The impact of the combined lactoperoxidase and pasteurisation treatment on the safety of goat milk and cottage cheese
Abstract (Summary)
The impact of the combined lactoperoxidase and pasteurisation
treatment on the safety of goat milk and cottage cheese.
By
Onneile Jacqueline Mariba
Supervisor: Prof E. M. Buys
Department: Food Science
Degree: Masters in Institutional Agriculture (Food production and processing)
This study investigated the effect of the Lactoperoxidase system (LPS) alone and in
combination with pasteurisation, on the growth of Listeria monocytogenes (LM) ATTC
7644 in goat milk and goat milk cottage cheese during a shelf life of 10 days at 4 °C.
Goat milk was inoculated with LM ATTC 7644 and divided into two samples, one the
control and Lactoperoxidase (LP) was activated in the other sample. Both the control
and LP activated samples were kept at ambient temperature for 6h. After 6h the control
and LP activated samples were again divided into two and one of the respective
samples was pasteurised at 72 °C for 15 s. All the four samples were analysed for LM
ATTC 7644 immediately after LP activation at 0h, after 6h of LP activation and after
pasteurisation. Goat milk cottage cheese was made with all four samples, i.e. control
raw, control pasteurised, LP activated raw and LP activated pasteurised goat milk and
analysed for LM ATTC 7644 on days 1, 2, 5, and 10.
Six hours after LP activation the mean LM ATTC 7644 count for the LP activated milk
decreased by log 0.5 cfu/ml where as the LM ATTC 7644 for the control increased by
log 0.5 cfu/ml. The reduction of LM ATTC 7644 count in LP activated milk when
compared to the control shows that goat milk lactoperoxidase is capable of reducing L.
monocytogenes when stored at ambient temperatures.
Furthermore, LM ATTC 7644 count in LP activated pasteurised goat milk decreased by
log 1.1 cfu/ml more, compared to the control pasteurised goat milk. Therefore,
pasteurisation together with LP activation may be more effective than pasteurisation
alone in controlling the growth of L. monocytogenes in goat milk.
For the control raw goat milk cottage cheese on day 10, the LM ATTC 7644 count was
90 % less than on first day of storage. The LP activated raw goat milk cottage cheese
count followed a similar trend to the control raw goat milk cottage cheese, and reached
levels of log 2.9 cfu/g on the last day of storage. The control pasteurised goat milk
cottage cheese LM ATTC 7644 count on day 10 was 92 % lower compared to day 1
where as the LP activated pasteurised goat milk cottage cheese LM ATTC 7644 count
was 98 % less than on day 1.
The results of this study indicate that the activation of the LPS significantly (p 0.05)
decreased the LM ATTC 7644 count in goat milk, during a period of 6h. Combined
pasteurisation and LP activation had a synergistic effect on the LM ATTC 7644 count
in goat milk. The LM ATTC 7644 count declined in cottage cheese made from both
control and LP activated goat milk. A greater decrease was observed in LP activated
pasteurised goat milk cottage cheese over the storage period of 10 days at 4 °C. This
combination may be used to reduce the multiplication of LM ATTC 7644 for
production of safer products like goat milk and goat milk cottage cheese.
Bibliographical Information:
Advisor:
School:University of Pretoria/Universiteit van Pretoria
School Location:South Africa
Source Type:Master's Thesis
Keywords:goat milk cottage cheese listeria monocytogenes
ISBN:
Date of Publication: