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Effect of the muscle nanostructure changes during post-mortem aging on tenderness of different beef breeds

OBJECTIVE: Tenderness is a very complex feature, and the process of its formation is very complicated and not fully understood. Its diversification is one of the most important problems of beef production, as a result beef aging is widely used to improve tenderness as it is believed to provide a hom...

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Autor principal: Soji, Zimkhitha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Animal Bioscience 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8563251/
https://www.ncbi.nlm.nih.gov/pubmed/33152214
http://dx.doi.org/10.5713/ajas.20.0488
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author Soji, Zimkhitha
author_facet Soji, Zimkhitha
author_sort Soji, Zimkhitha
collection PubMed
description OBJECTIVE: Tenderness is a very complex feature, and the process of its formation is very complicated and not fully understood. Its diversification is one of the most important problems of beef production, as a result beef aging is widely used to improve tenderness as it is believed to provide a homogeneous product to consumers. While few studies have evaluated the muscle structure properties in relation to tenderness from early post-mortem, there little to no information available on how the muscle nanostructure of beef carcasses changes during post-mortem ageing to determine the appropriate aging time for acceptable tenderness. METHODS: Muscle nanostructure (myofibril diameter [MYD], myofibril spacing [MYS], muscle fibre diameter [MFD], muscle fibre spacing [MFS], and sarcomere length [SL]), meat tenderness and cooking loss [CL]) were measured on 20 A2 longissimus muscles of Bonsmara, Beefmaster, Hereford, and Simbra at 45(mins), 1, 3, and 7 days post-slaughter. Muscle nanostructure was measured using a scanning electron microscope, while tenderness was measured using Warner Bratzler shear force. RESULTS: At 45 minutes post-slaughter, breed affected MYD and MYS only, while at 24(hrs) it also affected MFD and MFS. On day 3 breed effected MFS and SL, while on day 7 breed effected tenderness only. As the muscles matured, both MYD and MYS decreased while CL increased, and the muscles became tender. There was no uniformity on muscle texture features (surface structure, fibre separation, muscle contraction, and relaxation) throughout the ageing period. CONCLUSION: Meat tenderness can be directly linked to breed related myofibril structure changes during aging in particular the MYD, spacing between myofibrils and their interaction; while the MFD, spacing between muscle fibres, SL, and CL explain the non-uniformity in beef tenderness.
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spelling pubmed-85632512021-11-17 Effect of the muscle nanostructure changes during post-mortem aging on tenderness of different beef breeds Soji, Zimkhitha Anim Biosci Article OBJECTIVE: Tenderness is a very complex feature, and the process of its formation is very complicated and not fully understood. Its diversification is one of the most important problems of beef production, as a result beef aging is widely used to improve tenderness as it is believed to provide a homogeneous product to consumers. While few studies have evaluated the muscle structure properties in relation to tenderness from early post-mortem, there little to no information available on how the muscle nanostructure of beef carcasses changes during post-mortem ageing to determine the appropriate aging time for acceptable tenderness. METHODS: Muscle nanostructure (myofibril diameter [MYD], myofibril spacing [MYS], muscle fibre diameter [MFD], muscle fibre spacing [MFS], and sarcomere length [SL]), meat tenderness and cooking loss [CL]) were measured on 20 A2 longissimus muscles of Bonsmara, Beefmaster, Hereford, and Simbra at 45(mins), 1, 3, and 7 days post-slaughter. Muscle nanostructure was measured using a scanning electron microscope, while tenderness was measured using Warner Bratzler shear force. RESULTS: At 45 minutes post-slaughter, breed affected MYD and MYS only, while at 24(hrs) it also affected MFD and MFS. On day 3 breed effected MFS and SL, while on day 7 breed effected tenderness only. As the muscles matured, both MYD and MYS decreased while CL increased, and the muscles became tender. There was no uniformity on muscle texture features (surface structure, fibre separation, muscle contraction, and relaxation) throughout the ageing period. CONCLUSION: Meat tenderness can be directly linked to breed related myofibril structure changes during aging in particular the MYD, spacing between myofibrils and their interaction; while the MFD, spacing between muscle fibres, SL, and CL explain the non-uniformity in beef tenderness. Animal Bioscience 2021-11 2020-10-14 /pmc/articles/PMC8563251/ /pubmed/33152214 http://dx.doi.org/10.5713/ajas.20.0488 Text en Copyright © 2021 by Animal Bioscience https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Article
Soji, Zimkhitha
Effect of the muscle nanostructure changes during post-mortem aging on tenderness of different beef breeds
title Effect of the muscle nanostructure changes during post-mortem aging on tenderness of different beef breeds
title_full Effect of the muscle nanostructure changes during post-mortem aging on tenderness of different beef breeds
title_fullStr Effect of the muscle nanostructure changes during post-mortem aging on tenderness of different beef breeds
title_full_unstemmed Effect of the muscle nanostructure changes during post-mortem aging on tenderness of different beef breeds
title_short Effect of the muscle nanostructure changes during post-mortem aging on tenderness of different beef breeds
title_sort effect of the muscle nanostructure changes during post-mortem aging on tenderness of different beef breeds
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8563251/
https://www.ncbi.nlm.nih.gov/pubmed/33152214
http://dx.doi.org/10.5713/ajas.20.0488
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