Influence of Aging Temperature and Duration on Spoilage Organism Growth, Proteolytic Activity, and Related Chemical Changes in Vacuum-Packaged Beef Longissimus

Abstract

The objective was to evaluate the influence of vacuum-packaged aging temperature, duration, and their inter-action on spoilage organism growth, proteolytic activity, and resulting beef tenderness. Paired strip loins were collected from 60 USDA Low Choice beef carcasses (n=60), then assigned a storage temperature (−2°C, 0°C, or 4°C). Loins were portioned into half loins and assigned to an aging duration (14, 28, 42, or 56 d) and vacuum packaged. Loins were aged in commercial upright refrigerators. Half-loin packages, at their respective aging duration, were aseptically opened and cut surface swabbed for microbial analysis before fabrication into 2.54 cm strip steaks (n=5). Steaks assigned to slice shear force (SSF) were cooked to 71°C. A raw steak was used for microbial, proteolytic, and volatile analyses. Two-way interactions were observed for all spoilage organisms (P < 0.001). Aging for 42 and 56 d at−2°C produced lower microbial counts compared to individual aging durations at 4°C (P < 0.05). Loins aged for 14 d at 4°C had increased desmin and troponin-T degradation compared to aging for 14 at−2°C and 0°C (P < 0.05). Loins aged at 4°C produced more tender steaks compared to−2°C and 0°C (P = 0.001). Steaks aged for 42 and 56 d possessed the lowest SSF values (P < 0.05). Aging for 56 d at 4°C produced the greatest amount of total free amino acids (P < 0.001). Two-way interactions were observed for 7 compounds (alcohols, aldehydes, carboxylic acids, ketones, and sulfur-containing compounds; P < 0.05). Aging for 56 d at 4°C had the greatest ethanol concentration (P < 0.05). These data indicate aging at 4°C increases the rate of proteolysis and subsequent tenderness development and flavor precursor accumulation. However,extended aging at 4°C resulted in increased microbial counts. Many traits peaked at 42 d of aging.