Brightwell Gale, Clemens Robyn, Adam Katharine, Urlich Shelley, Boerema Jackie
Food Metabolism and Microbiology, AgResearch, Ruakura MIRINZ Centre, Private Bag 3123, Hamilton, Waikato, New Zealand.
Food Microbiol. 2009 May;26(3):283-8. doi: 10.1016/j.fm.2008.12.010. Epub 2009 Jan 7.
The diversity of microflora associated with peroxyacetic acid (POAA) treated and untreated beef was investigated by 16S rDNA gene cloning, DGGE analysis and conventional bacterial cultivation. Following vacuum packaging, POAA treated and untreated meat samples were stored for up to 18 weeks at -1.5 degrees C. Each culture independent method showed Carnobacterium spp. to predominate on both POAA treated and untreated meat. However, 16S rDNA gene analysis also detected the presence of psychrotolerant Clostridium spp. in the POAA-treated beef. Culture-dependent analysis did not distinguish Carnobacterium spp. from Lactobacilli. Although culture-dependent analysis showed an increase in the ratio of Enterobacteriaceae to lactic acid bacteria from weeks 6-18 in the POAA treated compared with the untreated meat, the numbers of Enterobacteriaceae were significantly less on POAA treated than on untreated meat. The combination of data collected by culture-dependent and independent techniques provided the most robust approach for elucidating the efficacy of chemical sanitization of chilled vacuum-packaged beef. If conventional cultivation is used for monitoring bacterial spoilage of vacuum-packaged chilled meats it is recommended that culture methods specific for Carnobacterium and Clostridium spp. should be included in order to provide a more complete indication of microbial diversity.
通过16S rDNA基因克隆、变性梯度凝胶电泳(DGGE)分析和传统细菌培养方法,研究了与过氧乙酸(POAA)处理和未处理牛肉相关的微生物群落多样性。真空包装后,将POAA处理和未处理的肉样在-1.5℃下储存长达18周。每种独立培养方法均显示,肉杆菌属在POAA处理和未处理的肉中均占主导地位。然而,16S rDNA基因分析还检测到在POAA处理的牛肉中存在耐冷梭菌属。基于培养的分析无法区分肉杆菌属和乳杆菌属。尽管基于培养的分析表明,与未处理的肉相比,POAA处理的肉在第6至18周期间肠杆菌科与乳酸菌的比例有所增加,但POAA处理的肉中肠杆菌科的数量明显少于未处理的肉。依赖培养和非依赖培养技术收集的数据相结合,为阐明冷藏真空包装牛肉化学消毒效果提供了最可靠的方法。如果使用传统培养方法监测真空包装冷藏肉的细菌腐败情况,建议采用针对肉杆菌属和梭菌属的培养方法,以便更全面地反映微生物多样性。