Magnetic biochar derived from rice straw and stainless steel pickling waste liquor for highly efficient adsorption of crystal violet.

Reducing the preparation cost of magnetic biochar is necessary for its large-scale application as an adsorbent. In this study, stainless steel pickling waste liquor and rice straw were successfully applied to synthesize of magnetic biochar (SPWL-MBC). Several iron oxides adhered on the biochar matrix, mainly FeO, FeO and FeO.

Analyzing scaling behavior of calcium sulfate in membrane distillation via optical coherence tomography.

Deepening the understanding of scaling processes would facilitate the improvement of membrane distillation (MD) as a promising technique for sustainable development. This study investigated the scaling of calcium sulfate in MD via an approach based on optical coherence tomography (OCT). The OCT-based characterization enabled an analysis that correlated the flux decline with the morphological evolution of the scaling layer.

Pyrolysis of different biomass pre-impregnated with steel pickling waste liquor to prepare magnetic biochars and their use for the degradation of metronidazole.

In this study, Fenton-like catalysts (magnetic biochar) were synthesised by pyrolysis the different biomass pre-impregnated with steel pickling waste liquor. The results of degradation of metronidazole illustrated that the catalytic performance of magnetic biochar was significantly affected by biomass feedstocks. Electron spin resonance (ESR) and radical quenching experiments showed that the hydroxide radicals (OH) were the key reactive oxygen species responsible for the metronidazole removal.

The humic acid influenced the behavior and reactivity of Ni/Fe nanoparticles in the removal of deca-brominated diphenyl ether from aqueous solution.

The removal of contaminants by iron-based nanomaterials was inevitably affected by the natural organic matter (NOM), which is one of the most abundant material on earth and exists in natural waters. This study was performed to investigate the main influence of humic acid (HA, representing NOM) on the behavior and reactivity of Ni/Fe nanoparticles in the removal of deca-brominated diphenyl ether (BDE209). Generally, the inhibitory effect of HA on the removal of BDE209 by Ni/Fe showed greater significance with an increase of HA concentration.

The mechanism of antifungal action of a new polyene macrolide antibiotic antifungalmycin 702 from Streptomyces padanus JAU4234 on the rice sheath blight pathogen Rhizoctonia solani.

Antifungalmycin 702, a new polyene macrolide antibiotic produced by Streptomycespadanus JAU4234, has a broad antifungal activity and may have potential future agricultural and/or clinical applications. However, the mechanism of antifungal action of antifungalmycin 702 remains unknown. Antifungalmycin 702 strongly inhibited mycelial growth and sclerotia formation/germination of Rhizoctonia solani.

In vitro antifungal activity of antifungalmycin 702, a new polyene macrolide antibiotic, against the rice blast fungus Magnaporthe grisea.

Antifungalmycin 702, a novel polyene macrolide antibiotic produced by Streptomyces padanus JAU4234, strongly inhibited mycelial growth of the rice blast fungus, Magnaporthe grisea, with EC50 of 37 μg/ml and EC90 of 136 μg/ml. Significant reduction in the number of conidia was observed at above 20 μg/ml. Conidia germination and appressorium formation were also suppressed and were not viable with >40 μg/ml.

[Inhibition effect of Ag-antibiotic 702 on plant pathogenic fungi and related mechanisms].

To explore the practical application value and action mechanisms of Ag-antibiotic 702 against pathogenic fungi, the inhibition spectrum of Ag-antibiotic 702 was studied by measuring the mycelium growth rate of pathogenic fungi, and the effects of Ag-antibiotic 702 on the membrane permeability of Rhizoctonia solani, a typical pathogenic fungus, were investigated, with the variations of mycelium electrolyte leakage and protein, nucleic acid, and Mg2+ and K+ contents under the action of Ag-antibiotic 702 determined, and the effects of Ag-antibiotic 702 on the cell membrane ergosterol biosynthesis and ultramicrostructure observed. The results showed that the active products of Ag-antibiotic 702 had stronger inhibition effect on 13 test pathogens, among which, Sclerotinia sclerotiorum was most sensitive, with the EC50 being 0.23 microg x mL(-1).

Characterization of Streptomyces padanus JAU4234, a producer of actinomycin X₂, fungichromin, and a new polyene macrolide antibiotic.

Strain JAU4234, identified as Streptomyces padanus, was isolated from soil collected in Jiangxi Province, China. It produced actinomycin X2, fungichromin, and a new polyene macrolide compound with antifungal activity, antifungalmycin 702. Antifungalmycin 702 had good general antifungal activity and may have potential future agricultural and/or clinical applications.

[Studies on the secondary metabolites of Coriolopsis sp. G066].

Objective: To study the secondary metabolites of Coriolopsis sp. G066.

Methods: The compounds were isolated by various chromatographic methods (silica gel, reverse silica gel, Sephadex LH-20, preparative TLC and so on).

Optimization of medium composition for actinomycin X2 production by Streptomyces spp JAU4234 using response surface methodology.

The effects of cultivation medium compositions including soybean meal, peptone, soybean oil and cornstarch for actinomycin X2 production by Streptomyces spp JAU4234 were accessed by using response surface methodology. The 2(4) full factorial designs and the paths of steepest ascent were effective in searching for the major factors of actinomycin X2 production. In this study, cornstarch and soybean oil showed negative effect on actinomycin X2 production based on the first-order regression coefficients derived from MINITAB software.

Identification of a gene cluster encoding meilingmycin biosynthesis among multiple polyketide synthase contigs isolated from Streptomyces nanchangensis NS3226.

A cluster encoding genes for the biosynthesis of meilingmycin, a macrolide antibiotic structurally similar to avermectin and milbemycin alpha11, was identified among seven uncharacterized polyketide synthase gene clusters isolated from Streptomyces nanchangensis NS3226 by hybridization with PCR products using primers derived from the sequences of aveE, aveF and a thioesterase domain of the avermectin biosynthetic gene cluster. Introduction of a 24.1-kb deletion by targeted gene replacement resulted in a loss of meilingmycin production, confirming that the gene cluster encodes biosynthesis of this important anthelminthic antibiotic compound.

A complete gene cluster from Streptomyces nanchangensis NS3226 encoding biosynthesis of the polyether ionophore nanchangmycin.

The PKS genes for biosynthesis of the polyether nanchangmycin are organized to encode two sets of proteins (six and seven ORFs, respectively), but are separated by independent ORFs that encode an epimerase, epoxidase, and epoxide hydrolase, and, notably, an independent ACP. One of the PKS modules lacks a corresponding ACP. We propose that the process of oxidative cyclization to form the polyether structure occurs when the polyketide chain is still anchored on the independent ACP before release.

[Determination of nanchangmycin and meilingmycin by high performance liquid chromatography].

A high performance liquid chromatographic method had been established for the separation and determination of two antibiotics produced by Streptomyces nanchangensis, polyether nanchangmycin and 16-membered macrolide meilingmycin. The latter is composed of several components. The operating conditions were Waters XTerra RP18 column (3.

'Streptomyces nanchangensis', a producer of the insecticidal polyether antibiotic nanchangmycin and the antiparasitic macrolide meilingmycin, contains multiple polyketide gene clusters.

Several independent gene clusters containing varying lengths of type I polyketide synthase genes were isolated from 'Streptomyces nanchangensis' NS3226, a producer of nanchangmycin and meilingmycin. The former is a polyether compound similar to dianemycin and the latter is a macrolide compound similar to milbemycin, which shares the same macrolide ring as avermectin but has different side groups. Clusters A-H spanned about 133, 132, 104, 174, 122, 54, 37 and 59 kb, respectively.