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1.
Molecules ; 25(11)2020 May 28.
Article in English | MEDLINE | ID: mdl-32481583

ABSTRACT

Crude glycerol (C3H8O3) is a major by-product of biodiesel production from vegetable oils and animal fats. The increased biodiesel production in the last two decades has forced glycerol production up and prices down. However, crude glycerol from biodiesel production is not of adequate purity for industrial uses, including food, cosmetics and pharmaceuticals. The purification process of crude glycerol to reach the quality standards required by industry is expensive and dificult. Novel uses for crude glycerol can reduce the price of biodiesel and make it an economical alternative to diesel. Moreover, novel uses may improve environmental impact, since crude glycerol disposal is expensive and dificult. Glycerol is a versatile molecule with many potential applications in fermentation processes and synthetic chemistry. It serves as a glucose substitute in microbial growth media and as a precursor in the synthesis of a number of commercial intermediates or fine chemicals. Chlorinated derivatives of glycerol are an important class of such chemicals. The main focus of this review is the conversion of glycerol to chlorinated derivatives, such as epichlorohydrin and chlorohydrins, and their further use in the synthesis of additional downstream products. Downstream products include non-cyclic compounds with allyl, nitrile, azide and other functional groups, as well as oxazolidinones and triazoles, which are cyclic compounds derived from ephichlorohydrin and chlorohydrins. The polymers and ionic liquids, which use glycerol as an initial building block, are highlighted, as well.


Subject(s)
Chlorohydrins/chemistry , Epichlorohydrin/chemistry , Glycerol/chemistry
2.
Molecules ; 24(20)2019 Oct 21.
Article in English | MEDLINE | ID: mdl-31640139

ABSTRACT

Nine monoamides were synthesized from carboxylic acids (C8-C18) and crude glycerol. The final monoamides were the result of a rearrangement of the acyl chain during the final hydrogenation process. The purity of the final compounds was determined by spectroscopic and mass spectrometry (MS) techniques. The thermophysical properties of solid monoamides were investigated to determine their capability to act as phase change materials (PCM) in thermal energy storage. Thermophysical properties were determined with a differential scanning calorimeter (DSC). The melting temperatures of the analyzed material ranged from 62.2 °C to 116.4 °C. The analyzed enthalpy of these monoamides ranged from 25.8 kJ/kg to 149.7 kJ/kg. Enthalpy values are analyzed considering the carbon chain and the formation of hydrogen bonds.


Subject(s)
Amides/chemical synthesis , Carboxylic Acids/chemistry , Glycerol/chemistry , Amides/chemistry , Calorimetry, Differential Scanning , Hot Temperature , Hydrogen Bonding , Mass Spectrometry , Molecular Structure , Thermodynamics
3.
Proc Natl Acad Sci U S A ; 115(33): E7854-E7862, 2018 08 14.
Article in English | MEDLINE | ID: mdl-30061386

ABSTRACT

The transmission of HIV can be prevented by the application of neutralizing monoclonal antibodies and lectins. Traditional recombinant protein manufacturing platforms lack sufficient capacity and are too expensive for developing countries, which suffer the greatest disease burden. Plants offer an inexpensive and scalable alternative manufacturing platform that can produce multiple components in a single plant, which is important because multiple components are required to avoid the rapid emergence of HIV-1 strains resistant to single microbicides. Furthermore, crude extracts can be used directly for prophylaxis to avoid the massive costs of downstream processing and purification. We investigated whether rice could simultaneously produce three functional HIV-neutralizing proteins (the monoclonal antibody 2G12, and the lectins griffithsin and cyanovirin-N). Preliminary in vitro tests showed that the cocktail of three proteins bound to gp120 and achieved HIV-1 neutralization. Remarkably, when we mixed the components with crude extracts of wild-type rice endosperm, we observed enhanced binding to gp120 in vitro and synergistic neutralization when all three components were present. Extracts of transgenic plants expressing all three proteins also showed enhanced in vitro binding to gp120 and synergistic HIV-1 neutralization. Fractionation of the rice extracts suggested that the enhanced gp120 binding was dependent on rice proteins, primarily the globulin fraction. Therefore, the production of HIV-1 microbicides in rice may not only reduce costs compared to traditional platforms but may also provide functional benefits in terms of microbicidal potency.


Subject(s)
Anti-HIV Agents , Antibodies, Monoclonal , Endosperm , HIV Antibodies , HIV Envelope Protein gp120/antagonists & inhibitors , HIV-1/chemistry , Oryza , Plants, Genetically Modified , Anti-HIV Agents/chemistry , Anti-HIV Agents/metabolism , Antibodies, Monoclonal/biosynthesis , Antibodies, Monoclonal/chemistry , Antibodies, Monoclonal/genetics , Endosperm/chemistry , Endosperm/genetics , Endosperm/metabolism , HIV Antibodies/biosynthesis , HIV Antibodies/chemistry , HIV Antibodies/genetics , HIV Envelope Protein gp120/chemistry , HIV Envelope Protein gp120/genetics , HIV Envelope Protein gp120/metabolism , Oryza/chemistry , Oryza/genetics , Oryza/metabolism , Plants, Genetically Modified/chemistry , Plants, Genetically Modified/genetics , Plants, Genetically Modified/metabolism
4.
Anal Bioanal Chem ; 386(2): 306-12, 2006 Sep.
Article in English | MEDLINE | ID: mdl-16868725

ABSTRACT

A specific, sensitive, precise, and accurate method for the determination of abscisic acid (ABA) in grapevine leaf tissues is described. The method employs high-performance liquid chromatography and electrospray ionization-mass spectrometry (LC-ESI-MS) in selected ion monitoring mode (SIM) to analyze ABA using a stable isotope-labeled ABA as an internal standard. Absolute recoveries ranged from 72% to 79% using methanol/water pH 5.5 (50:50 v/v) as an extraction solvent. The best efficiency was obtained when the chromatographic separation was carried out by using a porous graphitic carbon (PGC) column. The statistical evaluation of the method was satisfactory in the work range. A relative standard deviation (RDS) of < 5.5% and < 6.0% was obtained for intra-batch and inter-batch comparisons, respectively. As for accuracy, the relative error (%Er) was between -2.7 and 4.3%, and the relative recovery ranged from 95% to 107%.


Subject(s)
Abscisic Acid/analysis , Chromatography, Liquid/methods , Isotopes/chemistry , Plant Leaves/chemistry , Spectrometry, Mass, Electrospray Ionization/methods , Vitis/chemistry , Hydrogen-Ion Concentration , Indicator Dilution Techniques , Methanol/chemistry , Reproducibility of Results , Sensitivity and Specificity , Solvents/chemistry , Water/chemistry
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