Environmental assessment of Rhodosporidium toruloides-1588 based oil production using wood hydrolysate and crude glycerol.

Rhodosporidium toruloides, an oleaginous yeast, is a potential feedstock for biodiesel production due to its ability to utilize lignocellulosic biomass-derived hydrolysate with a considerably high lipid titer of 50-70 % w/w. Hence, for the first-time environmental assessment of large-scale R. toruloides-based biodiesel production from wood hydrolysate and crude glycerol was conducted. The global warming potential was observed to be 0.67 kg CO2 eq./MJ along with terrestrial ecotoxicity of 1.37 kg 1,4-DCB eq./MJ and fossil depletion of 0.13 kg oil eq./MJ. The highest impacts for global warming (∼45 %) and fossil depletion (∼37 %) are attributed to the use of chloroform for lipid extraction while fuel consumption for transportation contributed more than 50 % to terrestrial ecotoxicity. Further, sensitivity analysis revealed that maximizing biodiesel yield by increasing lipid yield and solid loading could contribute to reduced environmental impacts. In nutshell, this investigation reveals that environmental impact varies with the type of chemical utilized.

Genetic algorithm-assisted artificial neural network modelling for remediation and recovery of Pb (II) and Cr(VI) by manganese and cobalt spinel ferrite super nanoadsorbent.

MnFe2O4 and CoFe2O4 nanoparticles were hydrothermally synthesized to examine their capability in adsorption of Pb (II) and Cr (VI). The adsorbents exhibited a high rate of adsorption, reaching 90% of their adsorption capacity in less than 30 min. Furthermore, the adsorption capability of the Magnetic Nanoparticles (MNPs) was noticeably greater at initial pollutant concentrations smaller than 40 mg/L. Maximum adsorption capacity on MnFe2O4 and CoFe2O4 nanoparticles were 40 and 25.38 mg/g for Cr (VI) and 523.32 and 476.19 mg/g for Pb (II), respectively. A data-driven model of Artificial Neural Network was used for prediction of adsorption capacity at both equilibrium and non-equilibrium condition. The model parameters including the numbers of neuron (n = 7) and data portioning for training (49.5%), validation (40.5%), and testing (10%) were obtained using Genetic Algorithm. The results indicated that the model could predict the data with high accuracy (R2 = 0.998). The input parameters were initial concentration, time, pH, temperature, adsorbent dosage, and other parameters that is dependent to the physico-chemical properties of ions and adsorbents' surface (ε, α1, α2). The mechanism involved in Cr(VI) and Pb(II) adsorption are electrostatic physisorption and a combination of ion exchange chemisorption and electrostatic physisorption, respectively. Desorption capability and adsorbent reuse capability were also examined.

Extracellular polymeric substances overproduction strategy in Ferroplasma acidiphilum growth for biooxidation of low-grade gold bearing ore: Role of monosaccharides.

The adhesion of microorganisms to surfaces and the affecting factors is important in biomining pretreatment. In this research, the novelty is focused on studying the monosaccharide's impact on the adaptability and adhesivity of Ferroplasma acidiphilum for oxidization of sulfide-bearing ore containing pyrite harboring 98 % of gold in its crystal lattice. d-sucrose increased EPS production with the highest amount of pyrite dissolution (69 %) as compared to the other types of monosaccharides (d-galactose and d-fructose). Addition of 0.8 wt% d-sucrose enhanced the production of ferric ions 65 % for the ore load of 20 wt% while for the addition of 0.4 wt%, the ferric ions concentration was maximum up to 95 %. The results indicated that the addition of both yeast extract and d-sucrose with the concentration of 0.4 wt% enhanced the EPS (Extracellular Polymeric Substances) biovolume fraction from 7.5 to 32.5 v/v %.

A co-fermentation strategy with wood hydrolysate and crude glycerol to enhance the lipid accumulation in Rhodosporidium toruloides-1588.

Wood hydrolysate has been regarded as sustainable and renewable substrate to produce microbial lipids, a potential feedstock for the biodiesel industry. Moreover, the major by-product of biofuel industries is crude glycerol but its implementation as a carbon source is still constrained due to the presence of impurities resulting in low biomass production and low lipid titer. Thus, this study investigates the effect of different carbon ratios of hydrolysate and crude glycerol on R. toruloides-1588. Hydrolysate to crude glycerol ratio of 60:40 resulted in maximum lipid accumulation of 49% (w/w), more than 90% of sugars and glycerol consumption. Further, scale-up to bench-scale fermenter resulted in 12% higher lipid accumulation (56.3% w/w, 0.15 g/L∙h) in 50% less time than flask fermentation. Hence, the ability of R. toruloides-1588 to flourish on different carbohydrates and accumulate high lipid content will be beneficial for the further development of biorefinery industries.

Pilot-scale production and in-situ application of petroleum-degrading enzyme cocktail from Alcanivorax borkumensis.

Petroleum degrading enzymes can be used as an alternative way to improve petroleum bioremediation approaches. Alcanivorax borkumensis is an alkane-degrading bacteria that can produce petroleum degrading enzymes such as alkane hydroxylase and lipase. In this study, pilot-scale Alcanivorax borkumensis fermentation was developed for producing large volumes of petroleum degrading enzymes cocktail (∼900 L). Different process conditions, such as inoculum age 72 h and size 4% v/v, temperature 30 ± 1 °C, agitation speed at 150 rpm and, fermentation period 3 days were determined as the optimum for producing alkane hydroxylase and lipase activity. The oxygen transfer capacity was studied for obtaining better bacterial growth and higher enzyme activities in bioreactor process optimization as well as scale-up. Results showed that the maximum values of oxygen mass transfer coefficient (kLa), oxygen uptake rate (OUR), oxygen transfer rate (OTR), alkane hydroxylase, lipase, and cell count were 196.95 h-1, 0.92 mmol O2/L/h, 1.8 mmol O2/L/h, 222.49 U/mL, 325 U/mL, and 8.6 × 1010 CFU/mL, respectively. Compared with the bench-scale bioreactors, the 150 L fermenter showed a better oxygen transfer rate which affected the cell growth that doubled the number and enzymes production that increased. Then, the enzyme cocktail was used for a field test in a diesel source zone using a 5-spot well pattern. The results showed a significant reduction in concentrations of C10 - C50 (from 36% to > 99%) after one injection of enzyme cocktail, mainly for the contaminated soils located in the saturated zone of the unconfined aquifer. This study confirmed the scaling-up ofalkane-degrading enzyme production to an industrial-scale and its application for effective bioremediation of petroleum contaminated sites.

Antibiotic-metal complexes in wastewaters: fate and treatment trajectory.

Unregulated usage, improper disposal, and leakage from pharmaceutical use and manufacturing sites have led to high detection levels of antibiotic residues in wastewater and surface water. The existing water treatment technologies are insufficient for removing trace antibiotics and these residual antibiotics tend to interact with co-existing metal ions and form antibiotic-metal complexes (AMCs) with altered bioactivity profile and physicochemical properties. Typically, antibiotics, including tetracyclines, fluoroquinolones, and sulphonamides, interact with heavy metals such as Fe2+, Co2+, Cu2+, Ni2+, to form AMCs which are more persistent and toxic than parent compounds. Although many studies have reported antibiotics detection, determination, distribution and risks associated with their environmental persistence, very few investigations are published on understanding the chemistry of these complexes in the wastewater and sludge matrix. This review, therefore, summarizes the structural features of both antibiotics and metals that facilitate complexation in wastewater. Further, this work critically appraises the treatment methods employed for antibiotic removal, individually and combined with metals, highlights the knowledge gaps, and delineates future perspectives for their treatment.

Integrated wood biorefinery: Improvements and tailor-made two-step strategies on hydrolysis techniques.

This study categorized different pretreatment methods into mild (below 120 °C), normal (120-200 °C) and extreme conditions (above 200 °C) for selective approach with efficient wood hydrolysis for direct market applications. The model two-step strategy of selective normal-hydrolysis: steam explosion (170 °C for 30 min) with concentrating normal-hydrolysis: organosolv at (160 °C for 20 min) on hard/softwood will delivery individual fractions of hemicellulose, lignin, and cellulose with recovery rate above 95%. The first step releases C5 sugars with a recovery rate of 80% followed by the second step for C6 sugars with 95% rate and direct use of reduced sugars into C5 and C6 value-added products. The categorized conditions will ease the selection of the pretreatment method for the wood type and model strategy will increase the hydrolysis rate with greater simplicity and validity. The integrated wood biorefinery with two-step treatment is an in-house and closed-loop with endless industrial applications.

Enzymatic reactions in the production of biomethane from organic waste.

Enzymatic reactions refer to organic reactions catalyzed by enzymes. This review aims to enrich the documentation relative to enzymatic reactions occurring during the anaerobic degradation of residual organic substances with emphasis on the structures of organic compounds and reaction mechanisms. This allows to understand the displacement of electrons between electron-rich and electron-poor entities to form new bonds in products. The detailed mechanisms of enzymatic reactions relative to the production of biomethane have not yet been reviewed in the scientific literature. Hence, this review is novel and timely since it discusses the chemical behavior or reactivity of different functional groups, thereby allowing to better understand the enzymatic catalysis in the transformations of residual proteins, carbohydrates, and lipids into biomethane and fertilizers. Such understanding allows to improve the overall biomethanation efficiency in industrial applications.

Ciprofloxacin removal via sequential electro-oxidation and enzymatic oxidation.

The combination of electro-oxidation and enzymatic oxidation was tested to evaluate the potency of this system to remove ciprofloxacin (CIP), a fluoroquinolone antibiotic, from water. For the electro-oxidation boron-doped diamond (BDD) and mixed metal oxides anodes were tested, at three current densities (4.42, 17.7 and 35.4 A/cm2). BDD anode at 35.4 A/cm2 exhibited the highest removal efficiency in the shortest time (>90 % removal in 6 min). For the enzymatic oxidation, laccase from Trametes versicolor was chosen. Laccase alone was not able to remove CIP; hence the influence of redox mediators was investigated. The addition of syringaldehyde (SA) and 2,2'-azino-bis(3-ethylbenzothiazoline-6-sulphonic acid) (ABTS) resulted in enhanced CIP transformation. About 48.9±4.0 % of CIP remained after 4 h of treatment when SA-mediated laccase was applied and 87.8±6.6 % in the case of ABTS-mediated laccase. The coupling of enzymatic oxidation followed by electro-oxidation led to 73 % removal of the antibiotic. Additionally, the antimicrobial activity increased up to its original efficiency after the treatment. The combination of electro-oxidation followed by enzymatic oxidation led to 97-99 % removal of CIP. There was no antimicrobial activity of the solution after the treatment. The tests with wastewater confirmed the efficacy of the system to remove CIP from the complex matrix.

Immobilized laccase on polyimide aerogels for removal of carbamazepine.

Since it is known that conventional wastewater treatment plants cannot completely remove pharmaceutical compounds, such as carbamazepine, the need for their removal has intensified. The use of biocatalysts, such as enzyme is an environmentally friendly method for carbamazepine biodegradation. Nevertheless, enzyme immobilization is required to facilitate the recovery and reusability and avoid the loss of enzyme. In this work, laccase was immobilized on modified polyimide aerogels by means of covalent bonding. Results showed that the immobilized laccase on polyimide aerogels possesses significantly improved activity under acidic or basic pH range in comparison with the free enzyme. Furthermore, for all the temperature range the activity of the immobilized enzyme was higher compared to the free enzyme form. The storage stability improved by the immobilization on this support material. The reusability tests towards oxidation of 2, 2'-azino-bis (3-ethylbenzothiazoline-6-sulphonicacid) (ABTS) showed that the immobilized laccase maintained 22% of the initial activity after 7 cycles. Immobilized laccase on polyimide aerogels for carbamazepine (CBZ) degradation exhibited 76% and 74% removal in spiked water and secondary effluent, respectively. Furthermore, after 7 cycles the CBZ removal efficiency remained higher (50% and 65% for spiked water and secondary effluent, respectively).

Alternatives to antibiotics in poultry feed: molecular perspectives.

The discovery of the growth promoting property of antibiotics led to their use as antibiotic feed additives (AFAs) in animal feed at sub-therapeutic doses. Although this has been beneficial for animal health and productivity, it has been, essentially, a double-edged sword. The continued and non-judicious use of AFAs has led to the selection and dissemination of antibiotic-resistant strains of poultry pathogens such as Salmonella, Campylobacter and Escherichia coli. The rapid spread of drug-resistant pathogens as well as emergence of antibiotic-related environmental pollutants is of global concern. Hence, the identification and development of new and effective alternatives to antibiotics that do not hinder productivity is imperative. For this, it is essential to understand not only the molecular basis of development of resistance to AFAs but also the mechanisms of action of AFA alternatives and how they differ from AFAs. This review provides a molecular perspective on the alternatives to antibiotics that have been proposed till date and their current trends, as well as novel approaches such as development of improved delivery systems.

An insight into the adsorption of diclofenac on different biochars: Mechanisms, surface chemistry, and thermodynamics.

Biochars were prepared from feedstocks pinewood and pig manure. Biochar microparticles obtained through grinding were evaluated for the removal of emerging contaminant diclofenac (DCF) and the underlying mechanism were thoroughly studied. Characterization of biochar was carried out using particle size analyzer, SEM, BET, FT-IR, XRD, XPS and zeta potential instrument. Pig manure biochar (BC-PM) exhibited excellent removal efficiency (99.6%) over pine wood biochar (BC-PW) at 500 µg L-1 of DCF (environmentally significant concentration). Intraparticle diffusion was found to be the major process facilitated the adsorption. BC-PW followed pseudo first-order kinetics whereas BC-PM followed pseudo second-order kinetics. Pine wood biochar was largely affected by pH variations whereas for pig manure biochar, pH effects were minimal owing to its surface functional groups and DCF hydrophobicity. Thermodynamics, presence of co-existing ions, initial adsorbate concentration and particles size played substantial role in adsorption. Various isotherms models were also studied and results are presented.

Biodegradation of polycyclic aromatic hydrocarbons (PAHs) by fungal enzymes: A review.

Polycyclic aromatic hydrocarbons (PAHs) are a large group of chemicals. They represent an important concern due to their widespread distribution in the environment, their resistance to biodegradation, their potential to bioaccumulate and their harmful effects. Several pilot treatments have been implemented to prevent economic consequences and deterioration of soil and water quality. As a promising option, fungal enzymes are regarded as a powerful choice for degradation of PAHs. Phanerochaete chrysosporium, Pleurotus ostreatus and Bjerkandera adusta are most commonly used for the degradation of such compounds due to their production of ligninolytic enzymes such as lignin peroxidase, manganese peroxidase and laccase. The rate of biodegradation depends on many culture conditions, such as temperature, oxygen, accessibility of nutrients and agitated or shallow culture. Moreover, the addition of biosurfactants can strongly modify the enzyme activity. The removal of PAHs is dependent on the ionization potential. The study of the kinetics is not completely comprehended, and it becomes more challenging when fungi are applied for bioremediation. Degradation studies in soil are much more complicated than liquid cultures because of the heterogeneity of soil, thus, many factors should be considered when studying soil bioremediation, such as desorption and bioavailability of PAHs. Different degradation pathways can be suggested. The peroxidases are heme-containing enzymes having common catalytic cycles. One molecule of hydrogen peroxide oxidizes the resting enzyme withdrawing two electrons. Subsequently, the peroxidase is reduced back in two steps of one electron oxidation. Laccases are copper-containing oxidases. They reduce molecular oxygen to water and oxidize phenolic compounds.

Lignin preparation from oil palm empty fruit bunches by sequential acid/alkaline treatment--A biorefinery approach.

Lignin is an important raw material for the sustainable biorefineries and also the forerunner of high-value added products, such as biocomposite for chemical, pharmaceutical and cement industries. Oil palm empty fruit bunches (OPEFB) were used for lignin preparation by successive treatment with 1% (w/w) H2SO4 at 121°C for 60 min and 2.5% NaOH at 121°C for 80 min resulting in the high lignin yield of 28.89%, corresponding to 68.82% of the original lignin. The lignin obtained was characterized by gel permeation chromatography (GPC), Fourier transform infrared spectroscopy (FTIR) and nuclear magnetic resonance (NMR). The results indicated a lignin with molecular masses ramping from 4500 kDa to 12,580 kDa. FTIR and NMR of these lignins showed more syringyl and p-hydroxyphenyl than guaiacyl units. Moderate acid/alkaline treatment provided lignin with high industrial potential and acid hydrolyzates rich in fermentable sugars and highly porous cellulosic fibers.