Antioxidative Effect of Chlorella Pyrenoidosa Protein Hydrolysates and Their Application in Krill Oil-in-Water Emulsions

Chlorella pyrenoidosa is an excellent source of protein, and in this research, we assessed the antioxidant and emulsifying effects of Chlorella protein hydrolysate (CPH) using neutral proteases and alkaline proteases, as well as the properties of CPH-derived krill oil-in-water (O/W) emulsions. The CPHs exhibited the ability to scavenge several kinds of free radicals, including 1,1-diphenyl-2-picrylhydrazyl (DPPH), O₂⁻, hydroxyl, and ABTS. Additionally, the CPHs (5 mg/mL) scavenged approximately 100% of the DPPH and ABTS. The CPHs showed similar emulsifying activities to Tween 20 and excellent foaming activities (max FS 74%), which helped to stabilize the krill oil-in-water emulsion. Less than 10 mg/mL CPHs was able to form fresh krill oil-in-water emulsions; moreover, the CPHs (5 mg/mL) in a krill O/W emulsion were homogenous, opaque, and stable for at least 30 days. Based on their inhibitory effects on the peroxide value (POV) and thiobarbituric acid reactive substances (TRABS), the CPHs were found to be able to inhibit lipid oxidation in both emulsifying systems and krill O/W emulsions. Thus, the CPHs could improve superoxide dismutase (SOD) activities by 5- or 10-fold and decrease the high reactive oxygen species (ROS) level caused by the addition of H₂O₂ in vitro. In conclusion, health-promoting CPHs could be applied in krill oil-in-water emulsions as both emulsifiers and antioxidants, which could help to improve the oxidative and physical stability of emulsions.     

Chemical characterization of barks from Picea abies and Pinus sylvestris after fractioning into different particle sizes

The composition of Norway spruce (Picea abies (L.) Karst.) and Scots pine (Pinus sylvestris L.) barks was studied after grinding and fractioning into different particles sizes.Both barks fractionated well and with similar fraction yield profile. The yield of fines was low and the major fractions were larger particles, i.e. 2.4% and 3.1% of particles under 0.425 mm and 66.0% and 50.3% of particles over 2 mm, respectively for spruce and pine bark.The chemical composition of spruce and pine barks, as a mass weighed average of all granulometric fractions was, respectively: ash 3.3 and 4.6%; total extractives 21.6 and 18.8% (hydrophilic extractives were dominant), lignin 27.9 and 33.7% and holocellulose 42.7 and 37.6%. Suberin accounted for 1.3% and 1.6% of spruce and pine bark, respectively. The non-cellulosic monosaccharides showed in both barks predominance of arabinose followed by xylose and mannose.Ash elemental composition showed that N represented about 35% of the total inorganics, Ca 35% and K 17%. Zn, Cu, Ni, Cr and Pb were present in both barks at levels under 1% of the total inorganics. Spruce bark had in average higher contents compared to pine bark, except for Pb and Cr.Size reduction of spruce and pine bark did not apply randomly to the different components and instead resulted into partial separation of the inorganic and organic matter into different size particles. Fine particles concentrated higher amounts of inorganic material and of extractives.     

Some investigations on the pectin and amino acid composition of Dovyalis caffra W. fruit

Pectin was found in the fruits ofDovyalis caffra W. (3.7%). Acid hydrolysis of the isolated pectin material afforded galacturonic acid (63%), galactose (26.8%), arabinose (2.13%), xylose (1.42%), and rhamnose (0.3%). With sugar and acid, pectin gave a gel of 100-grade. The fruits were shown to contain 15 combined amino acids. Glutamic acid, aspartic acid, and leucine comprised 28.25, 13.56, and 10.60% of the total amino acid content, respectively.     

Conversion of starch from dry common beans (Phaseolus vulgaris L.) to ethanol

Dry common beans (Phaseolus vulgaris L.) were evaluated for potential conversion of starch to ethanol. Eight varieties of beans with average starch content of 46% (db) were assayed in a laboratory-scaled process based upon the commercial corn dry grind fermentation process. Ethanol yield was 0.43-0.51 g ethanol/g glucose (0.19-0.23 g ethanol/g beans). The average ethanol yield for the eight bean types was 92% of maximum theoretical yield, demonstrating that starch from beans could be efficiently converted to ethanol. Ethanol concentration obtained from 20% (w/w) solids loading was 3.5-4.4% (w/v). The residual fermentation solids contained, on a dry basis, 37.1-43.6% crude protein, 10.8-15.1% acid detergent fiber and 19.1-31.3% neutral detergent fiber.     

Chemical composition of oleo-gum-resin from Ferula gummosa

The chemical composition of oleo-gum-resin from Ferula gummosa collected in the northern part of Iran has been studied. The fraction of oleo-gum-resin soluble in ethanol (ca 67 wt.%) is composed by three major fractions: (i) monoterpenes and monoterpenoids (ca 15 wt.% fraction), (ii) sesquiterpenes and sesquiterpenoids (ca 30 wt.%) and (iii) triterpenes and triterpenoids (ca 55 wt.%). The major families of terpenes and terpenoids were identified employing gas chromatography coupled with mass spectrometry detector (GC-MS). Almost 25 wt.% of oleo-gum-resin was insoluble in ethanol and, according to wet chemistry analyses, assigned to arabinogalactane structurally associated with protein complex (AGP). This arabinogalactan possessed the molecular weight of ca 30 kDa, as revealed by size exclusion chromatography, and the main backbone was constituted by β-(1 → 3)/β-(1 → 3,6)-linked d-galactopyranosyl residues ramified predominantly by terminal α-l-arabinofuranosyl and β-d-glucuronopyranosyl residues, as assessed by 1D/2D ¹H NMR.     

超声-微波协同提取百香果皮果胶的工艺研究

以果胶得率为分析指标,采用超声-微波协同提取百香果干果皮果胶,利用响应面分析法优化其工艺条件。结果表明,百香果皮果胶超声-微波协同提取的最佳工艺参数为：液料比30 mL/g,pH 2.0,温度50 ℃,水浴60 min,超声功率50 W、微波功率600 W、超声-微波时间8.0 min,在此条件下,果胶得率可达(12.14±0.06)%。超声-微波协同法的提取效果与单独水提、超声、微波法的相比,得率分别提高了47.33%、34.74%和23.50%,3种提取方法的酯化度均≥50%,其说明百香果皮果胶属于高甲氧基果胶。扫描电镜结果显示,百香果皮细胞壁在超声-微波协同作用下破碎更为彻底,利于果胶溶出。     

Optimization of ethanol production by Saccharomyces cerevisiae UFPEDA 1238 in simultaneous saccharification and fermentation of delignified sugarcane bagasse

Ethanol production by Saccharomyces cerevisiae UFPEDA1238 was performed in simultaneous saccharification and fermentation of delignified sugarcane bagasse. Temperature (32 °C, 37 °C), agitation (80; 100 rpm), enzymatic load (20 FPU/g cellulose and 10%, v/v β-glucosidase or 10 FPU/g cellulose and 5% β-glucosidase) and composition of culture medium were evaluated. Ethanol concentration, enzymatic convertibility of cellulose and volumetric productivity were higher than 25 g/L, 72% and 0.70 g/L h, respectively, after 30 h, when the culture medium 1 and 20 FPU/g cellulose/10%, v/v β-glucosidase or the culture medium 2 and 10 FPU/g cellulose/5% β-glucosidase were used in SSF at 37 °C and 80 rpm. In the SSF with culture medium 2 (supplemented with ammonium, phosphate, potassium and magnesium), 150 L ethanol/t bagasse was achieved, with minimum enzyme loading (10 FPU/g cellulose and 5%, v/v β-glucosidase) for 8%, w/v of solids, which is often an important requirement to provide cost-efficient second generation ethanol processes.     

Antiviral activities of sulfated polysaccharides isolated from Sphaerococcus coronopifolius (Rhodophytha, Gigartinales) and Boergeseniella thuyoides (Rhodophyta, Ceramiales)

Water-soluble sulfated polysaccharides isolated from two red algae Sphaerococcus coronopifolius (Gigartinales, Sphaerococcaceae) and Boergeseniella thuyoides (Ceramiales, Rhodomelaceae) collected on the coast of Morocco inhibited in vitro replication of the Human Immunodeficiency Virus (HIV) at 12.5 μg/mL. In addition, polysaccharides were capable of inhibiting the in vitro replication of Herpes simplex virus type 1 (HSV-1) on Vero cells values of EC₅₀ of 4.1 and 17.2 μg/mL, respectively. The adsorption step of HSV-1 to the host cell seems to be the specific target for polysaccharide action. While for HIV-1, these results suggest a direct inhibitory effect on HIV-1 replication by controlling the appearance of the new generations of virus and potential virucidal effect. The polysaccharides from S. coronopifolius (PSC) and B. thuyoides (PBT) were composed of galactose, 3,6-anhydrogalactose, uronics acids, sulfate in ratios of 33.1, 11.0, 7.7 and 24.0% (w/w) and 25.4, 16.0, 3.2, 7.6% (w/w), respectively.     

Carbohydrate degrading enzyme production by plant pathogenic mycelia and microsclerotia isolates of Macrophomina phaseolina through koji fermentation

The ability of hydrolytic enzyme production by two different isolates of Macrophomina phaseolina was studied on apple pomace as a substrate for solid state fermentation (SSF). Initial moisture level, temperature and fermentation period was optimized so as to achieve higher output. Among the two different isolates, microsclerotial (MphP) and mycelial (MphM), MphP was observed as a potential source of different hydrolytic enzymes as compared to MphM. MphP gave higher enzyme activities (IU/gram dry substrate (gds): filter paper cellulase (FPase) activity 196.21 ± 16.3 (120 h), carboxymethyl cellulase (CMCase) 279.34 ± 28.25 (72 h), β-glucosidase (BGL) 129.82 ± 12.41 (96 h), xylanase 2527.88 ± 46.15 (120 h), and amylase 2780.72 ± 38.13 (96 h), respectively at 70% (v/w) IML. The incubation temperature was also found to have impact on the enzyme production ability of Macrophomina strains. The higher enzyme activities were achieved (IU/gds) as follows FPase 276.13 ± 25.02 (40 °C, 120 h), CMCase 278.11 ± 24.47 (35 °C, 144 h), BGL 189.47 ± 15.05 (30 °C, 144 h), xylanase 3845.77 ± 43.38 (35 °C, 144 h) and amylase activity of 3309.45 ± 29.22 (35 °C, 120 h), respectively using MphP at 70% (v/w) IML. This study reports for the first time the potential of carbohydrate degrading enzyme bioproduction by different isolates of M. phaseolina.     

Optimisation of a solvent for the complete extraction of prolamins from heated foods

Wheat bread was lyophilised, ground, extracted and centrifuged. The supernatants were analysed for gluten content by RP-HPLC and a commercial sandwich ELISA. Prolamin extraction solvents contained tris(2-carboxyethyl)phosphine (TCEP; 1, 2, 5, 10, 20, 50 mmol/L), guanidine hydrochloride (GUA; 0 or 2 mol/L) and a buffered salt solution. A commercial cocktail solution (250 mmol/L mercaptoethanol (ME), 2 mol/L GUA, buffered salt solution) as well as 60% (v/v) ethanol were used as control solvents. Wheat flour was the control for the extractability of the native prolamins. 60% ethanol only extracted 37% of the prolamins from wheat bread (cocktail = 100%). When ME was replaced by TCEP the protein yield increased from 35% at the lowest TCEP-level to 95% when 20–50 mmol/L TCEP were used. The use of GUA was essential to extract prolamins quantitatively. Comparative protein analysis using RP-HPLC and ELISA showed that both methods provided comparable prolamin (gliadin) concentrations of the wheat flour (40.3–45.7 mg/g), when 60% ethanol was used as extraction solvent. The extraction yields from bread were considerably lower (16.7–24.7 mg/g). Cocktail and TCEP extracted almost the same amount of protein from flour and bread with TCEP showing slightly lower yields. Total extractable protein (gliadin + glutenin) as determined by RP-HPLC was 70.5–75.3 mg/g, and total gliadin as determined by ELISA was 42.7–44.2 mg/g. Thus, the study has shown that TCEP in combination with GUA extracts proteins from heated, gluten-containing foods as effective as the commercial cocktail solution.     

Two fraction extraction of α-zein from DDGS and its characterization

Zein was recovered from corn distiller's dried grains with solubles (DDGS) by a modified method using 70% (w/w) aqueous 2-propanol (70-IPA) or 70% (v/v) aqueous ethanol (70-EtOH) solvents, and a commercial method using 88% (w/w) aqueous 2-propanol (88-IPA). Yield, purity, and film properties of the isolated zein were determined. The modified procedure extracted two fractions of zeins: a mostly α-zein fraction, and a mostly γ-zein fraction. The modified method increased α-zein yield from 4% to 14%. Enzyme cellulase pretreatment did not improve zein yield, but grinding did. The α-zein fraction showed electrophoretic bands at 40, 22, 19, and 10 kDa, corresponding to α-zein dimer, α₁-zein, α₂-zein, and δ-zein, respectively. The α-zein of DDGS retained its film forming capability. The α-zein film of unmodified DDGS was cloudy and rough, unlike the clear and smooth films of α-zeins isolated from corn gluten meal and enzyme-treated DDGS.     

菠萝皮果胶的分离纯化及组成分析

以热带水果菠萝皮为原料,采用漂烫灭酶、酸法提取和醇沉工艺提取果胶,对提取果胶的分离纯化和组成进行研究.结果表明:菠萝皮果胶经离子交换层析后分离纯化出1个中性组分,命名为PRP-N,2个酸性组分,命名为PRP-1、PRP-2.比对PRP-1、PRP-2的组成和结构发现,PRP-1的半乳糖醛酸含量较低,中性糖含量较高,单糖成分主要为鼠李糖、半乳糖和阿拉伯糖,以鼠李糖半乳糖醛酸Ⅰ型(RG-Ⅰ)结构为主,侧链主要成分为阿拉伯糖和半乳糖,通过4-O-Rha连接到主链上;PRP-2的半乳糖醛酸含量高,中性糖含量低,以半乳糖醛酸型(HG)和鼠李糖半乳糖醛酸Ⅱ型(RG-Ⅱ)结构为主,含有少量RG-Ⅰ型果胶分子结构.PRP-1比PRP-2的流体力学体积小,且聚合度分布更集中.     

The effects of onion and salt treatments on essential oil content and composition of Rosa damascena Mill

Due to the low oil content of Rosa damascena Mill., on one hand, and the wide spectrum of its application, on the other hand, it is desirable to find ways to increase the oil yield and also its quality. Therefore, in the present study the effects of chopped onion (1.0, 1.5, 2.0 and 4.0 g per 220 g of rose flower) and sodium chloride (11.0, 15.5, 22.0 and 30.0 g per 220 g of rose flower) which were added to rose flowers before distillation, were investigated on the quality and quantity of the oil. The quantity was measured as the ratio of oil to rose flower (w/w, %) and the quality was evaluated using the oil composition especially the content of monoterpene alcohols and hydrocarbons. Compared with corresponding control sample, treating with 1.5 g of chopped onion increased the oil content by 41% but it resulted in a lower quality; whereas in the presence of 1.0 g of onion, an increase of 30% and a decrease of 18% were observed in the percentage of monoterpene alcohols and hydrocarbons, respectively without any considerable change in the oil content. However, the effect of sodium chloride was somehow different from that of onion; such that in the optimal amount (22.0 g), the salt had no considerable effect on the quality but an increase of 21% in the oil yield.     

Potential uses for cuphea oil processing byproducts and processed oils

Cuphea spp. have seeds that contain high levels of medium chain fatty acids and have the potential to be commercially cultivated. In the course of processing and refining cuphea oil a number of byproducts are generated. Developing commercial uses for these byproducts would improve the economics of growing cuphea. Oil fractions and byproducts were obtained from processed seeds of cuphea germplasm line PSR 23 (Cuphea viscosissima × Cuphea lanceolata). We investigated the employment of oil byproducts as growth regulators and solid residues as organic soil amendments on Calabrese broccoli (Brassica oleracea L, family Brassicaceae) seedling growth. Seed processing solid residue fractions, included presscake, bin trash, stem trash and seed trash. These fractions were ground and mixed into soil to obtain concentrations of 0, 0.5, 1, 3, and 10% (w/w). Ground presscake and bin trash could be employed as an organic soil amendment up to 1% without detrimental effects on broccoli. Ground seed meal (seed trash) was detrimental to seedling growth at all concentrations tested. Stem trash employed at 1% caused fresh and dry weights to increase 26.8 and 29.8%, respectively, compared to untreated broccoli seedlings. Stem trash could be employed up to 10% without a detrimental effect on broccoli seedlings. Solvent extraction to remove residual oils from residue fractions was also conducted to generate improved soil amendments. Generally, solvent extraction of seed-processing residue fractions improved the broccoli seedling growth responses. Administration of processed oils and their byproduct fractions as foliar sprays on broccoli seedlings was conducted at rates of 0, 10, 30, and 50 g L⁻¹. Plants were evaluated 72 h after spraying. Refined and crude oils had no effect on broccoli seedlings; gums and soapstock sprays had no effect at 10 or 30 g L⁻¹ concentrations but at 50 g L⁻¹ it killed seedlings. Distilled fatty acid fraction sprays killed broccoli seedlings at all tested concentrations. Certain oil byproduct fractions from cuphea oil processing can be employed as “environmentally-friendly” herbicidal sprays. Calorific evaluation of cuphea ag-wastes were conducted and found to compare well to other biomass energy sources.     

High (1→3,1→4)-β-Glucan Barley Fractions in Bread Making and their Effects on Human Glycemic Response

Barley flour (BF) from whole naked grain and two (1→3,1→4)-β-glucan-enriched fractions, a sieved fraction (SF) and a water-extracted fraction (WF), were produced and mixed with bread wheat flour (BW), for bread-making quality evaluation. Bread was baked in a pilot plant and analysed for sensory properties, proximate composition and (1→3,1→4)-β-glucan content. Four kinds of bread were produced from different mixtures of barley ingredients and bread wheat flour: a 100% BW ((1→3,1→4)-β-glucan content: total, 0·1%; soluble, 0·1%); a 50% BW and 50% BF (2·4%; 2·0%); a 50% BW and 50% SF (4·2%; 2·8%); an 80% BW and 20% WF (6·3%; 5·7%). Eight adults were fed test meals of each of the four breads, containing the same amount (50 g) of available carbohydrate, and glycemic indices calculated from finger-prick capillary blood samples. A linear decrease in glycemic index was found for increasing (1→3,1→4)-β-glucan content. The 20% WF bread had a 28% lower glycemic index than the plain BW and also showed the best scores for sensory attributes. This research confirms the effectiveness of viscous (1→3,1→4)-β-glucan in reducing postprandial blood glucose levels, even in foods with a high glycemic index. The enrichment technique, and water extraction/freeze-drying technique, could enable the use of barley as a source of a high-value fibre for reducing the glycemic index of traditional wheat-based foods such as bread, without negatively affecting their sensory characteristics.     

Changes in phytochemical, antimicrobial and free radical scavenging activities of the Peruvian pepper tree (Schinus molle L.) as influenced by fruit maturation

The effect of stage of maturity on total lipids, fatty acids, yields and essential oil composition and their antimicrobial and free radical scavenging activities of the Schinus molle fruits was investigated. The content of total lipids varied from 2.87 to 5.35% (w/w, dw) and were rich in unsaturated fatty acids particularly linoleic acid. As maturation progress, the essential oil yield dropped from 5.18% to 1.15%. Monoterpene hydrocarbons with α-phellandrene (35.15-40.38%), limonene + β-phellandrene (21.47-36.62%), β-myrcene (7.61-24.96%) and α-pinene (1.92-2.58%) were found to be the main components. At the same time, the essential oils were evaluated for their antimicrobial and free radical scavenging activities. They were found to be active against Bacillus subtilis, Bacillus cereus, Salmonella typhymurium and Escherichia coli but they do not inhibit the growth of Candida albicans. Conversely, they showed very weak activity against the DPPH radical. In both assay, the oil derived from the intermediate stage was reported as more efficient.     

Cotyledon thermal behavior and pectic solubility as related to cooking quality in common beans

The characteristic of proteins, starch and pectic substances in cotyledons of two bean cultivars varying in cooking time were determined to investigate their possible contribution to bean cooking quality. Both cultivars showed the same enthalpies of starch gelatinization but different protein denaturation enthalpies. The proportion of hot water soluble pectins was higher in Michigan, the cultivar with the lower cooking time, than in Ojo de Cabra, the cultivar with the higher cooking time. These results were not due to differences in pectin methylation or in the ratio of monovalent to divalent cations in the tissue, suggesting that in fresh beans the β-elimination reaction is not the sole or predominant route of thermal pectin degradation. Overall, this study indicates that varietal differences in bean cooking quality may be reflections of the rate of pectin loss during soaking/heating and that the thermal properties of starch and protein fractions seem to have a minor contribution. Researchers involved in this study propose that in fresh beans, the thermal pectin loss results from a two step mechanism: pectin enzymic breakdown during the bean soaking followed by thermal solubilization rather than β-elimination during the bean heating.     

Characterization of Cell Wall Polysaccharides of Cherry (<Emphasis Type="Italic">Prunus cerasus</Emphasis> var. Schattenmorelle) Fruit and Pomace

The polysaccharide composition of cell wall of sour cherry (Prunus cerasus var. Schattenmorelle) fruit and pomace was investigated. Furthermore, the alcohol insoluble solids composition of ‘Kelleriis’ and ‘Dobreczyn Botermo’ varieties were studied too. Yield of alcohol insoluble solids for fruits was lower than 10%, and for pomaces circa 50%. Uronic acid was the main pectin component of alcohol insoluble solids. Enzymes used as juice processing aids decreased the content of uronic acid. Araban and galactan side chains bonded tightly to cellulose presence was suggested by high content of arabinose and galactose in hemicellulose fraction. The process of drying at below 70 °C did not influence polysaccharide composition of sour cherry pomaces. Alcohol insoluble solids of fruits expressed higher hydration properties than of pomaces.     

Fresh and ensiled forage plants—total composition,silage losses and the prediction of silage composition from the crop

Twenty ley and whole‐crop samples were analysed before and after ensiling to determine the proportion of dry matter (DM) that could be accounted for by the sum of 12 chemical assays for ash, ash‐excluded‐amylase‐treated neutral detergent fibre (aNDFom), starch, water‐soluble carbohydrates (WSC), pectin, crude protein (CP), CP in aNDFom (CPndf), ammonia, crude fat, phenolics, plant organic acids and liquid fermentation products (acids and alcohols). Crop components, utilized during silage fermentation and the possibility of predicting silage composition from that of the crop, were also investigated. Samples consisted of timothy and red and white clover, harvested at early and late maturities in two cuts per maturity and of whole‐crop barley, wheat and maize, harvested at early, intermediate and late stages of maturity. Ley crops were wilted to reach a DM content of approximately 400 g/kg, whereas whole crops (WC) were not wilted (151–757 g DM/kg) before ensiling. The average sum of analytes was 1022 and 981 g/kg DM for crops and silages respectively. An overall closeness to complete recovery indicates that no major plant components were missing from the analyses. Relative proportions of pectin, plant organic acids and phenolics, which are rarely analysed, were approximately 60:40:2 (w/w). Ash, aNDFom, crude fat and CP were almost completely recovered after ensiling, whereas partial metabolism reduced recoveries of starch (81%), CPndf (62%), plant organic acids (65%), pectin (64%) and WSC (29%). Only the four analytes with high silage recoveries could be reasonably well predicted from parent crop levels with mean prediction error from 0.065 for aNDFom to 0.167 for crude fat.     

Insecticidal formulation based on Xylopia aethiopica essential oil and kaolinite clay for maize protection

Insecticidal formulations based on the essential oil of Xylopia aethiopica (Annonaceae) and kaolinite-clay (particles size less than 50 μm) are efficient in protecting stored grains. Ingestion-contact insecticide tests have been conducted using the maize weevil Sitophilus zeamais (Motsch.) (Curculionidae). Residual action of terpenic constituents adsorbed on clay was assessed. Bioassays indicated that S. zeamais adult mortality increased with the quantity of active ingredient. The formulation based on essential oil and clay produced mortality rates ranging from 22% at 2.5% (w/w) to 100% at 10% (w/w). The lethal concentration producing a 50% mortality rate (LC50) was 4.35% (w/w). Efficacy also depended on storage conditions and duration of the formulation, decreasing from 91 to 37% for formulation stored in closed boxes and from 91 to 17% for formulation stored in open boxes, after 1 and 15 days respectively.