Karbowiak Marcelina, Okoń Anna, Łaszkiewicz Beata, Szymański Piotr, Zielińska Dorota
Institute of Human Nutrition Sciences, Warsaw University of Life Sciences (SGGW), Nowoursynowska 159c, 02-776 Warsaw, Poland.
Department of Meat and Fat Technology, Institute of Agricultural and Food Biotechnology-State Research Institute (IBPRS-PIB), Rakowiecka 36, 02-532 Warsaw, Poland.
Foods. 2025 May 29;14(11):1934. doi: 10.3390/foods14111934.
This study explored a novel application of bacterial preparations, derived from lactic acid bacteria (LAB) and acetic acid (AAB), to preserve ready-to-cook minced pork. Two LAB and AAB cell-free supernatant mixtures were evaluated as raw meat additives during nine refrigerated storage days. Both treatments effectively stabilized the meat's pH (final values around 5.54) and oxidation reduction potential (final ORP values around 336-349 mV), while preserving color parameters (*, *, *) without significant degradation. Lipid oxidation, measured by TBARS, was significantly reduced in treated samples (0.34-0.37 mg MDA/kg) compared to the control (0.43 mg MDA/kg) by day 9. Microbial counts were markedly lower: total viable counts in treated samples did not exceed 3.2 log CFU/g, whereas the count in the control reached 4.6 log CFU/g. Exploratory factor analysis (EFA) revealed that microbial growth was the dominant factor affecting quality deterioration, while lipid oxidation and color stability formed distinct quality axes. Functional principal component analysis (FPCA) showed that among treatments, the combination of O24 and KNS32 (T2) demonstrated the most effective biopreservation, achieving the best microbiological and oxidative stability. This study introduces the novel, synergistic use of LAB and AAB preparations as a clean-label biopreservation strategy for addressing minced meat products.
本研究探索了源自乳酸菌(LAB)和醋酸菌(AAB)的细菌制剂在即食碎猪肉保鲜中的新应用。在9天的冷藏储存期间,评估了两种LAB和AAB无细胞上清液混合物作为生肉添加剂的效果。两种处理均有效地稳定了肉的pH值(最终值约为5.54)和氧化还原电位(最终ORP值约为336 - 349 mV),同时保持了颜色参数(,,*)且无明显降解。到第9天,通过硫代巴比妥酸反应物(TBARS)测定,处理过的样品中的脂质氧化显著降低(0.34 - 0.37 mg丙二醛/千克),而对照样品为(0.43 mg丙二醛/千克)。微生物计数明显更低:处理过的样品中的总活菌数不超过3.2 log CFU/克,而对照样品中的计数达到4.6 log CFU/克。探索性因子分析(EFA)表明,微生物生长是影响质量劣化的主要因素,而脂质氧化和颜色稳定性形成了不同的质量轴。功能主成分分析(FPCA)表明,在各处理中,O24和KNS32(T2)的组合表现出最有效的生物保鲜效果,实现了最佳的微生物和氧化稳定性。本研究介绍了LAB和AAB制剂的新型协同使用,作为一种用于解决碎肉产品问题的清洁标签生物保鲜策略。