1 International Journal of Food Properties ISSN: (Print) (Online) Journal homepage: Characteristics of Microparticulated Particles from Mung Bean Protein Patinya Sirikulchayanont, Siripastr Jayanta, Pasawadee Pradipasena & Osato Miyawaki To cite this article: Patinya Sirikulchayanont, Siripastr Jayanta, Pasawadee Pradipasena & Osato Miyawaki (2007) Characteristics of Microparticulated Particles from Mung Bean Protein, International Journal of Food Properties, 10:3, , DOI: / To link to this article: Copyright Taylor and Francis Group, LLC Published online: 10 Aug Submit your article to this journal Article views: 322 View related articles Citing articles: 6 View citing articles Full Terms & Conditions of access and use can be found at
2 International Journal of Food Properties, 10: , 2007 Copyright Taylor & Francis Group, LLC ISSN: print / online DOI: / CHARACTERISTICS OF MICROPARTICULATED PARTICLES FROM MUNG BEAN PROTEIN Patinya Sirikulchayanont Department of Food Technology, Faculty of Science, Chulalongkorn University, Bangkok, Thailand Siripastr Jayanta Department of Chemistry, Faculty of Science, Chulalongkorn University, Bangkok, Thailand Pasawadee Pradipasena Department of Food Technology, Faculty of Science, Chulalongkorn University, Bangkok, Thailand Osato Miyawaki Department of Food Science, Ishikawa Prefectural University, Nonoichi, Ishikawa, Japan Mung bean protein was separated from wastewater of mung bean starch factory by utilizing an isoelectric precipitation method. The characteristics of freeze dried protein concentrate (having 88.93% protein content on dry basis) were oil absorption capacity, water absorption capacity, surface hydrophobicity and emulsifying activity index of 5.76 g/g, 2.41 g/g, 30, and 83, respectively. The lab scale procedure for production of microparticulated protein particle (MP 3 ) included heating 5% w/w solution of mung bean protein concentrate in deionized water at 83 C for 15 min, coupled with homogenization at 17,000 rpm, homogenization at 23,000 rpm for 15 min, and centrifugation at 1000 g for 10 min. The resulting supernatant produced 0.89 g of μm MP 3 per g of dry mung bean protein concentrate. Observations of MP 3 using SEM showed a particle round shape indicating the potential for MP 3 to provide creamy texture in oil-in-water emulsion foods to serve as a fat replacer. Keywords: Microparticulated protein particles, Protein, Mung bean. INTRODUCTION Microparticulated protein particles, MP 3, are considered as mixtures of both soluble and insoluble protein aggregates to controlled size. [1 2] They can be produced by thermal aggregation and/or chemical (acid or salt) precipitation under high shear conditions. [2 3] MP 3 are regarded as functional ingredients. The potential uses of MP 3 include fat replacer, Received 21 May 2005; accepted 6 October Address correspondence to Pasawadee Pradipasena, Department of Food Technology, Faculty of Science, Chulalongkorn University, Bangkok 10330, Thailand
3 622 SIRIKULCHAYANONT ET AL. texturizer, and stabilizer in food products and controlled release microcapsules in cosmetic, pharmaceutical, and medical applications. [3 4] The main application of MP 3 is a fat replacer. As a food ingredient, fat contributes key sensory and physical benefits such as mouthfeel, taste, creaminess, and appearance.  But high fat intake can increase risk of obesity, heart disease, and some types of cancer.  Also consumers, researchers, and manufacturers are interested in fat replacers having fat-like physical properties that can maintain palatable texture of food. [7 9] Fat replacers should provide less energy than fats and should provide mouthfeel similar to fats. [4,10 12] For fat replacer application, the size of particles has to be small enough that the tongue cannot feel the particles individually, but has the creamy rich texture of fats. [11,13] The critical characteristics of MP 3 to provide creamy mouthfeel were reported to be spherical shape and diameter of μm. [10 12] Most of the protein-based fat replacers or MP 3 were produced from whey protein by heating (at C) and shearing (at 500,000 min 1 ) to obtain spherical MP 3, having diameter of μm.  Starch from mung bean [Vigna radiata (L.) Wilczek] is used as main ingredient for Asian-special texturize noodle (called glass noodle). In Thailand, the high protein content wastewater (1.5% protein) produced from mung bean starch factories was estimated to be about 600 tons/day. Treatment of this wastewater, which is mainly removal of protein, is required prior to disposal. To reduce cost of wastewater treatment and to utilize protein, some factories precipitate protein at ph 4.5 with HCl, centrifuge and (oven or drum) dry. The resulting denatured protein product is used for animal feed. Proteins in mung bean are globular proteins consisting of globulins ( 70%), albumins ( 15 20%), and glutelins. The main globulin is vicilin, which has high content of acidic amino acid but low content of sulphur amino acid. [15 16] Regardless of its low nutritional value, mung bean proteins might be utilized as functional ingredients. While there are numerous studies on utilization of whey protein and soy protein, research on mung bean protein is limited. Unlike soy protein, mung bean protein has bland taste and no smell. Therefore, it can be added into foods without giving undesirable flavor. This research aimed to develop MP 3 from mung bean protein that is a by-product of mung bean starch production. MATERIALS AND METHODS Preparation of Mung Bean Protein Concentrate Mung bean protein concentrate was prepared from precipitant wastewater of mung bean starch factory (Thaiwah Food Products Co. Ltd., Nakorn Pathom, Thailand). The process included precipitation at ph 4.5 with HCl, centrifugation at 20 C and 2000 g for 20 min, washing of protein precipitate with distilled water (1:1 wt ratio) twice, centrifugation at 20 C and 2000 g for 20 min after each washing step, adjusting to ph 7 with 1 N NaOH, centrifugation at 20 C and 1500 g for 30 min, and freeze drying at chamber (or sample holder) pressure and condenser temperature lower than 0.5 Torr and 40 C, respectively. The contents of protein, moisture, fat and ash in this protein concentrate were determined using AOAC Methods , , , and , respectively.  Determination of Protein Functionality ph-solubility profile. Protein concentrate was dissolved in deionized water to obtain 1% w/v solution. The ph of protein solution was adjusted with 1 N HCl or 1 N
4 MICROPARTICULATED PARTICLES FROM MUNG BEAN PROTEIN 623 NaOH to cover the range 2 to 10 and then was centrifuged at 1500 g for 30 min. The content of nitrogen in supernatant was determined by Kjeldahl method.  Nitrogen solubility index was calculated as described by Vojdani.  NSI versus ph was plotted and the isoelectric point of mung bean protein was determined. Oil and water absorption capacity. To determine oil and water absorption capacity, the protein concentrate was mixed with oil (Soy bean oil, Thai Oil Co. Ltd., Nakorn Pathom, Thailand) or distilled water (at the weight ratio of 1 to 20) in a vortex mixer (MS1 Minishaker, IKA-Works, Inc., Wilmington, NC, USA) at 2500 rpm for 1 min. The mixture was allowed to stand at 27 C for 30 min and then was centrifuged at 3000 g for 30 min. The supernatant was weighed and the absorption capacities were calculated. The results were expressed on a dry weight basis. Surface hydrophobicity. Mung bean protein concentrate or bovine serum albumin (Sigma, St. Louis, MO, USA) was dissolved in 0.01 M phosphate buffer ph 7 to cover the concentration range to %w/v. To 4 ml protein solution, 20 μl of 8 mm solution of 1-anilinonapthalene-8-sulfonic acid (Sigma, St. Louis, MO, USA) in 0.1 M phosphate buffer (ph 7.4) was added. The fluorescent intensity of solution was measured by spectrofluorometer (Jasco FP-770, Japan Spectroscopic Co., Ltd., Tokyo, Japan) at excitation and emission wavelengths of 390 and 470 nm, respectively.  Emulsifying activity index. Mung bean protein solution of 0.5% w/v was prepared in 0.1 M phosphate buffer ph 7. It was then mixed with soy bean oil at a volume ratio of 3:1 using homogenizer (Ystral, Ballrechten-Dottingen, Germany) at speed No. 7 [which rpm was determined by digital tachometer (Digicon DT-240P, Digicon, Moorestown, NJ, USA) to be 25,000 rpm] for 2 min. The mixture was diluted 1000 times with 0.1% w/v solution of sodium dodecyl sulfate (Ajax, Auburn, N.S.W., Australia) in distilled water. Absorbency was measured at 500 nm and emulsifying activity index was calculated according to the method of Pearce and Kinsella.  Production of Microparticulated Particles from Mung Bean Protein Mung bean protein concentrate was dissolved in deionized water to obtain concentration of 5% w/w.  CaCl 2 was added to protein solution to cover the range 0 to 0.03 g/g of protein (wet weight basis) in order to enhance aggregation of heat denaturated protein. The protein solution was heated at 83 ± 1 C for 5 to 15 min. The denaturation temperature of mung bean protein concentrate was determined by differential scanning calorimetry to be 83 C. During heating, protein solution was stirred with a homogenizer (Ystral, Ballrechten- Dottingen, Germany) at speed No. 1 (equivalent to 17,000 rpm as determined by digital tachometer). To maximize the process parameters, effects of CaCl 2 concentration and heating time on size of protein aggregates were evaluated. To reduce the size of protein aggregates, suspension of heat denaturated mung bean protein was homogenized at speeds No. 5, 6, 7, and 8 for 5 min. Rpms were determined by digital tachometer to be 23,000, 24,000, 25,000, and 27,000 rpm, respectively. The effect of homogenization time (5 20 min) on MP 3 particle size was determined at 23,000 rpm. To precipitate protein aggregates of size higher than 3 μm, the homogenized suspension was centrifuged at g for 10 min. The effect of centrifugation force on particle size separation was evaluated by determination of size and size distribution of protein aggregates in precipitate and supernatant.
5 624 SIRIKULCHAYANONT ET AL. Characterization of Microparticulated Protein Particles (MP 3 ) Size and size distribution of MP 3 were determined by laser particle size analyzer (Mastersizer, Malvern Instruments Ltd., Malvern, UK). The following process had to be done in order to determined the shape of MP 3. After centrifugation, supernatant was diluted 50 times with distilled water, then filtered through 0.45 μm membrane. The membrane was dried and coated with gold. Two-dimensional micrograph of particles on the membrane was analyzed using Scanning Electron Microscope (JSM-5410LV, JEOL Ltd., Tokyo, Japan). RESULTS AND DISCUSSION Composition and Functionality of Mung Bean Protein Concentrate Prepared mung bean concentrate had a moisture content of 6.38 ± 0.45% (wet weight basis). On dry weight basis, the contents of protein, fat, and ash were ± 0.59%, 0.78 ± 0.78%, and 4.59 ± 0.04%, respectively. From a ph-solubility profile (Figure 1), mung bean concentrate had maximum solubility in term of nitrogen solubility index of 86.5% at ph 10 and ph 4.5 was its isoelectric point. Oil absorption capacity, water absorption capacity, surface hydrophobicity and emulsifying activity index of this protein concentrate were 5.76 g/g, 2.41 g/g, 30 and 83, respectively. Figure 1 Nitrogen solubility index of mung bean protein at various ph.
6 MICROPARTICULATED PARTICLES FROM MUNG BEAN PROTEIN 625 Production of Microparticulated Particles from Mung Bean Protein Protein denaturation and aggregation were induced by heating at 83 C. The purpose of homogenizing at 17,000 rpm was mainly to aid heat transfer within the sample. From particle size analysis, amount of aggregate having size smaller than 0.1 μm was about 1% in every treatment. Since CaCl 2 enhanced protein aggregation, increase in CaCl 2 concentration resulted in higher amount of particles having size larger than 3 μm.  The objective of MP 3 production is to produce an ingredient that could be used as a fat replacer, therefore, the target size was in the range of 0.1 to 3.0 μm to develop creamy mouthfeel in oil-in-water emulsion.  As shown in Figure 2, amount of particles in this size range decreased as CaCl 2 concentration increased. However, the number of particles in this size range increased with heating time while this effect was minimized as CaCl 2 increased. Heating the protein solution without CaCl 2 at 83 C for 15 min gave highest amount of μm particles of ± 16.76% (which that of > 3.0 μm particles was more than 50%). To increase amount of μm particles, homogenization was required to break down particles having size larger than 3.0 μm. The effect of further homogenizing at various rpm (0 27,000) for 5 min is shown in Figure 3. Even though further homogenation of the protein aggregate suspension at 23,000 27,000 rpm did not increase amount of μm particles significantly (p 0.05). But standard error (S.E.) of amount of μm particles was smaller when homogenized at 23,000 and 24,000 rpm. An increase in homogenizing time required to break more particles of size larger than 3.0 μm was studied at 23,000 rpm. The amount of μm particles increased with homogenizing time (Figure 4). Sample containing Figure 2 Effect of CaCl 2 concentration and heating time on amount of particles with diameter of μm. Results are presented as mean ± standard error (SE). Statistical analysis of the data was done by using analysis of variance and Duncans multiple range test. Bars, not sharing even one common letter (a, b, c, and e), are significantly different (p 0.05).
7 626 SIRIKULCHAYANONT ET AL. Figure 3 Effect of speed of hand-operating homogenizer at constant time (5 min) on amount of particles with diameter of μm. Results are presented as mean ± SE. Statistical analysis of the data was done by using analysis of variance and Duncans multiple range test. Bars bearing the letter ns (non-significant) indicate that means are not significantly different (p 0.05). Figure 4 Effect of homogenizing time at constant speed (23,000 rpm) on amount of particles with diameter of μm. Results are presented as mean ± SE. Statistical analysis of the data was done by using analysis of variance and Duncans multiple range test. Bars, not sharing even one common letter (a, b, c and e), are significantly different (p 0.05).
8 MICROPARTICULATED PARTICLES FROM MUNG BEAN PROTEIN 627 about ± 4.24% of this target size particles could be obtained by homogenizing for 15 min while increasing homogenizing time to 20 min did not increase the amount significantly (p 0.05). To precipitate particles larger than 3.0 μm, centrifugation was applied. By centrifugation at 2000 g for 10 min, all of the particles larger than 3.0 μm were in the precipitate, however the amount of μm particles in the supernatant decreased while that in the precipitate increased as centrifugation force increased (Table 1). Centrifugation at 1000 g for 10 min was sufficient for removal of particles larger than 3.0 μm (only about 0.01% of them left in supernatant). Under these conditions, the amount of the target particles was ± 0.40%. The yield of μm particles (in term of gram of μm particles per gram dry mung bean protein concentrate) was determined and illustrated in Table 2. The results showed that the yield in supernatant was 0.89 g/g dry protein when sample was centrifuged at 1000 g for 10 min. Increasing centrifugation force showed a tendency to decrease this yield. The round shape particles, shown in SEM image (Figure 5), indicated that the MP 3 produced from mung bean protein had spherical shape. Mung bean protein microparticulation was done using thermomechanical process. Heat and high shearing force unfolded/denatured protein. [3,24 25] Microparticles were formed by protein-protein interactions. These interactions were hydrogen bonds, van der Waals forces, hydrophobic interactions and disulfide linkages. The ph used in this process Table 1 Effect of centrifugation force on the amount of particle of supernatant and precipitate (centrifugation time=10 min). Amount of particles (%) in Supernatant with diameter Precipitate with diameter Force (x g) < 0.1 μm μm > 3.0 μm < 0.1 μm μm > 3.0 μm ± 0.42D ± 0.40A 0.01 ± 0.01E 0.30 ± 0.06i ± 0.46d ± 0.41e ± 0.39D ± 0.39A 0.00E 0.65 ± 0.18i ± 1.47c ± 1.29f ± 0.48D ± 0.48A 0.00E 1.44 ± 0.09i ± 1.87b ± 1.78g ± 0.15C ± 0.15B 0.00E 1.83 ± 0.31i ± 0.13a 8.03 ± 0.18h Results are presented as mean ± standard deviation (SD). Statistical analysis of the data was done by using analysis of variance and Duncans multiple range test. Numbers, not sharing even one common letter (uppercase for supernatant and lower case for precipitate), are significantly different (p 0.05). Table 2 Effect of centrifugation force on the yield of particle in the range of μm of supernatant and precipitate (centrifugation time=10 min). Yield of particles with diameter μm (g/g protein dry basis) Force (x g) Supernatant Precipitant
9 628 SIRIKULCHAYANONT ET AL. Figure 5 Scanning Electron Micrograph at 7500 times enlargement of μm MP 3 from mung bean protein concentrate. was 7, which was higher than the pi of the protein; therefore, the protein had a net negative charge. It was reported that formation of large particles was promoted by sulfhydryldisulfide interchange reactions at ph > pi. [3,26] However, this interchange reaction might be lower in mung bean protein comparing with whey protein and egg albumin. This might be because of the content of sulfur-containing amino acids in mung bean protein which is lower than those in whey protein and egg albumin.  In the presence of CaCl 2, saltbridges formed between calcium and the negatively charge amino acids, which exposed on the surface at ph 7. These interactions caused large protein aggregates. The microparticulated particles can be produced from proteins (milk, egg and soy) and polysaccharides (starch, dextran, cellulose and gellan gum). [1 3,6,9 13,26 29] They are used as fat replacers. [3,28,30] The most popular one in the market is Simplesse, produced from whey protein. The main function of microparticulated particles is to provide the creamy mouthfeel similar to fats. [1 3,6,10 14,26 30] To provide this sensory property, the required physical characteristics were reported to be spheroidal shape and a mean particle size distribution ranging between μm, with less than 30% of the total number of particles exceeding 5.0 μm in diameter. [10,13,22,29] The characters of MP 3 produced from mung bean protein met the above criteria. Therefore, they had the potential to be used as fat replacers, which provided creamy mouthfeel. They might be used in oil-in-water emulsion, such as low fat salad dressing and sandwich spread. [3,28,30 31] CONCLUSION Spherical shape microparticulated protein particles of μm could be produced from mung bean concentrate. The lab scale procedure included heating of 5% w/w solution of protein concentrate in deionized water at 83 C for 15 min while homogenized at 17,000 rpm, homogenizing at 23,000 rpm for 15 min, and centrifugation at 1000 g for 10 min. The resulting products contained 92% of μm MP 3 with 89% yield. The characteristics of this microparticulated particles produced from mung bean protein indicated that they could be used as fat replacer for oil-in-water emulsion.
10 MICROPARTICULATED PARTICLES FROM MUNG BEAN PROTEIN 629 ACKNOWLEDGMENTS We would like to thank the Ministry of University Affairs Chulalongkorn University Thesis Grant, Chulalongkorn University Graduate School Thesis Grant, TJTTP-JBIG, Chulalongkorn University Budget Funded for Research on Development of Agro-Industry/Food-Industry Project for giving us financial support, the Faculty of Pharmacy for providing the freeze dryer, and Thaiwah Food Products Co., Ltd., for supplying raw materials. REFERENCES 1. Renard, D.; Robert, P.; Faucheron, S.; Sanchez, C. Rheological Properties of Mixed Gels Made of Microparticulated Whey Proteins and β-lactoglobulin. Colloids and Surfaces B: Biointerfaces 1999, 12, Renard, D.; Lavenant, L.; Sanchez, C.; Hemar, Y.; Horne, D. Heat-induced Flocculation of Microparticulated Whey Proteins (MWP); Consequences for Mixed Gels Made of MWP and β-lactoglobulin. Colloids and Surfaces B: Biointerfaces 2002, 24, Sanchez, C.; Paquin, P. Protein and Protein-Polysaccharide Microparticles. In Food Protein and Their Applications; Damodaran, S.; Paraf, A.; Eds.; Marcel Dekker: NY, 1997; Alonso, M.J. Nanoparticulate Drug Carrier Technology. In Microparticulate Systems for the Delivery of Proteins and Vaccines. Drugs and the Pharmaceutical Sciences Vol. 77; Cohen, S.; Bernstein, H.; Eds.; CRC Press: Boca Raton, FL, 1996; Jones, S.A. Issues in Fat Replacement. In Handbook of Fat Replacer; Roller, S.; Jones, S. A.; Eds.; CRC Press: Boca Raton, FL, 1996; Akoh, C. C. Fat Substitute. Food Ingredients and Analysis International 1999, 21 (2), Clark, J.P. Processing. Food Technology 2005, 59 (3), Domagala, J.; Sady, M.; Grega, T.; Bonczar, G. The Influence of Storage Time on Rheological Properties and Texture of Yoghurts with the Addition of Oat-maltodextrin as the Fat Substitute. International Journal of Food Properties 2005, 8, Domagala, J.; Sady, M.; Grega, T.; Bonczar, G. Rheological Properties and Texture of Yoghurts When Oat-maltodextrin is Used as a Fat Substitute. International Journal of Food Properties 2006, 9, Singer, N.S.; Chang, H.-H.; Tang, P.; Dunn, J.M. Carbohydrate Cream Substitute. U.S. Patent 4,911,946, Filed June 24, 1988 and issued March 27, Singer, N.S.; Dunn, J.M. Protein Microparticulation: The Principle and the Process. J. Am. Coll. Nutr. 1990, 9 (4), Singer, N.S. Microparticulated Proteins as Fat Mimetics. In Handbook of Fat Replacer; Roller, S.; Jones, S.A.; Eds.; CRC Press: Boca Raton, FL, 1996; Ziegler, G.R. Process for Producing Microparticulated Protein and the Product thereof. U.S. Patent 5,147,677, Filed August 21, 1990 and issued September 15, Singer, N.S.; Yamamoto, S.; Latella, J. Protein Product Base. U.S. Patent 4,734,287, Filed May 4, 1984 and issued March 29, Evans, R.J.; Bandemer, S.L. Nutritive Value of Legume Seed Proteins. J. Agric. Food Chem. 1967, 15, Poehlman, J.M. The Mungbean; Westview Press: Boulder, CO, Association of Official Analytical Chemists. Official Method of Analysis, 16th ed.; AOAC: Washington, DC, American Oil Chemists Society. Official Methods and Recommended Practices of the American Oil Chemists Society; 3rd ed.; AOCS: Champaign, IL, Vojdani, F. Solubility. In Method of Testing Protein Functionality; Hall, G.H; Ed.; Blackie Academic & Professional: London, 1996,
11 630 SIRIKULCHAYANONT ET AL. 20. Alizadeh-Pasdar, N.; Li-Chan, C.Y. Comparison of Protein Surface Hydrophobicity Measured at Various ph Values Using Three Different Fluorescent Probes. J. Agric. Food Chem. 2000, 48, Pearce, K.N.; Kinsella, J.E. Emulsifying Properties of Proteins: Evaluation of a Turbidimetric Technique. J. Agric. Food Chem. 1978, 26, McCarthy, A.J.; Maegli, J.W. Protein Fat Replacer and Method of Manufacture Thereof. U.S. Patent 5,350,590, Filed December 15, 1992 and issued September 27, Tay, S.L.; Tan, H.Y.; Perera, C. The Coagulating Effects of Cations and Anions on Soy Protein. International Journal of Food Properties 2006, 9, Pradipasena, P.; Rha, C.K. Pseudoplastic and Rheopectic properties of a Globular Protein Solution. J. Texture Stud. 1977, 8, Ker, Y.C.; Toledo, R.T. Influence of Shear Treatments on Consistency and Gelling Properties of Whey Protein Isolate Suspensions. J. Food Sci. 1992, 57 (1), Cheftel, J.C.; Dumay, E. Microcoagulation of Proteins for Development of Creaminess. Food Rev. Int. 1993, 9 (4), Villagran, F.V.; Baughman, J.M. Low Fat Creamer Compositions. U.S. Patent 7,018,668, Filed February 6, 2003 and issued March 28, Akoh, C.C. Fat Replacers. Food Technology 1998, 52 (3), Amankonah, O.J.; Valli, R.C.; Zdanis, D.A. Oil-coated Microparticulated Gellan Gum. U.S. Patent 5,516,543, Filed November 30, 1994 and issued May 14, American Dietetic Association. Position of the American Dietetic Association: Fat Replacers. J. Amer. Dietetic Assoc. 2005, 105 (2), Cheung, I.; Gomes. F.; Ramsden, R.; Roberts, D.G. Evaluation of Fat Replacers Avicel, N Lite S, and Simplesse in Mayonnaise. Int. J. Consumer Studies. 2002, 26,
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CODEX STAN 243-2003 Page 1 of 5 1. SCOPE CODEX STANDARD FOR FERMENTED MILKS CODEX STAN 243-2003 This standard applies to fermented milks, that is Fermented Milk including, Heat Treated Fermented Milks,
Enzymes: Amylase Activity in Starch-degrading Soil Isolates Introduction This week you will continue our theme of industrial microbiologist by characterizing the enzyme activity we selected for (starch
Experiment 8 - Double Displacement Reactions A double displacement reaction involves two ionic compounds that are dissolved in water. In a double displacement reaction, it appears as though the ions are
SUCRALOSE Prepared at the 41st JECFA (1993), published in FNP 52 Add 2 (1993). Metals and arsenic specifications revised at the 63rd JECFA (2004). An ADI of 0-15 mg/kg bw was established at the 37th JECFA
ACUSOL 810A Detergent Grade Rheology Modifier and Stabilizer Description ACUSOL 810A is an Alkali Soluble acrylic polymer Emulsion (ASE). ACUSOL 810A can be directly incorporated into formulations without
Additional Lecture: TITRATION BASICS 1 Definition and Applications Titration is the incremental addition of a reagent solution (called titrant) to the analyte until the reaction is complete Common applications:
FLOCARE 2 About us SNF, a French company with headquarter in Andrézieux, is a leading producer of acrylamide based polymers with manufacturing sites in Andrézieux France, Savannah USA and Taixing China.
Assoc. Prof. Dr. M. Aylin DELİORMANLI EDUCATION Degree University Department / Program Undergrad Ege University Chemical Engineering 99 99 M.S. Izmir Institute of Tech. Materials Science and Engineering
Cat. No. CS-330 Amount 1 Kit For in vitro use only. Quality guaranteed for 3 months. Store at 4 C. Application Screen for thermal stability of proteins as a function of the FUNDAMENTAL variables ph and
Thom Huppertz Principal Scientist, Dairy and Ingredient Technology, NIZO food research Inge Gazi Project Manager, NIZO food research Milk protein concentrate functionality through optimised product-process
Phosphorus, colorimetry, phosphomolybdate, automated-segmented flow Parameter and code: Phosphorus, total-in-bottom-material, dry weight, I-6600-88 (mg/kg as P): 00668 1. Application This method is used
THE SOLUBILITY OF A SALT IN WATER AT VARIOUS TEMPERATURES 2007, 1995, 1991 by David A. Katz. All rights reserved. Permission for academic use provided the original copyright is included. OBJECTIVE To measure
Supporting Information Copyright Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, 2013 A Study of Commercial Nanoparticulate g-al 2 O 3 Catalyst Supports Yahaya Rozita, [a] Rik Brydson,* [a] Tim P. Comyn,
LAB 3: DIGESTION OF ORGANIC MACROMOLECULES INTRODUCTION Enzymes are a special class of proteins that lower the activation energy of biological reactions. These biological catalysts change the rate of chemical
Proc. Estonian Acad. Sci. Chem., 26, 55, 2, 78 84 Preparation of chitosan powder and investigation of its properties Marianna Laka * and Svetlana Chernyavskaya Latvian State Institute of Wood Chemistry,
FluoroTag FITC Conjugation Kit Product Number FITC1 Storage Temperature 2 8 C TECHNICAL BULLETIN Product Description The FluoroTag FITC Conjugation Kit is suitable for the conjugation of polyclonal and
Chapter 3 Formulas, Equations and Moles Interpreting Chemical Equations You can interpret a balanced chemical equation in many ways. On a microscopic level, two molecules of H 2 react with one molecule
ELIANE The New Waxy Potato Starch of AVEBE Detmold, 2006 Contents Introduction to ELIANE Characteristics of ELIANE, differences with other starches ELIANE in several food applications 2 What is ELIANE?
International Journal of Engineering Inventions ISSN: 2278-7461, www.ijeijournal.com Volume 1, Issue 7 (October2012) PP: 44-50 REMOVAL OF PHOSPHATE FROM WASTEWATER USING LOW-COST ADSORBENTS Dr. C.R.Ramakrishnaiah
Chapter 2 The Chemistry of Life Worksheets (Opening image courtesy of David Iberri, http://en.wikipedia.org/wiki/file:camkii.png, and under the Creative Commons license CC-BY-SA 3.0.) Lesson 2.1: Matter
Zein is a major component of corn proteins, called a prolamine soluble in aqueous ethanol. Zein is extracted from gluten meal separated under corn starch production. The acquisition of deodorized and decolourised
ACUSOL 805S HASE Rheology Modifier and Stabilizer for High Surfactant Containing Detergent or Cleaner Formulations Description ACUSOL 805S rheology modifier is a synthetic hydrophobically-modified acrylic
Standard Operating Procedure (SOP) Title: Direct Fluorescent Antibody Test (DFAT) for the detection of Renibacterium salmoninarum in tissues Number: BACT-3 Version: 02 Created December 14, 2011 Approval:
Spectroscopic Characterization of Cytochrome C Entrapped in AOT Reverse Micelles Kristen Grinstead Chemistry Department Marshall University One John Marshall Drive Huntington, WV 25755 email@example.com
Proteins Functionality & Application Anneke Martin Content Functionality Techno-functionality of proteins Interfacial properties Gelation properties Type of protein networks Water holding Texturizing of
Assessment Chapter Test A Elements, Compounds, and Mixtures MULTIPLE CHOICE Write the letter of the correct answer in the space provided. 1. What is a pure substance made of two or more elements that are
PET Recycling Nicholas Robusto Maggie Ifarraguerri Nathaniel Lawton Isabel Hefner OBJECTIVES Hydrolyze a sample of Polyethylene Terephthalate (PET) obtained from used soda bottles, and synthesize a dimer
Experiment 3 Separation by Solvent Extraction Objectives To separate a mixture consisting of a carboxylic acid and a neutral compound by using solvent extraction techniques. Introduction Frequently, organic
Working With Enzymes a world of learning Presented by Peter J Ball, Southern Biological. For further information, please contact the author by phone (03) 9877-4597 or by email firstname.lastname@example.org.
Conduct A Qualitative Test For Starch, Fat, A Reducing Sugar, A Protein Biology Leaving Cert Experiments Materials/Equipment Starch solution (1%) Iodine Solution Glucose Solution (1%) 100 C) Benedict s
CHEMICAL PRECIPITATION: WATER SOFTENING Submitted to: Dr. Hashsham Research Complex Engineering Department of Civil and Environmental Engineering Michigan State University East Lansing, MI 4884 Authors
Determination of calcium by Standardized EDTA Solution Introduction The classic method of determining calcium and other suitable cations is titration with a standardized solution of ethylenediaminetetraacetic
Experiment #10: Liquids, Liquid Mixtures and Solutions Objectives: This experiment is a broad survey of the physical properties of liquids. We will investigate solvent/solute mixtures. We will study and
LIFE SCIENCE I TECHNICAL BULLETIN ISSUE N 11 /JULY 2008 PARTICLE CHARACTERISATION IN EXCIPIENTS, DRUG PRODUCTS AND DRUG SUBSTANCES AUTHOR: HILDEGARD BRÜMMER, PhD, CUSTOMER SERVICE MANAGER, SGS LIFE SCIENCE