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- Author:
- Skretas, Georgios; Makino, Tomohiro; Varadarajan, Navin; Pogson, Mark; Georgiou, George
- Source:
- Metabolic engineering 2012 v.14 no.5 pp. 591-602
- ISSN:
- 1096-7176
- Subject:
- physical properties; protein folding; nitrogen; fluorescence; lipoproteins; G-protein coupled receptors; stress response; gene expression; genes; mammals; bacteria; Escherichia coli
- Abstract:
- ... Low yields of recombinant expression represent a major barrier to the physical characterization of membrane proteins. Here, we have identified genes that globally enhance the production of properly folded G protein-coupled receptors (GPCRs) in Escherichia coli. Libraries of bacterial chromosomal fragments were screened using two separate systems that monitor: (i) elevated fluorescence conferred by ...
- DOI:
- 10.1016/j.ymben.2012.05.001
- PubMed:
- 22609824
- PubMed Central:
- PMC3428473
-
http://dx.doi.org/10.1016/j.ymben.2012.05.001
- Author:
- Leighty, Robert W.; Antoniewicz, Maciek R.
- Source:
- Metabolic engineering 2012 v.14 no.5 pp. 533-541
- ISSN:
- 1096-7176
- Subject:
- Escherichia coli; carbon; carbon dioxide; chi-square distribution; enzymes; glucose; inoculum; isotope labeling; metabolites; model validation; models; stable isotopes; transporters
- Abstract:
- ... ¹³C-metabolic flux analysis (MFA) is a widely used method for measuring intracellular metabolic fluxes in living cells. ¹³C MFA relies on several key assumptions: (1) the assumed metabolic network model is complete, in that it accounts for all significant enzymatic and transport reactions; (2) ¹³C-labeling measurements are accurate and precise; and (3) enzymes and transporters do not discriminate ...
- DOI:
- 10.1016/j.ymben.2012.06.003
-
http://dx.doi.org/10.1016/j.ymben.2012.06.003
- Author:
- Joe Shaw, A.; Covalla, Sean F.; Miller, Bethany B.; Firliet, Brian T.; Hogsett, David A.; Herring, Christopher D.
- Source:
- Metabolic engineering 2012 v.14 no.5 pp. 528-532
- ISSN:
- 1096-7176
- Subject:
- Thermoanaerobacterium saccharolyticum; ammonium salts; ethanol; ethanol production; fermentation; genes; osmolality; pH; urea; urease
- Abstract:
- ... Genes encoding the enzyme urease were integrated in a Thermoanaerobacterium saccharolyticum ethanologen. The engineered strain hydrolyzed urea, as evidenced by increased cellular growth and elevated final pH in urea minimal medium and urease activity in cell free extracts. Interestingly, replacement of ammonium salts with urea resulted in production of 54g/L ethanol, one of the highest titers repo ...
- DOI:
- 10.1016/j.ymben.2012.06.004
-
http://dx.doi.org/10.1016/j.ymben.2012.06.004
- Author:
- Reyes, Luis H.; Almario, Maria P.; Winkler, James; Orozco, Margarita M.; Kao, Katy C.
- Source:
- Metabolic engineering 2012 v.14 no.5 pp. 579-590
- ISSN:
- 1096-7176
- Subject:
- DNA shuffling; Escherichia coli; biocatalysts; biofuels; butanol; feedstocks; gene expression regulation; gene overexpression; mutants; phenotype; population growth; population structure; regulon; sequence analysis; toxicity; transcriptome; transcriptomics
- Abstract:
- ... Toxicity of products or feedstock components poses a challenge in the biocatalyst-based production of fuels and chemicals. The genetic determinants that are involved in increased resistance to an inhibitor form the adaptive landscape for the phenotype; so in order to engineer more robust biocatalysts, a better understanding of the adaptive landscape is required. Here, we used an adaptive laborator ...
- DOI:
- 10.1016/j.ymben.2012.05.002
-
http://dx.doi.org/10.1016/j.ymben.2012.05.002
- Author:
- Fan, Ziyan; Keum, Young Soo; Li, Qing X.; Shelver, Weilin L.; Guo, Liang-Hong
- Source:
- Journal of environmental monitoring 2012 v.14 no.5 pp. 1345
- ISSN:
- 1464-0333
- Subject:
- DNA; antibodies; antigens; benzopyrene; cross reaction; detection limit; equipment performance; estradiol; ethers; fluorescent dyes; fluorescent labeling; glass; immunoassays; microarray technology; pollutants; proteins; river water; screening; water pollution
- Abstract:
- ... Indirect competitive immunoassays were developed on protein microarrays for the sensitive and simultaneous detection of multiple environmental chemicals in one sample. In this assay, a DNA/SYTOX Orange conjugate was employed as an antibody label to increase the fluorescence signal and sensitivity of the immunoassays. Epoxy-modified glass slides were selected as the substrate for the production of ...
- Handle:
- 10113/54134
- DOI:
- 10.1039/c2em10956e
- PubMed:
- 22437995
-
https://dx.doi.org/10.1039/c2em10956e
- Author:
- Pang, Min; Liu, Chunyan; Xia, Wei; Muhler, Martin; Liang, Changhai
- Source:
- Green chemistry 2012 v.14 no.5 pp. 1272-1276
- ISSN:
- 1463-9270
- Subject:
- activated carbon; carbides; catalysts; green chemistry; hydrogenation; microwave radiation; molybdenum; naphthalene
- Abstract:
- ... The selective hydrogenation of naphthalene to tetralin has been conducted on Mo₂C/AC prepared by microwave irradiation, and achieved a lasting high conversion with 100% selectivity up to 60 hours. The choice of activated carbon as a support is critical in gaining an ideal balance between high activity and good stability of the catalyst. ...
- DOI:
- 10.1039/c2gc35177c
-
http://dx.doi.org/10.1039/c2gc35177c
- Author:
- Wang, Deping; Zhang, Fuxing; Kuang, Daizhi; Yu, Jiangxi; Li, Junhua
- Source:
- Green chemistry 2012 v.14 no.5 pp. 1268-1271
- ISSN:
- 1463-9270
- Subject:
- arylation; bromides; catalysts; catalytic activity; chlorides; green chemistry; imidazoles; ligands; organoiodine compounds
- Abstract:
- ... 6,7-Dihydroquinolin-8(5H)-one oxime (L3) was found to serve as a superior ligand for the CuI-catalyzed N-arylation of imidazoles with aryl iodides, bromides, and electron-deficient chlorides in water. Moreover, the CuI/L3 catalyst system enabled the coupling reactions to take place smoothly with high yields under a low catalyst loading (0.1–1 mol% CuI and 0.2–2 mol% L3). ...
- DOI:
- 10.1039/c2gc35077g
-
http://dx.doi.org/10.1039/c2gc35077g
- Author:
- Jiang, Chang; Liu, Zhi-Hua; Li, Li; Lin, Bin-Bin; Yang, Fan; Qin, Min-Jian
- Source:
- Journal of Asian natural products research 2012 v.14 no.5 pp. 491-495
- ISSN:
- 1477-2213
- Subject:
- Liliaceae; Liriope muscari; chemical structure; glycogen; glycosides; nuclear magnetic resonance spectroscopy; palmitic acid; phosphorylase; roots; sesquiterpenoids
- Abstract:
- ... A new eudesmane sesquiterpene glycoside, ophiopogonoside B (1), along with five known compounds, ophiopogonoside A (2), ruscogenin-1-O-[β-d-glucopyranosyl (1 → 2)]-[β-d-xylopyranosyl (1 → 3)]-β-d-fucopyranoside (3), palmitic acid (4), palmitic acid glyceride (5), and β-sitosterol-d-glucopyranoside (6),was isolated from the tuberous roots of Liriope muscari (Decn.) Bailey (Liliaceae). Their structu ...
- DOI:
- 10.1080/10286020.2012.668533
-
http://dx.doi.org/10.1080/10286020.2012.668533
- Author:
- Suthiwong, Jittra; Poopasit, Kitisak; Yenjai, Chavi
- Source:
- Journal of Asian natural products research 2012 v.14 no.5 pp. 482-485
- ISSN:
- 1477-2213
- Subject:
- benzaldehyde; coumarin; monoacylglycerols; nuclear magnetic resonance spectroscopy; squalene; stigmasterol; triterpenoids
- Abstract:
- ... Thirteen compounds were isolated from the stem of Hymenocardia wallichii Tul. A new phenolic compound, wallinol (1), was found in this plant. The other chemical components were squalene (2), stigmasterol (4), homopterocarpin (5), two triterpenes (3 and 13), two benzaldehyde derivatives (6 and 9), three cinnamyl derivatives (7, 11, and 12), a coumarin (8), and a monoglyceride (10). Their structures ...
- DOI:
- 10.1080/10286020.2012.669377
-
http://dx.doi.org/10.1080/10286020.2012.669377
- Author:
- Dohi, Toshifumi; Fukushima, Kei-ichiro; Kamitanaka, Tohru; Morimoto, Koji; Takenaga, Naoko; Kita, Yasuyuki
- Source:
- Green chemistry 2012 v.14 no.5 pp. 1493-1501
- ISSN:
- 1463-9270
- Subject:
- aldehydes; catalysts; filtration; green chemistry; iodine; iodobenzenes; ketones; methanol; oxidation; recycling; solvents
- Abstract:
- ... Using a recyclable hypervalent iodine reagent 1, the authors have constructed versatile and green methods for the hypervalent iodine and nitroxyl radical-mediated selective oxidation of alcohols to aldehydes and ketones. The recyclable reagent 1 having a unique tetraphenyladamantane structure exhibited almost the same reactivity as the ordinary reagent, phenyliodine diacetate (PIDA), in the hyperv ...
- DOI:
- 10.1039/c2gc16632a
-
http://dx.doi.org/10.1039/c2gc16632a
- Author:
- Wohlgemuth, Stephanie-Angelika; White, Robin Jeremy; Willinger, Marc-Georg; Titirici, Maria-Magdalena; Antonietti, Markus
- Source:
- Green chemistry 2012 v.14 no.5 pp. 1515-1523
- ISSN:
- 1463-9270
- Subject:
- aerogels; carbon; catalysts; catalytic activity; electrochemistry; green chemistry; hydrothermal carbonization; nitrogen; pyrolysis; sulfur; synergism
- Abstract:
- ... A one-pot, hydrothermal synthesis of nitrogen and sulfur dual doped carbon aerogels is presented, derived from our previously published hydrothermal carbonization approach. Two co-monomers, S-(2-thienyl)-l-cysteine (TC) and 2-thienyl carboxaldehyde (TCA), were used for sulfur incorporation, giving rise to distinct morphologies and varying doping levels of sulfur. Nitrogen-doping levels of 5 wt% an ...
- DOI:
- 10.1039/c2gc35309a
-
http://dx.doi.org/10.1039/c2gc35309a
- Author:
- Chawla, Ruchi; Kapoor, Ritu; Singh, Atul K.; Yadav, Lal Dhar S.
- Source:
- Green chemistry 2012 v.14 no.5 pp. 1308-1313
- ISSN:
- 1463-9270
- Subject:
- catalysts; catalytic activity; epoxides; green chemistry; regioselectivity; sodium
- Abstract:
- ... A highly efficient LiBr catalysed regioselective synthesis of vinyl sulfones from readily available terminal epoxides and sodium sulfinates in a one-pot procedure using water as a reaction medium is reported. The protocol is adorned with several attributes of green chemistry like recycling of the catalyst, atom-economy and an aqueous medium. ...
- DOI:
- 10.1039/c2gc16664j
-
http://dx.doi.org/10.1039/c2gc16664j
- Author:
- Fu, Jian-Jun; Wang, Li-Yan; Li, Hong-Lin; Qin, Jiang-Jiang; Shen, Yun-Heng; Cheng, Jia-Gao; Jin, Hui-Zi; Zhang, Wei-Dong
- Source:
- Journal of Asian natural products research 2012 v.14 no.5 pp. 496-502
- ISSN:
- 1477-2213
- Subject:
- Incarvillea; chemical structure; circular dichroism spectroscopy; roots; sesquiterpenoid lactones; spectral analysis
- Abstract:
- ... Argutalactone (1), a novel sesquiterpenoid lactone featuring an unprecedented 6/5/7 rigid skeleton, was isolated from the roots of Incarvillea arguta. The structure and relative configuration of 1 were established by extensive analysis of spectroscopic data. The absolute configuration of 1 was determined as 2R,5S,10R,12S based on the analysis of biogenetical transformation, comparison of the optic ...
- DOI:
- 10.1080/10286020.2012.668535
-
http://dx.doi.org/10.1080/10286020.2012.668535
- Author:
- Do, Phuong T. M.; Foster, Andrew J.; Chen, Jingguang; Lobo, Raul F.
- Source:
- Green chemistry 2012 v.14 no.5 pp. 1388-1397
- ISSN:
- 1463-9270
- Subject:
- alcohols; aluminum oxide; biofuels; catalysts; cobalt; green chemistry; hydrogen; hydrogenation; nickel; platinum; toluene
- Abstract:
- ... The hydrodeoxygenation (HDO) of meta-cresol, a typical phenolic compound in bio-oils, is investigated in the vapor-phase on γ-Al₂O₃-supported Pt catalysts at near atmospheric hydrogen pressure. The HDO reaction yields two major hydrocarbons: toluene and methylcyclohexane. The deoxygenation of meta-cresol proceeds through two consecutive steps: hydrogenation of the aromatic ring on the Pt metal fol ...
- DOI:
- 10.1039/c2gc16544a
-
http://dx.doi.org/10.1039/c2gc16544a
- Author:
- Zhu, Meng; Liu, Xiao-Yu; Chen, Qiao-Hong; Wang, Feng-Peng
- Source:
- Journal of Asian natural products research 2012 v.14 no.5 pp. 441-449
- ISSN:
- 1477-2213
- Subject:
- alkaloids; biomimetics; oxidation
- Abstract:
- ... The first biomimetic conversion from the aconitine-type C₁₉-diterpenoid alkaloids to the corresponding alkaloids of lactone-type C₁₉-diterpenoid alkaloid has been achieved. Chasmanine was used as starting material with Baeyer–Villiger oxidation as a key reaction. It was also observed that the oxygenated group at C-16 did not change the relative migration tendencies of C-13 and C-9 during the oxida ...
- DOI:
- 10.1080/10286020.2012.669378
-
http://dx.doi.org/10.1080/10286020.2012.669378
- Author:
- Zhang, Zhan-Hui; Zhang, Xiao-Nan; Mo, Li-Ping; Li, Yong-Xiao; Ma, Fei-Ping
- Source:
- Green chemistry 2012 v.14 no.5 pp. 1502-1506
- ISSN:
- 1463-9270
- Subject:
- aldehydes; ammonium acetate; biodegradability; green chemistry; ketones; melting; oxidation; solvents
- Abstract:
- ... Low melting mixture of maltose–dimethylurea (DMU)–NH₄Cl was found to be an inexpensive, non-toxic, easily biodegradable and effective reaction medium in the catalyst-free synthesis of quinazoline derivatives. This simple and efficient method furnished the corresponding quinazolines in high yields via one-pot three-component reaction of 2-aminoaryl ketones, aldehyde, and ammonium acetate under aero ...
- DOI:
- 10.1039/c2gc35258c
-
http://dx.doi.org/10.1039/c2gc35258c
- Author:
- Kumar, Ajeet; Aerry, Swati; Saxena, Amit; de, Arnab; Mozumdar, Subho
- Source:
- Green chemistry 2012 v.14 no.5 pp. 1298-1301
- ISSN:
- 1463-9270
- Subject:
- additives; alkynes; ambient temperature; azides; catalysts; catalytic activity; copper nanoparticles; green chemistry; guar gum
- Abstract:
- ... Cu-nanoparticulates in Guar-gum at room temperature were investigated for the first time as a recyclable catalytic system in organic synthesis. The catalytic potential of these materials were evaluated in the Huisgen [3 + 2]-cycloaddition of azides and alkynes without additives under ambient conditions which offers several advantages, viz. high yields, clean reactions, short reaction times, recycl ...
- DOI:
- 10.1039/c2gc35070j
-
http://dx.doi.org/10.1039/c2gc35070j
- Author:
- Bähr, Moritz; Bitto, Alexandro; Mülhaupt, Rolf
- Source:
- Green chemistry 2012 v.14 no.5 pp. 1447-1454
- ISSN:
- 1463-9270
- Subject:
- carbon dioxide; carbon dioxide fixation; carbonates; carbonation; catalysts; catalytic activity; citric acid; crosslinking; diamines; glass transition temperature; green chemistry; limonene; modulus of elasticity; molecular weight; polyethyleneimine; polyols; polyurethanes; resins; silica; tetrabutylammonium compounds
- Abstract:
- ... Herein we report a very versatile new route to linear as well as cross-linked terpene-based non-isocyanate poly(hydroxyurethanes) (NIPUs) and prepolymers derived from the novel cyclic limonene dicarbonate (CL). The catalytic carbonation of epoxidized limonene with CO₂ was monitored in the presence of both homogeneous tetrabutylammonium bromide (TBAB) and heterogeneous silica supported 4-pyrrolidin ...
- DOI:
- 10.1039/c2gc35099h
-
http://dx.doi.org/10.1039/c2gc35099h
- Author:
- Metin, Önder; Alp, Nurdan Alcan; Akbayrak, Serdar; Biçer, Abdullah; Gültekin, Mehmet Serdar; Özkar, Saim; Bozkaya, Uğur
- Source:
- Green chemistry 2012 v.14 no.5 pp. 1488-1492
- ISSN:
- 1463-9270
- Subject:
- acetone; alkenes; ambient temperature; catalysts; catalytic activity; dihydroxylation; green chemistry; hydrogen peroxide; nanoparticles; osmium
- Abstract:
- ... Addressed herein is a novel, eco-friendly, recoverable, reusable and bottleable catalytic system developed for the dihydroxylation of various olefins yielding 1,2-cis-diols. In our protocol, zeolite-confined osmium(0) nanoclusters (zeolite-Os⁰) are used as reusable catalyst and H₂O₂ served as a co-oxidant. Zeolite-Os⁰ are found to be highly efficient and selective catalysts for the dihydroxylation ...
- DOI:
- 10.1039/c2gc16616j
-
http://dx.doi.org/10.1039/c2gc16616j
- Author:
- Liu, Xiaoying; Jensen, Klavs F.
- Source:
- Green chemistry 2012 v.14 no.5 pp. 1471-1474
- ISSN:
- 1463-9270
- Subject:
- aldehydes; amides; catalysts; green chemistry; hydrogen peroxide; secondary amines
- Abstract:
- ... A practical and economical protocol has been developed for the direct oxidative amidation of aromatic aldehydes with secondary amines to synthesize amides in a single operation under mild conditions within 15–40 min. The utilization of aqueous hydrogen peroxide affords a clean synthetic route. No catalysts or promoting reagents are required. ...
- DOI:
- 10.1039/c2gc35078e
-
http://dx.doi.org/10.1039/c2gc35078e