Nutritional Composition of Oven Dried Eggs Produced from Isa-Brown Hens Fed Composite Leaf Meal-Based Diets
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Specialties of the House!
7167 MG_FullMenu_709904 MG_FullMenu 4/1/11 3:20 PM Page 1 EGG SPECIALTIES APPLE PANCAKE DUTCH BABY Peanut Oil is used in many items. Please talk to a manager ARE SERVED WITH 3 BUTTERMILK PANCAKES OR* TOAST. Specialties An Oven-Baked Confection with Granny Smith An Oven-Baked, Light and Delicate, if you have concerns. OR AN AVAILABLE SUBSTITUTE FOR AN EXTRA CHARGE. Apples and a Premium Sinkiang Cinnamon Glaze. BACON AND EGGS of the “German” Pancake. Served with Lemon Three thick sliced bacon and two large fresh eggs, Wedges, Whipped Butter, and Extra Powdered *These items can be prepared served any style. $9.25 10.25 Maple Grove Sugar for a Truly Special Treat. Gluten Free upon request. SAUSAGE AND EGGS House! Additional $1.00 Our special recipe patty sausage and two large fresh eggs, Served with Whipped Cream or served any style. $8.25 Häagen-Dazs Ice Cream 1.50 9.25 LINKS AND EGGS Our special recipe link sausage and two large fresh eggs, served any style. $8.25 HAM AND EGGS A thick slice of honey maple ham and two large fresh eggs, FRUITS & CEREALS served any style. $8.95 YOGURT AND GRANOLA POTATO CANADIAN BACON AND EGGS BLUEBERRY Four slices of Canadian bacon and two large fresh eggs, WITH FRESH FRUIT $8.95 PANCAKES GEORGIA PEANUT BUTTER STRAWBERRY Crisp Potato Cakes BUTTERMILK PANCAKES* THE 2 X 4* SOURDOUGH * * served any style. $9.25 * PECAN PANCAKES* PANCAKES PANCAKES FRESH FRUIT served with your choice PANCAKES Loaded with Blueberries Two Eggs, Four PANCAKES Served with Buttermilk, Strawberries, Served with Whipped Fresh Pecans With that Special HASHBROWNS AND EGGS Strawberries or other Berries. -
Near Infrared Spectroscopy – a Potentially Useful Method for Rapid
European Journal of Clinical Nutrition (2000) 54, 20±23 ß 2000 Macmillan Publishers Ltd. All rights reserved 0954±3007/00 $15.00 www.nature.com/ejcn Near infrared spectroscopy Ð a potentially useful method for rapid determination of fat and protein content in homogenized diets K Almendingen1, HM Meltzer1,2*, JI Pedersen1,3, BN Nilsen4 and M Ellekjñr4 1Institute for Nutrition Research, Faculty of Medicine, University of Oslo, Blindern, Oslo, Norway; 2Department of Environmental Medicine, National Institute of Public Health, Torshov, Oslo, Norway; 3Akershus College, Bekkestua, Norway; and 4Norwegian Food Research Institute, AÊ s, Norway Objective: To investigate the potential of near-infrared re¯ectance (NIR) spectroscopy as a rapid and non- destructive method to determine total fat and protein in mixed, homogenized and freeze-dried human diets. Design: 29 students collected duplicate portions of their diet for four consecutive days. In addition, a detailed food diary was kept. The duplicate portions were analysed for total protein and fat content both by traditional chemical analysis (Kjeldahl and Folch methods) and through the recently developed NIR spectroscopy method. In addition, traditional computerized estimation of nutrient composition was performed. Results: Plotting of the NIR-predicted fat content against the chemically analysed fat content gave a correlation coef®cient of 0.99. Plotting of the NIR-predicted protein content against the Kjeldahl-analysed protein gave a correlation coef®cient of 0.81. Conclusion: NIR-spectroscopy seems to be able to determine fat content in mixed, homogenized diets to a high degree of accuracy. In surveys involving duplicate portion sampling this will save time and money. -
Egg Powder — Specification
DUS 1683 DRAFT UGANDA STANDARD First Edition 2017-mm-dd Egg powder — Specification Reference number DUS 1683: 2017 © UNBS 2017 DUS 1683: 2017 Compliance with this standard does not, of itself confer immunity from legal obligations A Uganda Standard does not purport to include all necessary provisions of a contract. Users are responsible for its correct application © UNBS 2017 All rights reserved. Unless otherwise specified, no part of this publication may be reproduced or utilised in any form or by any means, electronic or mechanical, including photocopying and microfilm, without prior written permission from UNBS. Requests for permission to reproduce this document should be addressed to The Executive Director Uganda National Bureau of Standards P.O. Box 6329 Kampala Uganda Tel: +256 414 333 250/1/2/3 Fax: +256 414 286 123 E-mail: [email protected] Web: www.unbs.go.ug ii © UNBS 2017 – All rights reserved DUS 1683:2017 Contents Page Foreword ............................................................................................................................................................ iv Introduction ......................................................................................................................................................... v 1 Scope ...................................................................................................................................................... 1 2 Normative references ........................................................................................................................... -
Many Modifications of the Kjeldahl Method Have Been Accepted for the Estimation of Protein in Organic Materials
PROTE.01-1 PROTEIN (Kjeldahl) PRINCIPLE Many modifications of the Kjeldahl method have been accepted for the estimation of protein in organic materials. It comprises sample oxidation and conversion of nitrogen to ammonia, which reacts with excess sulfuric acid, forming ammonium sulfate. The solution is made alkaline and the ammonia is determined by distilling into an excess of standard acid, followed by titrating the excess acid. SCOPE The procedure is applicable to the determination of protein nitrogen in corn, corn starches, corn syrups, feedstuffs and steepwater when suitable amounts of sample, sulfuric acid and catalyst are employed. Without additional modification, it is not applicable to the estimation of total nitrogen in the presence of nitrates and nitrites. SAFETY NOTE Person(s) performing this method should be trained in the handling and disposal of concentrated acids and alkalis, with emphasis on preparation of aqueous solutions, and in coping with potential spills. Accordingly, they should wear appropriate protective equipment and prepare samples and solutions under a fume hood. They should also understand the performance limits and exhaust (scrubber) requirements of the Kjeldahl apparatus available to them. Glassware should be carefully inspected for defects before use. Dispose of spent copper and selenium catalyst according to Good Laboratory Practice and existing regulations. SPECIAL APPARATUS Standard Kjeldahl digestion and distillation equipment in conjunction with 800 mL capacity Kjeldahl flasks and suitable connecting bulbs are recommended. Analytical Methods of the Member Companies of the Corn Refiners Association, Inc. PROTE.01-2 PROTEIN continued REAGENTS 1. Sulfuric Acid, Concentrated: Reagent grade (96% H 2SO 4, sp g 1.84) 2. -
Dumas Or Kjeldahl for Reference Analysis? Comparison and Considerations for Nitrogen/Protein Analysis of Food and Feed
A White Paper from FOSS Dumas or Kjeldahl for reference analysis? Comparison and considerations for Nitrogen/Protein analysis of food and feed By: Dr. Jürgen Müller Print: June 2017. GB The Dumas method The Dumas combustion method is an absolute method for the determination of the total Nitrogen content in a usually organic matrix. The sample is combusted at high temperature in an oxygen atmosphere. Via subsequent oxidation and reduction tubes, nitrogen is quantitatively converted to N2. Other volatile combustion products are ei- ther trapped or separated. A Thermal Conductivity Detector measures Nitrogen gas. Results are given as % or mg Nitrogen, which may be converted into protein by using conversion factors (table 1). Table 1 – Nitrogen to Protein conversion factors (examples from ISO 16634-1:2008) Commodity Conversion factor Barley 5,88 Coconut meal 5,30 Oats 5,50 Rice 5,95 Rye 5,83 Sun flower (seed, meal) 5,30 Soy bean (seeds, flour or products) 5,71 Triticale 5,78 Wheat (whole meal, flour or bulgur) 5,83 Wheat (bran) 5,26 According to ISO/TS 16634-2:2009 the generally agreed conversion factor for the product analysed, is equal to 5,7 for wheat, rye and their milled products and 6,25 for all other products falling within the scope of this ISO standard. During the 1990’s the Dumas method gained recognition versus the traditional Kjeldahl method that was the dominating method for Crude Protein analysis for more than 100 years. The Dumas method has the advantage of being easy to use and automated. It is also considerably faster than the Kjeldahl method, taking a few minutes per measurement, as compared to an hour or more for Kjeldahl. -
The Effect of Storage Temperature and Time on the Quality of Spray Dried Egg Powder" (2017)
Louisiana State University LSU Digital Commons LSU Master's Theses Graduate School 2017 The ffecE t of Storage Temperature and Time on The Quality of Spray Dried Egg Powder Fallon Polette Salinas Gonzalez Louisiana State University and Agricultural and Mechanical College Follow this and additional works at: https://digitalcommons.lsu.edu/gradschool_theses Part of the Life Sciences Commons Recommended Citation Salinas Gonzalez, Fallon Polette, "The Effect of Storage Temperature and Time on The Quality of Spray Dried Egg Powder" (2017). LSU Master's Theses. 4583. https://digitalcommons.lsu.edu/gradschool_theses/4583 This Thesis is brought to you for free and open access by the Graduate School at LSU Digital Commons. It has been accepted for inclusion in LSU Master's Theses by an authorized graduate school editor of LSU Digital Commons. For more information, please contact [email protected]. THE EFFECT OF STORAGE TEMPERATURE AND TIME ON THE QUALITY OF SPRAY DRIED EGG POWDER A Thesis Submitted to the Graduate Faculty of the Louisiana State University and Agricultural and Mechanical College in partial fulfillment of the requirements for the degree of Master of Science in The School of Nutrition and Food Sciences by Fallon Polette Salinas Gonzalez B.S., Louisiana State University, 2014 August 2017 ACKNOWLEDGMENTS I would like to express my grateful feelings to everyone who helped me and supported me in a various way during my master’s degree study. First, I would like to thank God for leading me into a career path that I feel passionate about, brings me rewarding feelings and inspires me to never stop improving. -
Application Notes
Application Notes Monitoring pH and Salt During AN #: 07_020_11_001 Market: Food & Dairy Powdered Egg Processing Subcategory: Eggs and Egg Products Product: HI902C, HI4115 Description: Powdered eggs, also known as dried eggs, are fully dehydrated eggs, and are one of the most common products from the poultry industry. The realized value of powdered eggs versus fresh eggs is extensive. Dried eggs are more cost- effective, occupy less storage space, have a reduced weight per volume, and eliminate the need for refrigeration. When stored properly, powdered eggs exhibit a shelf-life of 5 to 10 years; certain products such as freeze-dried eggs exhibit a shelf-life of up to 25 years. There is a wide range of dried egg products, including whole egg pow- der with and without sugar, egg yolk powder, and egg white powder. The process to manufacture egg powder is performed in specialized processing plants. The typical process starts with the breaking of eggs, followed by the separation of albu- men (egg white), yolk, and eggshell. The albumen may be processed independently for the production of egg white powder, in which the albumen liquid undergoes filtration, chilling at approximately 4°C, fermentation to remove glucose, and spray drying before packaging. Fermentation of albumen liquid is necessary as glucose may react with amino acids during the spray drying process, in which a brown color may be produced. Whole egg powder and egg yolk powder are processed by chilling the liquid at approximately 4°C, dry pasteuriz- ing at temperatures around 64 to 70°C for short periods of time to remove bacteria, and subsequently spray drying prior to final packaging. -
Protein Determination by Kjeldahl Method
Protein determination by Kjeldahl method Item Type book_section Authors Lim, Pang Yong Publisher Marine Fisheries Research Department, Southeast Asian Fisheries Development Center Download date 27/09/2021 04:31:09 Link to Item http://hdl.handle.net/1834/40994 PROTEIN DETERMINATION BY KJELDAHL METHOD LIM P.Y. INTRODUCTION In the presence of sulphuric acid and catalyst, the nitrogen atom in the nitrogenous organic compound is converted to ammonium sulphate. The ammonia is then distilled from an alkaline medium and absorbed in boric acid. The ammonia is then determined by titration with a standard mineral acid. Taking protein as an example, it is as follows:- h2so4 Protein N (NH4)2SO4 + CO2 ↑ + H2O Catalyst (NH4)2SO4 + NaOH → Na2SO4 + 2NH4OH NH4OH → NH3 + H2O 3NH3 + H3BO3 → NH4 + BO3 BO3 + 3H+ → H3BO3 I APPARATUS Kjeldahl digestion and assembly (“Tecator” brand) Kjeldahl digestion tube, 250 ml Kjeldahl distillation apparatus (“Tecator” brand) Conical flask 250 ml Automatic burettes 50 ml with 2000 ml reservoir bottle Magnetic stirrer II REAGENTS a) Sulphuric acid (H2SO4), nitrogen free b) Catalyst Mix 9 parts of potassium sulphate (K2SO4) anhydrous, nitrogen free with 1 part of copper sulphate (CuSO4), anhydrous, nitrogen free. c) NaOH solution (40% w/v) Dissolve sodium hydroxide (NaOH), technical grade, mini pearls, in distilled water. d) Boric acid (4% w/v) e) Anti-bumping granules f) Ethanol (95% v/v) g) Standard 0.1N Sulphuric acid Break ampoule for preparation of standard solution, empty content into 1 L volumetric flask and dilute with nitrogen free distilled water until the mark. Cap and invert the volumetric flask until solution well mix. -
The Practitioner's Guide to Delayed Food Sensitivities
The Practitioner’s Guide to Delayed Food Sensitivities Brent L. Dorval, Ph.D. and Marissa Mirenda, M.S. Version: 1.4-04APR17 About the Authors Dr. Dorval has over 25 years of experience in strategic management of research, manufacturing and regulatory affairs in the area of medical devices and diagnostics. Previously, Dr. Dorval held a number of management positions and served as an advisor to the World Health Organization committee on vaccines and diagnostics. Dr. Dorval has several patents covering rapid assays, novel biomarkers and a novel Polio Virus vaccine. Dr. Dorval holds a Ph.D. in Medical Microbiology and Immunology from the College of Medicine, The Ohio State University and performed postdoctoral studies and was a Visiting Scholar in the Department of Chemistry at the Massachusetts Institute of Technology. Marissa Mirenda, M.S. performed her undergraduate studies in Biology and Psychology at Rutgers University and her graduate studies in BioMedical Forensics at Boston University School of Medicine. She currently works at KBMO Diagnostics in Hopedale, Massachusetts performing clinical lab work using the FIT test to study food sensitivities in patients from all over the world. 2 Table of Contents Section Page Introduction to Food Sensitivities 4 Differentiation of Food Allergies, Food Sensitivities and Food Intolerance 4 Comparison of Food Sensitivity, Food Allergies and Food Intolerance (Table) 4 Food Allergies: Type I, Immediate Hypersensitivity 4-5 Food Sensitivities: Types II & III, Delayed Hypersensitivity 5 Food Sensitivities: Food Intolerance 6 The Food Inflammation Test (FIT Test) Format 6 Comparison of the FIT Test with other available Tests 6-7 Interpretation of the FIT Test Results 7 Implementation of the FIT Test Results and Report 7 Elimination, Rotation and Challenge Diets based on the FIT Test Results 7-8 Food Sensitivity Testing of the Eight most common Food Groups using The FIT Test 8 I. -
Many Modifications of the Kjeldahl Method Have Been Accepted for the Estimation of Protein in Organic Materials
Steepwater Analysis J-56-1 PROTEIN PRINCIPLE Many modifications of the Kjeldahl method have been accepted for the estimation of protein in organic materials. It comprises sample oxidation and conversion of nitrogen to ammonia which reacts with excess sulfuric acid, forming ammonium sulfate. The solution is made alkaline and the ammonia is determined by distilling into an excess of standard acid, followed by titrating the excess acid. SCOPE The method applies to the determination of protein nitrogen in steepwater, (Note 1), feedstuffs, syrups, sugars, starches and other protein-bearing materials when suitable amounts of sample, sulfuric acid and catalyst are employed. Without additional modification, it is not applicable to estimation of nitrogen in mixtures containing nitrates and nitrites. SPECIAL APPARATUS Standard Kjeldahl digestion and distillation equipment together with 800 mL Kjeldahl flasks and suitable connecting bulbs are recommended. REAGENTS 1. Sulfuric Acid, Concentrated: Reagent grade (96% H2SO4, sp g 1.84) 2. Potassium Sulfate: Reagent grade potassium sulfate (K2SO4), free from nitrogen 3. Copper Selenite: Reagent grade copper selenite (CuSeO3•2H2O); available from Bodman Chemicals, Media, PA 19063 4. Sodium Hydroxide Solution, 50% 5. Sodium Hydroxide Solution, 0.1 N: Standard Analytical Methods of the Member Companies of the Corn Refiners Association, Inc. Accepted 9-17-76 Revised 9-30-97 Steepwater Analysis J-56-2 PROTEIN ⎯ continued 6. Sulfuric Acid Solution, 0.1 N: Standard 7. Methyl Red-Bromcresol Green Indicator: Dissolve 0.3 g bromcresol green and 0.66 g methyl red dyes in 1 L of 95% ethyl alcohol. Add sufficient 0.1 N sodium hydroxide solution to produce a green color; add dropwise just sufficient 0.1 N hydrochloric acid solution to produce a deep wine-red color. -
PITTCON Conference and Expo 2016
PITTCON Conference and Expo 2016 Abstracts Atlanta, Georgia, USA 6 - 10 March 2016 Volume 1 of 2 ISBN: 978-1-5108-2394-5 Printed from e-media with permission by: Curran Associates, Inc. 57 Morehouse Lane Red Hook, NY 12571 Some format issues inherent in the e-media version may also appear in this print version. Copyright© (2016) by Pittsburgh Conference All rights reserved. Printed by Curran Associates, Inc. (2016) For permission requests, please contact Pittsburgh Conference at the address below. Pittsburgh Conference 300 Penn Center Boulevard Suite 332 Pittsburgh, PA 15235-5503 USA Phone: (412) 825-3220 (800) 825-3221 Fax: (412) 825-3224 [email protected] Additional copies of this publication are available from: Curran Associates, Inc. 57 Morehouse Lane Red Hook, NY 12571 USA Phone: 845-758-0400 Fax: 845-758-2633 Email: [email protected] Web: www.proceedings.com TECHNICAL PROGRAM 3:35 (40-4) Old Photochemistry Brings New Capabilities in Unsaturated Lipid Analysis YU XIA, Purdue University, Zheng Ouyang, Xiaoxiao Ma, Craig Stinson 4:10 (40-5) Evaluating Small Molecule Histone Inhibitors with High Resolution Mass SUNDAY, MARCH 6, 2016 Spectrometry and 3D Cell Cultures AMANDA B HUMMON, University of Notre AFTERNOON Dame, Simone Sidoli, Peter E Feist, Monica M Schroll, Benjamin A Garcia Sunday Afternoon Sunday SYMPOSIUM Session 50 The Wallace H. Coulter Lecture Session 10 Enabling Sample Preconcentration Methods for Bioanalysis The Wallace H. Coulter Lecture arranged by Adam T Woolley, Brigham Young University Sunday Afternoon, Sidney Marcus Auditorium, Bldg A, Level 4 Sunday Afternoon, Room B304 Adam T Woolley, Brigham Young University, Presiding 5:00 (10-1) How Optical Single-Molecule Detection in Solids Led to Super-Resolution Nanoscopy in Cells and Beyond W.E. -
Methods of Protein Analysis and Variation in Protein Results
Methods of Protein Analysis and Variation in Protein Results C. E. McDonald Premiums on high-protein hard red spring wheat has created much interest in the protein test. The Kjeldahl method, a chemical procedure for nitrogen, is still the basic method used for protein analysis. The Kjeldahl method, the Udy dye binding method and the new infrared reflectance method for determining protein are described in this paper. In the analysis of wheat protein by the Kjeldahl method, the moximum amount of variance in results expected between different laboratories and within the same laboratory is larger than the increments of pro tein on which price premiums have been paid. The causes of protein variance and ways of reducing the variance are discussed. In the past year, the price of hard red spring Table I. Basis of Kjeldahl Protein Procedure. wheat has been substantially influenced by the 1. Protein made of amino acid building blocks. protein content. Price premiums have been paid on increased increments of 0.1 percentage points 2. Amino acids made of carbon, hydrogen, oxygen, of protein. The price expected for wheat on the sulfur, nitrogen. basis of protein as determined by a North Dakota laboratory sometimes is changed because the pro 3. Protein calculated from measurement of nitro tein found later at Minneapolis or Duluth differs gen. more than the protein increment required for 4. Per cent nitrogen x 5.7 = per cent crude pro premium. With barley, an unexpected discount tein of wheat. may be applied against the seller because the pro Per cent nitrogen X 6.25 = per cent protein of tein is found to be over the discount protein level other grains.