Source: OKLAHOMA STATE UNIVERSITY submitted to NRP
MEAT AND DAIRY BY-PRODUCT PROTEIN RECOVERY AND UTILIZATION
Sponsoring Institution
National Institute of Food and Agriculture
Project Status
COMPLETE
Funding Source
Reporting Frequency
Annual
Accession No.
0185357
Grant No.
(N/A)
Cumulative Award Amt.
(N/A)
Proposal No.
(N/A)
Multistate No.
(N/A)
Project Start Date
Oct 1, 2000
Project End Date
Sep 30, 2004
Grant Year
(N/A)
Program Code
[(N/A)]- (N/A)
Recipient Organization
OKLAHOMA STATE UNIVERSITY
(N/A)
STILLWATER,OK 74078
Performing Department
ANIMAL SCIENCE
Non Technical Summary
Both the meat and dairy industries produce by-products whose full utilization and potential is, to date, still unrealized. The purpose of this study is to determine if an alternative protein recovery process can enhance the functionality and stability of underutilized, low valued by-products from the meat and dairy industries.
Animal Health Component
70%
Research Effort Categories
Basic
30%
Applied
70%
Developmental
(N/A)
Classification

Knowledge Area (KA)Subject of Investigation (SOI)Field of Science (FOS)Percent
4033320102030%
4033520102020%
5013320102030%
5013520102020%
Goals / Objectives
The primary objective of this study is to determine if a novel process involving manipulations of pH and ionic strength for the recovery of protein in the surimi seafood industry can be successfully applied to improve the functionality and stability of a surimi-like product from traditionally low valued beef and pork by-products (i.e. heart muscle and mechanically separated meat-MSM). It will involve optimization of the new seafood protein recovery process for use on meat by-products. Once optimization parameters are established physical, chemical, and functional properties from product produced using the new method will be compared to product produced by the traditional surimi process. In addition, storage stability of recovered by-product protein will be compared to skeletal protein. The secondary objective of this study is to determine if the principles used for the recovery of a functional protein from meat by-product can be applied to recover and improve the functionality of acid whey.
Project Methods
In order to optimize the new recovery process pH-solubility profiles will first be collected on bovine and swine cardiac muscle and MSM. This will involve adjusting acidity, followed by centrifugation, and determination of soluble protein in the supernatant. For meat, data will be collected on pre-rigor and post-rigor samples. Once solubility profiles are established, they can be used to optimize the various steps involved in the production of surimi-like material using the new process. Soluble protein will be used to measure protein recovery at each stage of the process. SDS-PAGE will be utilized to determine changes in the protein profile. To determine the effect the process has on product composition, proximate analysis will be conducted on by-product before and after processing. A colorimeter will be used to monitor color changes. Standard Plate Count Agar will be used for enumeration of both psychrotrophic and mesophilic bacteria in the sample at various stages in the process. Lipid oxidation will be measured. Protein carbonyls will be used as an index of protein oxidation by reacting proteins with 2,4-dinitrophenylhydrazine. Once optimized, by-product protein recovered using the new process will be compared with by-product protein recovered using the traditional surimi manufacturing process. Characteristics compared will be proximate composition, bacterial numbers, emulsifying activity index, emulsion stability, and water holding capacity. Dynamic rheological properties and gel strength will also be determined. Surimi made from skeletal muscle utilizing both methods will serve as a positive control. Differences in color will be measured with a colorimeter. Both lipid oxidation and protein oxidation will be monitored as described previously. SDS-PAGE will be used to characterize the effect of treatment on protein patterns. Storage stability of by-product and skeletal protein recovered using the new process will be compared. Samples will be blended with cryoprotectant prior to frozen storage at -15 C, -30 C, and -80 C up to 52 weeks. Functional stability will be monitored by measuring protein solubility, gel forming ability, cook yield and water holding capacity, and emulsifying properties. Both lipid oxidation and protein oxidation will be monitored as described previously. Acid whey from cottage cheese production will be collected from a commercial processor. Protein interactions will be studied by constructing pH and ionic strength solubility-type profiles of whey protein. Protein will then be recovered via an isoelectric precipitation similar to that used in the new process for meat by-product. If a significant amount of the protein can be concentrated using these types of alterations, then additional studies will be conducted to determine the effect the recovery process has on concentrated whey protein physicochemical properties. In addition, investigations will be made to determine if adjustments in acidity and/or ionic strength can significantly improve functional properties in whey protein concentrated by alternative means.

Progress 10/01/00 to 09/30/04

Outputs
This work determined that protein solubilization of red meat is achieved optimally with the following conditions, pH 2.5, 1 part meat to 9 parts 2 mM Citric Acid. Recovery is maximized at pH 5.5. It was also determined that protein gels formed from solubilized proteins have higher water binding capacity and gel strength than those from non-solubilized proteins. In addition, protein gels formed without the aid of salt from solubilized proteins have higher gel strength than non-solubilized proteins and have a gel strength equivalent to, or better than protein gels formed with the aid of salt and non-solubilized proteins. These results have not only functional significance for processed meat formulation, but nutritional ones as well. In terms of processed meat formulations, results suggest that water binding and gel strength can be improved through the application of solubilized proteins. Improved water binding and gel strength enhances not only quality, but shelf-life of processed meats. The nutritional implications are that solubilized proteins could possibly be used in place of salt and phosphates in processed meat formulations. The role of salt is two-fold, salt solubilization of proteins to improve bind (water and protein) and enhance meat flavor. Many times salt addition is dictated by its effect on protein functionality as opposed to flavor enhancement. The addition of solubilized proteins to processed meat formulations might allow salt addition to be dictated by flavor instead of functionality improvements. For consumers susceptible to hypertension, products with lower salt would be more appealing. In addition, phosphates are also added to enhance bind. However, like salt, phosphate usage also has its drawbacks. From the highest permitted level, 0.5%, to about 0.3% phosphates can produce an astringent metallic flavor. Phosphates can react with fat during the cooking process to produce a soapy flavor. High dietary phosphate intake also reduces calcium adsorption, which can lead to osteoporosis in post menopausal women and the development of brittle bones in renal patients. Replacing phosphate enhancement with same source solubilized proteins would remove an additive from the processed meat label and again enhance consumer product appeal.

Impacts
The work from this study suggests that protein solubilization is a process that recovers a highly functional and valuable protein from low valued red meat. The recovered protein is very low in fat (<1%) and has the ability to form strong gels with good water holding capacity without the addition of salt. Typically the level of salt added in processed meats is dictated by the amount needed to improve their binding ability. Usually processed meats are made from low-valued red meat with low binding ability. Almost 2% salt is needed to help the proteins bind properly. Fat also plays an important role in the binding ability of these emulsified products. Low salt and low fat formulations are typically plagued with not being able to hold water and bind as well as higher salt and fat formulations. Protein recovered using this process could therefore be utilized to improve the binding ability of low salt and fat processed meats. Salt and fat could just be added for flavor. This could have a significant impact on improving the nutritional quality of processed red meat products in order to help consumers challenged with obesity and/or high blood pressure.

Publications

  • James JM, Bellmer D, Mireles DeWitt CA. 2004. Changes in gel attributes of beef heart when treated by acid solubilization-isoelectric precipitation and the surimi process. J Food Sci 69(6):C473-479.
  • Mireles DeWitt CA, Gomez G, James JM. 2002. Protein extraction from beef heart utilizing acid solubilization. J Food Sci 67(9):3335-3341.


Progress 10/01/02 to 09/30/03

Outputs
The objective of this research was to determine the applicability of protein solubilization on red meat and characterize the functionality of the product recovered from this process. The applicability of the protein solubilization process was initially tested on a red meat by-product, beef heart. Results from that study have been published and demonstrate that acid protein solubilization recovers almost 60% of the total protein from beef heart (Mireles DeWitt et al., 2002). SDS-PAGE analysis demonstrated that the recovered protein was primarily myofibrillar protein and chemical analysis demonstrated it was low in collagen. The albumins (sarcoplasmic proteins) were the major fraction characterized in the wastewater. Since the myofibrillar fraction typically represents about 60-70% of meat protein, our results suggests that a significant amount of the myofibrillar protein fraction was recovered. This has important implications with regard to improving protein functionality as the myofibrillar proteins are typically responsible for the gel binding ability of red meat. Proteins such as collagen and the sarcoplasmic proteins are typically credited with interfering with gel formation. Further work focused on characterizing the gels formed from protein solubilized beef heart (James and Mireles DeWitt). In addition, a study characterizing gels from pork, heart and ground (not de-boned) picnic shoulder, was also performed (James and Mireles DeWitt, 2003). Results from both studies have demonstrated that gel attributes of red meat proteins are markedly improved when processed by protein solubilization. For example, in the first study characterizing gels from beef heart, water holding capacity was improved almost 2-fold as a result of acid solubilization. Addition of salt only improved water holding capacity of the acid solubilized protein slightly. The improved water holding capacity directly translated to improvements in cook yield. When salt was not added, the cook yield improved from 68% in untreated beef heart to 99% in acid solubilized beef heart. In addition, results from ground (not deboned) pork picnic shoulder demonstrated that the recovered protein from a red meat product high in ash and connective tissue had improved cook yield and water holding capacity. Overall, data from these studies demonstrated that red meat treated by protein solubilization had significantly improved protein functionality. Protein functionality is important to the quality and economic value of processed muscle food products. Cooked products formulated with an excessive amount of low binding (or low water holding capacity) meat often experience excessive purge through loss of water, gelatin and/or fat. Purge loss is often viewed as a quality defect by the consumer and results in significant economic losses for the commercial processor. The most significant finding from these studies has been that salt is not necessary to produce strong gels from protein recovered by protein solubilization.

Impacts
The work from this study suggests that protein solubilization is a process that recovers a highly functional and valuable protein from low valued red meat. The recovered protein is very low in fat (<1%) and has the ability to form strong gels with good water holding capacity without the addition of salt. Typically the level of salt added in processed meats is dictated by the amount needed to improve their binding ability. Usually processed meats are made from low-valued red meat with low binding ability. Almost 2% salt is needed to help the proteins bind properly. Fat also plays an important role in the binding ability of these emulsified products. Low salt and low fat formulations are typically plagued with not being able to hold water and bind as well as higher salt and fat formulations. Protein recovered using this process could therefore be utilized to improve the binding ability of low salt and fat processed meats. Salt and fat could just be added for flavor. This could have a significant impact on improving the nutritional quality of processed red meat products in order to help consumers challenged with obesity and/or high blood pressure.

Publications

  • James JM, Mireles DeWitt CA. 2003. Application of Acid Solubilization Isoelectric Precipitation to Low Value Red Meat. Oklahoma State University Animal Science Research Report. Available on web: http://www.ansi.okstate.edu/research/researchreport/index.html
  • James JM, Mireles DeWitt CA. Composition, Color, and Gel Attributes of Beef Heart When Treated by Acid Solubilization Isoelectric Precipitation and the Surimi Process. J Food Sci, submitted November 2003.


Progress 10/01/01 to 09/30/02

Outputs
Results to date demonstrated the applicability of the acid solubilization-isoelectric precipitation process on a red meat by-product, beef heart. These results have also demonstrated that nutritional composition of by-product with respect to fat content, cholesterol content and ash content is significantly improved upon treatment with acid solubilization. On going work has focused on characterizing the gels formed from beef heart, pork heart, and whole ground (not de-boned) pork picnic shoulder treated by this processes. Results have demonstrated that gel attributes are markedly improved as a result of acid solubilization treatment. In addition, salt solubilization does not appear to be critical to gel formation in treated by-product as it is in untreated by-product. Untreated beef heart without salt, had an average water holding capacity of about 1.2 g bound water/g protein. When salt was added to untreated beef heart, average water holding capacity increased to about 1.4 g bound water/g protein. However, when the same beef heart was treated by acid solubilization the average water holding capacity increased by a factor of almost 1.8 without the addition of salt (2.2 g bound water/g protein) and a factor 2 with the addition of salt (2.4 g bound water/g protein). Cook yield improved from 68% in untreated beef heart to 99% in acid solubilized beef heart without the addition of salt. In every attribute measured by texture profile analysis, the attribute was in some measure increased as a result of treatment with acid solubilization. In addition, results from whole ground (i.e. not deboned) pork picnic shoulder treated by acid solubilization demonstrated that the recovered protein from a pork product initially high in ash/bone and connective tissue had improved cook yield, water holding capacity, and significant increases in many other of the gel attributes measured by texture profile analysis. Data demonstrates that application of an acid solubilization process not only significantly alters gel attributes, but improves many of these attributes with respect to their potential ingredient functionality.

Impacts
Improvments in nutritional composition and protein functionality of meat by-product will enhance its value to food and pet food processors. Our research is quantifying how acid solubilization can be utilized to improve composition and protein functionality in red meat by-product.

Publications

  • Mireles DeWitt, C.A., Gomez, G., and James, J.M. 2002. Protein Extraction from Beef Heart using Acid Solubilization. J Food Sci. 67(9): 3335-3341.


Progress 10/01/00 to 09/30/01

Outputs
The focus of this project was initially to apply a protein solubilization process to meat and dairy by-products for the recovery of value-added functional protein concentrates. Attempts to apply this process to meat by-products have so far been very promising. Attempts to apply this process to dairy by-products, such as acid whey, have not been successful. As a result, the project has focused more on the recovery of protein concentrates from meat by-products. To date, we have successfully applied protein solubilization to meat by-product using beef heart as a model. Process parameters have been maximized for pH solubilization and subsequent isoelectric precipitation. The effect of salt addition on protein solubilization was evaluated. Results indicated that additon of NaCl at levels as low as 50 mM adversely affected protein solubilization. Maximum protein recovery was achieved without the addition of salt and calculated recovery yields have ranged between 75-85% of the functional protein fraction. These yields are similar to results reported for seafood filets using a similar process. Compositional studies have also demonstrated that in addition to producing a functional protein concentrate, the resulting product has significantly reduced lipid, cholesterol, collagen, and ash content when compared to the starting material. Current research is focusing on maximizing production of sufficient protein concentrate on a lab-scale in order to quantitate protein functionality through texture profile analysis. Further measures of functionality will be quantitated by water-holding capacity, cook yield, emulsion stability, and emulsion activity index. In addition, we will also evaluate the role of this process as a microbial intervention step. These measurements are needed to gain a basic understanding of the potential value this type of functional protein concentrate may contribute when incorporated into processed foods. In addition, preliminary research is also looking at how this product affects sensory properties when incorporated into a formulated product. Initial results, to date, have demonstrated that at the level of incorporation we have looked at (about 2%) no significant off-flavors or unacceptable colors are produced. Initial test have also demonstrated that the process does not significantly produce TBARS as a result of its application. However, this does not necessarily relate to long-term storage stability of either the lipid or protein fraction. As a result, future research will look at the frozen storage lipid and protein stability of the protein concentrate. In addition, in order to show practical application of the process we plan to apply the process parameters determined on beef heart to more complex meat by-product streams that typically are rendered. A mass balance of each of the value-added outputs from this process (protein concentrate, ash and collagen, neutral lipids) will also be made.

Impacts
Effective and responsible utilization of natural resources has become increasingly important as a result of increased awareness of the environmental consequences of waste. The question is no longer just are we not dumping resources, but are we maximizing the potential value and gain from our resources. The long-term goal of this project is to enhance the value of meat by-product through the successful application of a protein solubilization process. It is our belief that this process can be utilized to capture value from meat by-product by diverting part of it from the traditional rendering process. If this type of concentrate produced by protein solubilization can be demonstrated to compete with more traditional protein concentrates (whey and soy) in certain product formulations, there would be substantial potential value to the food industry.

Publications

  • No publications reported this period


Progress 10/01/99 to 09/30/00

Outputs
This project began October 1, 2000, and there is no progress to report this period.

Impacts
(N/A)

Publications

  • No publications reported this period