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Cembranoid Diterpenes from the Soft Coral Lobophytum crassum and Their Anti-inflammatory Activities
Cuong, Nguyen Xuan,Thao, Nguyen Phuong,Luyen, Bui Thi Thuy,Ngan, Nguyen Thi Thanh,Thuy, Dinh Thi Thu,Song, Seok Bean,Nam, Nguyen Hoai,Kiem, Phan Van,Kim, Young Ho,Minh, Chau Van Pharmaceutical Society of Japan 2014 Chemical & pharmaceutical bulletin Vol.62 No.2
Cuong, Nguyen Xuan,Thao, Nguyen Phuong,Luyen, Bui Thi Thuy,Ngan, Nguyen Thi Thanh,Thuy, Dinh Thi Thu,Song, Seok Bean,Nam, Nguyen Hoai,Kiem, Phan Van,Kim, Young Ho,Minh, Chau Van WILEY‐VCH Verlag 2014 Chem Inform Vol.45 No.28
<P><B>Abstract</B></P><P>isolation, structure determination and antiinflammatory effects of nine cembranoid diterpenes including four new compounds, crassumols D—G (I)—(IV), respectively</P>
Nguyen, Dinh Chuong,Tran, Duy Thanh,Luyen Doan, Thi Luu,Kim, Nam Hoon,Lee, Joong Hee American Chemical Society 2019 Chemistry of materials Vol.31 No.8
<P>Developing efficient and cost-effective bifunctional electrocatalysts for both oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) is highly important for fabricating energy conversion and storage technologies, such as fuel cells, water electrolyzers, and metal-air batteries. Herein, we report a facile and economical route for synthesizing ultrasmall molybdenum phosphide (MoP<SUB><I>y</I></SUB>) nanocrystal-attached mesoporous manganese phosphides on N,P-codoped graphene nanosheets, which display equivalent ORR (OER) activity to that of Pt/C (RuO<SUB>2</SUB>) catalysts. This is manifested by the positive onset potential (0.969 V) and half-wave potential (0.842 V) for ORR, as well as a mere overpotential of 301 mV at a current density of 20 mA·cm<SUP>-2</SUP> and a small Tafel slope of 105 mV·dec<SUP>-1</SUP> for OER in alkaline medium. It also demonstrates remarkable stability in comparison with Pt/C and RuO<SUB>2</SUB> for both ORR and OER, respectively. The excellent performance can be attributed to the mesoporous structure with enhanced multiple types of electroactive sites, which highly favors the adsorption and catalyzation of reactants, as well as efficient reagent/product mass transport. The findings can pave a new way for the synthesis and usage of a hybrid as a bifunctional catalyst with high efficiency and outstanding longevity to enable next generation of energy conversion and storage.</P> [FIG OMISSION]</BR>
( Christiane Liers ),( Rene Ullrich ),( Harald Kellner ),( Do Huu Chi ),( Dang Thu Quynh ),( Nguyen Dinh Luyen ),( Le Mai Huong ),( Martin Hofrichter ),( Do Huu Nghi ) 한국미생물 · 생명공학회 2021 Journal of microbiology and biotechnology Vol.31 No.10
A bifunctional glycoside hydrolase GH78 from the ascomycete Xylaria polymorpha (XpoGH78) possesses catalytic versatility towards both glycosides and esters, which may be advantageous for the efficient degradation of the plant cell-wall complex that contains both diverse sugar residues and esterified structures. The contribution of XpoGH78 to the conversion of lignocellulosic materials without any chemical pretreatment to release the water-soluble aromatic fragments, carbohydrates, and methanol was studied. The disintegrating effect of enzymatic lignocellulose treatment can be significantly improved by using different kinds of hydrolases and phenoloxidases. The considerable changes in low (3 kDa), medium (30 kDa), and high (> 200 kDa) aromatic fragments were observed after the treatment with XpoGH78 alone or with this potent cocktail. Synergistic conversion of rape straw also resulted in a release of 17.3 mg of total carbohydrates (e.g., arabinose, galactose, glucose, mannose, xylose) per gram of substrate after incubating for 72 h. Moreover, the treatment of rape straw with XpoGH78 led to a marginal methanol release of approximately 17 μg/g and improved to 270 μg/g by cooperation with the above accessory enzymes. In the case of beech wood conversion, the combined catalysis by XpoGH78 and laccase caused an effect comparable with that of fungal strain X. polymorpha in woody cultures concerning the liberation of aromatic lignocellulose fragments.