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Sirloin steaks were obtained from a local supermarket in Guelph, ON and stored at 4°C. Fat, protein, and moisture contents of the beef were determined with the MEAT TracTM (CEM Corporation, Matthews, NC, United States), Sprint, Rapid Protein Analyser (CEM Corporation), and Smart Turbo (CEM Corporation), respectively. Meat slurries were prepared by grinding sirloin steaks in a food processor (Bowl Scraping Food Processor, Hamilton Beach, Glen Allen, VA, United States). For each 100 g of ground meat, 30 g of liquid (SM buffer for control samples, or phage preparation, or bacterial subculture for inoculating samples), and NaCl (2% w/w, final concentration) were added and mixed thoroughly using a food processor and stored frozen in freezer bags until use. All experiments detailed in the manuscript were conducted in triplicate from a single batch of frozen meat slurry thawed before each experiment. For each sample, 10 g of meat slurry was transferred to a 18 × 30 cm commercial meat barrier bags (oxygen transmission rate 40–50 cc m2 24 h−1; Winpak Ltd., Winnipeg, MB, Canada) and rolled using a 2 mm ridged roller pin resulting in sheets of meat slurry with an uniform thickness of 2 mm. The pH of the slurry (uncooked) was determined using a flat surface pH probe (sympHonyTM Handheld Meters, B106, VWR International, Radnor, PA, United States).

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