deposition time of 300 s. The analytical performance of the NCBFE was evaluated in the presence of dissolved oxygen, with the determination limits of 0.35 µg·L−1 for Pb and 0.72 µg·L−1 for Cd and recoveries of 87.8% –105.4% for Pb and 89.5% –108.5% for Cd obtained from different samples. The Pb and Cd concentrations in the studied samples have been also determined by graphite furnace atomic absorption spectrometry (GFAAS), suggesting that there was a satisfactory agreement between the two techniques, with relative errors lower than 6.5% in all cases. The great advantages of the proposed method over the spectroscopic method were characterized by its simplicity, selectivity and short analysis time, simultaneous analysis of different metals and cost-efficiency.

Platinum nanoparticles/carbon nanotubes (Ptnano/CNTs) were rapidly synthesized by microwave radiation, and applied for the oxidative determination of arsenic(III). The transmission electron microscopy (TEM) revealed the size of synthesized Pt nanoparticles with nominal diameter of 15 ± 3 nm. Ptnano/CNTs modified glassy carbon electrode (Ptnano/CNTs/GCE) exhibited better performance for arsenic(III) analysis than that of Pt nanoparticles modified GCE (Ptnano/GCE) by electrochemical deposition or Pt foil electrode. Excellent reproducibility of the Ptnano/CNTs/GCE was obtained with the relative standard deviation (RSD) of 3.5% at 20 repeated analysis of 40 μM As(III), while the RSD was 9.8% for Ptnano/GCE under the same conditions. The limit of determination (LOD) of the Ptnano/CNTs/GCE was 0.12 ppb, which was 1–2 orders of magnitude lower than that of Ptnano/GCE or Pt foil electrode. Keywords: Microwave-irradiated synthesis, Platinum nanoparticles, Voltammetry, Carbon nanotubes, Arsenic

In situ adsorption of human serum albumin (HSA) and ovalbumin (OVA) was real-time monitored by piezoelectric quartz crystal impedance (PQCI) technique to fully understand the initial cellular response on hydroxyapatite/chitosan (HAP/CS) composite. The PQCI parameters, such as resonant frequency ( f ), static capacitance ( C s ), and motional resistance ( R m ) were measured for investigating the kinetic adsorption behaviors of both proteins. The change in frequency shifts (Δ f ) depends on the amount of the adsorbed protein, and the change in motional resistance (Δ R m ) results from the microporosity variation of HAP/CS coating. The results show that the amount of the absorbed HSA is much greater than that of OVA on HAP/CS coating because of the unique construction of HSA as well as a flexible protein. Furthermore, Δ f and Δ R m data were fitted according to the kinetic exponential decay equations. It can be seen that there is only one adsorption process for OVA, but the absorption process for HSA is followed by a rearrangement process, and the former process is faster than the rearrangement process. Subsequently, the composite binding with proteins were demonstrated by the Fourier transform infrared (FTIR), cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS).

Mercury electrodes have been traditionally employed for achieving high reproducibility and sensitivity of the stripping technique. However, new alternative electrode materials are highly desired because of the toxicity of mercury. Bismuth is an electrode material characterized by its low toxicity and its ability to form alloys with some metals such as cadmium, lead and zinc, allowing their preconcentration at the electrode surface. In this work, we reported the simultaneous determination of Pb(II), Cd(II) and Zn(II) at the low μg/l concentration levels by differential pulse anodic stripping voltammetry (DPASV) on a Nafion-coated bismuth film electrode (NCBFE) plated in situ, and investigated the application of NCBFE to heavy metals analysis in vegetable samples. The analytical performance of NCBFE was evaluated for simultaneous determination of Pb(II), Cd(II) and Zn(II) in non-deaerated solution, with the limits of determination of 0.30 μg/l for Zn, 0.17 μg/l for Cd and Pb at a preconcentration time of 180 s. High reproducibility for NCBFE was indicated from the relative standard deviations of 2.4% for Pb, 2.0% for Cd and 3.4% for Zn at the 15 μg/l level (n = 15). The NCBFE was successfully applied to determine Pb and Cd in vegetable samples, and the results were in agreement with those of graphite furnace atomic absorption spectrometry (GFAAS).