Pharmacological significance of marine microbial bioactive compounds

Environmental Chemistry Letters - The continuous growth of the world population has raised heatlh issues such as the inefficiency of common drugs, such as antibiotics, due to...     

Toxins and bioactive compounds from cyanobacteria and their implications on human health

Many species of cyanobacteria (blue-green algae) produce secondary metabolites with potent biotoxic or cytotoxic properties. These metabolites differ from the intermediates and cofactor compounds that are essential for cell structural synthesis and energy transduction. The mass growth of cyanobacteria which develop in fresh, brackish and, marine waters commonly contain potent toxins. Cyanobacterial toxins or cyanotoxins are responsible for or implicated in animal poisoning, human gastroenteritis, dermal contact irritations and primary liver cancer in humans. These toxins (microcystins, nodularins, saxitoxins, anatoxin-a, anatoxin-a(s), cylindrospermopsin) are structurally diverse and their effects range from liver damage, including liver cancer to neurotoxicity. Several incidents of human illness and more recently, the death of 60 haemodialysis patients in Caruaru, Brazil, have been linked to the presence of microcystins in water. In response to the growing concern about the non-lethal acute and chronic effects of microcystins, World Health Organization has recently set a new provisional guideline value for microcystin-LR of 1.0 microg/L in drinking water. Cyanobacteria including microcystin-producing strains produce a large number of peptide compounds, e.g. micropeptins, cyanopeptolins, microviridin, circinamide, aeruginosin, with varying bioactivities and potential pharmacological application. This article discusses briefly cyanobacterial toxins and their implications on human health.     

Induction of metamorphosis in larvae of the oyster Crassostrea gigas using neuroactive compounds

Chemical (neuroactive compounds at different concentrations and exposure times) and physical (water agitation, light) factors with potential effects on the metamorphosis of larvae of the oyster Crassostrea gigas (Thunberg) larvae have been studied. The neurotransmitters l-dihydroxyphenylalanine (DO), epinephrine (EP), norepinephrine (NE), and acetylcholine (AC) have been identified as very active inducers of metamorphosis, whilst serotonin (SE), dopamine (DA) and potassium (K) were less effective inducers. The -aminobutyric acid (GA) and ammonium (AM) were found ineffective at the concentrations tested. Exposure to 10^-4 M EP for 15 min was sufficient to promote >80% metamorphosis within 48 h, whereas NE required 2 h to exert comparable induction. Maximum induction by DO (>50%) was achieved after 2 h exposure to 10^-4 M. However, unlike EP and NE, DO was lethal at that concentration in the long term. Maximum induction by AC (30% metamorphosis) was achieved at a concentration of 10^-4 M. In contrast to other neurotransmitters, AC induced settlement behaviour, cementation and eventual metamorphosis, yielding postlarvae which were all attached to the substratum. EP and NE triggered the morphogenetic changes, by-passing settlement and leading to postlarvae not cemented to the substratum. DO induced mostly attached spat at low concentrations (10^-5 M) and unattached spat at high concentrations (10^-4 M), and a similar pattern was apparent for the weaker inducers SE and DA. Regarding physical factors, a highly reflectant surface significantly increased the percentage of attached spat obtained, compared to a dark bottom. No consistent effect of water current or light was detected on the production of unattached spat. The three different forms of induction are discussed in relation to different regulatory pathways of settlement and metamorphosis.     

Encapsulation in cyclodextrins to widen the applications of essential oils

Environmental Chemistry Letters - There is a growing interest for aromatic and biological properties of essential oils as alternatives to synthetic chemicals and drugs. However, essential oils and...     

Control of chlorinated aromatic compounds from a municipal solid waste incinerator using limestone addition

In this study, limestone powder was directly added to synthetic MSW, which was fed into a small‐scale fluidized bed incinerator. The concentration of CBzs and CPs in the flue gas were measured before and after a secondary combustion air injection. Finally, the PCDDs and PCDFs concentrations were also measured in the flue gas after the secondary combustion zone. The CaCO₃ added to synthetic MSW not only controls HCl in the flue gas, but suppresses the formation of chlorinated aromatic compounds like CBzs, CPs, PCDDs, and PCDFs. The main mechanisms to control the formation of chlorinated aromatic compounds was more likely related to the suppression of catalytic capability of flyash than the HCl reduction in the flue gas. However, the NO concentration was increased by catalytic reaction of limestone in the fluidized bed.     

Environmental benefits of using magnesium carbonate minerals as new wildfire retardants instead of commercially available,phosphate-based compounds

A serial batch leaching experiment has been carried out to evaluate the release of elements from the ash of Pinus halepensis needles burned under two test conditions—with and without treatment of the forest species with the carbonate minerals (huntite and hydromagnesite) in aqueous solution (pH 6). The ash (before and after leaching) and leachates were analyzed using atomic absorption spectroscopy and X-ray diffraction. Compared with data from samples treated with the commercially available, phosphate-based fire retardant diammonium phosphate (DAP), we found that use of huntite or hydromagnesite was much more successful in obstructing the release of the toxic elements present in the ash, probably because of the alkaline conditions resulting from decomposition of the minerals during burning. In contrast, DAP tended to be more able to facilitate the extraction of some toxic metals (e.g., Zn, Cu, Mn), probably because of the acidic conditions resulting from its decomposition to phosphoric acid. Data from this study thus lend strong support to the use of magnesium carbonate minerals as new wildfire retardants, because they were shown to be more friendly to the environment (e.g., soil, ground, and underground water streams) than those currently in use (e.g., phosphate or sulfate salt type).     

Simultaneous analysis of five taste and odor compounds in surface water using solid-phase extraction and gas chromatography-mass spectrometry

In this paper, a method using solid-phase extraction (SPE) and gas chromatography-mass spectrometry (GC-MS) was developed to simultaneously analyze five taste and odor compounds in surface water, i.e., 2-methylisoborneol (2-MIB), 2,4,6-trichloroanisole (TCA), 2-isopropyl-3-methoxy pyrazine (IPMP), 2-isobutyl-3-methoxy pyrazine (IBMP), and trans-1,10-dimethyl-trans-9-decalol (geosmin, GSM). The mass spectrometry was operated in selective ion monitoring (SIM) mode. Three kinds of SPE columns and three eluting solvents were compared, the C18 column was chosen as optimum SPE column, and methanol was chosen as the optimum eluting solvent. It was found that the method showed good linearity in the range of 1–200 ng·L^-1 and gave detection limits of 0.5–1.5 ng·L^-1 for individual compounds. Good recoveries (93.5%–108%) and relative standard deviations (1.58%–7.31%) were also obtained. Additionally, concentrations of these taste and odor compounds in Jinan’s surface and drinking water were analyzed by applying this method, and the results showed that GSM and 2-MIB were the dominant taste and odor compounds in Jinan’s raw water.     

Toxicology of perfluorinated compounds

Perfluorinated compounds [PFCs] have found a wide use in industrial products and processes and in a vast array of consumer products. PFCs are molecules made up of carbon chains to which fluorine atoms are bound. Due to the strength of the carbon/fluorine bond, the molecules are chemically very stable and are highly resistant to biological degradation; therefore, they belong to a class of compounds that tend to persist in the environment. These compounds can bioaccumulate and also undergo biomagnification. Within the class of PFC chemicals, perfluorooctanoic acid and perfluorosulphonic acid are generally considered reference substances. Meanwhile, PFCs can be detected almost ubiquitously, e.g., in water, plants, different kinds of foodstuffs, in animals such as fish, birds, in mammals, as well as in human breast milk and blood. PFCs are proposed as a new class of 'persistent organic pollutants'. Numerous publications allude to the negative effects of PFCs on human health. The following review describes both external and internal exposures to PFCs, the toxicokinetics (uptake, distribution, metabolism, excretion), and the toxicodynamics (acute toxicity, subacute and subchronic toxicities, chronic toxicity including carcinogenesis, genotoxicity and epigenetic effects, reproductive and developmental toxicities, neurotoxicity, effects on the endocrine system, immunotoxicity and potential modes of action, combinational effects, and epidemiological studies on perfluorinated compounds).     

Effect of co-existing organic compounds on adsorption of perfluorinated compounds onto carbon nanotubes

Co-existing organic compounds may affect the adsorption of perfluorinated compounds (PFCs) and carbon nanotubes in aquatic environments. Adsorption of perfluorooctane sulfonate (PFOS), perfluorooctane acid (PFOA), perfluorobutane sulfonate (PFBS), and perfluorohexane sulfonate (PFH_xS) on the pristine multi-walled carbon nanotubes (MWCNTs-Pri), carboxyl functionalized MWCNTs (MWCTNs-COOH), and hydroxyl functionalized MWCNTs (MWCNTs-OH) in the presence of humic acid, 1-naphthol, phenol, and benzoic acid was studied. Adsorption kinetics of PFOS was described well by the pseudo-second-order model and the sorption equilibrium was almost reached within 24 h. The effect of co-existing organic compounds on PFOS adsorption followed the decreasing order of humic acid>1-naphthol>benzoic acid>phenol. Adsorbed amounts of PFOS decreased significantly in the presence of co-existing or preloaded humic acid, and both adsorption energy and effective adsorption sites on the three MWCNTs decreased, resulting in the decrease of PFOS adsorption. With increasing pH, PFOS removal by three MWCNTs decreased in the presence of humic acid and phenol. The adsorbed amounts of different PFCs on the MWCNTs increased in the order of PFBSxS相似文献   

Characterization of bioactive plant ellagitannins by chromatographic, spectroscopic and mass spectrometric methods

Ellagitannins are widely distributed plant polyphenols showing potent anti-herbivore activities, but rather complex chemical structures. Here we show how ellagitannins with different structures can be efficiently characterized from plant extracts by utilizing the information obtained from four universal methods used for ellagitannin analysis: Sephadex LH-20 gel chromatography, high-performance liquid chromatography, ultraviolet spectroscopy, and mass spectrometry. We show that by combining the information obtained from the ellagitannins’ chromatographic elution order, specific shapes of the ultraviolet spectra, molecular masses and characteristic mass spectral fragmentations, it is possible to classify these polyphenols into different ellagitannin sub-groups, and even characterize the structures within the sub-groups. These findings aid in the fast screening of complex plant samples for their ellagitannin composition without having to isolate compounds for individual characterization.     

Ecotoxicity studies of some organotin compounds

The ecotoxicities of three organic compounds containing spacer groups, an intermediate organotin premonomer, four organotin monomers, their homopolymers and six copolymers of tributylin α‐chloroacrylate (TCA) are reported against two microorganisms viz., Pseudomonas aeruginosa and Sarcina lutea and a larval species Anemia salina (Nauplii II). The organic compounds containing spacer group were less toxic whereas the monomers were found to be highly toxic. The homopolymers were found to be more toxic than that of tributyltin acrylate (TBTAA), tributyltin methacrylate (TBTMA) and tributyltin α‐Chloroacrylate (TCA). The toxicity of TCA copolymers increased with the increase in tributyltin (TBT) content in the polymer. From this study it was not possible to establish any relationship between the chemical nature of the comonomer with its toxicity.     

Determination of selected semi-volatile organic compounds in water using automated online solid-phase extraction with large-volume injection/gas chromatography/mass spectrometry

A rapid, sensitive, and cost-effective analytical method was developed for the analysis of selected semi-volatile organic compounds in water. The method used an automated online solid-phase extraction technique coupled with programmed-temperature vaporization large-volume injection gas chromatography/mass spectrometry. The water samples were extracted by using a fully automated mobile rack system based on x-y-z robotic techniques using syringes and disposable 96-well extraction plates. The method was validated for the analysis of 30 semivolatile analytes in drinking water, groundwater, and surface water. For a sample volume of 10 mL, the linear calibrations ranged from 0.01 or 0.05 to 2.5 ??g·L^?1, and the method detection limits were less than 0.1 ??g·L^?1. For the reagent water samples fortified at 1.0 ??g·L^?1 and 2.0 ??g·L^?1, the obtained mean absolute recoveries were 70%?C130% with relative standard deviations of less than 20% for most analytes. For the drinking water, groundwater, and surface water samples fortified at 1.0 ??g·L^?1, the obtained mean absolute recoveries were 50%?C130% with relative standard deviations of less than 20% for most analytes. The new method demonstrated three advantages: 1) no manipulation except the fortification of surrogate standards prior to extraction; 2) significant cost reduction associated with sample collection, shipping, storage, and preparation; and 3) reduced exposure to hazardous solvents and other chemicals. As a result, this new automated method can be used as an effective approach for screening and/or compliance monitoring of selected semi-volatile organic compounds in water.     

Consequences of manganese compounds: a review

Manufacturing of manganese (Mn) compounds, their industrial applications as well as mining overburden, has generated a potential environmental pollutant. Occupational exposure to elevated levels of Mn occurs during mining, welding, smelting and other industrial anthropogenic sources. Chronic and acute exposure of this metal pollutant leads to adverse consequences and is clinically categorized by various symptoms of neurotoxicity including cognitive, psychiatric symptoms, Parkinson's disease, extra pyramidal signs, manganism, dystonia, and motor system dysfunction. The aim of this review is to summarize the possible mechanism underlying Mn compounds-mediated neurotoxicity leading to neurodegenerative diseases. Our review endeavours to examine recent advances in research on Mn-related environmental pollution, Mn-induced poisoning, molecular mechanisms underlying Mn-induced neurotoxicity with case studies as well as current approaches employed for treatment and prevention of Mn exposure.     

Simultaneous removal of hydrogen sulfide and volatile organic sulfur compounds in off-gas mixture from a wastewater treatment plant using a two-stage bio-trickling filter system

A two-stage BTF system was established treating odorous off-gas mixture from a WWTP. The two-stage BTF system showed resistance for the lifting load of H₂S and VOSC. Miseq Illumina sequencing showed separated functional microbial community in BTFs. Avoiding H₂S inhibition and enhancement of VOSC degradation was achieved. Key control point was discussed to help industrial application of the system. Simultaneous removal of hydrogen sulfide (H₂S) and volatile organic sulfur compounds (VOSCs) in off-gas mixture from a wastewater treatment plant (WWTP) is difficult due to the occasional inhibitory effects of H₂S on VOSC degradation. In this study, a two-stage bio-trickling filter (BTF) system was developed to treat off-gas mixture from a real WWTP facility. At an empty bed retention time of 40 s, removal efficiencies of H₂S, methanethiol, dimethyl sulfide, and dimethyl disulfide were 90.1, 88.4, 85.8, and 61.8%, respectively. Furthermore, the effect of lifting load shock on system performance was investigated and results indicated that removal of both H₂S and VOSCs was slightly affected. Illumina Miseq sequencing revealed that the microbial community of first-stage BTF contained high abundance of H₂S-affinity genera including Acidithiobacillus (51.43%), Metallibacterium (25.35%), and Thionomas (8.08%). Analysis of mechanism demonstrated that first stage of BTF removed 86.1% of H₂S, mitigating the suppression on VOSC degradation in second stage of BTF. Overall, the two-stage BTF system, an innovative bioprocess, can simultaneously remove H₂S and VOSC.     

Bioconcentration of butyltin compounds by round crucian carp

Bioconcentration factors (BCF) by round crucian carp and partition coefficients between n‐octanol and water (Pow) were measured for dibutyltin, tributyltin and triphenyltin compounds. Pow was 0.97–3.66 for 7 organotin compounds. BCF of tributyltin and triphenyltin compounds was 1.70–2.77 for muscle, 1.70–2.66 for vertebra, 2.05–3.70 for liver and 1.49–3.50 for kidney.     

Standard purity and response factors of perfluorinated compounds

It has been reported that the relative response factors of isotopically labeled standards and unlabeled standards of the same perfluorinated compounds could be different. Individual (100 ng mL^?1) solutions of perfluorooctanoic acid (PFOA) and perfluorooctane sulfonate (PFOS) were analyzed using high-performance liquid chromatography tandem mass-spectrometry under negative-ion electrospray to detect any impurities present down to 0.5%–0.1% relative to the major component. Purity of the standards ranged from approximately 86% to ≥ 97%. Standard solutions of unlabeled and isotopically labeled materials were analyzed to compare the response factors of isotopically labeled analytes versus their nonlabeled counterparts in three different matrices at equivalent concentrations: organic solvent (methanol), serum extract, and water present individually and concurrently. Not all labeled analytes have the same response factor as their nonlabeled complement, and in at least one case the matrix in which the standard is present may cause significant suppression of response. Standard solutions of electrochemical fluorination produced PFOA and PFOS were quantified under multiple reaction monitoring mode, using calibration curves prepared from standards consisting primarily of linear standards only. The use of linear only standards may cause under-prediction of concentrations, and that the working range of these standards may be limited.     

Pollution survey of carbonyl compounds in train air

The train is an important vehicle in China, but its air quality has important impacts on passengers’ health. In this work, pollution from carbonyl compounds was measured in the air of six trains. The objectives of this work were to investigate carbonyl compound levels in selected air from trains, identify their emission sources, and assess the intake of carbonyl compounds for passengers. The methods for sampling and analyzing 10 carbonyl compounds such as formaldehyde, acetaldehyde, acrolein, acetone, propionaldehyde, crotonaldehyde, butyraldehyde, benzaldehyde, cyclohexanone, and valeraldehyde in indoor air were proposed with the sampling efficiency, recovery, and detection limit being 92%–100%, 91%–104%, and 0.26–0.82 ng/m³, respectively. It was indicated that the total concentrations of carbonyl compounds were 0.159–0.2828 mg/m³ with the average concentration of 0.2330 mg/m³. The average concentrations of form aldehyde, acetaldehyde and acetone were 0.0922, 0.0499, and 0.0580 mg/m³, accounting for 42.6%, 21.4%, and 24.9% of the total concentrations of carbonyl compounds, respectively. The carbonyl compounds probably came from woodwork and cigarette smoking. The intake of carbonyl compounds for the passengers was approximately 0.043–0.076 mg/h. The carbonyl compounds in train air could be harmful to human health.     

The determination of partition coefficients of organic compounds in technical products and waste waters for the estimation of their bioaccumulation potential using reversed phase thin layer chromatography

Reversed phase thin layer chromatography (RPTLC) has been investigated for the estimation of octanol/water partition coefficients (P), an important parameter for the prediction of the environmental behaviour of organic chemicals. A strong correlation between P derived from the traditional octanol/water system and RPTLC has been established over five orders of magnitude. RPTLC data are likewise correlated to results obtained by high performance chromatography (HPLC). Due to the low costs, simplicity and separation power RPTLC is especially suited for the investigation and screening of mixtures of compounds before more complicated tests are involved.

Results from a round robin test on the determination of partition coefficients by HPLC, RPTLC and the batch method indicate the simplicity and accuracy of the RPTLC technique. Applications of the RPTLC‐technique on technical products and industrial waste waters are described.     

硝基芳香化合物的植物作用研究进展

硝基芳香化合物是环境中难以降解的污染物之一。因其用途广泛,大量残留于土壤,水体和大气中,造成的环境污染日趋严重。多种植物对该类污染物具有吸收、富集和代谢降解作用,利用植物对其环境污染进行治理是一种有效的方法。文章在总结国内外有关硝基芳香化合物的植物作用研究基础上,重点阐述了植物对硝基芳香化合物的吸收、转运和代谢过程,分析了吸收、代谢机理以及影响吸收的因素;硝基芳香化合物的理化特性、浓度和植物自身特性及其它外界条件都会影响植物对该类化合物的吸收,植物可以通过体内降解、体外联合代谢、根部释放酶催化的机制实现该类化合物的降解。目前,硝基芳香化合物进入植物细胞膜的机理认知不足,模拟模型缺乏有力数据验证;代谢机制中参与反应的酶、化合物等体系和反应产物环境特性仍不明确,植物修复可行性缺乏有力证据。未来将在模型预测构建、降解机理和修复工程的实际应用方面作进一步探究,以形成系统的认知,为硝基芳香化合物污染土壤和农产品的生态风险评价以及植物修复提供理论依据。     

Air revitalization compounds: A literature survey

Chemical processes for air revitalization are attractive alternatives for some closed life support systems in the applications of space and marine explorations. A review of the literature is given for the purpose of evaluating potential candidates as air revitalizing chemicals based upon a set of criteria including toxicity in use, removal of airborne contaminants and bacteria, theoretical oxygen yields, chemical reactivity to breathing atmospheres, and commercial availability. The preliminary evaluation shows potassium and sodium Superoxides as prime candidates for further evaluation against the practical considerations of actual use. Upon closer scrutiny, potassium Superoxide is the desired chemical for air revitalization in closed life support systems according to the present technology. Kinetic reaction rates for the simple hydration of KO₂ were reported to increase for increasing pressures to 12 atm making it a promising air revitalization chemical at the hyperbaric conditions encountered in deep diving.