Evaluation of stored lamb bio-preserved using a three-strain cocktail of Lactobacillus sakei
Introduction
A significant proportion of fresh meat produced in New Zealand is exported as vacuum-packaged chilled product that can spend up to 8 weeks travelling to overseas markets. During storage a range of bacterial populations can develop from small numbers of psychrotrophic organisms acquired by meat surfaces during processing. Typically, such populations tend to develop from the uncontrolled but fortuitous acquisition of benign strains of lactic acid bacteria (LAB) resulting in a wide degree of variability in the microflora of individual packs (Jones, 2004). During processing undesirable contaminants may also be acquired and these can contribute towards spoilage when organisms such as Brochothrix thermosphacta and gas-producing species of clostridia are involved (Broda et al., 1999, Gardner, 1981). The presence of such pathogens as Listeria monocytogenes, Campylobacter jejuni and toxigenic strains of Escherichia coli are also of concern for public health and market access reasons (Anonymous, 2000, Bosilevac et al., 2007, Dykes and Moorhead, 2001, Stern, 1981). Pro-active seeding of fresh meat with small numbers of inhibitory LAB “bio-preservation” offers both a way to improve the microbial consistency of product while reducing the opportunity of unwanted organisms to survive using a range of mechanisms including the production of inhibitory molecules such as bacteriocins (Jones et al., 2009, Kostrzynska and Bachand, 2006, Vermeiren et al., 2006).
Lactobacillus sakei is a meat adapted LAB species commonly isolated from stored products (Chaillou et al., 2005). In a recent study (Jones et al., 2009) the ability of three L. sakei strains (27, 44 and 63) to dominate the microflora of stored meat and inhibit the development of one or more of L. monocytogenes, C. jejuni and Clostridium estertheticum was demonstrated. To be useful for bio-preservation, such strains must also be able to develop on stored meat without detracting from the overall eating quality of the finished product (Stiles, 1996). In this report experiments performed to evaluate the microbiological profile and sensory acceptance of chill-stored vacuum-packaged lamb after treatment with a cocktail of three L. sakei strains are described.
Section snippets
Strain selection inoculation and storage
L. sakei strains 27, 44 and 63 were selected based on their abilities to inhibit L. monocytogenes, C. jejuni and B. thermosphacta during chilled meat storage. Inhibitory activities involved mechanisms such as acid production and bacteriocin-like molecules (Jones et al., 2008, Jones et al., 2009). In order to differentiate seeded strains from background LAB, streptomycin resistant (smr) sub-populations of L. sakei 63 were prepared by sequential sub-culture in a gradient concentration of
Microbial populations
Between 6 and 14 weeks storage mean anaerobic populations ranged between 6.2 and 8.3 log cfu cm−2 for packs inoculated with L. sakei (Fig. 1). Average inoculation levels for each of the three L. sakei strains were approximately 1.2 log cfu cm−2 and 3.2 log cfu cm−2 for low and high levels respectively and all three inoculated L. sakei strains were detected at each sampling period in proportions ranging between 1% and 92% of the L. sakei population. L. sakei populations developing from inoculated strains (
Conclusion
These results demonstrate that when inoculated onto lamb at levels as low as 1.2 log cfu cm2, inhibitory L. sakei strains 27, 44 and 63 are capable of developing into dominant components of stored meat bacterial flora under standard commercial chilled storage conditions without reducing the sensory acceptance of the cooked product.
Acknowledgements
The authors would like to acknowledge Michael Agnew and Nicole More for GC analysis of drip samples. We are also grateful to Kevin Taukiri and to Crusader Meats Ltd. (NZ) for assistance in sample collection and use of materials and facilities.
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