Jinshao Ye

Biosorption of chromium from aqueous solution and electroplating wastewater using mixture of Candida lipolytica and dewatered sewage sludge

In this study, the objective was to investigate Cr removal from aqueous solutions, as well as Cr, Cu, Ni and Zn from electroplating wastewaters by the mixture of Candida lipolytica and sewage sludge. The bioreduction ratios of Cr(VI) and the removal ratios of total Cr showed that initial pH, biosorbent dosage and contact time were the important parameters for Cr biosorption. The range of optimal pH for the mixture (1-5) was wider than C. lipolytica (1-4) and sewage sludge (2-4), respectively. Biosorption and bioreduction potentials of living C. lipolytica were better than those of cell wall and cytoplasm. Bonded hydroxyl group, CH(2) asymmetric stretch, amide I, amide II, amide III, secondary amide, pyridine(I)beta(C-H) and pyridine(II)beta(C-H) were detected in the biosorbent and they were the functional groups for binding Cr. The effect of Cu and Zn in combination was significant on the removal of total Cr and the bioreduction of Cr(VI).

Biodegradation of anthracene by Aspergillus fumigatus

An anthracene-degrading strain, identified as Aspergillus fumigatus, showed a favorable ability in degradation of anthracene. The degradation efficiency could be maintained at about 60% after 5d with initial pH of the medium kept between 5 and 7.5, and the optimal temperature of 30 °C. The activity of this strain was not affected significantly by high salinity. Exploration on co-metabolism showed that the highest degradation efficiency was reached at equal concentration of lactose and anthracene. Excessive carbon source would actually hamper the degradation efficiency. Meanwhile, the strain could utilize some aromatic hydrocarbons such as benzene, toluene, phenol etc. as sole source of carbon and energy, indicating its degradation diversity. Experiments on enzymatic degradation indicated that extracellular enzymes secreted by A. fumigatus could metabolize anthracene effectively, in which the lignin peroxidase may be the most important constituent. Analysis of ion chromatography showed that the release of anions of A. fumigatus was not affected by addition of anthracene. GC-MS analysis revealed that the molecular structure of anthracene changed with the action of the microbe, generating a series of intermediate compounds such as phthalic anhydride, anthrone and anthraquinone by ring-cleavage reactions.

Removal of Cr(VI) and Ni(II) from aqueous solution by fused yeast: Study of cations release and biosorption mechanism

Biosorption of Cr(VI) and Ni(II) by a fused yeast from Candida tropicalis and Candida lipolytica under varying range of pH, initial metal concentration and reaction time was investigated. Net cation release and Cr removal reached 2.000 mmol/l and 81.37% when treating 20mg/l Cr(VI) at pH 2 with 25mg/l biomass for 30 min, while for Ni were 0.351 mmol/l and 64.60%, respectively. Trace metal elements such as Co, Cu, Mn, Mo, Se and Zn played active role in biosorption as important ingredients of functional enzymes. Cr(VI) was reduced to less toxic Cr(III) and chelated with extracellular secretions, and further accumulated inside the cells. For Ni biosorption, however, largely a passive uptake process influenced by ion gradient led to lower adsorption capacity and cations release. Fourier transform infrared (FTIR) spectrum analysis indicated that amide and pyridine on cells were involved in binding with Cr, but for Ni, bound-OH and nitro-compounds were the main related functional groups. Scanning electron microscopy (SEM) and atomic force microscopy (AFM) analysis confirmed that considerable amounts of metals precipitated on cell surface when dealing with high concentration metals.

Aerobic biotransformation of decabromodiphenyl ether (PBDE-209) by Pseudomonas aeruginosa

Aerobic biodegradation of decabromodiphenyl ether (PBDE-209) by Pseudomonas aeruginosa under the influence of co-metabolic substrates and heavy metal cadmium ion was studied, The results showed that certain amount of co-metabolic substrates, such as glucose, sucrose, lactose, starch, and beef extract, would promote the biodegradation of PBDE-209, among which glucose most favorably accelerated PBDE-209 degradation by about 36% within 5d. The highest degradation efficiency was reached at the ratio of PBDE-209 and glucose 1:5 while excessive carbon source would actually hamper the degradation efficiency. Exploration of influences of cadmium ion on PBDE-209 biodegradation indicated that degradation efficiency was stimulated at low concentrations of Cd(2+) (0.5-2 mg L(-1)) while inhibited at higher levels (5-10 mg L(-1)), inferring that the heavy metals of different concentrations possessed mixed reactions on PBDE-209 bioremoval. Bromine ion was produced during the biotransformation process and its concentration had a good negative correlation with the residues of PBDE-209. Two nonabromodiphenyl ethers (PBDE-208, PBDE-207), four octabromodiphenyl ethers (PBDE-203, PBDE-202, PBDE-197, PBDE-196) and one heptabromodiphenyl ethers (PBDE-183) were formed with the decomposition of PBDE-209, demonstrating that the main aerobic transformation mechanism of PBDE-209 was debromination.

Influence of co-existed benzo[a]pyrene and copper on the cellular characteristics of Stenotrophomonas maltophilia during biodegradation and transformation.

Microbial remediation has been proposed as a promising technique to remove pollutions, however, its application has been hindered by the lack of understanding the mechanisms involved in contaminants conversion and the influence of pollutants on cellular characteristics. To address this problem, biodegradation and transformation of BaP-Cu(II) by Stenotrophomonas maltophilia, along with interactions of these pollutants with microbial cells through FCM assay were investigated. The results indicated that BaP and Cu(II) were rapidly removed by S. maltophilia on the 1st d, but only less than 10% BaP was broken down due to temporary store in cells, instead of being decomposed immediately. The key ATP enzymes in cells were then activated by BaP to promote bacteria to further decompose BaP. Stimulation of co-existed contaminants strengthened cell membrane permeability and altered cell structure, but a higher esterase activity and DNA in cells of S. maltophilia were still retained.

Biosorption and biodegradation of triphenyltin by Brevibacillus brevis

Triphenyltin (TPT) is an endocrine disruptor highly toxic to non-target organisms, and has contaminated the environment worldwide. To accelerate TPT elimination, the study on the behavior and mechanism of TPT biosorption and biodegradation by Brevibacillus brevis was conducted. The results revealed that TPT and coexisted Cu2+, Cd2+, Pb2+ and Zn2+ in solution could be adsorbed effectively by B. brevis, and TPT was further transformed to diphenyltin, monophenyltin and tin intracellularly. The removal efficiency of 0.5 mg L(-1) TPT after degradation by 0.3 g L(-1) biomass for 5d was about 60%. Suitable kinds and levels of oxygen, nutrient, surfactant and metals obviously improved TPT biodegradation. When concentrations of H2O2, glucose, rhamnolipid, Cu2+ and Zn2+ varied from 1.5 to 6 mmol L(-1), 0.5 to 5 mg L(-1), 5 to 25 mg L(-1), 0.5 to 6 mg L(-1) and 0.5 to 1 mg L(-1), separately, TPT biodegradation efficiencies increased 15-25%.

Effect of cadmium ion on biodegradation of decabromodiphenyl ether (BDE-209) by Pseudomonas aeruginosa

The influence of Cd(II) ions on the degradation of decabromodiphenyl ether (BDE-209) by an aerobic degrading strain, Pseudomonas aeruginosa, was investigated. The results demonstrated that the strain P. aeruginosa exhibited a high level of resistance against cadmium toxicity, and Cd(II) ions of different concentrations possessed mixed reactions on BDE-209 bioremoval. The degradation efficiency was stimulated at low concentrations of Cd(II) ions (≤ 1 mg L(-1)) but inhibited at higher levels (≥ 5 mg L(-1)). Subsequent analyses revealed that the increase of cell hydrophobicity and membrane permeability were two main factors for Cd(II) ions of low concentrations to accelerate BDE-209 degradation. However, inhibition effect by high concentrations of Cd(II) ions was mainly attributed to the negative impact of metals on growth and metabolism of the strain. It was also showed through cellular distribution of BDE-209 that different concentration of Cd(II) ions affected the amount of BDE-209 inside or outside the cell at different incubation time.

Effect of copper(II) on biodegradation of benzo[a]pyrene by Stenotrophomonas maltophilia

Benzo[a]pyrene (BaP) biodegradation by Stenotrophomonas maltophilia was studied under the influence of co-existed Cu(II) ions. About 45% degradation was achieved within 3d when dealing with 1 mg L(-1) BaP under initial natural pH at 30 °C; degradation reached 48% in 2 d at 35 °C. Efficacy of BaP biodegradation reached the highest point at pH 4. In the presence of 10 mg L(-1) Cu(II) ions, the BaP removal ratio was 45% on 7th day, and maintained stable from 7 to 14 d at 30 °C under natural pH. The favorable temperature and pH for BaP removal was 25 °C and 6.0 respectively, when Cu(II) ions coexisted in the solutions. Experiments on cometabolism indicated that S. maltophilia performed best when sucrose was used as an additional carbon source. GC-MS analysis revealed that the five rings of BaP opened, producing compounds with one or two rings which were more bioavailable.

Improvement of chromium biosorption by UV–HNO2 cooperative mutagenesis in Candida utilis

The present study focused on the improvement of chromium resistance and biosorption efficiency in Candida utilis CR-001 utilizing protoplast mutagenesis technology. Through ultraviolet (UV) radiation, HNO(2) treatment and chromium acclimatization, six preferred mutants of C. utilis CR-001 were screened out, namely, CRU132-26, CRC7-2, CRC2811-1, CRC2811-2, CRC2814-8 and CRY182-1. The removal efficiency of these mutants for 20mg/L Cr(VI) solutions were 85.6%, 95.2%, 87.0%, 82.5%, 94.7% and 82.7%, respectively, noticeably greater than that of the parent strain CR-001 (79.5%). Furthermore, CRC2811-1 exhibited outstanding application potential with high removal efficiency and low dosage over a wide range of pH. Cell surface and inner details of CRC2811-1 and its parent strain CR-001 were analyzed by scanning electron microscopy (SEM) and atomic force microscopy (AFM) in order to explore possible changes caused by inducement. The results showed that Cr-sorption of CR-001 mainly depended on intracellular accumulation, but for CRC2811-1, cell surface deposition was also involved in improving its chromium biosorption capacity.

Biosorption and biodegradation of triphenyltin by Stenotrophomonas maltophilia and their influence on cellular metabolism

Triphenyltin (TPT), an endocrine disruptor, is polluting the global environment through its worldwide use. However, information concerning the mechanisms of TPT biodegradation and cellular metabolism is severely limited. Therefore, these processes were elucidated through experiments involving TPT biosorption and degradation, intracellular metabolite analysis, nutrient use, ion and monosaccharide release, cellular membrane permeability and protein concentration quantification. The results verified that TPT was initially adsorbed by the cell surface of Stenotrophomonas maltophilia and was subsequently transported and degraded intracellularly with diphenyltin and monophenyltin production. Cl(-), Na(+), arabinose and glucose release, membrane permeability and the extracellular protein concentration increased during TPT treatment, whereas K(+) and PO4(3-) utilization and intracellular protein concentration declined. The biosorption, degradation and removal efficiencies of TPT at 0.5mgL(-1) by 0.3gL(-1) viable cells at 10 d were 3.8, 77.8 and 86.2%, respectively, and the adsorption efficiency by inactivated cells was 72.6%.