The synthesis of nanocrystals is in the limelight in modern nanotechnology. Biosynthesis of nanoparticles by plant extracts is currently under exploitation. Not only could silver nanoparticles ranging from 55 to 80 nm in size be fabricated, but also triangular or spherical shaped gold nanoparticles could be easily modulated by reacting the novel sundried biomass of Cinnamomum camphora leaf with aqueous silver or gold precursors at ambient temperature. The marked difference of shape control between gold and silver nanoparticles was attributed to the comparative advantage of protective biomolecules and reductive biomolecules. The polyol components and the water-soluble heterocyclic components were mainly responsible for the reduction of silver ions or chloroaurate ions and the stabilization of the nanoparticles, respectively. The sundried leaf in this work was very suitable for simple synthesis of nanoparticles.

A new polymerizable imidazolium salt monomer, 1-(4-vinylbenzyl)-3-methyl-imidazolium chloride ([VBMI]Cl), has been readily synthesized by reaction of 4-vinylbenzyl chloride with 1-methylimidazole. Novel anion exchange membranes (AEMs) based on the copolymers of [VBMI]Cl and styrene have been prepared and characterized. Excellent thermostability of the membranes is observed through the thermo-gravimetric analysis (TGA) curves. Water uptake and ion exchange capacity (IEC) of the OH(-) form AEMs range from 26.1% to 61.9% and from 0.95 to 1.45 mmol g(-1), respectively. This type of AEM displays significant ionic conductivities over the order of 10(-2) S cm(-1) in deionized water at room temperature, and the membranes are stable in 10 mol L(-1) NaOH solution at 60 degrees C for 120 h. For the H(2)/air single fuel cell at 30 degrees C with this novel AEM, the peak power density of 33 mW cm(-2) is obtained at a current density of 59 mA cm(-2).High-Tech Research and Development Program of China[2008AA05Z107]; National Nature Science Foundation of China[20876129

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Xanthophyllomyces dendrorhous is a promising source of natural astaxanthin due to its ability to accumulate high amounts of astaxanthin. This study showed that 6-benzylaminopurine (6-BAP) is an effective substrate that enhances cell biomass and astaxanthin accumulation in X. dendrorhous. In the current study, the biomass and astaxanthin content in X. dendrorhous were determined to be improved by 21.98% and 24.20%, respectively, induced by 6-BAP treatments. To further understand the metabolic responses of X. dendrorhous to 6-BAP, time-course metabolomics and gene expression levels of X. dendrorhous cultures with and without 6-BAP feeding were investigated. Metabolome analysis revealed that 6-BAP facilitated glucose consumption, promoted the glycolysis, suppressed the TCA cycle, drove carbon flux of acetyl-CoA into fatty acid and mevalonate biosynthesis, and finally facilitated the formation of astaxanthin. ROS analysis suggested that the antioxidant mechanism in X. dendrorhous can be induced by 6-BAP. Additionally, the process of 6-BAP significantly upregulated the expression of six key genes involved in pathways related to astaxanthin biosynthesis. This research demonstrates the metabolomic mechanism of phytohormone stimulation of astaxanthin production iNn X. dendrorhous and presents a new strategy to improve astaxanthin production to prevent the dilemma of choosing between accumulation of astaxanthin and cell biomass.

The polyketide synthase (PKS) cluster genes are supposed to synthesize polyunsaturated fatty acids (PUFAs) in S. limacinum. In this study, two enyolreductase (ER) genes located on PKS cluster were knocked out through homologous recombination to explore their functions. The knock-out of OrfB-ER (located on OrfB subunit) decreased lipid content and had obvious decrease on PUFAs content, indicating OrfB-ER domain played a vital role on PUFAs synthesis; the knock-out of OrfC-ER (located on OrfC subunit) decreased SFAs content and increased total lipid content, indicating OrfC-ER domain was likely to be related with SFAs synthesis, and lipid production could be improved by down-regulating OrfC-ER domain expression. Therefore, the addition of triclosan as a reported regulator of ER domain induced the increase of PUFAs production by 51.74% and lipids yield by 47.63%. Metabolic analysis indicated triclosan played its role through inhibiting the expression of OrfC-ER to reduce the feedback inhibition of SFAs and further to enhance NADPH synthesis for lipid production, and by weakening mevalonate pathway and tricarboxylic acid (TCA) cycle to shift precursors for lipid and PUFAs synthesis. This research illuminates functions of two ER domains in S. limacinum and provides a potential targets for improving lipid production.