Análise electroforética da farinha de trigo sarraceno em comazaçao com a farinha de trigo suave / Electrophoretic analysis of meal of buckwheat in comparison with common wheat flour

A composiçao das proteínas alcool (prolaminas) obtidas das farinhas de trigo suave por dois procedimentos foram analizadas por el electroforense a pH 3,1 e, após disociaçao, na presença de dodecil sulfato de sódio a pH 8,0. Os perfis obtidos da fracâo prolamina do trigo sarraceno muito diferentes tanto qualitativamente como quantitativamente daqueles da prolamina, do trigo suave. Parece, portanto, provável que ofeitos adversos associados com alimentares contendo gliadina de trigo a pacientes celíacos seriam reduzidos e possivelmente evitados se a farinha de trigo fosse substituida pela farinha de trigo sarraceno

Biological evaluation of protein quality of sorghum as affected by insect infestation

Protein quality of sorghum grains having 25, 50 and 75 percent infestation caused by mixed population of Trogoderma granarium Everts and Rhizopertha dominica Fabricius was biologically evaluated by rat growth and nitrogen balance studies. Feeding of diet containing insect infested sorghum grains (50 and 75 percent) resulted in marked decrease in food intake, protein intake, gain in body weight, food efficiency ratio, protein efficiency ratio, nitrogen consumption, nitrogen absorption, biological value, net protein utilization, dry matter digestibility, net protein retention and protein retention efficiency. These parameters showed negative association with insect infestation levels. However, 25 percent level of grain infestation did not affect these parameters significantly (AU)

Available carbohydrates of cereal grains as affected by storage and insect infestation

Total soluble sugar, reducing sugar, non-reducing sugar and starch contents of wheat, maize and sorghum grains were affected adversely at 25, 50 and 75 percent insect infestation caused by Trogoderma granarium Everts and Rhizopertha dominica Fabricius, separately and mixed population. R. dominica caused significant (P < 0.05) reduction in available carbohydrates at 50 and 75 percent. Mixture of both insect species caused intermediate losses. Storage of cereal grains up to 4 months resulted in substantial increase in sugars and decrease in starch content, but storage for a shorter period of time did not cause any significant changes in levels of carbohydrates (Summary)

Características físicas, tecnológicas y proteícas de frijoles (Phaseolus Vulgaris L.) silvetres y cultivados / Physical, technological and proteinic characteristics of wild and cultivated beans (Phaseolus Vulgaris L.)

El objetivo principal de este trabajo fue el de observar y comparar algunas características físicas, tecnológicas y proteínicas de cuatro cultivares de frijol desarrollados en México, semillas de ocho accesiones silvetres de frijol colectados en México semillas de cuatro accesiones silvestres colectadas en América del Sur, todas ellas pertenecen a la especie Phaseolus vulgaris. El tamaño de la semilla en los materiales Sudamericanos fue muy similar (X = 10.4 g/100 semillas), sin embargo, el porcentaje de absorción de agua fue variable (36.0 - 64.0%), los porcentajes de testa y de sólidos de las aguas de cocción fueron estadísticamente iguales, el rango del contenido de proteína vario de 23.8 a 27.2% (b.s.) En los frijoles silvestres mexicanos se encontraron las semillas más pequeñas (2.8 g/100) semillas) y también en los que el porcentaje de absorción de agua fue muy pequeño, estas dos variables se encuentran correlacionadas (r = 0.83 ); tienen la mayor cantidad de testa y la cantidad de sólidos liberados durante la cocción fue pequeña. El rango del contenido de proteína fue de 21.3 a 24.6% )b.s.). El contenido de lisina fue bajo (X = 0.98%). El material cultivado tuvo las mejores características físicas y tecnológicas, pero el porcentaje promedio de proteína del grupo (X = 22.3%) fue el más bajo, los contenidos de lisina y triptófano fueron de 1.14 y 0.36%, respectivamente. El coeficiente de regresión lineal entre el tiempo de cocción y el porcentaje de semillas cocidas fue diferente entre los miembros de cada grupo. Después de 200 minutos, en el matrial Sudamericano, solamente el 85% de las semillas se había cocido, en tanto que en la accesión silvestre mexicana 153 solamente se cocieron 40%; las accesiones 147, 148, 153 y 175 forman un grupo que es irregular y necesitan un tiempo largo para cocerse; las accesiones 631,882,900 y 939, al igual que los cultivos Bayomex y Negro Puebla necesitaron de 140 minutos para estar 100% cocidos. Jamapa necesitó solamente 100 minutos para estar 100% cocidos

Characterization of glucosylceramide from plasma membranes of plant root cells.

Plasma membranes of oat root cells were isolated from intracellular membranes by subfractionation of the microsomal fraction using an aqueous polymer two-phase system. The plasma membranes originated from oat plants which were acclimated to dehydration by exposure to a repeated water-deficit stress program. Glucosylceramides was a major component of the plasma membrane lipids and amounted to 9% of the lipid of control plants and 5% of the lipid of acclimated plants. Structural analysis using FAB-MS showed only one type of glucosylceramides. The constituent monosaccharide was exclusively glucose and the sphingosine base was 4,8-sphingadienine. The fatty acid composition was determined to 24:1-OH, with only trace levels of non-hydroxy acids. The decrease in the level of glucosylceramides during acclimation to dehydration was accompanied by a corresponding decrease in phospholipids and increase in free sterols.

GroEL-related molecular chaperones are present in the cytosol of oat cells.

In eukaryotic cells GroEL-related molecular chaperones (cpn 60) are considered to be restricted to plastids and mitochondria. Re-evaluation of the intracellular localization of chaperonins by electron microscopy, using two different anti-chaperonin antisera, revealed additionally their presence in the cytosol of oat primary leaf and coleoptile cells. The distribution of cpn 60 is not influenced by heat or light treatments.

Utilisation of pearl millet (Pennisetum typhoides) for egg production.

1. The performance of White Leghorn laying hens on diets providing pearl millet (Pennisetum typhoides) at 300 and 600 g/kg to replace maize, part per part, or "maize mix" isoenergetically and isonitrogenously in the first experiment and at 600 g/kg diet to replace maize in toto, part per part, in the second experiment were examined. In the first experiment, 3 groups of 12 laying hens were placed on each of the 5 dietary treatments for 3 x 28 d, whereas in the second experiment, each of the two diets was offered to 10 groups of 15 laying hens for 6 x 28 d. 2. Inclusion of pearl millet in the diet at the expense of maize, part per part, did not significantly influence hen-day egg production, feed intake, feed efficiency and body weight in either experiment. Incorporation of pearl millet isoenergetically at the expense of "maize mix" at any level, i.e. 300 g or 600 g/kg (Experiment 1), also did not influence hen-day egg production but at the end of periods 2 and 3 did result in decreased feed intakes with consequent improvements in feed efficiency. 3. Egg weight in general showed a tendency to improve with diets providing pearl millet at 600 g/kg. 4. Profits from egg sales over feed cost were directly proportional to the inclusion of pearl millet in the diet either at the expense of maize, part per part, or "maize mix" isoenergetically.

Spectrophotometric method for the determination of paraquat in water, grain and plant materials.

A sensitive spectrophotometric method for the determination of paraquat using ascorbic acid (an easily available reducing agent) is described. Paraquat is reduced with ascorbic acid in alkaline solution to give a blue radical ion with an absorbance maximum at 600 nm. Beer's law is obeyed in the range 12-96 micrograms of paraquat in 10 ml of the final solution (1.2-9.6 ppm). The important analytical parameters and the optimum reaction conditions were evaluated. The method was applied successfully to the determination of paraquat in water, grain and plant materials.

Contents of Fusarium toxins in Finnish and imported grains and feeds.

The aim of the present study was to investigate the levels of trichothecenes in representative samples of Finnish and imported cereals and feeds from the 1987 and 1988 crops. Trichothecene concentrations were determined in samples as trimethylsilylether derivatives by a gas chromatograph equipped with a mass selective detector (GC-MSD) using selected ion monitoring (SIM) which proved to be a reliable and sufficiently sensitive technique. Representative samples of Finnish and imported oats, wheat, barley, rye, maize gluten, soy granules, rapeseed, turnip rapeseed, fish meal, poultry feed and pig feed were analysed employing 19-nortestosterone as an internal standard. Almost all grain and feed samples contained deoxynivalenol (DON) from 7 to 300 micrograms/kg and smaller amounts (13-120 micrograms/kg) of 3-acetyldeoxynivalenol (3-AcDON). The most toxic trichothecenes, T-2, HT-2 toxins and nivalenol (NIV) and also zeralenone (ZEN) were found at low concentrations in some samples. Six lots of oats containing 1.3-2.6 mg/kg of DON and 0.2-0.6 mg/kg of 3-AcDON were found in the Finnish grain samples. Silo samples of almost all imported grains contained DON but at levels below 50 micrograms/kg. Imported grains contained no other trichothecenes. DON, 3-AcDON and ZEN were found in imported feedstuffs at low concentrations.

Immunochemical assessment of mycotoxins in 1989 grain foods: evidence for deoxynivalenol (vomitoxin) contamination.

To assess the potential for mycotoxin contamination of the human food supply following the 1988 U.S. drought, 92 grain food samples were purchased from retail outlets in the summer of 1989 and surveyed for aflatoxin B1, zearalenone, and deoxynivalenol (DON [vomitoxin]) by monoclonal antibody-based competitive enzyme-linked immunosorbent assay (ELISA). Only one sample (buckwheat flour) was found to contain aflatoxin B1 (12 ng/g), whereas zearalenone was found in 26% of the samples at a mean concentration of 19 ng/g. In contrast, the DON ELISA was positive in 50% of the samples at a detection level of 1.0 micrograms/g. Between 63 and 88% of corn cereals, wheat flour/muffin mixes, rice cereals, and corn meal/muffin mixes yielded positive results for DON, whereas 25 to 50% of oat cereals, wheat- and oat-based cookies/crackers, corn chips, popcorn, and mixed-grain cereals were positive for DON. The mean DON content of the positive samples was 4.0 micrograms/g, and the minimum and maximum levels were 1.2 and 19 micrograms/g, respectively. When positive ELISA samples were also analyzed by high-performance liquid chromatography, a strong correlation between the two methods was found. The presence of DON in the two highest samples, corn meal and mixed-grain cereal, which contained 19 and 16 micrograms/g, respectively, was quantitatively confirmed by gas chromatography-mass spectrometry. The results indicated that DON was present in 1989 retail food products at concentrations that exceeded those found in previous market surveys and that have been experimentally associated with impaired animal health.

Estimating human exposure through multiple pathways from air, water, and soil.

This paper describes a set of multipathway, multimedia models for estimating potential human exposure to environmental contaminants. The models link concentrations of an environmental contaminant in air, water, and soil to human exposure through inhalation, ingestion, and dermal-contact routes. The relationship between concentration of a contaminant in an environmental medium and human exposure is determined with pathway exposure factors (PEFs). A PEF is an algebraic expression that incorporates information on human physiology and lifestyle together with models of environmental partitioning and translates a concentration (i.e., mg/m3 in air, mg/liter in water, or mg/kg in soil) into a lifetime-equivalent chronic daily intake (CDI) in mg/kg-day. Human, animal, and environmental data used in calculating PEFs are presented and discussed. Generalized PEFs are derived for air----inhalation, air----ingestion, water----inhalation, water----ingestion, water----dermal uptake, soil----inhalation, soil----ingestion, and soil----dermal uptake pathways. To illustrate the application of the PEF expressions, we apply them to soil-based contamination of multiple environmental media by arsenic, tetrachloroethylene (PCE), and trinitrotoluene (TNT).

[Assay of moniliformin content in household grains from families in patients with Keshan disease].

Ion-pairing extraction and high-performance liquid chromatography (HPLC) were employed for assaying moniliformin (a fungal toxin) content in the corn (Shaanxi) and rice (Yunnan) samples collected from families suffering from Ke-shan disease. The highest contents were found to be 264 micrograms/kg (corn) and 252 micrograms/kg (rice), while a rice sample from Beijing market showed none. The identity of moniliformin was confirmed by 2D-UV detection and co-HPLC with a synthetic toxin sample. These results strongly support the view that moniliformin is a pathogenic factor of Ke-shan disease.

Analysis of triallate residues in cereals and soil by gas chromatography with ion-trap detection.

Triallate residues in barley seedlings and soil samples were determined by gas chromatography with ion-trap detection. Soil was extracted with methanol on a mechanical shaker, and plants were extracted with acetonitrile in a Sorvall homogenizer. After evaporation of the organic solvents, the residue was dissolved in hexane, and plants extracts were cleaned-up on an alumina column. Gas chromatographic analysis was carried out using a BP-1 fused-silica capillary column with helium as carrier gas. To quantitate residues the total-ion chromatogram was obtained and then the selected-ion monitoring chromatograms were displayed at m/z 86 for triallate and at m/z 154 for the internal standard, methyl-(4-amino-2-chloro)-benzoate. The average recovery through the method from barley and soil samples was always higher than 80%. The limit of detection in the selected-ion mode was 0.01 mg/kg. Barley and soil samples treated with triallate were also analysed. A good agreement was observed between results obtained by this method and by gas chromatography with nitrogen-phosphorus detection.

The assessment of radiocaesium intake from food using duplicate diet and whole-body monitoring techniques.

A duplicate diet study has been carried out on a group of Harwell employees in order to investigate the food types in which radiocaesium from Chernobyl was most likely to be found, and also the intake of radiocaesium in food with relation to observed whole-body levels. The duplicate diet study indicated that the highest levels of radiocaesium were in milk and meat or fruit and vegetables. Radiocaesium concentrations in food of all types are small compared to the most restrictive generalized derived limit. Daily intakes of radiocaesium measured by the diet study, of the order of 2-3 Bq day-1, generally agreed with values calculated from whole-body measurements. Committed does from radiocaesium have been estimated from dietary intakes to be in the range 3-29 muSv year-1, while whole-body measurements indicate a range of 6-18 muSv year-1; these doses are small compared to other sources of internal irradiation and to recommended limits.

Determination of phytic acid in cereals using ICP-AES to determine phosphorus.

A novel approach for determination of phytic acid in cereals has been applied in 2 traditional methods. In the first, phytic acid in a sample extract is first separated and concentrated by ion-exchange chromatography. The phytic acid concentrate is then quantitatively determined as phosphorus by inductively coupled plasma atomic emission spectrometry (ICP-AES). In the second method, extracted phytic acid is first precipitated by FeCl3 solution. The complexed iron is converted to ferric hydroxide by adding NaOH, thus releasing phytic acid as soluble sodium phytate. Phytate is then quantitatively determined as phosphorus by ICP-AES. In these methods, both the difficult acid digestion and the spectrometric determination of phosphorus found in traditional methods are eliminated by using ICP-AES. This results in a method that is simpler, faster, and more accurate than earlier procedures.

Improved enzymatic method to measure processing effects and starch availability in sorghum grain.

A modified enzymatic method to measure processing effects and starch availability in steam-flaked sorghum grain (SFSG) was developed. To establish the method, experiments were conducted to determine the required enzyme concentration, color reagents, precipitants, sample particle size, shaking frequency and buffer pH. Glucose release at different incubation times (0 to 48 h) from uncooked (UNC) or fully cooked (CK, 100% gelatinized) ground sorghum grain, a 50:50 mixture of UNC and CK (C50) and SFSG was determined. Glucose release from UNC, CK and SFSG was expressed as one-component equations with rate constant k and r2 of .119 and .98, 1.781 and .98, and .368 and .99, respectively; C50 was characterized by having two starch components, one with a fast rate constant, 2.624/h, and one with a slow rate constant, .066/h (R2 = .99). Different degrees of gelatinization were obtained by mixing different proportions of CK and UNC. Glucose release from these samples was highly correlated with starch gelatinization (r2 = .99). By adjusting the tension between mill rollers, five SFSG samples with bulk densities ranging from 476 to 283 g/liter (37 to 22 lb/bu) were produced; respective roller mill electrical load ranged from 21 to 51.5 amps. Enzymatic determination of glucose release resulted in values of 422, 512, 588, 618 and 678 mg/g, which were more closely related to bulk density than birefringence measurements. The modified method for starch availability determination was found to be relatively simple, fast and sensitive, and is recommended.

Determination of trace amount of cobalt in feed grains and forages by solvent extraction and graphite furnace atomic absorption spectrometry.

A method is described for the determination of trace amounts of cobalt in feed grains and forages with a detection limit of 1 ng g-1. Samples are ashed in a muffle furnace and complexed with 2-nitroso-1-naphthol. Following solvent extraction, cobalt is determined using graphite furnace atomic absorption spectrometry. The assay can be carried out in a normal analytical laboratory without the need for special "clean" rooms. Reagents have been selected to keep reagent blank values at low levels, and heptan-2-one is used as extracting solvent to avoid problems with evaporation. The assay has been used for diagnostic purposes and to formulate special low cobalt diets for sheep for experimental purposes.