Citation
Mohamed, Khadra Yousuf
(2018)
Antimicrobial properties of different types of honey and effects of tualang honey as a marinating agent and vacuum packaging on chicken.
Masters thesis, Universiti Putra Malaysia.
Abstract
The antimicrobial activity of honey is mainly credited to its acidity, osmolarity and
enzymatic generation of hydrogen peroxide via glucose oxidase. Additional honey
components, such as aromatic acids or phenolic compounds, might also contribute to
the overall antimicrobial activity. The level of antimicrobial activities found in honey
varies with different types of honey, and these differences are mainly due to the
composition, percentage as well as the nature of the sugars present in the honey.
Chicken meat is widely consumed, and it is the most common and popular poultry
species in the world. The diverse nutritional composition of chicken meat makes it an
ideal environment for the growth and propagation of meat spoilage microorganisms
and common foodborne pathogens. It is therefore essential that adequate preservation
is applied to maintain its safety and quality. Due to the widespread of antibiotic
resistance there is a need to replace modern chemical medicines and preservatives with
safer natural remedies to increase the shelf life of chicken. The antimicrobial
properties of local (Malaysia) honey are still very limited. Chicken is a perishable
commodity, application of honey as a natural preservative could increase the shelf life.
The aims of this study were therefore (i) to evaluate the antimicrobial activity of four
types of honey namely Tualang Honey (TH1), Tualang Honey (TH2), Acacia Honey
(AH) and Yemeni Sumur Honey (YSH), and (ii) to evaluate the effect of honey
marinated chicken in different packaging on the microbiological and physicochemical
characteristics. Nine bacterial strains were used. Disc Diffusion Assay, Well Diffusion
Assay, Minimum Inhibitory Concentration (MIC), Minimum Bactericidal
Concentration (MBC) and time-kill methods were performed to reveal the
antimicrobial potentials of the honey samples. The diameter of inhibition zone (DIZ)
was between 11.17 mm to 35.50 mm for 12.5, 25 and 50% (w/v), respectively. The
MIC ranged between 12.5 to 50% for both TH1 and YSH while for TH2, and AH it
ranged between 25 to 50%. For MBC, it ranged from 25 to 50%. The time-kill with TH1 of Staphylococcus aureus (food isolate) was 6 h in 2 × MIC and for S. aureus
ATCC 29737 was 3.84 log CFU/g at 6 h. For TH2 and AH, the time-kill was decreased
from 7 to 5 log CFU/g. While for YSH S. aureus (food isolate) at 2 × MIC was
decreased from 6.42 to 3.68 log CFU/g in 6 h, for S. aureus ATCC 29737 at 1× MIC
it was decreased from 6.66 to 5.16 log CFU/g and for the 2 × MIC it reached 4.26 log
CFU/g at 6 h, for Salmonella Typhimurium ATCC 13311 at 2 × MIC was decreased
from 6.56 to 3.83 lo CFU/g at 6 h. Physicochemical quality of honey resulted as
follows: the pH of the honey samples were acidic ranging from 3.69 to 3.94, and the
aw of the honey samples were between 0.53 to 0.69. For colur analysis, maximum
lightness and yellowness were seen in YSH, and maximum redness was seen in TH1,
while AH had minimum lightness, redness, and yellowness. For the marinated chicken
at different temperatures (25, 10 and 5°C) overall 5°C with vacuum packaging showed
increased shelf life and less microbial count for S. aureus, Salmonella Typhimurium
and Escherichia coli. While Listeria monocytogenes was not detected in any of the
marinated chicken. Therefore, honey marinated chicken with vacuum packaging
(HCVP) treatment might be used as an alternative preservative method for storage of
chicken and could be recommended to be used for other poultry. The remarkable
inhibitory activity of honey might attribute them as potential antimicrobial agent and
natural preservative.
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