Effect of sodium dodecyl sulfate on lipase ofCandida lipolytica

The effects of sodium dodecyl sulfate on extracellular lipase produced byCandida lipolytica have been studied. The microorganism was grown in culture medium containing different sodium dodecyl sulfate concentrations added to the culture at different intervals of growth. The extracellular lipase activity was not detected when the treated culture supernatants were directly tested in Yeast Mold Agar-Triolein-Rhodamine plates, regardless of surfactant addition time and concentrations. However, after ammonium sulfate precipitation and dialysis, the extracellular lipase activity could be recovered. Therefore, the surfactant, under the experimental conditions used here, does not seem to be able to inhibit lipase production, but it does inhibit the enzyme activity because of its presence in the mixture of the reaction.     

Bioemulsifier production in batch culture using glucose as carbon source by Candida lipolytica

The yeast Candida lipolytica IA 1055 produced an inducible extracellular emulsification activity while utilizing glucose at different concentrations as carbon source during batch fermentation at 27°C. In all glucose concentrations studied, maximum production of emulsification activity was detected in the stationary phase of growth, after pH reached minimal values. The bioemulsifier isolated was a complex biopolymer constituting proteins, carbohydrates, and lipids. The results obtained in this work show that the biosynthesis of a bioemulsifier is not simply a prerequisite for the degradation of extracellular hydrocarbon.     

Naturally engineered glycolipid biosurfactants leading to distinctive self-assembled structures

Self-assembling properties of "natural" glycolipid biosurfactants, mannosyl-erythritol lipids A and B (MEL-A, MEL-B), which are abundantly produced from yeast strains, were investigated by using the fluorescence-probe method, dynamic light-scattering (DLS) analysis, freeze-fracture transmission electron microscopy (FF-TEM), and synchrotron small/wide-angle X-ray scattering (SAXS/WAXS) analysis, among other methods. Both MEL-A and MEL-B exhibit excellent self-assembly properties at extremely low concentrations; they self-assemble into large unilamellar vesicles (LUV) just above their critical-aggregation concentration (CAC). The CAC(I) value was found to be 4.0x10(-6) M for MEL-A and 6.0x10(-6) M for MEL-B. Moreover, the self-assembled structure of MEL-A above a CAC(II) value of 2.0x10(-5) M was found to drastically change into sponge structures (L3) composed of a network of randomly connected bilayers that are usually obtained from a complicated multicomponent "synthetic" surfactant system. Interestingly, the average water-channel diameter of the sponge structure was 100 nm. This is relatively large compared with those obtained from "synthetic" surfactant systems. In addition, MEL-B, which has a hydroxyl group at the C-4' position on mannose instead of an acetyl group, gives only one CAC; the self-assembled structure of MEL-B seems to gradually move from LUV to multilamellar vesicles (MLV) with lattice constants of 4.4 nm, depending on the concentration. Furthermore, the lyotropic-liquid-crystal-phase observation at high concentrations demonstrates the formation of an inverted hexagonal phase (H2) for MEL-A, together with a lamella phase (L(alpha)) for MEL-B, indicating a difference between MEL-A and MEL-B molecules in the spontaneous curvature of the assemblies. These results clearly show that the difference in spontaneous curvature caused by the single acetyl group on the head group probably decides the direction of self-assembly of glycolipid biosurfactants. The unique and complex molecular structures with several chiral centers that are molecularly engineered by microorganisms must have led to the sophisticated self-assembling properties of the glycolipid biosurfactants.     

Separation of Co(II) from dilute aqueous solutions by precipitate and adsorbing colloid flotation

Ion, precipitate and adsorbing colloid flotation of cobalt(II) have been investigated at different pH values, using N-dodecylpyridinium chloride (DPCl), A strong cationic surfactant, and sodium lauryl sulfate (NaLS), a strong anionic surfactant, as collectors. In case of adsorbing colloid flotation, hydrous manganese dioxide was used as an adsorbent. The precipitate flotation curves experimentally obtained with the two tested collectors were compared with the corresponding theoretical one calculated from the data published for Co(II) hydrolysis. The effects of the collector concentration, ageing of the water-MnO₂–Co(II) system, bubbling time period, cobalt(II) concentration and foreign salts on the percent removal of Co(II) by adsorbing colloid flotation using DPCl as collector were determined. Removals approaching 100% could be achieved under the optimum conditions.     

Efficient synthesis of antifungal pyrimidines via palladium catalyzed Suzuki/Sonogashira cross-coupling reaction from Biginelli 3,4-dihydropyrimidin-2(1H)-ones

An efficient regioselective approach to the synthesis of tetrasubstituted pyrimidines was developed by sequential functionalization of easily available Biginelli 3,4-dihydropyrimidine-2(1H)-ones via dehydrogenation, chlorination followed by palladium catalyzed C–C Suzuki/Sonogashira coupling reaction. All the synthesized compounds were evaluated in vitro for their antifungal activities against Candida albicans, Cryptococcus neoformans, Benjaminiella poitrasii, Yarrowia lipolytica, and Fusarium oxysporum, and antibacterial activities against Gram-negative Escherichia coli and Gram-positive Staphylococcus aureus.     

Removal of radionuclides from acid mine waters by retention on adsorbing materials

Summary This study proposes a method for decontamination of acid drainage water from a uranium mine, as an alternative process to lime treatment. The research embodied the recovery of uranium with an ion-exchange resin, treatment of effluent resin with lime, or with inorganic adsorbents and biosorbents. The uranium decontamination level using the resin process was 94% and allowed the recovery of this element as a commercial product. Among the inorganic adsorbents studied, phosphogypsum was effective for ²²⁶Ra, ²²⁸Ra, and ²¹⁰Pb removal. Among the biosorbents, Sargassum sp.was superior in relation to its specific capacity to accumulate and remove ²²⁶Ra.     

Continuous fermentation for the production of citric acid from glucose

Citric acid is finding new areas of use each year and the demand for the acid is constantly increasing. Being a bulk chemical, the continuous production of citric acid would be advantageous. The paper presents the results from ammonia limited batch and continuous fermentations using the yeast strainSaccharomycopsis (Candida) lipolytica (NRRL Y-7576). Mathematical models were developed for growth and glucose utilization in batch and continuous culture. Cell and acid yields appeared to be almost the same in batch and continuous culture. The specific production rates were found to be constant, equal to 0.053 g/g h, in the batch fermentations but varied in the continuous experiments from 0 to 0.11 g/g h depending on the fermentation conditions. Continuous production in a single stage CSTR was studied for over 1,000 hours without shutdown.     

Biosurfactant production by Bacillus subtilis using cassava-processing effluent

A cassava flour-processing effluent (manipueira) was evaluated as a substrate for surfactant production by two Bacillus subtilis strains. B. subtilis ATCC 21332 reduced the surface tension of the medium to 25.9 mN/m, producing a crude biosurfactant concentration of 2.2 g/L. The wild-type strain, B. subtilis LB5a, reduced the surface tension of the medium to 26.6 mN/m, giving a crude biosurfactant concentration of 3.0 g/L. A decrease in surfactant concentration observed for B. subtilis ATCC 21332 seemed to be related to an increase in protease activity. The biosurfactant produced on cassava effluent medium by B. subtilis LB5a was similar to surfactin.     

Decolorization of textile dye effluent by genetically improved bacterial strains

Synthetic dyes are released into the environment from textile industrial effluents. The discharge of this colored wastewater into rivers and lakes leads to a reduction in sunlight penetration in natural water bodies, which, in turn, decreases both photosynthetic activity and dissolved oxygen concentration and is toxic to living beings. Bacterial isolates are optimized for growth and biomass production before using them for decolorizing dye effluent. The bacterial isolates Bacillus sp. 1 and Bacillus sp. 2 were employed at different percentages by volume with standard nutrient concentration. Of these bacterial isolates Bacillus sp. 2 recorded maximum color reduction. The pH and electrical conductivity (EC) were reduced in the decolorized effluent, and a reduction in biologic oxygen demand, chemical oxygen demand, total suspended solids, and total dissolved solids (TDS) were also observed.     

Adsorption on stainless steel surfaces of biosurfactants produced by gram-negative and gram-positive bacteria: Consequence on the bioadhesive behavior of Listeria monocytogenes

The ability of adsorbed biosurfactants (Pf and Lb) obtained from gram-negative bacterium (Pseudomonas fluorescens) or gram-positive bacterium (Lactobacillus helveticus) to inhibit adhesion of four listerial strains to stainless steel was investigated. These metallic surfaces were characterized using the following complementary analytical techniques: contact-angle measurements (CAM), atomic force microscopy (AFM), polarization modulation-infrared reflection-adsorption spectroscopy (PM-IRRAS) and X-ray photoelectron spectroscopy (XPS). Contact-angles with polar liquids (water and formamide) indicated that the stainless steel surface covered with adsorbed biosurfactant was more hydrophilic and electron-donating than bare stainless steel. The surface characterization by XPS and PM-IRRAS revealed that conditioning the stainless steel changes the substrate in two ways, by modifying the surface alloy composition and by leaving an thin adsorbed organic layer. AFM observations enabled to say that the layer covered entirely the surface and was probably thicker (with patches) in the case of Pf-conditioned surfaces compared to the Lb-conditioned ones, which seemed to be less homogeneous. Though the added layer was thin, significant chemical changes were observed that can account for drastic modifications in the surface adhesive properties. As a matter of fact, adhesion tests showed that both used biosurfactants were effective by decreasing strongly the level of contamination of stainless steel surfaces by the four strains of Listeria monocytogenes. The more important decrease concerned the CIP104794 and CIP103573 strains (>99.7%) on surface conditioned by L. helveticus biosurfactant. A less reduced phenomenon (75.2%) for the CIP103574 strain on stainless steel with absorbed biosurfactant from P. fluorescens was observed. Whatever the strain of L. monocytogenes and the biosurfactant used, this antiadhesive biologic coating reduced both total adhering flora and viable and cultivable adherent bacteria on stainless steel surfaces. This study confirms that biosurfactants constitute an effective strategy to prevent microbial colonization of metallic surfaces by pathogenic bacteria like the food-borne pathogen L. monocytogenes.     

Competitive adsorption of -α-lysophosphatidylcholine/β-lactoglobulin mixtures at the interfaces of foams and foam lamellae

The stability of foams formed with the protein β-lactoglobulin as a function of increasing concentration of the lipid analogue -α-lysophosphatidylcholine were investigated using a microconductivity technique. The drainage, surface diffusion and thickness properties of thin liquid films (foam lamallae) were also studied using optical microscopy including epi-illumination, fluorescence recovery after photobleaching and film interferometry techniques. In addition, the surfactant binding properties of the protein were examined. The addition of small quantities of -α-lysophosphatidylcholine to β-lactoglobulin (molar ratio, R < 7:1) increased the foam stability, whereas a slightly higher concentration of surfactant in the mixture (R = 10) caused foam destabilisation. The explanation of these observations is based on changes in the composition and structure of the adsorbed interfacial layers of the thin films caused by competitive displacement of the protein by the surfactant.     

Lipase‐Catalyzed transformation of Poly(trimethylene carbonate) into Cyclic Monomer,Trimethylene Carbonate: A New Strategy for Sustainable Polymer Recycling Using an Enzyme

The enzymatic degradation and polymerization using an enzyme were carried out with respect to the establishment of a sustainable chemical recycling system for poly(trimethylene carbonate) [P(TMC)] which is a potentially biodegradable synthetic plastic. The enzymatic transformation of P(TMC)s having an M_n of 3000~48000 using Candida antarctica lipase (lipase CA) in acetonitrile at 70 °C afforded the corresponding cyclic monomer, trimethylene carbonate (TMC: 1,3‐dioxan‐2‐one), in a yield of up to 80%. Thus obtained TMC readily polymerized again using both fresh lipase CA and recovered lipase CA.     

Chemical composition and antimicrobial evaluation of the essential oils of Bocageopsis pleiosperma Maas

Essential oils from the leaves, twigs and barks of Bocageopsis pleiosperma Maas were obtained by using hydrodistillation and analysed by using gas chromatography coupled to mass spectrometry. Several compounds (51) were detected and identified, being β-bisabolene the main component in all aerial parts of the plant, with higher concentration in the leaves (55.77%), followed by barks (38.53%) and twigs (34.37%). In order to increase the biological knowledge about the essential oil of Bocageopsis species, antimicrobial activities were evaluated against the microorganisms Escherichia coli, Staphylococcus epidermidis, Enterobacter aerogenes, Candida tropicalis, Candida dubliniensis, Candida glabrata and Candida albicans. The essential oil obtained from the barks exhibited a moderate effect against S. epidermidis ATCC 1228 (MIC = 250 μg/mL), while the other oils did not exhibit antimicrobial activity. These results represent the first report about the chemical composition of B. pleiosperma and the first antimicrobial evaluation with a Bocageopsis species.     

Continuous production of citric acid from raw glycerol by <Emphasis Type="Italic">Yarrowia lipolytica</Emphasis> in cell recycle cultivation

The kinetics of continuous citric acid (CA) fermentation, using two acetate-negative mutants of Yarrowia lipolytica (Wratislavia AWG7 and Wratislavia 1.31) with long-term cell recycle, were investigated at a dilution rate (D) of 0.011 h⁻¹. The capacity of the mutants to produce CA from raw glycerol under steady state conditions was compared. The process involving the Wratislavia AWG7 strain showed that this strain was a better producer of CA than the Wratislavia 1.31 strain in this regime. In steady state, the concentration of CA in the effluent was constant and amounted to 116 g dm⁻³. This corresponded to a volumetric CA production rate of 1.3 g dm⁻³ h⁻¹. A stable high-level production of CA was maintained for over 400 h of operation. The Wratislavia AWG7 strain employed remained highly stable throughout the experiment and demonstrated good viability, high genetic and phenotypic stability over the long-term continuous fermentation process.     

Selective oxidation surface analysis on metals and minerals

Selective Oxidation Surface Analysis (SOSA) studies were made on (a) metal surfaces containing high molecular weight carbonaceous impurities (i.e. greases, oils) and (b) mineral particles containing adsorbed “surfactant collectors”.The principle of the technique consists of heating the sample in a stream of oxygen. The surface carbon species are selectively oxidized over characteristic temperature ranges and the effluent gas fed over a catalyst. The resulting carbon dioxide was continuously analyzed by an I.R. detection system. The method was shown to capable of differentiating and quantifying the various carbonaceous compounds.SOSA could prove useful in the mineral and metallurgical industries.     

A Photocleavable Masked Nuclear‐Receptor Ligand Enables Temporal Control of C. elegans Development

The development and lifespan of C. elegans are controlled by the nuclear hormone receptor DAF‐12, an important model for the vertebrate vitamin D and liver X receptors. As with its mammalian homologues, DAF‐12 function is regulated by bile acid‐like steroidal ligands; however, tools for investigating their biosynthesis and function in vivo are lacking. A flexible synthesis for DAF‐12 ligands and masked ligand derivatives that enable precise temporal control of DAF‐12 function was developed. For ligand masking, photocleavable amides of 5‐methoxy‐N‐methyl‐2‐nitroaniline (MMNA) were introduced. MMNA‐masked ligands are bioavailable and after incorporation into the worm, brief UV irradiation can be used to trigger the expression of DAF‐12 target genes and initiate development from dauer larvae into adults. The in vivo release of DAF‐12 ligands and other small‐molecule signals by using photocleavable MMNA‐masked ligands will enable functional studies with precise spatial and temporal resolution.     

Hydrolysis of Hydrophobic Esters in a Bicontinuous Microemulsion Catalysed by Lipase B from Candida antarctica

Selective enzyme‐catalysed biotransformations offer great potential in organic chemistry. However, special requirements are needed to achieve optimum enzyme activity and stability. A bicontinuous microemulsion is proposed as reaction medium because of its large connected interface between oil and water domains at which a lipase can adsorb and convert substrates in the oil phase of the microemulsion. Herein, a microemulsion consisting of buffer–n‐octane–nonionic surfactant C_iE_j was used to investigate the key factors that determine hydrolyses of p‐nitrophenyl esters catalysed by the lipase B from Candida antarctica (CalB). The highest CalB activity was found around 44 °C in the absence of NaCl and substrates with larger alkyl chains were better hydrolysed than their short‐chained homologues. The CalB activity was determined using two different co‐surfactants, namely the phospholipid 1,2‐dioleoyl‐sn‐glycero‐3‐phosphocholine (DOPC) and the sugar surfactant decyl β‐D ‐glucopyranoside (β‐C₁₀G₁). The results show the CalB activity as linear function of both enzyme and substrate concentration with an enhanced activity when the sugar surfactant is used as co‐surfactant.     

Structure determination of candidine,a violet indolic constituent from culture solutions of Candida lipolytica

A violet indolic constituent, candidine, isolated from culture solutions of Candida lipolytica has been identified as 6,12-dihydro-6-(3-oxoindolid-2-ene)-12-oxoindolo[2,1-b]quinazoline by an independent synthesis (condensation of 6,12-dihydro-6,12-dioxoindolo[2,1-b]quinazoline with 1-acetylindoxyl).     

Enhancement of Paenibacillus sp. D9 Lipopeptide Biosurfactant Production Through the Optimization of Medium Composition and Its Application for Biodegradation of Hydrophobic Pollutants

Interests in biosurfactant in industrial and environmental applications have increased considerably in recent years, owing to their potential benefits over synthetic counterparts. The present study aimed at analyzing the stability and oil removal efficiency of a new lipopeptide biosurfactant produced by Paenibacillus sp. D9 and its feasibility of its use in biotechnological applications. Paenibacillus sp. D9 was evaluated for optimal growth conditions and improved production yield of lipopeptide biosurfactant with variations in different substrate parameters such as carbon (C), nitrogen (N), C:N: ratio, metal supplements, pH, and temperature. Enhanced biosurfactant production was observed when using diesel fuel and ammonium sulfate as carbon and nitrogen source respectively. The maximum biosurfactant yield of 4.11 g/L by Paenibacillus sp. D9 occurred at a C/N ratio of 3:1, at pH 7.0, 30 °C, 4.0 mM MgSO₄, and 1.5% inoculum size. The D9 biosurfactant was found to retain surface-active properties under the extreme conditions such as high thermal, acidic, alkaline, and salt concentration. The ability to emulsify further emphasizes its potential usage in biotechnological application. Additionally, the lipopeptide biosurfactant exhibited good performance in the degradation of highly toxic substances when compared with chemical surfactant, which proposes its probable application in biodegradation, microbial-enhanced oil recovery or bioremediation. Furthermore, the biosurfactants were effective in a test to stimulate the solubilization of hydrophobic pollutants in both liquid environments removing 49.1 to 65.1% diesel fuel including hydrophobic pollutants. The study highlights the usefulness of optimization of culture parameters and their effects on biosurfactant production, high stability, improved desorption, and solubilization of hydrophobic pollutants.

     

Ion and Adsorbing Colloid Flotation of Auramine

Auramine, a cationic dye, was removed from synthetic wastewater by ion flotation of auramine‐sodium lauryl sulfate complex. Over 98% of auramine was removed from the solution in 15 min. A stoichiometric amount of surfactant (1 mol of surfactant to 1 mol of dye) was found to be most effective for auramine removal. The rate of separation and ultimate removal of auramine increased with increasing the rate of air flow and decreased with increasing concentration of NaNO₃. Auramine was also removed by adsorbing colloid flotation technique using ferric hydroxide as the coagulant. Sodium lauryl sulfate was used as the collector, and over 95% of auramine was removed in 10 min. The separation efficiency decreased with increasing ionic strength of the solution. The deleterious effect of neutral salt was compensated somewhat with the aid of aluminum ions as the activator. Both ion flotation and adsorbing colloid flotation are promising approaches for the removal of cationic dye from wastewater.