Solid state fermentation of olive mill residues by wood- and dung-dwelling Agaricomycetes: Effects on peroxidase production,biomass development and phenol phytotoxicity

The in vivo conversion of dry olive mill residue (DOR) by wood- and dung-dwelling fungi − Auricularia auricula-judae, Bjerkandera adusta and Coprinellus radians − increases peroxidase secretion up to 3.2–3.5-fold (∼1.3, 3.5 and 7.0 U g⁻¹ DOR for dye-decolorizing peroxidase, manganese peroxidase and aromatic peroxygenases, respectively). The incubation of DOR with these fungi produced a sharp decrease in total phenolic content (100% within 4 wk), a reduction in phytotoxicity as well as a certain degree of plant growth caused by the stimulating effect of fungal-treated DOR. These findings correlate with a characteristic shift in the fragmentation pattern of water-soluble aromatics (detected at 280 nm) from low (0.2, 1.5 and 2.2 kDa, respectively) to high molecular mass (35 to >200 kDa), which demonstrates the presence of a polymerization process. Phenol-rich agricultural residues are a useful tool for enzyme expression and production studies of peroxidase-producing Agaricomycetes which could make DOR a valuable organic fertilizer.     

GDX-502对一元酚动态吸附曲线和吸附容量的研究

测定了GDX-502树脂对水中9种一元酚的动态吸附曲线和吸附容量,讨论了可能的吸附机理?实验结果表明,水中各种酚对GDX-502存在着竞争吸附,若水样体积足够大,则水也参与竞争吸附?浓度高的酚,竞争能力强,被吸附容量大?相同浓度的酚,溶解度越小,偶极矩适当大,并能做为电子受体与树脂形成较强的π-键合作用力,则竞争占优势,被吸附容量大?动态吸附曲线上负吸附现象的存在是竞争吸附,特别是水处于优势吸附时的结果      

有机微污染物在污水处理过程中的变化研究

多环芳烃等有毒有机微污染物对污水处理综合指标BOD、COD和TOC等的贡献极小,但危害却很大.采用固相萃取的前处理方法和GC/MS、GC/μECD的分析方法,针对北京市某污水处理厂的总泵进水、二沉出水以及混凝沉淀出水中有机氯农药、多环芳烃和酚类的浓度进行分析.研究结果表明,在不同处理工艺段中,有机氯农药、多环芳烃和酚类的质量浓度分别为nd～10、nd～835、nd～3 248 μg/L.所有检出化合物均未超出中国污水与地表水相应标准限值,其中多环芳烃和酚残留水平较高,应为重点监测对象.这些污染物多数能够在二级处理过程中得到有效去除,但混凝沉淀并没有显著地进一步去除效果.     

Urinary concentrations of phenols, oxidative stress biomarkers and thyroid cancer: Exploring associations and mediation effects

Phenols have been shown to influence the cellular proliferation and function of thyroid in experimental models. However, few human studies have investigated the association between phenol exposure and thyroid cancer, and the underlying mechanisms are also poorly understood. We conducted a case-control study by age- and sex-matching 143 thyroid cancer and 224 controls to investigate the associations between phenol exposures and the risk of thyroid cancer, and further to explore the mediating role of oxidative stress. We found that elevated urinary triclosan (TCS), bisphenol A (BPA) and bisphenol S (BPS) levels were associated with increased risk of thyroid cancer (all P for trends < 0.05), and the adjusted odds ratios (ORs) comparing the extreme exposure groups were 3.52 (95% confidence interval (CI): 2.08, 5.95), 2.06 (95% CI: 1.06, 3.97) and 7.15 (95% CI: 3.12, 16.40), respectively. Positive associations were also observed between urinary TCS, BPA and BPS and three oxidative stress biomarkers measured by 8-hydroxy-2′-deoxyguanosine (8-OHdG), 8-iso-prostaglandin F_2α (8-isoPGF_2α) and 4-hydroxy-2-nonenal-mercapturic acid (HNE-MA), as well as between urinary 8-isoPGF_2α and HNE-MA and the risk of thyroid cancer. Mediation analysis showed that urinary 8-isoPGF_2α mediated 28.95%, 47.06% and 31.08% of the associations between TCS, BPA and BPS exposures and the risk of thyroid cancer, respectively (all P < 0.05). Our results suggest that exposure to TCS, BPA and BPS may be associated with increased risk of thyroid cancer and lipid peroxidation may be an intermediate mechanism. Further studies are warranted to confirm the findings.     

芳香类污染物的厌氧生物降解研究

综述了国内外芳香类污染物厌氧降解的研究进展,详细阐述了含氮芳香类、氯代芳香类和酚类污染物厌氧降解的微生物类群与机理.提出了芳香类污染物生物降解今后发展方向的重点是共基质条件下生物降解性研究、厌氧-好氧条件下的生物降解性研究、高效工程菌和固定化细胞技术应用研究、构建基因工程菌和遗传学研究等技术领域.     

Coupled biodegradation of p-nitrophenol and p-aminophenol in bioelectrochemical system: Mechanism and microbial functional diversity

Biodegradation mechanisms and microbial functional diversity during coupled p-nitrophenol (PNP) and p-aminophenol (PAP) degradation were studied in a bioelectrochemical system. PNP in the biocathode and PAP in the bioanode were almost completely removed within 28hr and 68hr respectively. The degradation followed the steps including hydrating hydroxyalkylation, dehydrogenating carbonylation, and hydrolating ring cleavage, etc. Metagemomic analysis based on the KEGG and eggNOG database annotations revealed the microbial composition and functional genes/enzymes related to phenol degradation in the system. The predominant bacteria genera were Lautropia, Pandoraea, Thiobacillus, Ignavibacterium, Truepera and Hyphomicrobium. The recognized biodegradation genes/enzymes related to pollutant degradation were as follows: pmo, hbd, & ppo for phenol degradation, nzba, amie, & badh for aromatic degradation, and CYP & p450 for xenobiotics degradation, etc. The co-occurrence of ARGs (antibiotic resistant genes), such as adeF, MexJ, ErmF, PDC-93 and Escherichia_coli_mdfA, etc., were annotated in CARD database during the biodegradation process. The Proteobacteria & Actinobacteria phylum was the primary host of both the biodegradation genes & ARGs in this system. The microbial functional diversity ensured the effective biodegradation of the phenol pollutants in the bioelectrochemical system.     

The conversion of chicken manure to biooil by fast pyrolysis II. Analysis of chicken manure,biooils, and char by curie-point pyrolysis-gas chromatography/mass spectrometry (Cp Py-GC/MS)

The initial chicken manure and the three fractions derived from it by fast pyrolysis, that is, the two biooils Fractions I and II as well as the residual char were analyzed by Curie-point pyrolysis-gas chromatography/mass spectrometry (Cp Py-GC/MS). The individual compounds identified were grouped into the following six compound classes: (a) N-heterocyclics; (b) substituted furans; (c) phenol and substituted phenols; (d) benzene and substituted benzenes; (e) carbocyclics; and (f) aliphatics. Of special interest were the relatively high concentrations of N-heterocyclics in biooil Fraction II which was obtained in the highest yield and had the highest calorific value. Prominent N-heterocyclics in biooil Fraction II were methyl-and ethyl-substituted pyrroles, pyridines, pyrimidine, pyrazines, and pteridine. Also noteworthy was the high abundance of aliphatics in biooil Fraction I and the char. The alkanes and alkenes in biooil Fraction I ranged from n-C₇ to n-C₁₈ and C_7:1 to C_18:1, respectively, and those in the char from n-C₇ to n-C₁₉ and C_7:1 to C_19:1, respectively. The N-heterocyclics in the two biooil Fractions came from the chicken manure, from proteinaceous materials during fast pyrolysis or were formed during the fast pyrolysis manure conversion by the Maillard reaction which involved the formation of N-heterocyclics by amino acids interacting with sugars.     

黄河水中细菌对18种酚的降解作用研究

为了掌握酚污染物在黄河水中的生物降解情况,采用苯酚为唯一碳源的液体培养基富集黄河水中的降酚微生物,并研究富集微生物对18种酚的降解作用.结果表明:黄河水中含有降解苯酚的微生物,该微生物属于细菌;降酚细菌对实验用的15种酚均有降解能力,其中对二元酚分解能力较强;但是,对4-氨基苯酚、2,4,6-三氯苯酚、五氯苯酚无分解能力;混合细菌的降酚能力可以代表黄河水体的降酚能力.