Biomedical subjects

Lizhong Zhu

Publications and source records attributed to Lizhong Zhu.

12 recordsLinked to original sources

PubMed2024

Sulfonamide-induced DNA hypomethylation disturbed sugar metabolism in rice (Oryza sativa L.).

DNA methylation is well-accepted as a bridge to unravel the complex interplay between genome and environmental exposures, and its alteration regulated the cellular metabolic responses towards pollutants. However, the mechanism underlying site-specific aberrant DNA methylation and metabolic disorders under pollutant stresses remained elusive. Herein, the multilevel omics interferences of sulfonamides (i.e., sulfadiazine and sulfamerazine), a group of antibiotics pervasive in farmland soils, towards rice in 14 days of 1 mg/L hydroponic exposure were systematically evaluated. Metabolome and transcriptome analyses showed that 57.1-71.4 % of mono- and disaccharides were accumulated, and the differentially expressed genes were involved in the promotion of sugar hydrolysis, as well as the detoxification of sulfonamides. Most differentially methylated regions (DMRs) were hypomethylated ones (accounting for 87-95 %), and 92 % of which were located in the CHH context (H = A, C, or T base). KEGG enrichment analysis revealed that CHH-DMRs in the promoter regions were enriched in sugar metabolism. To reveal the significant hypomethylation of CHH, multi-spectroscopic and thermodynamic approaches, combined with molecular simulation were conducted to investigate the molecular interaction between sulfonamides and DNA in different sequence contexts, and the result demonstrated that sulfonamides would insert into the minor grooves of DNA, and exhibited a stronger affinity with the CHH contexts of DNA compared to CG or CHG contexts. Computational modeling of DNA 3D structures further confirmed that the binding led to a pitch increase of 0.1 Å and a 3.8° decrease in the twist angle of DNA in the CHH context. This specific interaction and the downregulation of methyltransferase CMT2 (log2FC = -4.04) inhibited the DNA methylation. These results indicated that DNA methylation-based assessment was useful for metabolic toxicity prediction and health risk assessment.

DNA Methylation↗

PubMed2004

Solubilization of pyrene by anionic-nonionic mixed surfactants.

Surfactant-enhanced remediation (SER) is an effective approach for the removal of sorbed hydrophobic organic compounds from contaminated soils. The solubilization of pyrene by four anionic-nonionic mixed surfactants, sodium dodecyl sulfate (SDS) with Triton X-405 (TX405), Brij35, Brij58, and Triton X-100 (TX100), has been studied from measurements of the molar solubilization ratio (MSR), the micelle-water partition coefficient (Kmc), and the critical micelle concentration (CMC). The MSRs of pyrene in mixed surfactants are found to be larger than those predicted according to an ideal mixing rule. The mixing effect of anionic and nonionic surfactants on MSR for pyrene follows the order of SDS-TX405 > SDS-Brij35 > SDS-Brij58 > SDS-TX100 and increases with an increase in the hydrophile-lipophile balance (HLB) value of nonionic surfactant in mixed systems. In addition, the mixture of anionic and nonionic surfactants cause the Kmc value for pyrene to be greater than the ideal value in SDS-TX405 mixed system, but to be smaller than the ideal value in SDS-Brij35, SDS-Brij58, and SDS-TX100 mixed systems. Meanwhile, in the four mixed systems, the experimental CMCs are lower than the ideal CMCs at almost all mixed surfactant solution compositions. The mixing effect of anionic and nonionic surfactants on MSR for pyrene can be attributed to the conjunct or the net result of the negative deviation of the CMCs from ideal mixture and the increasing or decreasing Kmc.

Anions↗

PubMed2004

Characterization of sorption mechanisms of VOCs with organobentonites using a LSER approach.

To fully utilize the sorption traits of organobentonites to control volatile organic compounds (VOCs) pollution, the sorption mechanisms of VOCs with organobentonites need to be understood adequately. The sorption of VOCs as vapors to a typical organobentonite, modified with cetyltrimethylammonium bromide (CTMAB-bentonite), was characterized using a linear solvation energy relationship (LSER) of the type log Kc = c + rR2 + s pi2H + a sigma(alpha2)H + b sigma(beta2)H + l log L16. The fitted LSER equation, log Kc = 0.434 + 0.968R2 - 0.0886pi2H + 2.170sigma(alpha2)H + 1.611sigma(beta2)H + 0.417 log L16, was obtained by a multiple regression of the partition coefficients of 22 probe solutes against the solvation parameters of the solutes. The coefficients of the LSER equation show that CTMAB-bentonite is a sorbent with nonsignificant dipolarity/polarizability, interacts with solutes partly through pi-/n-electron pairs, behaves both as hydrogen-bond donor and hydrogen-bond acceptor, and can interact with solutes by cavity/dispersion interactions. The related terms in LSER suggest that the potential factors governing the sorption of VOCs onto CTMAB-bentonite are dispersion interactions, hydrogen-bond acidity interactions, hydrogen-bond basicity interactions, and pi-/n-electron interactions. The dispersion interaction is recognized to be the predominant parameter for most solutes, whereas the contributions of the other parameters depend on specific solutes. The derived LSER equation successfully predicted the VOC partition coefficients and the selectivity of CTMAB-bentonite for the VOCs. The relationship between LSER and adsorption/partition model was compared. The classification of sorption mechanisms by LSER goes on the molecular interaction types between sorbate and sorbent, and classification by adsorption/partition model goes on the property difference among various components of sorbent. The LSER approach coupled with inverse gas chromatography (IGC) is a comparatively simple and reliable tool to rapidly characterize the sorption mechanism of VOCs with solid sorbents such as CTMAB-bentonite, and may potentially be applied to the design of an organoclay sorbent for control of VOCs.

Adsorption↗

PubMed2004

Plant uptake, accumulation and translocation of phenanthrene and pyrene in soils.

Uptake, accumulation and translocation of phenanthrene and pyrene by 12 plant species grown in various treated soils were comparatively investigated. Plant uptake and accumulation of phenanthrene and pyrene were correlated with their soil concentrations and plant compositions. Root or shoot accumulation of phenanthrene and pyrene in contaminated soils was elevated with the increase of their soil concentrations. Significantly positive correlations were shown between root concentrations or root concentration factors (RCFs) of phenanthrene and pyrene and root lipid contents. The RCFs of phenanthrene and pyrene for plants grown in contaminated soils with initial phenanthrene concentration of 133 mgkg(-1) and pyrene of 172 mgkg(-1) were 0.05-0.67 and 0.23-4.44, whereas the shoot concentration factors of these compounds were 0.006-0.12 and 0.004-0.12, respectively. For the same soil-plant treatment, shoot concentrations and concentration factors of phenanthrene and pyrene were generally much lower than root. Translocations of phenanthrene and pyrene from shoots to roots were undetectable. However, transport of these compounds from roots to shoots usually was the major pathway of shoot accumulation. Plant off-take of phenanthrene and pyrene only accounted for less than 0.01% of dissipation enhancement for phenanthrene and 0.24% for pyrene in planted versus unplanted control soils, whereas plant-promoted biodegradation was the predominant contribution of remediation enhancement of soil phenanthrene and pyrene in the presence of vegetation.

Analysis of Variance↗

PubMed2003

Interactions of organic contaminants with mineral-adsorbed surfactants.

Sorption of organic contaminants (phenol, p-nitrophenol, and naphthalene) to natural solids (soils and bentonite) with and without myristylpyridinium bromide (MPB) cationic surfactant was studied to provide novel insightto interactions of contaminants with the mineral-adsorbed surfactant. Contaminant sorption coefficients with mineral-adsorbed surfactants, Kss, show a strong dependence on surfactant loading in the solid. At low surfactant levels, the Kss values increased with increasing sorbed surfactant mass, reached a maximum, and then decreased with increasing surfactant loading. The Kss values for contaminants were always higher than respective partition coefficients with surfactant micelles (Kmc) and natural organic matter (Koc). At examined MPB concentrations in water the three organic contaminants showed little solubility enhancement by MPB. At low sorbed-surfactant levels, the resulting mineral-adsorbed surfactant via the cation-exchange process appears to form a thin organic film, which effectively "adsorbs" the contaminants, resulting in very high Kss values. At high surfactant levels, the sorbed surfactant on minerals appears to form a bulklike medium that behaves essentially as a partition phase (rather than an adsorptive surface), with the resulting Kss being significantly decreased and less dependent on the MPB loading. The results provide a reference to the use of surfactants for remediation of contaminated soils/sediments or groundwater in engineered surfactant-enhanced washing.

Adsorption↗

PubMed2003

A multi-component statistic analysis for the influence of sediment/soil composition on the sorption of a nonionic surfactant (Triton X-100) onto natural sediments/soils.

The contents of soil/sediment organic carbon and clay minerals (i.e. montmorillonite, kaolinite, illite, gibbsite and 1.4 nm minerals) for 21 natural soil/sediment samples and the sorption of Triton X-100 on these samples were determined. A multi-component statistic analysis was employed to investigate the importance of soil/sediment organic matters and clay minerals on their sorption of Triton X-100. The sorption power of soil/sediment composition for Triton X-100 conforms to an order of montmorillonite>organic carbon>illite>1.4 nm minerals (vermiculite+chlorite+1.4 nm intergrade mineral)>>kaolinite. The sorption of Triton X-100 on a montmorillonite, a kaolinite and a humic acid were also investigated and consistent with the result of multi-component statistic analysis. It is clear that the sorption of Triton X-100 on soils or sediments is the combined contribution of soil/sediment organic matters and clay minerals, which depended on both the contents of soil/sediment organic matters and the types and contents of clay minerals. The important influence of illite on the sorption of nonionic surfactants onto soils/sediments is suggested and demonstrated in this paper. Surfactants for aquifer remediation application may be more efficient for the contaminated soils/sediments that contain little clay minerals with 2:1 structure because of the less sorption of nonionic surfactants on these soils/sediments.

Adsorption↗

PubMed2003

Sources and patterns of polycyclic aromatic hydrocarbons pollution in kitchen air, China.

Twelve polycyclic aromatic hydrocarbons, multi-ringed compounds known to be carcinogenic in air of six domestic kitchens and four commercial kitchens of China were measured in 1999-2000. The mean concentration of total PAHs in commercial kitchens was 17 microg/m3, consisting mainly of 3- and 4-ring PAHs, and 7.6 microg/m3 in domestic kitchens, where 2- and 3-ring PAHs were predominant, especially naphthalene. The BaP levels in domestic kitchens were 0.0061-0.024 microg/m3 and 0.15- 0.44 microg/m3 in commercial kitchens. Conventional Chinese cooking methods were responsible for such heavy PAHs pollution. The comparative study for PAH levels in air during three different cooking practices: boiling, broiling and frying were conducted. It was found that boiling produced the least levels of PAHs. For fish, a low-fat food, frying it produced a larger amount of PAHs compared to broiling practice, except pyrene and anthracene. In commercial kitchens, PAHs came from two sources, cooking practice and oil-fumes, however the cooking practice had a more predominant contribution to PAHs in commercial kitchen air. In domestic kitchens, except for cooking practice and oil-fumes, there were other PAHs sources, such as smoking and other human activities in the domestic houses, where 3-4 ring PAHs mainly came from cooking practice. Naphthalene (NA, 2-ring PAHs) was the most predominant kind, mostly resulting from the evaporation of mothball containing a large quantity of NA, used to prevent clothes against moth. A fingerprint of oil-fumes was the abundance of 3-ring PAHs. Heating at the same temperature, the PAHs concentrations in different oil-fumes were lard > soybean oil > rape-seed oil. An increase in cooking temperature increased the levels of PAHs, especially acenaphthene.

Air Pollutants, Occupational↗

PubMed2003

Synergistic solubilization of polycyclic aromatic hydrocarbons by mixed anionic-nonionic surfactants.

Water solubility enhancements of naphthalene (Naph), acenaphthylene (Acen), anthracene (An), phenanthrene (Phen) and pyrene (Py) by micellar solutions of single and mixed anionic-nonionic surfactants were measured and compared. Effects of typical inorganic ions, such as NH(4)(+), Na(+) and Mg(2+) coexisted with the organic pollutants (in soils) on water solubilities of polycyclic aromatic hydrocarbons (PAHs) in the presence of single and mixed surfactants were also investigated. Solubilities of PAHs in water are greatly enhanced in a linear fashion by each of Triton X-100 (TX100), Triton X-305 (TX305), Brij 35, and sodium dodecyl sulfate (SDS). Solubility enhancement efficiencies of surfactants above the critical micelle concentration (CMC) follow the order of TX100>Brij 35>TX305>SDS. PAHs are solubilized synergistically in mixed anionic-nonionic surfactant solutions, especially at low surfactant concentrations. The synergistic power of the mixed surfactants is SDS-TX305>SDS-Brij 35>SDS-TX100. Synergistic effect of a given mixed-surfactant solution on different PAHs also appears to be linearly related to the solute logK(ow). The noted synergism for the mixed surfactants is attributed to the formation of mixed micelles, the lower CMC of the mixed-surfactant solutions, and the increase of the solute's molar solubilization ratio or micellar partition coefficients (K(mc)) because of the lower polarity of the mixed micelles. Suitable quantity of inorganic cations can enhance the solubilization capacities of anionic-nonionic mixed surfactants, the effect being Mg(2+)>NH(4)(+)>Na(+). The water solubility of pyrene was slightly increased by anthracene and significantly increased by 1,2,3-TCB in the presence of SDS-Brij 35. Mixed surfactants may improve the performance of surfactant-enhanced remediation of soils and sediments by decreasing the applied surfactant level and thus the remediation cost.

Biodegradation, Environmental↗

PubMed2003

[PAHs pollution in air of coke plant and health risk assessment].

12 PAHs in air of different production sector in coking plant were measured with the result showing that, the total PAHs concentrations ranged from 11.75 to 46.66 micrograms/m3, among which, BaP was 0.050-1.054 micrograms/m3 descending following the order: the outlet of coke oven, the top of coke oven, the gate, the point of flaming out coke. BaP pollution in air of the top and the outlet of coke oven were much heavier than in the soot and in air of arterial road. The toxic equivalency factors (TEF) adjusted concentrations of total PAHs were 0.3875-1.714 micrograms/m3, and in this way, workers' daily exposure to PAHs were 3.100-13.71 micrograms/m3.

Air Pollutants, Occupational↗

PubMed2003

[Enhanced sorption of naphthalene into bentonites in water containing myristylpyridinium bromide and its mechanism].

The influence of myristylpyridinium bromide (MPB) on sorption behavior of naphthalene into two bentonites in aqueous solution and its mechanism were investigated. The apparent sorption coefficients (Kd*) of naphthalene on two bentonites with surfactant was dependent on MPB equilibrium concentration (X). When X was less than 1/10CMC, the Kd* value increased rapidly with increasing MPB primary concentration (X0) that was mainly contributed to increasing the organic carbon contents (foc) of bentonites for partitioning naphthalene. The Kd* value decreased slowly with increasing X0 when X was intermediate 1/10CMC and 1 CMC, because the adding MPB increased foc for sorption naphthalene was less than MPB monomer for enhancement solubility of naphthalene. Then The Kd* value decreased sharply with increasing X0 when X was larger than 1 CMC, which resulted from that the addition of MPB only increased micelle concentration for enhancement solubility of naphthalene. The mechanism was explained by apparent partition coefficient normalized by foc(i. e. Koc*) for the first time. The relationship of 1/Koc* and X was linear. The value of Koc, Kmn and Kmc can be calculated from the intercept and slope of the linear, which will provide theoretical gist for organobentonite applied on organic contaminant remediation.

Adsorption↗

PubMed2003

[Research on PAHs fingerprints of vehicle discharges].

Air samples of 14 PAHs were collected from vehicle discharges of different types, oils, and mileages and analyzed by HPLC. It showed that the total PAHs discharged from the vehicle in 30 minutes were 41.53-121.1 micrograms/m3, among which, BaA was the most predominant, about 33.3%, followed by Naphthalene, Benzo (ghi) pyrene and In (1,2,3-cd) pyrene, about 16.8%, 12.9% and 12.1%, respectively. Diesel vehicle discharged more total PAHs compared to gasoline vehicle. The two vehicles all exhausted much BaA and Naph, however diesel vehicle mainly emitted Ac, Fluor, Bghip, In, while gasoline discharged mainly Bghip, In, BkF. PAHs with five or more rings in gasoline discharges were relatively higher than those in diesel discharges, however to 3-ring PAHs, diesel vehicle produced more than gasoline vehicle. As for vehicle of different mileage, there was a clear increase for almost all PAHs, especially Flur, Py, BaP, Bghip.

Polycyclic Aromatic Hydrocarbons↗

PubMed2003

[Main mechanism and affecting factors of phytoremediation of organic contaminated soil].

In this paper, the main mechanisms of phytoremediation of organic contaminated soil, such as adsorption and degradation in rhizosphere, plant uptake, and transformation, and phytoremediation model were illuminated in detail, and their affecting factors, including properties of pollutants, plant species, soil properties, coexisted pollutants, and climate conditions were analyzed. The main topics that need further research were prospected, e.g., deepening the mechanism of phytoremediation, consummating phytoremediation models, approaching on the mechanism and appliance of microbe associated phytoremediation systems, building efficient surfactants enhancing phytoremediation systems, and strengthening the research on phytoremediation of combined organic pollution.

Biodegradation, Environmental↗