نتایج جستجو برای: bisabolene

تعداد نتایج: 122  

Journal: :Molecules 2016
Yu-Jen Jou Chun-Hung Hua Chen-Sheng Lin Ching-Ying Wang Lei Wan Ying-Ju Lin Su-Hua Huang Cheng-Wen Lin

γ-Bisabolene has demonstrated antiproliferative activities against several human cancer cell lines. This study first discloses the antiproliferative and apoptosis induction activities of γ-bisabolene to human neuroblastoma TE671 cells. A CC50 value of γ-bisabolene was 8.2 μM to TE671 cells. Cell cycle analysis with PI staining showed γ-bisabolene elevating the sub-G1 fractions in a time-depende...

Journal: :Applied and environmental microbiology 2014
James Kirby Minobu Nishimoto Ruthie W N Chow Venkata N Pasumarthi Rossana Chan Leanne Jade G Chan Christopher J Petzold Jay D Keasling

To facilitate enzyme and pathway engineering, a selection was developed for improved sesquiterpene titers in Saccharomyces cerevisiae. α-Bisabolene, a candidate advanced biofuel, was found to protect yeast against the disruptive action of nonionic surfactants such as Tween 20 (T20). An experiment employing competition between two strains of yeast, one of which makes twice as much bisabolene as ...

2011
Pamela P. Peralta-Yahya Mario Ouellet Rossana Chan Aindrila Mukhopadhyay Jay D. Keasling Taek Soon Lee

Rising petroleum costs, trade imbalances and environmental concerns have stimulated efforts to advance the microbial production of fuels from lignocellulosic biomass. Here we identify a novel biosynthetic alternative to D2 diesel fuel, bisabolane, and engineer microbial platforms for the production of its immediate precursor, bisabolene. First, we identify bisabolane as an alternative to D2 die...

2014
Fiona K. Davies Victoria H. Work Alexander S. Beliaev Matthew C. Posewitz

The plant terpenoids limonene (C10H16) and α-bisabolene (C15H24) are hydrocarbon precursors to a range of industrially relevant chemicals. High-titer microbial synthesis of limonene and α-bisabolene could pave the way for advances in in vivo engineering of tailor-made hydrocarbons, and production at commercial scale. We have engineered the fast-growing unicellular euryhaline cyanobacterium Syne...

Journal: :The Journal of organic chemistry 2004
James R Vyvyan Celeste Loitz Ryan E Looper Cheryl S Mattingly Emily A Peterson Steven T Staben

Aromatic bisabolene derivatives were prepared by two methods involving cross-coupling of organozinc reagents. The first synthesis of (+/-)-glandulone A (10), as well as syntheses of (+/-)-curcuhydroquinone (8) and (+/-)-curcuquinone (9), were accomplished via coupling of a secondary alkyl zinc reagent (1,5-dimethyl-4-hexenylzinc halide, 18) to protected bromohydroquinones using Pd(dppf)Cl(2) as...

Journal: :Planta medica 2015
Ana Carolina B C Rodrigues Larissa M Bomfim Sara P Neves Leociley R A Menezes Rosane B Dias Milena B P Soares Ana Paula N Prata Clarissa A Gurgel Rocha Emmanoel V Costa Daniel P Bezerra

Duguetia gardneriana, popularly known in the Brazilian northeast as "jaquinha", is a species belonging to the family Annonaceae. The aim of this work was to assess the chemical composition and antitumor properties of the essential oil from the leaves of D. gardneriana in experimental models. The chemical composition of the essential oil was analyzed via gas chromatography-flame ionization detec...

Journal: :Plant physiology 1971
A C Thompson D N Baker R C Gueldner P A Hedin

When atmosphere from cotton plants (Gossypium hirsutum L., var. Deltapine Smoothleaf) was condensed by passing it over the expansion coil of an air conditioner and three 1-hour collections per day (early morning, noon, and late afternoon) were made, the total essential oils were found to consist of 50 to 60% beta-bisabolol (I(k) 1660) and gamma-bisabolene (I(k) 1550) and 30 to 40% geraniol (I(k...

1998
JÖRG BOHLMANN JOHN CROCK REINHARD JETTER RODNEY CROTEAU

E)-a-Bisabolene synthase is one of two wound-inducible sesquiterpene synthases of grand fir (Abies grandis), and the olefin product of this cyclization reaction is considered to be the precursor in Abies species of todomatuic acid, juvabione, and related insect juvenile hormone mimics. A cDNA encoding (E)-a-bisabolene synthase was isolated from a wound-induced grand fir stem library by a PCR-ba...

2017
Junko Yaegashi James Kirby Masakazu Ito Jian Sun Tanmoy Dutta Mona Mirsiaghi Eric R. Sundstrom Alberto Rodriguez Edward Baidoo Deepti Tanjore Todd Pray Kenneth Sale Seema Singh Jay D. Keasling Blake A. Simmons Steven W. Singer Jon K. Magnuson Adam P. Arkin Jeffrey M. Skerker John M. Gladden

BACKGROUND Economical conversion of lignocellulosic biomass into biofuels and bioproducts is central to the establishment of a robust bioeconomy. This requires a conversion host that is able to both efficiently assimilate the major lignocellulose-derived carbon sources and divert their metabolites toward specific bioproducts. RESULTS In this study, the carotenogenic yeast Rhodosporidium torul...

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