Small Molecular Organic Compounds Research Articles

The effect of non-Saccharomyces yeasts on biogenic amines in Sauvignon Blanc wine and Gewürztraminer wine

Biogenic amine (BA) is a class of nitrogen-containing small molecular organic compounds with biological activity. Excessive BAs in wine affect flavor and quality of wine and are hazardous to human health. However, little attention has been paid to the effect of non-Saccharomyces yeasts and Saccharomyces cerevisiae mixed fermentation on BAs in white wine. The effect of mixed fermentation on BAs and amino acids in wine was investigated using two white grapes of Sauvignon Blanc and Gewürztraminer. Higher levels of total amino acids and BAs in Gewürztraminer wine compared to Sauvignon Blanc wine may be due to different grape varieties. Mixed fermentation did not influence BA profiles in Sauvignon Blanc wine, while it increased total BAs content. VL3 (VL) fermented wine has 33.7% less BAs content than EC1118 (EC) single-strain fermented wine. Similar phenomenon was found in Gewürztraminer wine produced by different fermentation combinations except that cadaverine was only detected in wine produced by Hanseniaspora uvarum participated in mixed fermentations. Principal coordinate analysis (PCoA) and permutational multivariate analysis of variance (PERMANOVA) revealed that the effects on BAs were related to grape varieties and yeast species in white wine. Ethanolamine, tryptamine, isoamylamine and histamine content in wine were related to grape varieties. Collectively, mixed fermentation increased BAs content in Sauvignon Blanc and Gewürztraminer wine. The content of BAs in wine fermented by VL single-strain fermentation was lower than that fermented by EC single-strain fermentation, which is more suitable for the winemaking of white wine.

Potential hazards of typical small molecular organic matters in shale gas wastewater for wheat irrigation: 2-butoxyethanol and dimethylbenzylamine

2-butoxyethanol (BE) and dimethylbenzylamine (DMBA) are small molecular organic compounds commonly found in shale gas wastewater (SGW) and environmental samples, yet their environmental risks in exposure and irrigation reuse have not been thoroughly studied. From the perspectives of physicochemical properties and toxicity, seven groups of irrigation treatment were designed for wheat irrigation according to the concentration gradient. Overall, wheat growth was normal, but higher DMBA concentrations resulted in more severe growth inhibition. The absorption of BE by various tissues of wheat was positively correlated with its concentration, while the absorption of DMBA by wheat stems showed the same trend. Interestingly, there was no significant difference in the absorption of DMBA by wheat grains in different groups. The detection results of nutritional and heavy metal elements in wheat tissues showed that the presence of organic compounds changed the relative sensitivity of wheat leaves and grains to some elements (such as Mg, Mn, Mo, etc.) enrichment. The Cd and Pb contents of wheat grains in all groups complied with national safety standards, but the As or Cr concentration in wheat grains treated with BE or DMBA exceeded the limits in some cases. Transcriptome sequencing, GO annotation, and KEGG enrichment analysis revealed similar gene functions and metabolic pathways enriched by BE and DMBA. The safe and sustainable agricultural reuse of SGW still has great potential as a promising water resources management strategy.

Clindamycin removal from aqueous solution by non-thermal air plasma treatment: performance, degradation pathway and ensuing antimicrobial activity.

The present study set out to investigate clindamycin (CLN) removal from aqueous solution using non-thermal plasma (NTP) under atmospheric air conditions and to address the effects of some variables including pH, initial concentration of CLN, and working voltage on CLN degradation. The result showed that the NTP system exhibited excellent degradation rate and mineralization efficiency on CLN in 15 min under neutral conditions, which exceeded 90 and 45%, respectively, demonstrating its conversion to other organic by-products. Furthermore, CLN degradation was largely dependent upon the initial pH of solution, applied voltage, and reaction time. Specifically, under acidic conditions (pH = 3), working voltage of 24 kV and after 15 min of reaction, almost 100% of CLN was degraded. NTP-initiated CLN degradation products through LC-MS/MS analysis, determined within 10 min of reaction, inferred that the complex structure of CLN has undergone deterioration by active radical species which subsequently generated small molecular organic compounds. Chemical processes involved in CLN degradation were found to be demethylation, desulfonylation, dechlorination, hydroxylation and deamination. Lastly, antimicrobial susceptibility tests revealed that the activity of CLN was reduced following NTP treatment, which is also in good agreement with the minimum inhibitory concentration (MIC) values obtained from microdilution analyses.

Liquid Organic Fertilizer Amendment Alters Rhizosphere Microbial Community Structure and Co-occurrence Patterns and Improves Sunflower Yield Under Salinity-Alkalinity Stress.

Response of rhizosphere microbial community structure and co-occurrence patterns to liquid organic fertilizer in sunflower cropland was investigated. Moderate and severe saline-alkaline soils were treated with liquid organic fertilizer containing mainly small molecular organic compounds (450g L-1) at a rate of 4500 L ha-1year-1 over 2years. Compared with the untreated soils, organic fertilizer treatment increased soil nutrient concentrations by 13.8-137.1% while reducing soil pH and salinity by 5.6% and 54.7%, respectively. Organic fertilizer treatment also improved sunflower yield, plant number, and plant height by 28.6-67.3%. Following organic fertilizer treatment, fungal α-diversity was increased, and the effects of salinity-alkalinity stress on rhizosphere microbial communities were alleviated. The relative abundances of some halotolerant microbes and phytopathogenic fungi were reduced in organic fertilizer-treated soils, in contrast to increases in the relative abundances of plant growth-promoting microbes and organic matter decomposers, such as Nocardioides, Rhizophagus, and Stachybotrys. Network analysis revealed that severe salinity-alkalinity stress stimulated cooperation among bacteria, while organic fertilizer treatment tended to stimulate the ecosystem functions of fungi with higher proportions of fungi-bacteria and fungi-fungi links. More keystone taxa (e.g., Amycolatopsis, Variovorax, and Gemmatimonas) were positively correlated with soil nutrient concentrations and crop yield-related traits in organic fertilizer-treated soils. Overall, liquid organic fertilizer amendment could attenuate the adverse effects of salinity-alkalinity stress on sunflower yield by improving soil quality and optimizing rhizosphere microbial community structure and co-occurrence patterns.

Effect of superfine pulverization of powdered activated carbon on adsorption of carbamazepine in natural source waters

The purpose of this study is to investigate adsorptive removal of carbamazepine from natural source waters by superfine pulverized powdered activated carbon. Superfine pulverization is becoming an increasingly attractive approach to decrease the diffusion path of a target adsorbate molecule and improve the overall the kinetics of activated carbon adsorption. Here we report the impact of pulverization on powdered activated carbon characteristics, and carbamazepine adsorption behavior in distilled and deionized water and natural organic matter solutions. The superfine pulverization decreased the particle size of activated carbon by 50 folds and the specific surface area by 24%. In addition, the micropore volume of the activated carbon decreased from 0.23 cm3/g to 0.14 cm3/g, while mesopore and macropore volumes increased from 0.15 cm3/g and 0.11 cm3/g to 0.18 cm3/g and 0.48 cm3/g, respectively. In terms of surface chemistry, the oxygen and iron contents of the activated carbon increased notably after pulverization. Despite the decrease in surface area and increase in surface polarity, the pulverization improved the adsorption kinetics especially for short contact times i.e., < 6-h. In general, the dissolved organic carbon concentration negatively influenced the kinetic advantage of superfine pulverized activated carbon. Isotherm results indicated that the parent adsorbent has a higher adsorption capacity than superfine activated carbon in distilled and deionized water and in natural waters. This was attributed to the losses in specific surface area and favorable sorption sites inside micropores. Our literature analysis indicated that unlike the small molecular weight hydrophilic organic compounds, the pseudo-equilibrium adsorption capacity could be increased or at least not deteriorated for hydrophobic molecules (Kow > 3). Therefore, superfine pulverization of PAC can serve as a promising approach to remove micropollutants from natural source waters with a kinetic advantage.

Effects of organic fertilizers via quick artificial decomposition on crop growth

Applying organic matters into the soil would help to improve soil quality and sustain crop production. In addition, the small molecular organic matters could be active in influencing soil nutrient cycling and crop development. Thus, this study has firstly induced a new technology of quick artificial decomposition to produce fertilizers containing small molecular organic compounds from crop residues and other biological wastes. The fertilizers were produced via the quick artificial decomposition from biological wastes. The small organic species in the fertilizers were identified by the LC–MS. Field experiments of kiwifruit were conducted to test the effects of fertilizers. In total, 341 species of small organic matters have been determined in the produced fertilizers. The results showed that the organic fertilizers could significantly increase the yields of kiwifruit by 15.2% in contrast with mineral fertilizer treatments. Whereas, the organic fertilizers could enhance the contents of nutritive components in kiwifruits. These results proved that the organic fertilizers containing more small organic matter could be more efficient in promoting crop production.

Effect of high pressure processing on migration characteristics of polypropylene used in food contact materials

ABSTRACT The migration of small molecular mass organic compounds from polypropylene (PP) copolymer films into food simulants during and after high pressure processing (HPP) was studied. An overlapping temperature profile was developed to isolate the pressure effect of HPP (700 MPa, 71°C, 5 min) from equivalent thermal processing (TP) at atmospheric pressure (0.1 MPa). Chloroform, toluene, methyl salicylate, and phenylcyclohexane were chosen as surrogate compounds, and were spiked into test polymer films at concentrations of 762–1152 mg kg–1 by a solvent soaking technique. Migration (w/w) of surrogate compounds from loaded PP films into Miglyol 812 (a medium-chain triglyceride mixture) and 10% ethanol was quantified by headspace GC/MS during HPP and TP, and subsequent storage at 25°C for up to 10 days. HPP significantly delayed migration of the surrogates from PP into both food simulants relative to TP. The average migrations into Miglyol after TP and HPP were 92.2–109% and 16–60.6%, respectively. Diffusion coefficients estimated by migration modelling showed a reduction of more than two orders of magnitude for all surrogate compounds under high pressure at 700 MPa ( = 8.0) relative to equivalent TP at 0.1 MPa ( = 13.1). The relative Tg increase of PP copolymer under compression at 700 MPa was estimated as Tg+94°C. For 10% ethanol, average migrations after TP and HPP were 9.3–50.9% and 8.6–22.8%, respectively. During extended storage, migration into both simulants from HPP-treated samples was initially slower than that from untreated or TP-treated films. However, after 8–24 hours of storage, the differences in percent migration of selected surrogates were not significant (p > .05) among the treated PP films. Therefore, the physical changes of PP films that occur during HPP appear to be reversible with a return to their original dimensions and diffusion properties after decompression.

Electrochemical/Peroxymonosulfate/NrGO-MnFe2O4 for Advanced Treatment of Landfill Leachate Nanofiltration Concentrate

A simple one-pot method was used to successfully embed manganese ferrite (MnFe2O4) nanoparticles on the nitrogen-doped reduced graphene oxide matrix (NrGO), which was used to activate peroxymonosulfate to treat the landfill leachate nanofiltration concentration (LLNC) with electrochemical enhancement. NrGO-MnFe2O4 and rGO-MnFe2O4 were characterized by various means. This indicates that nitrogen-doped could induce more graphene oxide (GO) spall and reduction to produce more active centers, and was favorable for uniformly loading MnFe2O4 particles. The comparison between electrochemical/peroxymonosulfate/NrGO-MnFe2O4 (EC/PMS/NrGO-MnFe2O4) system and different catalytic systems shows that electrochemical reaction, NrGO and MnFe2O4 can produce synergies, and the chemical oxygen demand (COD) removal rate of LLNC can reach 72.89% under the optimal conditions. The three-dimensional (3D-EEM) fluorescence spectrum shows that the system has a strong treatment effect on the macromolecules with intense fluorescence emission in LLNC, such as humic acid, and degrades into substances with weak or no fluorescence characteristics. Gas chromatography-mass spectrometry (GC-MS) indicates that the complex structure of refractory organic compounds can be simplified, while the simple small molecular organic compounds can be directly mineralized. The mechanism of catalytic degradation of the system was preliminarily discussed by the free radical quenching experiment. Therefore, the EC/PMS/NrGO-MnFe2O4 system has significant application potential in the treatment of refractory wastewater.

Water Purification Effect and Saline-alkali Tolerance Improvement Mechanism of Suaeda salsa in the Estuary Area

The pollution load of nitrogen and phosphorus in pollutants entering the sea is high, which seriously affects the water quality of coastal water. It is necessary to strengthen land-sea coordination. However, affected by the seawater encroachment, the salt and alkali content of the water in the estuary area is high and the variation range is large, which leads to difficulty in plant growth. The ability of plants to remove nitrogen and phosphorus is reduced. How to improve the survival ability of plants is an urgent problem to be solved. In this study, the addition of appropriate concentrations of Ca2+ and K+ can improve the salinity tolerance of plants and reduce the risk of eutrophication. The results showed that under the condition of pH 8 and salinity 20‰, the removal efficiency of total nitrogen and total phosphorus was the highest in the hydroponic experiment with exogenous Ca2+ and K+ concentrations of 8mmol·L-1 and 10mmol·L-1 respectively, which were 1.53-1.87 times those in the control group. At this time, the growth rate of Suaeda salsa was the best, and the maximum relative growth rates (RGR) were 2.4 times and 2.0 times that of the control group, respectively. The remission effect of Ca2+ was greater than that of K+ at the same concentration. The mechanism by which exogenous Ca2+ and K+improve the salt-alkali tolerance ability of Suaeda salsa was mainly manifested as improving osmotic regulation ability. In the aspect of inorganic osmotic regulation, exogenous ions improved the water-holding capacity of the plant, among which the correlation coefficients of inorganic ion content and water content in leaves and roots were all above 0.966. In terms of organic osmotic regulation, exogenous Ca2+ and K+ all promoted the accumulation of small molecular organic compounds such as betaine in Suaeda salsa, and alleviated plasma membrane peroxidation in leaves. Among them, the largest reductions of malondialdehyde content in leaves were 72.9% and 61.7%, respectively. Therefore, exogenous Ca2+ and K+can enhance the osmotic adjustment ability and promote the growth of Suaeda salsa, thereby improving the removal rate of nitrogen and phosphorus. The results provide a theoretical basis for improving the water purification effect and reducing eutrophication risk in coastal waters.

Degradation of liquid phase N,N-dimethylformamide by dielectric barrier discharge plasma: Mechanism and degradation pathways

The degradation of liquid phase N,N-dimethylformamide (DMF) using the dielectric barrier discharge (DBD) plasma was studied in the present study. The results showed that 1000 mg L−1 DMF could be degraded by DBD plasma under different input power, treatment time and initial pH values of aqueous solution. After 40 min with DBD plasma discharge, 52.2% degradation efficiency was achieved at DMF concentration of 1000 mg L−1 with an input power of 16.19 W under initial pH of 11.14 in aqueous solution, and the energy efficiency of the system was 13.2 mg kJ−1. The removal efficiency decreased with the presence of radical scavenger, manifesting that •OH plays a critical role in the degradation process. The value of TOC in DMF aqueous solution decreased from 790 mg L−1 to 507 mg L−1 in 40 min, which indicated that DBD plasma has the ability to mineralize a portion of DMF in liquid directly. Additionally, the analysis of FTIR, HPLC and the small molecular organic compounds before and after the DBD plasma degradation indicated that the intermediates of DMF in degradation process were N-methylformamide, methanol, formaldehyde and formic acid, which were finally mineralized into ammonia nitrogen, CO2 and H2O. Moreover, the possible degradation mechanism and pathways were proposed.

Desitrificación en simulación de agua subterránea usando lignito como fuente de carbono orgánico en fase sólida

To ensure safety standards of drinking water, it is essential to perform NO3 remediation in groundwater. Owing to the lack of organic carbon in groundwater, heterotrophic denitrification is not quite effective in groundwater. Few studies have reported about how Chinese lignite can be used as an organic carbon source for denitrification. In simulated conditions of groundwater, we determined whether the four lignite types (Lignite was obtained from Sanjitun, Lingshi, Wangniutan, and Zhaotong in China.) could be used as a solid-phase organic carbon source for denitrification; the analyses were performed in a test water column. For denitrification, the most effective carbon source was the lignite obtained from Wangniutan. It showed the highest efficacy of 34% in nitrate (NO3) removal for an influent NO3-N concentration of 30 mg• L−1. The effluent NO3-N concentrations below 20 mg L−1 and the water samples showed no acute toxicity when they were subjected to luminescent bacteria test. We performed static carbon release test and infrared spectral analysis on all the four lignite types, and we found that there was a direct relation between NO3 removal and the lignite’s ability for static carbon release. When NO3 concentrations were high and the rate of static carbon release was low, the efficacy of denitrification was greater. This effect was achieved when the molecular structure of lignite contained small molecular organic compounds in free states; these compounds primarily included the following functional groups: alcohols, phenols, and organic acids. These compounds were primarily used by the denitrifying bacteria.

Degradation of high-chemical oxygen demand concentration pesticide wastewater by 3D electrocatalytic oxidation

The treatment of difficult biodegradable industrial wastewater by electrocatalytic oxidation technology has positive significance for the prevention and control of industrial pollution. In this study, particle electrode Ti–Ag/γ-Al2O3 was prepared and used as a catalyst in the 3D electrocatalytic oxidation reaction system for pretreatment of high-chemical oxygen demand (COD) concentration pesticide wastewater. Electrolysis conditions for high-COD concentration pesticide wastewater were discussed and optimized, and single-factor experiment results showed that the maximum COD removal rate was 82.50% with an energy consumption of 10.91 (kW h) kg−1 COD at conductivity of 4000 μS cm−1, current density of 30 mA cm−2, initial pH of 2.0, electrode distance of 3.0 cm, air flow of 3.0 L min−1, and filling proportion of 50.0%. The UV–visible absorption spectrum analysis of pesticide wastewater at different electrolysis times showed that the organic macromolecules containing long-chain, heterocyclic, and other structures were degraded into small molecular organic compounds. After the 3D electrocatalytic oxidation reaction, the BOD5/COD value of pesticide wastewater increased from 0.041 to 0.308, indicating that the biodegradability of the pesticide wastewater was improved significantly.

Hydrophilic Silver Nanoparticles Induce Selective Nanochannels in Thin Film Nanocomposite Polyamide Membranes.

Thin-film nanocomposite (TFN) membranes have been widely studied over the past decade for their desalination applications. For some cases, the incorporation of nonporous hydrophilic nanofillers has been reported to greatly enhance membrane separation performance, yet the underlying mechanism is poorly understood. The current study systematically investigates TFN membranes incorporated with silver nanoparticles (AgNPs). For the first time, we reveal the formation of nanochannels of approximately 2.5 nm in size around the AgNPs, which can be attributed to the hydrolysis of trimesoyl chloride monomers and thus the termination of interfacial polymerization by the water layer around each hydrophilic nanoparticle. These nanochannels nearly tripled the membrane water permeability for the optimal membrane. In addition, this membrane showed increased rejection against NaCl, boron, and a set of small-molecular organic compounds (e.g., propylparaben, norfloxacin, and ofloxacin), thanks to its combined effects of improved size exclusion, enhanced Donnan exclusion, and suppressed hydrophobic interaction. Our work provides fundamental insights into the formation and transport mechanisms involved in solid-filler incorporated TFN membranes. Future studies should take advantage of this spontaneous nanochannel formation in the design of TFN to overcome the classical membrane permeability-selectivity trade-off.

Separation of methyl glycosides and glycerol from aqueous fraction of methyl bio-oils using nanofiltration

The feasibility of separating small molecular organic compounds in the aqueous fraction of methyl bio-oils (AFMBO) using nanofiltration (NF) and reverse osmosis (RO) membranes was studied. Four kinds of commercially available NF and RO membranes were studied preliminarily by using model solutions (aqueous solution of methyl glycosides and glycerol). The membrane module was spiral wound, which is a more suitable format for industrialization than the flat-sheet format for dead-end filtration. The NF400-600 membrane exhibited the best separation performance; the permeate flux was 48.6 L/(m2·h), the methyl glucosides (MEG) rejection ratio was 95.4%, and the transmission of glycerol was 81.0% with an initial concentration of 10 g/L (0.4 MPa, 45 ºC). Compared with the model solution, the NF performance of AFMBO, which included permeate flux, rejection of MEG, transmission of glycerol, and separation of the other components in AFMBO, was investigated. The more complex constituents of AFMBO led to NF400-600 permeability and separating property decline compared with the model solution in the same operating conditions; meanwhile more serious and even irreversible membrane fouling occurred. This research provided a reference for membrane separation industrial feasibility and application of AFMBO.

An integrated permanganate and ozone process for the treatment of textile dyeing wastewater: Efficiency and mechanism

Textile dyeing effluent has been the focus of considerable research because of its adverse effects on aquatic biota. Here, we present the first comprehensive study of a combined permanganate and ozone (KMnO4O3) technique to treat different kinds of textile dyeing wastewater. We investigated the effects of process parameters on TOC and COD removal and the toxicity of the wastewater after KMnO4O3 treatment. The synergistic mechanism involved in the KMnO4O3 process is also discussed. The results indicate that KMnO4O3 treatment is efficient in treating many kinds of textile dyeing wastewater. The TOC, COD, and toxicity were reduced by approximately 70%, 80%, and 34.4–95.5%, respectively, using a KMnO4 dosage of 1.5 mM, an O3 dosage of 10 mg/L, a pH value of 7, and a reaction time of 30 min. Furthermore, biodegradability was increased to 0.33–0.68. The combined use of KMnO4 and O3 provided synergetic and complementary advantages. On the one hand, oxidation of pollutants on suspended solid surfaces and in the aqueous phase was enhanced by the stirring action of O3 molecule bubbles. On the other hand, small molecular organic compounds and fine particles were coagulated by KMnO4 and its intermediate oxidations. X-ray photoelectron spectroscopy results indicate that the valence state of manganese changed after KMnO4O3 treatment, and the manganese intermediate catalysing O3 process contributed to the removal of 20% of COD and 19% of TOC. It was therefore determined that the KMnO4O3 treatment is a promising method for use in the treatment of textile dyeing wastewater.

Folding Kinetics of Single Human Telomeric G-Quadruplex Affected by Cisplatin.

G-Quadruplex DNA structure has been proven to be a binding target for small molecular organic compounds and hence regarded as a promising pharmacological target. Cisplatin is a widely used chemotherapy drug that targets duplex DNA and was recently shown to react also with G-quadruplex, implying that cisplatin actually may also target G-quadruplex. In this work, we employed magnetic tweezers to investigate the influence of cisplatin on the folding kinetics of single human telomeric G-quadruplex. It was revealed that cisplatin and G-quadruplex interact in two different and competitive ways that depend on cisplatin concentration.

Prechlorination of algae-laden water: The effects of transportation time on cell integrity, algal organic matter release, and chlorinated disinfection byproduct formation

The prechlorination-induced algal organic matter (AOM) released from Microcystis aeruginosa (M. aeruginosa) cells has been reported to serve as a source of precursors for chlorinated disinfection byproducts (DBPs). However, previous studies have mainly focused on the precursors either extracted directly from the cell suspension or derived immediately after algal suspension prechlorination. This study aims to investigate the impacts of water transportation time after algal suspension prechlorination on cell integrity, AOM release, and DBP formation during the dissolved phase chlorination. The damage to cell integrity after prechlorination was indicated to depend not only on chlorine dose but also on transportation time. The highest dissolved organic carbon (DOC) and dissolved organic nitrogen (DON) values were observed at 2 mg/L chlorine preoxidation before transportation, but were obtained at 0.4 mg/L chlorine after 480-min simulated transportation. The variation of DON with transportation time was indicated to be mainly influenced by the small molecular weight nitrogenous organic compounds, such as amino acids. Additionally, formation of the corresponding chlorinated carbonaceous disinfection byproducts (C-DBPs) and nitrogenous disinfection byproducts (N-DBPs) during the dissolved phase chlorination showed the same variation tendency as DOC and DON respectively. The highest C-DBP (98.4 μg/L) and N-DBP (5.5 μg/L) values were obtained at 0.4 mg/L chlorine preoxidation after 480-min simulated transportation. Therefore, when prechlorination is applied for algae-laden water pretreatment, not only chlorine dose but also transportation time needs to be considered with regard to their effects on cell integrity, AOM release, and chlorinated DBP formation.

Study on small molecular organic compounds pyrolysed from rubber seed oil and its sodium soap.

Rubber seed oil (RSO) and its sodium soap were pyrolysed in a batch reactor to obtain low molar mass organic substances. The pyrolitic oil of RSO was redistilled and the distillates were characterized by GC–MS and FTIR. Density, acid value, saponification value and ester values were also measured according to the ASTM standard methods. A similar analysis was done for samples taken out at different time intervals from the reaction mixture. Industrially important low molar mass alkanes, alkenes, aromatics, cyclic compounds and carboxylic acids were identified in the pyrolysis process of rubber seed oil. However, pyrolysis of the sodium soap of rubber seed oil gave a mixture of hydrocarbons in the range of C14–C17 and hence it has more applications as a fuel.

Metabolite profiling of the ripening ofMangoes Mangifera indica L. cv. 'Tommy Atkins' by real-time measurement of volatile organic compounds.

Real-time profiling of mango ripening based on proton transfer reaction-time of flight-mass spectrometry (PTR–ToF–MS) of small molecular weight volatile organic compounds (VOCs), is demonstrated using headspace measurements of ‘Tommy Atkins’ mangoes. VOC metabolites produced during the ripening process were sampled directly, which enabled simultaneous and rapid detection of a wide range of compounds. Headspace measurements of ‘Keitt’ mangoes were also conducted for comparison. A principle component analysis of the results indicated that several mass channels were not only key to the ripening process but could also be used to distinguish between mango cultivars. The identities of 22 of these channels, tentatively speciated using contemporaneous GC–MS measurements of sorbent tubes, are rationalized through examination of the biochemical pathways that produce volatile flavour components. Results are discussed with relevance to the potential of headspace analysers and electronic noses in future fruit ripening and quality studies.

A Review on Bio-macromolecular Imprinted Sensors and Their Applications

Abstract Molecular imprinted technology has been maturely applied to analyze and detect small molecular organic compounds, also increasingly applied in biological macromolecules assay. This review addresses the perspective of bio-macromolecular imprinted sensors and their applications, including optical molecular imprinted sensors, electrochemical molecular imprinted sensors and mass-sensitive molecular imprinted sensors. In addition, the opportunities, challenges, and further research orientations of molecular imprinted sensors for bio-macromolecules detection were prospected.